Rhincodon typus isolate 14 chromosome 11, sRhiTyp1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Rhincodontidae; Rhincodon.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038808.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-associated and SH3 domain-containing protein A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
heat shock transcription factor 2 binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: polyA evidence [ECO:0006239]
cystathionine beta-synthase a, transcript variant X1
cystathionine beta-synthase a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
U2 small nuclear RNA auxiliary factor 1, transcript variant X4
U2 small nuclear RNA auxiliary factor 1, transcript variant X3
U2 small nuclear RNA auxiliary factor 1, transcript variant X2
U2 small nuclear RNA auxiliary factor 1, transcript variant X1
U2 small nuclear RNA auxiliary factor 1, transcript variant X5
splicing factor U2AF 35 kDa subunit isoform X4
splicing factor U2AF 35 kDa subunit isoform X1
splicing factor U2AF 35 kDa subunit isoform X3
splicing factor U2AF 35 kDa subunit isoform X2
splicing factor U2AF 35 kDa subunit isoform X5
crystallin, alpha A, transcript variant X2
crystallin, alpha A, transcript variant X1
salt-inducible kinase 1, transcript variant X2
salt-inducible kinase 1, transcript variant X1
serine/threonine-protein kinase SIK1 isoform X2
serine/threonine-protein kinase SIK1 isoform X1
NADH:ubiquinone oxidoreductase subunit V3
WD repeat domain 4, transcript variant X1
WD repeat domain 4, transcript variant X2
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit wdr4 isoform X1
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit wdr4 isoform X2
WD repeat domain 4, transcript variant X5
WD repeat domain 4, transcript variant X3
WD repeat domain 4, transcript variant X4
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit wdr4 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A
solute carrier family 37 member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
solute carrier family 37 member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ribosomal RNA processing protein 1 homolog A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pyridoxal (pyridoxine, vitamin B6) kinase a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 18 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X1
1-acylglycerol-3-phosphate O-acyltransferase 3, transcript variant X2
1-acyl-sn-glycerol-3-phosphate acyltransferase gamma
trafficking protein particle complex subunit 10
glutamine amidotransferase class 1 domain containing 3
glutamine amidotransferase-like class 1 domain-containing protein 3, mitochondrial
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
roundabout, axon guidance receptor, homolog 2 (Drosophila)
lipase member H-like, transcript variant X2
lipase member H-like, transcript variant X3
lipase member H-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
splicing regulator RBM11-like, transcript variant X1
splicing regulator RBM11-like, transcript variant X2
lysozyme C-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lysozyme C-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
heat shock protein 70 family, member 13, transcript variant X3
heat shock protein 70 family, member 13, transcript variant X2
heat shock protein 70 family, member 13, transcript variant X1
SAM domain-containing protein SAMSN-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SAM domain-containing protein SAMSN-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
SAM domain-containing protein SAMSN-1 isoform X2
SAM domain-containing protein SAMSN-1 isoform X1
nuclear receptor interacting protein 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor interacting protein 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nuclear receptor interacting protein 1a, transcript variant X3
uncharacterized protein LOC767695 homolog, transcript variant X1
uncharacterized protein LOC767695 homolog, transcript variant X2
uncharacterized protein LOC767695 homolog, transcript variant X3
ubiquitin specific peptidase 25, transcript variant X1
ubiquitin specific peptidase 25, transcript variant X3
ubiquitin specific peptidase 25, transcript variant X5
ubiquitin specific peptidase 25, transcript variant X2
ubiquitin specific peptidase 25, transcript variant X4
ubiquitin specific peptidase 25, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 25 isoform X1
ubiquitin carboxyl-terminal hydrolase 25 isoform X3
ubiquitin carboxyl-terminal hydrolase 25 isoform X5
ubiquitin carboxyl-terminal hydrolase 25 isoform X2
ubiquitin carboxyl-terminal hydrolase 25 isoform X4
ubiquitin carboxyl-terminal hydrolase 25 isoform X6
uncharacterized LOC109918524, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC109918524, transcript variant X2
uncharacterized LOC125484430, transcript variant X2
uncharacterized LOC125484430, transcript variant X1
CXADR Ig-like cell adhesion molecule, transcript variant X2
CXADR Ig-like cell adhesion molecule, transcript variant X1
coxsackievirus and adenovirus receptor homolog isoform X2
coxsackievirus and adenovirus receptor homolog isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
tripartite motif-containing protein 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125484378, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125484378, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
39S ribosomal protein L39, mitochondrial
ATP synthase peripheral stalk subunit F6, transcript variant X3
ATP synthase peripheral stalk subunit F6, transcript variant X4
ATP synthase peripheral stalk subunit F6, transcript variant X2
ATP synthase peripheral stalk subunit F6, transcript variant X5
ATP synthase peripheral stalk subunit F6, transcript variant X1
ATP synthase-coupling factor 6, mitochondrial isoform X1
ATP synthase-coupling factor 6, mitochondrial isoform X2
GA binding protein transcription factor subunit alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
GA binding protein transcription factor subunit alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
GA binding protein transcription factor subunit alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
GA binding protein transcription factor subunit alpha, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
GA-binding protein alpha chain isoform X1
GA-binding protein alpha chain isoform X2
amyloid beta (A4) precursor protein a, transcript variant X2
amyloid beta (A4) precursor protein a, transcript variant X1
amyloid beta (A4) precursor protein a isoform X2
amyloid beta (A4) precursor protein a isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
A disintegrin and metalloproteinase with thrombospondin motifs 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP-binding cassette sub-family G member 1 isoform X1
ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP-binding cassette sub-family G member 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain-containing protein 21, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 21, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 21 isoform X1
zinc finger and BTB domain-containing protein 21, transcript variant X5
zinc finger and BTB domain-containing protein 21, transcript variant X3
zinc finger and BTB domain-containing protein 21, transcript variant X4
zinc finger and BTB domain-containing protein 21, transcript variant X6
zinc finger and BTB domain-containing protein 21, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
C2 domain-containing protein 2 isoform X2
C2 domain-containing protein 2 isoform X3
C2 domain-containing protein 2 isoform X5
C2 domain-containing protein 2 isoform X4
zinc finger and BTB domain-containing protein 21, transcript variant X9
zinc finger and BTB domain-containing protein 21, transcript variant X8
C2 domain-containing protein 2 isoform X6
PR domain containing 15, transcript variant X1
PR domain containing 15, transcript variant X2
PR domain containing 15, transcript variant X3
PR domain containing 15, transcript variant X4
PR domain containing 15, transcript variant X5
PR domain containing 15, transcript variant X6
PR domain zinc finger protein 15 isoform X1
PR domain zinc finger protein 15 isoform X2
PR domain zinc finger protein 15 isoform X3
PR domain zinc finger protein 15 isoform X4
PR domain zinc finger protein 15 isoform X5
PR domain zinc finger protein 15 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
receptor-interacting serine-threonine kinase 4
receptor-interacting serine/threonine-protein kinase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
interferon-induced GTP-binding protein Mx3-like, transcript variant X3
interferon-induced GTP-binding protein Mx3-like, transcript variant X4
interferon-induced GTP-binding protein Mx3-like, transcript variant X1
interferon-induced GTP-binding protein Mx3-like, transcript variant X2
interferon-induced GTP-binding protein Mx3-like
interferon-induced GTP-binding protein Mx3
interferon-induced GTP-binding protein Mx-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: interferon-induced GTP-binding protein Mx-like
interferon-induced GTP-binding protein Mx1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 30 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
FAM3 metabolism regulating signaling molecule B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Down syndrome cell adhesion molecule-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
E3 ubiquitin-protein ligase DZIP3-like, transcript variant X2
E3 ubiquitin-protein ligase DZIP3-like, transcript variant X1
E3 ubiquitin-protein ligase DZIP3-like isoform X1
E3 ubiquitin-protein ligase DZIP3-like isoform X2
VPS26 endosomal protein sorting factor C, transcript variant X2
VPS26 endosomal protein sorting factor C, transcript variant X1
vacuolar protein sorting-associated protein 26C isoform X2
vacuolar protein sorting-associated protein 26C isoform X1
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, a, transcript variant X5
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, a, transcript variant X2
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, a, transcript variant X1
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A, a, transcript variant X4
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X1
dual specificity tyrosine-phosphorylation-regulated kinase 1A isoform X2
potassium inwardly rectifying channel subfamily J member 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 138 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 2
potassium inwardly rectifying channel subfamily J member 15
ATP-sensitive inward rectifier potassium channel 15
ETS transcription factor ERG, transcript variant X4
ETS transcription factor ERG, transcript variant X2
ETS transcription factor ERG, transcript variant X3
ETS transcription factor ERG, transcript variant X6
ETS transcription factor ERG, transcript variant X1
ETS transcription factor ERG, transcript variant X5
ETS transcription factor ERG, transcript variant X7
transcriptional regulator ERG isoform X2
transcriptional regulator ERG isoform X4
transcriptional regulator ERG isoform X1
transcriptional regulator ERG isoform X3
transcriptional regulator ERG isoform X5
v-ets avian erythroblastosis virus E26 oncogene homolog 2
proteasome (prosome, macropain) assembly chaperone 1, transcript variant X1
proteasome (prosome, macropain) assembly chaperone 1, transcript variant X2
proteasome assembly chaperone 1 isoform X1
proteasome assembly chaperone 1 isoform X2
bromodomain and WD repeat-containing protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
bromodomain and WD repeat-containing protein 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
bromodomain and WD repeat-containing protein 1-like, transcript variant X3
bromodomain and WD repeat-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
bromodomain and WD repeat-containing protein 1-like isoform X3
bromodomain and WD repeat-containing protein 1-like isoform X2
bromodomain and WD repeat-containing protein 1-like, transcript variant X1
bromodomain and WD repeat-containing protein 3-like isoform X1
non-histone chromosomal protein HMG-14-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
non-histone chromosomal protein HMG-14-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
non-histone chromosomal protein HMG-14-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
non-histone chromosomal protein HMG-14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
non-histone chromosomal protein HMG-14-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
non-histone chromosomal protein HMG-14-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
non-histone chromosomal protein HMG-14-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized protein LOC109910421 isoform X2
uncharacterized protein LOC109910421 isoform X1
non-histone chromosomal protein HMG-14-like, transcript variant X12
non-histone chromosomal protein HMG-14-like, transcript variant X8
non-histone chromosomal protein HMG-14-like, transcript variant X10
non-histone chromosomal protein HMG-14-like, transcript variant X9
non-histone chromosomal protein HMG-14-like, transcript variant X11
non-histone chromosomal protein HMG-14-like isoform X4
non-histone chromosomal protein HMG-14-like isoform X3
guided entry of tail-anchored proteins factor 1, transcript variant X1
guided entry of tail-anchored proteins factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
guided entry of tail-anchored proteins factor 1 isoform X1
guided entry of tail-anchored proteins factor 1 isoform X2
SH3 domain-binding glutamic acid-rich-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 22 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
SH3 domain-binding glutamic acid-rich-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol glycan anchor biosynthesis, class P
phosphatidylinositol N-acetylglucosaminyltransferase subunit P
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC109930483, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109930483, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC109930483, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC109930483, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC109930483 isoform X6
uncharacterized protein LOC109930483 isoform X5
uncharacterized protein LOC109930483 isoform X4
uncharacterized protein LOC109930483 isoform X2
uncharacterized LOC109930483, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC109930483 isoform X3
uncharacterized LOC109930483, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC109930483 isoform X1
uncharacterized LOC125484442, transcript variant X1
uncharacterized LOC125484442, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
MORC family CW-type zinc finger protein 3-like, transcript variant X1
MORC family CW-type zinc finger protein 3-like, transcript variant X3
MORC family CW-type zinc finger protein 3-like, transcript variant X2
MORC family CW-type zinc finger protein 3-like, transcript variant X4
MORC family CW-type zinc finger protein 3-like isoform X1
MORC family CW-type zinc finger protein 3-like isoform X3
MORC family CW-type zinc finger protein 3-like isoform X2
MORC family CW-type zinc finger protein 3-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
SET domain containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 18 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SET domain-containing protein 4 isoform X1
SET domain containing 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain containing 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain-containing protein 4 isoform X3
SET domain containing 4, transcript variant X2
SET domain-containing protein 4 isoform X2
SET domain-containing protein 4 isoform X4
intersectin 1 (SH3 domain protein), transcript variant X5
intersectin 1 (SH3 domain protein), transcript variant X3
intersectin 1 (SH3 domain protein), transcript variant X4
intersectin 1 (SH3 domain protein), transcript variant X1
intersectin 1 (SH3 domain protein), transcript variant X2
intersectin 1 (SH3 domain protein), transcript variant X6
crystallin, zeta (quinone reductase)-like 1, transcript variant X3
crystallin, zeta (quinone reductase)-like 1, transcript variant X4
crystallin, zeta (quinone reductase)-like 1, transcript variant X2
crystallin, zeta (quinone reductase)-like 1, transcript variant X1
crystallin, zeta (quinone reductase)-like 1, transcript variant X5
quinone oxidoreductase-like protein 1 isoform X1
quinone oxidoreductase-like protein 1 isoform X2
uncharacterized LOC125484415, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125484415, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium/myo-inositol cotransporter, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 long SRA reads, 74 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium/myo-inositol cotransporter, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, 74 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
sodium/myo-inositol cotransporter, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium/myo-inositol cotransporter, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
sodium/myo-inositol cotransporter, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sodium/myo-inositol cotransporter, transcript variant X7
sodium/myo-inositol cotransporter, transcript variant X8
sodium/myo-inositol cotransporter, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP synthase peripheral stalk subunit OSCP
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125484433, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125484433, transcript variant X3
uncharacterized LOC125484433, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily E member 2, transcript variant X1
potassium voltage-gated channel subfamily E member 2, transcript variant X5
potassium voltage-gated channel subfamily E member 2 isoform X1
potassium voltage-gated channel subfamily E member 2 isoform X2
potassium voltage-gated channel subfamily E member 2, transcript variant X4
potassium voltage-gated channel subfamily E member 2, transcript variant X2
potassium voltage-gated channel subfamily E member 2, transcript variant X3
chloride intracellular channel protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
RUNX family transcription factor 1, transcript variant X3
RUNX family transcription factor 1, transcript variant X2
RUNX family transcription factor 1, transcript variant X4
RUNX family transcription factor 1, transcript variant X1
runt-related transcription factor 1 isoform X2
runt-related transcription factor 1 isoform X3
runt-related transcription factor 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins
DNA replication fork stabilization factor DONSON, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DNA replication fork stabilization factor DONSON, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein downstream neighbor of Son isoform X1
protein downstream neighbor of Son isoform X2
SON DNA and RNA binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SON DNA and RNA binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
SON DNA and RNA binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphoribosylglycinamide formyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
trifunctional purine biosynthetic protein adenosine-3
DnaJ (Hsp40) homolog, subfamily C, member 28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
trifunctional purine biosynthetic protein adenosine-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
interleukin-10 receptor subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109928467, transcript variant X3
uncharacterized LOC109928467, transcript variant X1
uncharacterized LOC109928467, transcript variant X2
uncharacterized LOC109928467, transcript variant X4
uncharacterized protein LOC109928467 isoform X1
uncharacterized protein LOC109928467 isoform X2
uncharacterized protein C21orf62, transcript variant X3
uncharacterized protein C21orf62, transcript variant X1
uncharacterized protein C21orf62, transcript variant X5
uncharacterized protein C21orf62, transcript variant X2
uncharacterized protein C21orf62, transcript variant X4
uncharacterized protein C21orf62, transcript variant X6
uncharacterized protein C21orf62, transcript variant X7
uncharacterized protein C21orf62, transcript variant X8
uncharacterized LOC125484475, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125484475, transcript variant X2
oligodendrocyte transcription factor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins
oligodendrocyte transcription factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
cilia and flagella associated protein 298, transcript variant X2
cilia and flagella associated protein 298, transcript variant X1
cilia- and flagella-associated protein 298
uncharacterized LOC109915940, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC109915940, transcript variant X5
uncharacterized LOC109915940, transcript variant X3
uncharacterized LOC109915940, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC109915940, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
PAX3 and PAX7 binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PAX3 and PAX7 binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sorting nexin-9-like, transcript variant X3
sorting nexin-9-like, transcript variant X2
sorting nexin-9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sorting nexin-9-like, transcript variant X4
eva-1 homolog C (C. elegans), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
eva-1 homolog C (C. elegans), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
eva-1 homolog C (C. elegans), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
eva-1 homolog C (C. elegans), transcript variant X1
oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial
hormonally up-regulated Neu-associated kinase
hormonally up-regulated neu tumor-associated kinase homolog A
melanocortin-2 receptor accessory protein 2-like
URB1 ribosome biogenesis homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
URB1 ribosome biogenesis homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
URB1 ribosome biogenesis homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nucleolar pre-ribosomal-associated protein 1 isoform X2
nucleolar pre-ribosomal-associated protein 1 isoform X1
nucleolar pre-ribosomal-associated protein 1 isoform X3
N-6 adenine-specific DNA methyltransferase 1, transcript variant X2
N-6 adenine-specific DNA methyltransferase 1, transcript variant X5
N-6 adenine-specific DNA methyltransferase 1, transcript variant X1
N-6 adenine-specific DNA methyltransferase 1, transcript variant X4
N-6 adenine-specific DNA methyltransferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC569013 homolog, transcript variant X1
uncharacterized protein LOC569013 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxytryptamine (serotonin) receptor 1Fa, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
5-hydroxytryptamine (serotonin) receptor 1Fa, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
POU class 1 homeobox 1, transcript variant X3
POU class 1 homeobox 1, transcript variant X4
POU class 1 homeobox 1, transcript variant X6
POU class 1 homeobox 1, transcript variant X1
POU class 1 homeobox 1, transcript variant X2
pituitary-specific positive transcription factor 1 isoform X1
pituitary-specific positive transcription factor 1 isoform X2
pituitary-specific positive transcription factor 1 isoform X3
pituitary-specific positive transcription factor 1 isoform X4
pituitary-specific positive transcription factor 1 isoform X6
POU class 1 homeobox 1, transcript variant X5
POU class 1 homeobox 1, transcript variant X7
pituitary-specific positive transcription factor 1 isoform X5
pituitary-specific positive transcription factor 1 isoform X7
vestigial-like family member 3, transcript variant X1
vestigial-like family member 3, transcript variant X2
transcription cofactor vestigial-like protein 3 isoform X1
transcription cofactor vestigial-like protein 3 isoform X2
proto-oncogene tyrosine-protein kinase ROS-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
proto-oncogene tyrosine-protein kinase ROS
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin ligase TRAF3IP2-like, transcript variant X2
E3 ubiquitin ligase TRAF3IP2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized protein LOC109936155 isoform X2
E3 ubiquitin ligase TRAF3IP2-like isoform X1
chromodomain helicase DNA binding protein 1-like, transcript variant X2
chromodomain helicase DNA binding protein 1-like, transcript variant X1
chromodomain helicase DNA binding protein 1-like, transcript variant X3
chromodomain-helicase-DNA-binding protein 1-like isoform X1
chromodomain-helicase-DNA-binding protein 1-like isoform X3
chromodomain-helicase-DNA-binding protein 1-like isoform X2
adenosine deaminase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
adenosine deaminase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 long SRA reads, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
translocase of outer mitochondrial membrane 70 homolog A (S. cerevisiae)
mitochondrial import receptor subunit TOM70
TBC1 domain family, member 23, transcript variant X2
TBC1 domain family, member 23, transcript variant X1
cms1 ribosomal small subunit homolog, transcript variant X3
cms1 ribosomal small subunit homolog, transcript variant X2
cms1 ribosomal small subunit homolog, transcript variant X1
discoidin, CUB and LCCL domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
discoidin, CUB and LCCL domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
discoidin, CUB and LCCL domain-containing protein 2 isoform X2
discoidin, CUB and LCCL domain-containing protein 2 isoform X1
collagen, type VIII, alpha 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
collagen, type VIII, alpha 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
type 2 lactosamine alpha-2,3-sialyltransferase, transcript variant X5
type 2 lactosamine alpha-2,3-sialyltransferase, transcript variant X2
type 2 lactosamine alpha-2,3-sialyltransferase, transcript variant X4
type 2 lactosamine alpha-2,3-sialyltransferase, transcript variant X3
type 2 lactosamine alpha-2,3-sialyltransferase, transcript variant X1
type 2 lactosamine alpha-2,3-sialyltransferase
adhesion G-protein coupled receptor G7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
trafficking from ER to golgi regulator, transcript variant X2
trafficking from ER to golgi regulator, transcript variant X1
interphotoreceptor matrix proteoglycan 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
interphotoreceptor matrix proteoglycan 2
zinc finger and BTB domain-containing protein 11
PEST proteolytic signal-containing nuclear protein
tRNA methyltransferase 10 homolog C, transcript variant X2
tRNA methyltransferase 10 homolog C, transcript variant X1
tRNA methyltransferase 10 homolog C isoform X2
tRNA methyltransferase 10 homolog C isoform X1
uncharacterized LOC109928028, transcript variant X3
uncharacterized LOC109928028, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC109928028, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC109928028, transcript variant X1
uncharacterized protein LOC109928028 isoform X1
uncharacterized protein LOC109928028 isoform X2
NXPE family member 3-like, transcript variant X4
NXPE family member 3-like, transcript variant X10
NXPE family member 3-like, transcript variant X11
NXPE family member 3-like, transcript variant X12
NXPE family member 3-like, transcript variant X2
NXPE family member 3-like, transcript variant X7
NXPE family member 3-like, transcript variant X1
NXPE family member 3-like, transcript variant X3
NXPE family member 3-like, transcript variant X9
NXPE family member 3-like, transcript variant X14
NXPE family member 3-like, transcript variant X6
NXPE family member 3-like, transcript variant X13
NXPE family member 3-like, transcript variant X5
NXPE family member 3-like, transcript variant X8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NXPE family member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ephrin type-A receptor 5-like, transcript variant X2
ephrin type-A receptor 5-like, transcript variant X5
ephrin type-A receptor 5-like, transcript variant X4
ephrin type-A receptor 5-like, transcript variant X3
ephrin type-A receptor 5-like isoform X2
ephrin type-A receptor 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 61% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC125484453 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida-like domain containing 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida-like domain-containing protein 1a
zona pellucida-like domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
E3 ubiquitin-protein ligase DZIP3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
E3 ubiquitin-protein ligase DZIP3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin-protein ligase DZIP3-like, transcript variant X5
activated leukocyte cell adhesion molecule a
E3 ubiquitin-protein ligase CBL-B-like, transcript variant X1
E3 ubiquitin-protein ligase CBL-B-like, transcript variant X2
E3 ubiquitin-protein ligase CBL-B-like isoform X2
E3 ubiquitin-protein ligase CBL-B-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase CBL-B-B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
BBX high mobility group box domain containing, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
BBX high mobility group box domain containing, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
HMG box transcription factor BBX isoform X1
HMG box transcription factor BBX isoform X2
uncharacterized LOC109912944, transcript variant X1
uncharacterized LOC109912944, transcript variant X2
uncharacterized protein LOC109912944 isoform X1
uncharacterized protein LOC109912944 isoform X2
immunoglobulin lambda-1 light chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein CIP2A homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein CIP2A homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC100000923 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
T-cell receptor-associated transmembrane adapter 1, transcript variant X1
T-cell receptor-associated transmembrane adapter 1, transcript variant X2
T-cell receptor-associated transmembrane adapter 1 isoform X1
T-cell receptor-associated transmembrane adapter 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
suppressor of tumorigenicity 14 protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125484455, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125484455, transcript variant X1
protein CREG1-like, transcript variant X5
protein CREG1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
protein CREG1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
protein CREG1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein CREG1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
immunoglobulin-like domain-containing receptor 1
immunoglobulin-like domain containing receptor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
immunoglobulin-like domain containing receptor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin-like domain-containing receptor 2
protein maelstrom homolog, transcript variant X3
protein maelstrom homolog, transcript variant X2
protein maelstrom homolog, transcript variant X1
protein maelstrom homolog, transcript variant X4
cell surface A33 antigen, transcript variant X1
cell surface A33 antigen, transcript variant X2
dual specificity phosphatase 27, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dual specificity phosphatase 27, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dual specificity phosphatase 27, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dual specificity phosphatase 27, transcript variant X1
serine/threonine/tyrosine-interacting-like protein 2 isoform X1
serine/threonine/tyrosine-interacting-like protein 2 isoform X2
POU domain, class 2, transcription factor 1
T-cell surface glycoprotein CD3 zeta chain isoform X2
T-cell surface glycoprotein CD3 zeta chain isoform X1
T-cell surface glycoprotein CD3 zeta chain isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 58
glycogen synthase kinase 3 beta, genome duplicate a
cilia and flagella associated protein 91
cilia- and flagella-associated protein 91
TATA-box binding protein associated factor 13
transcription initiation factor TFIID subunit 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
syntaxin binding protein 5L, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
syntaxin binding protein 5L, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
syntaxin-binding protein 5-like isoform X2
syntaxin-binding protein 5-like isoform X1
general transcription factor IIE, polypeptide 1, alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
general transcription factor IIE, polypeptide 1, alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
general transcription factor IIE subunit 1
RAB, member of RAS oncogene family-like 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
homogentisate 1,2-dioxygenase, transcript variant X1
homogentisate 1,2-dioxygenase, transcript variant X2
homogentisate 1,2-dioxygenase, transcript variant X3
homogentisate 1,2-dioxygenase isoform X1
homogentisate 1,2-dioxygenase isoform X2
homogentisate 1,2-dioxygenase isoform X3
homogentisate 1,2-dioxygenase, transcript variant X4
homogentisate 1,2-dioxygenase isoform X4
NADH:ubiquinone oxidoreductase subunit B4
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4
fatty acid amide hydrolase-like, transcript variant X3
fatty acid amide hydrolase-like, transcript variant X1
fatty acid amide hydrolase-like, transcript variant X2
fatty acid amide hydrolase-like isoform X1
fatty acid amide hydrolase-like isoform X2
fatty acid amide hydrolase-like isoform X3
extracellular calcium-sensing receptor-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: extracellular calcium-sensing receptor-like
family with sequence similarity 162 member A
importin subunit alpha-5, transcript variant X2
importin subunit alpha-5, transcript variant X1
transmembrane protein 39A, transcript variant X5
transmembrane protein 39A, transcript variant X4
transmembrane protein 39A, transcript variant X9
transmembrane protein 39A, transcript variant X6
transmembrane protein 39A, transcript variant X3
transmembrane protein 39A, transcript variant X7
transmembrane protein 39A, transcript variant X1
transmembrane protein 39A, transcript variant X2
transmembrane protein 39A, transcript variant X8
transmembrane protein 39A, transcript variant X10
hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1
LOW QUALITY PROTEIN: sperm-associated antigen 17
tryptophanyl tRNA synthetase 2, mitochondrial
2-Hydroxyacid oxidase 2-like, transcript variant X1
2-Hydroxyacid oxidase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC109936871, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC109936871, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized protein LOC109936871 isoform X1
uncharacterized protein LOC109936871 isoform X2
kelch-like protein 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kelch-like protein 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kelch-like protein 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 40 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
WD repeat domain 3, transcript variant X3
WD repeat domain 3, transcript variant X1
WD repeat domain 3, transcript variant X2
WD repeat-containing protein 3 isoform X2
WD repeat-containing protein 3 isoform X1
ganglioside induced differentiation associated protein 2, transcript variant X1
ganglioside induced differentiation associated protein 2, transcript variant X2
ganglioside induced differentiation associated protein 2, transcript variant X3
ganglioside induced differentiation associated protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ganglioside-induced differentiation-associated protein 2 isoform X1
ganglioside induced differentiation associated protein 2, transcript variant X5
ganglioside-induced differentiation-associated protein 2 isoform X2
terminal nucleotidyltransferase 5C, transcript variant X3
terminal nucleotidyltransferase 5C, transcript variant X1
terminal nucleotidyltransferase 5C isoform X1
terminal nucleotidyltransferase 5C, transcript variant X5
terminal nucleotidyltransferase 5C, transcript variant X2
terminal nucleotidyltransferase 5C, transcript variant X4
terminal nucleotidyltransferase 5C isoform X2
mannosidase, alpha, class 1A, member 2, transcript variant X2
mannosidase, alpha, class 1A, member 2, transcript variant X1
mannosyl-oligosaccharide 1,2-alpha-mannosidase IB isoform X2
mannosyl-oligosaccharide 1,2-alpha-mannosidase IB isoform X1
uncharacterized LOC125484447, transcript variant X2
uncharacterized LOC125484447, transcript variant X1
transcription termination factor, RNA polymerase II
immunoglobulin superfamily member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins
prostaglandin F2 receptor negative regulator-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109936276, transcript variant X2
uncharacterized protein LOC109936276 isoform X2
uncharacterized LOC109936276, transcript variant X3
uncharacterized LOC109936276, transcript variant X1
uncharacterized protein LOC109936276 isoform X1
uncharacterized protein LOC109936276 isoform X3
uncharacterized LOC125484425, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125484425, transcript variant X1
uncharacterized LOC125484425, transcript variant X3
sodium/potassium-transporting ATPase subunit alpha
solute carrier family 22 member 15, transcript variant X2
solute carrier family 22 member 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 22 member 15 isoform X2
solute carrier family 22 member 15 isoform X1
nescient helix loop helix 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nescient helix loop helix 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
coiled-coil domain containing 181, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
coiled-coil domain containing 181, transcript variant X2
coiled-coil domain-containing protein 181
basic leucine zipper nuclear factor 1, transcript variant X1
basic leucine zipper nuclear factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium-transporting ATPase subunit beta-1
DDB1- and CUL4-associated factor 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
DDB1- and CUL4-associated factor 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DDB1- and CUL4-associated factor 6-like isoform X2
DDB1- and CUL4-associated factor 6-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
DDB1- and CUL4-associated factor 6-like, transcript variant X3
DDB1- and CUL4-associated factor 6-like isoform X3
G protein-coupled receptor 161a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 20 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G protein-coupled receptor 161a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 20 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
G protein-coupled receptor 161a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 20 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
G-protein coupled receptor 161 isoform X1
G-protein coupled receptor 161 isoform X2
thiamine transporter 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
thiamine transporter 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
thiamine transporter 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
thiamine transporter 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coagulation factor V, transcript variant X1
coagulation factor V, transcript variant X2
coagulation factor V, transcript variant X3
solute carrier family 35 member A5, transcript variant X1
solute carrier family 35 member A5, transcript variant X2
probable UDP-sugar transporter protein SLC35A5 isoform X1
solute carrier family 35 member A5, transcript variant X3
probable UDP-sugar transporter protein SLC35A5 isoform X2
coiled-coil domain containing 80, transcript variant X1
coiled-coil domain-containing protein 80 isoform X1
coiled-coil domain containing 80, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
coiled-coil domain-containing protein 80 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
lysine (K)-specific demethylase 6A, transcript variant X3
lysine (K)-specific demethylase 6A, transcript variant X1
lysine (K)-specific demethylase 6A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
lysine-specific demethylase 6A isoform X2
lysine-specific demethylase 6A isoform X1
lysine (K)-specific demethylase 6A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
lysine-specific demethylase 6A isoform X3
FUN14 domain containing 1, transcript variant X1
FUN14 domain containing 1, transcript variant X4
FUN14 domain-containing protein 1 isoform X1
FUN14 domain-containing protein 1 isoform X4
FUN14 domain containing 1, transcript variant X2
FUN14 domain containing 1, transcript variant X5
FUN14 domain-containing protein 1 isoform X2
FUN14 domain-containing protein 1 isoform X5
FUN14 domain containing 1, transcript variant X3
FUN14 domain-containing protein 1 isoform X3
EF-hand domain (C-terminal) containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
EF-hand domain-containing family member C2
peripheral plasma membrane protein CASK-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin specific peptidase 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ubiquitin specific peptidase 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X1
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X2
uncharacterized LOC125484431, transcript variant X1
uncharacterized LOC125484431, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125484431, transcript variant X3
uncharacterized LOC125484431, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125484431, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 14
uncharacterized protein CXorf38, transcript variant X2
uncharacterized protein CXorf38, transcript variant X1
uncharacterized protein CXorf38, transcript variant X3
uncharacterized protein CXorf38 isoform X1
uncharacterized protein CXorf38 isoform X2
ATPase H+ transporting accessory protein 2
uncharacterized LOC125484365, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 90% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125484365, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125484365, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125484365, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: BCL-6 corepressor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ornithine transcarbamylase, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
LOW QUALITY PROTEIN: X-linked retinitis pigmentosa GTPase regulator
sushi-repeat-containing protein SRPX-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
synaptotagmin-like 5, transcript variant X3
synaptotagmin-like 5, transcript variant X1
synaptotagmin-like 5, transcript variant X2
X-linked Kx blood group (McLeod syndrome)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid type A receptor subunit rho3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid type A receptor subunit rho3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid type A receptor subunit rho3, transcript variant X2
gamma-aminobutyric acid receptor subunit rho-3 isoform X1
gamma-aminobutyric acid receptor subunit rho-3 isoform X2
TIP41, TOR signaling pathway regulator-like (S. cerevisiae), transcript variant X4
TIP41, TOR signaling pathway regulator-like (S. cerevisiae), transcript variant X2
TIP41, TOR signaling pathway regulator-like (S. cerevisiae), transcript variant X1
TIP41, TOR signaling pathway regulator-like (S. cerevisiae), transcript variant X3
ribosomal oxygenase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ribosomal oxygenase 2, transcript variant X2
ribosomal oxygenase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ADP-ribosylation factor-like 6, transcript variant X2
ADP-ribosylation factor-like 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
NOP2/Sun RNA methyltransferase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NOP2/Sun RNA methyltransferase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tRNA (cytosine(34)-C(5))-methyltransferase, mitochondrial isoform X2
tRNA (cytosine(34)-C(5))-methyltransferase, mitochondrial isoform X1
ADP-ribosylation factor-like 13b, transcript variant X4
ADP-ribosylation factor-like 13b, transcript variant X3
ADP-ribosylation factor-like 13b, transcript variant X2
ADP-ribosylation factor-like 13b, transcript variant X1
ADP-ribosylation factor-like protein 13B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein si:ch211-214p13.7
cell surface glycoprotein CD200 receptor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
T-cell immunoreceptor with Ig and ITIM domains-like
zinc finger and BTB domain-containing protein 20-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 20-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and BTB domain-containing protein 20-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain-containing protein 20-like, transcript variant X1
zinc finger and BTB domain-containing protein 20-like, transcript variant X4
zinc finger and BTB domain-containing protein 20-like isoform X1
zinc finger and BTB domain-containing protein 20-like isoform X2
growth associated protein 43, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
growth associated protein 43, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
limbic system associated membrane protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
limbic system-associated membrane protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
eukaryotic translation initiation factor 2, subunit 3 gamma
eukaryotic translation initiation factor 2 subunit 3
uncharacterized LOC125484460, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125484460, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger X-chromosomal protein-like, transcript variant X4
zinc finger X-chromosomal protein-like, transcript variant X2
zinc finger X-chromosomal protein-like, transcript variant X1
zinc finger X-chromosomal protein-like, transcript variant X3
zinc finger X-chromosomal protein-like isoform X1
zinc finger X-chromosomal protein-like isoform X2
organic solute transporter subunit alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
organic solute transporter subunit alpha-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
organic solute transporter subunit alpha-like, transcript variant X3
organic solute transporter subunit alpha-like isoform X1
organic solute transporter subunit alpha-like isoform X2
pyruvate dehydrogenase kinase, isozyme 3a, transcript variant X2
pyruvate dehydrogenase kinase, isozyme 3a, transcript variant X1
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 3, mitochondrial isoform X1
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 3, mitochondrial isoform X2
choline-phosphate cytidylyltransferase B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interleukin 1 receptor accessory protein-like 1b
interleukin-1 receptor accessory protein-like 1-B
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nuclear receptor subfamily 0, group B, member 1
nuclear receptor subfamily 0 group B member 1
TLR adapter interacting with SLC15A4 on the lysosome, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TLR adapter interacting with SLC15A4 on the lysosome, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TLR adapter interacting with SLC15A4 on the lysosome
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X3
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X4
TGF-beta-activated kinase 1 and MAP3K7-binding protein 3 isoform X4
TGF-beta-activated kinase 1 and MAP3K7-binding protein 3 isoform X2
TGF-beta-activated kinase 1 and MAP3K7-binding protein 3 isoform X3
TGF-beta-activated kinase 1 and MAP3K7-binding protein 3 isoform X1
TGF-beta-activated kinase 1 and MAP3K7-binding protein 3 isoform X5
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TGF-beta activated kinase 1 (MAP3K7) binding protein 3, transcript variant X10
TGF-beta-activated kinase 1 and MAP3K7-binding protein 3 isoform X6
cilia and flagella-associated protein 47-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
transmembrane gamma-carboxyglutamic acid protein 1-like, transcript variant X4
transmembrane gamma-carboxyglutamic acid protein 1-like, transcript variant X1
transmembrane gamma-carboxyglutamic acid protein 1-like, transcript variant X2
transmembrane gamma-carboxyglutamic acid protein 1-like, transcript variant X3
transmembrane gamma-carboxyglutamic acid protein 1-like, transcript variant X5
transmembrane gamma-carboxyglutamic acid protein 1-like
SR-related CTD-associated factor 4a, transcript variant X2
SR-related CTD-associated factor 4a, transcript variant X1
SR-related and CTD-associated factor 4 isoform X1
SR-related and CTD-associated factor 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
superoxide dismutase [Cu-Zn]-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 38 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
superoxide dismutase [Cu-Zn]-like, transcript variant X9
superoxide dismutase [Cu-Zn]-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 38 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
superoxide dismutase [Cu-Zn]-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 39 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
superoxide dismutase [Cu-Zn]-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 38 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
superoxide dismutase [Cu-Zn]-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 38 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
superoxide dismutase [Cu-Zn]-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 38 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
superoxide dismutase [Cu-Zn]-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 38 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
superoxide dismutase [Cu-Zn]-like, transcript variant X1
superoxide dismutase [Cu-Zn]-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 38 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
superoxide dismutase [Cu-Zn]-like isoform X3
superoxide dismutase [Cu-Zn]-like isoform X5
superoxide dismutase [Cu-Zn]-like isoform X8
superoxide dismutase [Cu-Zn]-like isoform X7
superoxide dismutase [Cu-Zn]-like isoform X4
superoxide dismutase [Cu-Zn]-like isoform X2
superoxide dismutase [Cu-Zn]-like isoform X1
superoxide dismutase [Cu-Zn]-like isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
TIAM Rac1 associated GEF 1b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TIAM Rac1 associated GEF 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TIAM Rac1 associated GEF 1b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TIAM Rac1 associated GEF 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor TIAM1 isoform X1
rho guanine nucleotide exchange factor TIAM1 isoform X2
rho guanine nucleotide exchange factor TIAM1 isoform X3
rho guanine nucleotide exchange factor TIAM1 isoform X4
TIAM Rac1 associated GEF 1b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor TIAM1 isoform X5
TIAM Rac1 associated GEF 1b, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TIAM Rac1 associated GEF 1b, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TIAM Rac1 associated GEF 1b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
rho guanine nucleotide exchange factor TIAM1 isoform X6
TIAM Rac1 associated GEF 1b, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TIAM Rac1 associated GEF 1b, transcript variant X10
rho guanine nucleotide exchange factor TIAM1 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
map3k7 C-terminal like, transcript variant X2
map3k7 C-terminal like, transcript variant X3
map3k7 C-terminal like, transcript variant X1
MAP3K7 C-terminal-like protein isoform X1
MAP3K7 C-terminal-like protein isoform X2
uncharacterized LOC125484476, transcript variant X1
uncharacterized LOC125484476, transcript variant X6
uncharacterized LOC125484476, transcript variant X2
uncharacterized LOC125484476, transcript variant X3
uncharacterized LOC125484476, transcript variant X10
uncharacterized LOC125484476, transcript variant X9
uncharacterized LOC125484476, transcript variant X4
uncharacterized LOC125484476, transcript variant X8
uncharacterized LOC125484476, transcript variant X12
uncharacterized LOC125484476, transcript variant X5
uncharacterized LOC125484476, transcript variant X7
uncharacterized LOC125484476, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 16-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 16-like isoform X1
ubiquitin carboxyl-terminal hydrolase 16-like isoform X2
ubiquitin carboxyl-terminal hydrolase 16-like isoform X3
RWD domain containing 2B, transcript variant X1
RWD domain-containing protein 2B isoform X1
RWD domain containing 2B, transcript variant X2
RWD domain-containing protein 2B isoform X2
listerin E3 ubiquitin protein ligase 1, transcript variant X1
listerin E3 ubiquitin protein ligase 1, transcript variant X2
E3 ubiquitin-protein ligase listerin isoform X1
E3 ubiquitin-protein ligase listerin isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
kelch-like family member 15, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
kelch-like family member 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
kelch-like family member 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kelch-like family member 15, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
kelch-like family member 15, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kelch-like family member 15, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like, transcript variant X2
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like
UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
beta-1,4-galactosyltransferase 4 isoform X1
UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
beta-1,4-galactosyltransferase 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X1
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X3
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X2
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X1
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X5
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X6
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X4
coiled-coil domain containing 191, transcript variant X1
coiled-coil domain-containing protein 191 isoform X1
coiled-coil domain containing 191, transcript variant X2
coiled-coil domain-containing protein 191 isoform X2
zinc finger DHHC-type palmitoyltransferase 23b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
GTP binding protein 8 (putative), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
GTP binding protein 8 (putative), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
GTP binding protein 8 (putative), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
GTP binding protein 8 (putative), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
GTP binding protein 8 (putative), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
connector enhancer of kinase suppressor of Ras 2a
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: connector enhancer of kinase suppressor of ras 2
MSL complex subunit 3, transcript variant X1
MSL complex subunit 3, transcript variant X2
MSL complex subunit 3, transcript variant X5
MSL complex subunit 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
male-specific lethal 3 homolog isoform X5
male-specific lethal 3 homolog isoform X1
male-specific lethal 3 homolog isoform X2
male-specific lethal 3 homolog isoform X3
MSL complex subunit 3, transcript variant X4
male-specific lethal 3 homolog isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
FERM and PDZ domain-containing protein 4
ribose-phosphate pyrophosphokinase 2, transcript variant X1
ribose-phosphate pyrophosphokinase 2 isoform X1
ribose-phosphate pyrophosphokinase 2, transcript variant X2
ribose-phosphate pyrophosphokinase 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 222 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
toll-like receptor 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
toll-like receptor 7, transcript variant X1
toll-like receptor 7, transcript variant X3
uncharacterized LOC109915053, transcript variant X2
uncharacterized LOC109915053, transcript variant X1
transcription elongation factor A N-terminal and central domain-containing protein, transcript variant X2
transcription elongation factor A N-terminal and central domain-containing protein, transcript variant X1
transcription elongation factor A N-terminal and central domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trafficking protein particle complex subunit 2
OFD1 centriole and centriolar satellite protein
oral-facial-digital syndrome 1 protein homolog
glycoprotein M6Bb, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
glycoprotein M6Bb, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
glycoprotein M6Bb, transcript variant X3
gem (nuclear organelle) associated protein 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 96% coverage of the annotated genomic feature by RNAseq alignments
motile sperm domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
motile sperm domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
motile sperm domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
motile sperm domain-containing protein 2 isoform X1
motile sperm domain-containing protein 2 isoform X2
motile sperm domain-containing protein 2 isoform X3
mitogen-activated protein kinase kinase kinase 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
pyruvate dehydrogenase E1 component subunit alpha, mitochondrial-like
adhesion G-protein coupled receptor G4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
adhesion G-protein coupled receptor G2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
RALBP1 associated Eps domain containing 2, transcript variant X4
RALBP1 associated Eps domain containing 2, transcript variant X5
RALBP1 associated Eps domain containing 2, transcript variant X3
RALBP1 associated Eps domain containing 2, transcript variant X2
RALBP1 associated Eps domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RALBP1 associated Eps domain containing 2, transcript variant X6
RALBP1 associated Eps domain containing 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RALBP1 associated Eps domain containing 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RALBP1 associated Eps domain containing 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RALBP1 associated Eps domain containing 2, transcript variant X11
ralBP1-associated Eps domain-containing protein 2 isoform X4
ralBP1-associated Eps domain-containing protein 2 isoform X5
ralBP1-associated Eps domain-containing protein 2 isoform X1
ralBP1-associated Eps domain-containing protein 2 isoform X3
ralBP1-associated Eps domain-containing protein 2 isoform X2
ralBP1-associated Eps domain-containing protein 2 isoform X8
ralBP1-associated Eps domain-containing protein 2 isoform X6
RALBP1 associated Eps domain containing 2, transcript variant X7
ralBP1-associated Eps domain-containing protein 2 isoform X7
Nance-Horan syndrome protein, transcript variant X1
Nance-Horan syndrome protein, transcript variant X2
Nance-Horan syndrome protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
BEN domain-containing protein 2-like, transcript variant X3
BEN domain-containing protein 2-like, transcript variant X9
BEN domain-containing protein 2-like, transcript variant X2
BEN domain-containing protein 2-like, transcript variant X4
BEN domain-containing protein 2-like, transcript variant X6
BEN domain-containing protein 2-like, transcript variant X1
BEN domain-containing protein 2-like isoform X1
BEN domain-containing protein 2-like isoform X9
BEN domain-containing protein 2-like isoform X3
BEN domain-containing protein 2-like isoform X2
uncharacterized protein LOC109927206 isoform X4
uncharacterized protein LOC109927206 isoform X6
BEN domain-containing protein 2-like, transcript variant X7
BEN domain-containing protein 2-like, transcript variant X5
BEN domain-containing protein 2-like isoform X5
BEN domain-containing protein 2-like isoform X7
BEN domain-containing protein 2-like, transcript variant X8
BEN domain-containing protein 2-like isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Scm polycomb group protein like 2, transcript variant X4
Scm polycomb group protein like 2, transcript variant X3
Scm polycomb group protein like 2, transcript variant X1
Scm polycomb group protein like 2, transcript variant X2
Scm polycomb group protein like 2, transcript variant X6
Scm polycomb group protein like 2, transcript variant X5
sex comb on midleg-like protein 2 isoform X4
cyclin-dependent kinase-like 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclin-dependent kinase-like 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclin-dependent kinase-like 5, transcript variant X3
cyclin-dependent kinase-like 5 isoform X1
cyclin-dependent kinase-like 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SH3 domain-containing kinase-binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribosomal protein S6 kinase alpha-3, transcript variant X5
ribosomal protein S6 kinase alpha-3, transcript variant X2
ribosomal protein S6 kinase alpha-3, transcript variant X4
ribosomal protein S6 kinase alpha-3, transcript variant X3
ribosomal protein S6 kinase alpha-3, transcript variant X1
ribosomal protein S6 kinase alpha-3, transcript variant X9
ribosomal protein S6 kinase alpha-3, transcript variant X8
ribosomal protein S6 kinase alpha-3, transcript variant X7
ribosomal protein S6 kinase alpha-3, transcript variant X6
ribosomal protein S6 kinase alpha-3 isoform X9
ribosomal protein S6 kinase alpha-3 isoform X7
ribosomal protein S6 kinase alpha-3 isoform X8
ribosomal protein S6 kinase alpha-3 isoform X6
ribosomal protein S6 kinase alpha-3 isoform X4
ribosomal protein S6 kinase alpha-3 isoform X3
ribosomal protein S6 kinase alpha-3 isoform X2
ribosomal protein S6 kinase alpha-3 isoform X5
ribosomal protein S6 kinase alpha-3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125484393, transcript variant X1
uncharacterized LOC125484393, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125484393, transcript variant X3
E3 ubiquitin-protein ligase Midline-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
shroom family member 2a, transcript variant X1
shroom family member 2a, transcript variant X2
shroom family member 2a, transcript variant X3
shroom family member 2a, transcript variant X4
shroom family member 2a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
dehydrogenase/reductase (SDR family) member 12, transcript variant X1
dehydrogenase/reductase (SDR family) member 12, transcript variant X2
dehydrogenase/reductase SDR family member 12 isoform X1
dehydrogenase/reductase SDR family member 12 isoform X2
WD repeat and FYVE domain containing 2, transcript variant X2
WD repeat and FYVE domain containing 2, transcript variant X1
WD repeat and FYVE domain-containing protein 2 isoform X2
WD repeat and FYVE domain-containing protein 2 isoform X1
integrator complex subunit 6, transcript variant X1
integrator complex subunit 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
integrator complex subunit 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
integrator complex subunit 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
integrator complex subunit 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
integrator complex subunit 6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
ribonuclease H2, subunit B, transcript variant X2
ribonuclease H2, subunit B, transcript variant X1
ribonuclease H2, subunit B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125484468, transcript variant X1
uncharacterized LOC125484468, transcript variant X2
putative potassium channel regulatory protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fibronectin type III domain containing 3A, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fibronectin type III domain containing 3A, transcript variant X4
fibronectin type III domain containing 3A, transcript variant X1
fibronectin type III domain containing 3A, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibronectin type III domain containing 3A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fibronectin type III domain containing 3A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
fibronectin type III domain containing 3A, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
fibronectin type III domain containing 3A, transcript variant X2
fibronectin type-III domain-containing protein 3A isoform X6
fibronectin type-III domain-containing protein 3A isoform X1
fibronectin type-III domain-containing protein 3A isoform X3
fibronectin type-III domain-containing protein 3A isoform X7
fibronectin type-III domain-containing protein 3A isoform X5
fibronectin type-III domain-containing protein 3A isoform X4
fibronectin type III domain containing 3A, transcript variant X3
fibronectin type-III domain-containing protein 3A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 44 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
growth hormone secretagogue receptor type 1
cytidine and dCMP deaminase domain containing 1, transcript variant X1
cytidine and dCMP deaminase domain containing 1, transcript variant X2
cytidine and dCMP deaminase domain-containing protein 1 isoform X1
cytidine and dCMP deaminase domain-containing protein 1 isoform X2
calcium binding protein 39-like, transcript variant X2
calcium binding protein 39-like, transcript variant X1
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X1
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
histone-lysine N-methyltransferase SETDB2 isoform X1
histone-lysine N-methyltransferase SETDB2 isoform X3
histone-lysine N-methyltransferase SETDB2 isoform X2
histone-lysine N-methyltransferase SETDB2 isoform X5
histone-lysine N-methyltransferase SETDB2 isoform X6
histone-lysine N-methyltransferase SETDB2 isoform X4
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 2, transcript variant X10
histone-lysine N-methyltransferase SETDB2 isoform X9
histone-lysine N-methyltransferase SETDB2 isoform X7
histone-lysine N-methyltransferase SETDB2 isoform X8
PHD finger protein 6-like, transcript variant X1
PHD finger protein 6-like, transcript variant X3
PHD finger protein 6-like, transcript variant X2
PHD finger protein 6-like, transcript variant X6
uncharacterized protein LOC109919656 isoform X1
uncharacterized protein LOC109919656 isoform X3
uncharacterized protein LOC109919656 isoform X2
PHD finger protein 6-like, transcript variant X4
PHD finger protein 6-like, transcript variant X5
uncharacterized protein LOC109919656 isoform X4
uncharacterized protein LOC109919656 isoform X5
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X1
RCC1 and BTB domain-containing protein 1 isoform X1
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RCC1 and BTB domain-containing protein 1 isoform X4
RCC1 and BTB domain-containing protein 1 isoform X5
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X3
regulator of chromosome condensation (RCC1) and BTB (POZ) domain containing protein 1, transcript variant X2
RCC1 and BTB domain-containing protein 1 isoform X2
RCC1 and BTB domain-containing protein 1 isoform X3
cysteinyl leukotriene receptor 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 13 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cysteinyl leukotriene receptor 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cysteinyl leukotriene receptor 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
cysteinyl leukotriene receptor 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
cysteinyl leukotriene receptor 2-like, transcript variant X4
cysteinyl leukotriene receptor 2-like isoform X1
cysteinyl leukotriene receptor 2-like isoform X2
RCC1 and BTB domain-containing protein 2-like, transcript variant X3
RCC1 and BTB domain-containing protein 2-like, transcript variant X1
RCC1 and BTB domain-containing protein 2-like, transcript variant X2
RCC1 and BTB domain-containing protein 2-like isoform X3
RCC1 and BTB domain-containing protein 2-like isoform X1
RCC1 and BTB domain-containing protein 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
integral membrane protein 2B, transcript variant X1
integral membrane protein 2B, transcript variant X2
mediator complex subunit 4, transcript variant X1
mediator complex subunit 4, transcript variant X2
mediator of RNA polymerase II transcription subunit 4
nudix (nucleoside diphosphate linked moiety X)-type motif 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 11 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nucleotide triphosphate diphosphatase NUDT15
succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 22 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 18 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X3
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X1
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X1
leucine-rich repeats and calponin homology (CH) domain containing 1, transcript variant X5
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X2
rubicon like autophagy enhancer, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
rubicon like autophagy enhancer, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rubicon like autophagy enhancer, transcript variant X5
rubicon like autophagy enhancer, transcript variant X3
rubicon like autophagy enhancer, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein associated with UVRAG as autophagy enhancer isoform X1
protein associated with UVRAG as autophagy enhancer isoform X3
protein associated with UVRAG as autophagy enhancer isoform X4
protein associated with UVRAG as autophagy enhancer isoform X2
rubicon like autophagy enhancer, transcript variant X6
rubicon like autophagy enhancer, transcript variant X7
protein associated with UVRAG as autophagy enhancer isoform X5
leucine-rich repeat-containing protein 63-like, transcript variant X2
leucine-rich repeat-containing protein 63-like, transcript variant X4
leucine-rich repeat-containing protein 63-like, transcript variant X3
leucine-rich repeat-containing protein 63-like, transcript variant X1
leucine-rich repeat-containing protein 63-like isoform X3
uncharacterized protein LOC109917213 isoform X2
uncharacterized protein LOC109917213 isoform X1
carboxypeptidase B2 (plasma), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
carboxypeptidase B2 (plasma), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
zinc finger CCCH domain-containing protein 13
conserved oligomeric Golgi complex subunit 3
tumor protein, translationally-controlled 1, transcript variant X1
translationally-controlled tumor protein homolog isoform X1
tumor protein, translationally-controlled 1, transcript variant X2
translationally-controlled tumor protein homolog isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00322
general transcription factor IIF subunit 2, transcript variant X2
general transcription factor IIF subunit 2, transcript variant X1
general transcription factor IIF subunit 2 isoform X2
general transcription factor IIF subunit 2 isoform X1
potassium channel tetramerization domain containing 4
LOW QUALITY PROTEIN: BTB/POZ domain-containing protein KCTD4
laccase (multicopper oxidoreductase) domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
laccase (multicopper oxidoreductase) domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
purine nucleoside phosphorylase LACC1 isoform X1
purine nucleoside phosphorylase LACC1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ecto-NOX disulfide-thiol exchanger 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and SOCS box protein 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and SOCS box protein 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ankyrin repeat and SOCS box protein 9, transcript variant X3
ankyrin repeat and SOCS box protein 9 isoform X1
ankyrin repeat and SOCS box protein 9 isoform X2
phosphatidylinositol glycan anchor biosynthesis, class A
phosphatidylinositol N-acetylglucosaminyltransferase subunit A
vascular endothelial growth factor D, transcript variant X2
vascular endothelial growth factor D, transcript variant X1
vascular endothelial growth factor D isoform X1
vascular endothelial growth factor D isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
collectrin, amino acid transport regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide exchange factor DBS-like, transcript variant X2
guanine nucleotide exchange factor DBS-like, transcript variant X1
guanine nucleotide exchange factor DBS-like, transcript variant X3
guanine nucleotide exchange factor DBS-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
growth hormone-regulated TBC protein 1-A
cilia- and flagella-associated protein 44-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 55 Proteins
lysosomal associated membrane protein 1a
lysosome-associated membrane glycoprotein 1a
potassium-transporting ATPase subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mitochondrial translational release factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
mitochondrial translational release factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitochondrial translational release factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
peptide chain release factor 1, mitochondrial isoform X3
peptide chain release factor 1, mitochondrial isoform X1
peptide chain release factor 1, mitochondrial isoform X2
kelch repeat and BTB (POZ) domain containing 7
kelch repeat and BTB domain-containing protein 7
transmembrane and coiled-coil domains 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane and coiled-coil domains 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane and coiled-coil domains 3, transcript variant X7
transmembrane and coiled-coil domains 3, transcript variant X2
transmembrane and coiled-coil domains 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane and coiled-coil domains 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transmembrane and coiled-coil domains 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane and coiled-coil domains 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transmembrane and coiled-coil domain-containing protein 3 isoform X4
transmembrane and coiled-coil domain-containing protein 3 isoform X2
transmembrane and coiled-coil domain-containing protein 3 isoform X3
transmembrane and coiled-coil domain-containing protein 3 isoform X1
transmembrane and coiled-coil domains 3, transcript variant X11
transmembrane and coiled-coil domains 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane and coiled-coil domains 3, transcript variant X9
transmembrane and coiled-coil domain-containing protein 3 isoform X5
uncharacterized protein LOC103911624 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC103911624 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein LOC103911624 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC103911624 homolog, transcript variant X6
uncharacterized protein LOC103911624 homolog, transcript variant X4
uncharacterized protein LOC103911624 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC103911624 homolog, transcript variant X7
uncharacterized protein wu:fc50b12 isoform X1
uncharacterized protein wu:fc50b12 isoform X2
patched domain containing 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
patched domain containing 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
patched domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
patched domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
patched domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
patched domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
patched domain-containing protein 1 isoform X2
patched domain-containing protein 1 isoform X1
acyl-coenzyme A thioesterase 9, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125484361, transcript variant X2
uncharacterized LOC125484361, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 long SRA reads, 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
pleckstrin homology-like domain, family B, member 2b
pleckstrin homology-like domain family B member 1
phosphatidylinositol-specific phospholipase C, X domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: MICOS complex subunit MIC26
membrane-bound transcription factor peptidase, site 2, transcript variant X1
membrane-bound transcription factor peptidase, site 2, transcript variant X2
membrane-bound transcription factor site-2 protease
phosphate regulating endopeptidase homolog, X-linked
phosphate-regulating neutral endopeptidase PHEX
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
PCI domain containing 2, transcript variant X1
PCI domain containing 2, transcript variant X2
coagulation factor X-like, transcript variant X2
coagulation factor X-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
BCLAF1 and THRAP3 family member 3, transcript variant X1
BCLAF1 and THRAP3 family member 3, transcript variant X2
BCLAF1 and THRAP3 family member 3 isoform X1
BCLAF1 and THRAP3 family member 3 isoform X2
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein phosphatase, EF-hand calcium binding domain 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
serine/threonine-protein phosphatase with EF-hands 1
phosphorylase b kinase regulatory subunit alpha, liver isoform-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphorylase b kinase regulatory subunit alpha, liver isoform-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphorylase b kinase regulatory subunit alpha, liver isoform-like isoform X1
phosphorylase b kinase regulatory subunit alpha, liver isoform-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
adaptor related protein complex 1 subunit sigma 2
zinc finger (CCCH type), RNA-binding motif and serine/arginine rich 2
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 43% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain containing 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
von Willebrand factor A domain containing 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
von Willebrand factor A domain containing 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
von Willebrand factor A domain containing 8, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
von Willebrand factor A domain-containing protein 8 isoform X3
von Willebrand factor A domain-containing protein 8 isoform X2
von Willebrand factor A domain-containing protein 8 isoform X1
von Willebrand factor A domain-containing protein 8 isoform X4
von Willebrand factor A domain containing 8, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
A kinase (PRKA) anchor protein 11, transcript variant X11
A kinase (PRKA) anchor protein 11, transcript variant X1
A kinase (PRKA) anchor protein 11, transcript variant X3
A kinase (PRKA) anchor protein 11, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
A kinase (PRKA) anchor protein 11, transcript variant X15
A kinase (PRKA) anchor protein 11, transcript variant X13
A kinase (PRKA) anchor protein 11, transcript variant X4
A kinase (PRKA) anchor protein 11, transcript variant X12
A kinase (PRKA) anchor protein 11, transcript variant X10
A kinase (PRKA) anchor protein 11, transcript variant X7
A kinase (PRKA) anchor protein 11, transcript variant X2
A kinase (PRKA) anchor protein 11, transcript variant X8
A kinase (PRKA) anchor protein 11, transcript variant X6
A kinase (PRKA) anchor protein 11, transcript variant X9
A kinase (PRKA) anchor protein 11, transcript variant X5
TNF superfamily member 11, transcript variant X1
TNF superfamily member 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 10 isoform X1
tumor necrosis factor ligand superfamily member 10 isoform X2
epithelial stromal interaction 1, transcript variant X1
epithelial-stromal interaction protein 1 isoform X1
epithelial stromal interaction 1, transcript variant X3
epithelial stromal interaction 1, transcript variant X2
epithelial-stromal interaction protein 1 isoform X3
epithelial-stromal interaction protein 1 isoform X2
gastrula zinc finger protein XlCGF26.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 60 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X3
NACHT, LRR and PYD domains-containing protein 3-like isoform X1
NACHT, LRR and PYD domains-containing protein 3-like isoform X3
NACHT, LRR and PYD domains-containing protein 3-like isoform X2