Rhincodon typus isolate 14 chromosome 8, 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\nCM038805.1.\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.
spectrin repeat containing, nuclear envelope family member 3, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
spectrin repeat containing, nuclear envelope family member 3, transcript variant X2
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: 7 Proteins, and 44% 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: calcium permeable stress-gated cation channel 1
zinc finger DHHC-type palmitoyltransferase 22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 32% 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 93% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
feline leukemia virus subgroup C receptor-related protein 2-like
DNA mismatch repair protein Mlh3-like, transcript variant X3
DNA mismatch repair protein Mlh3-like, transcript variant X1
DNA mismatch repair protein Mlh3-like, transcript variant X2
DNA mismatch repair protein Mlh3-like isoform X1
DNA mismatch repair protein Mlh3-like isoform X3
DNA mismatch repair protein Mlh3-like isoform X2
eukaryotic translation initiation factor 2B, subunit 2 beta
translation initiation factor eIF-2B subunit beta
basic leucine zipper transcription factor, ATF-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
basic leucine zipper transcriptional factor ATF-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase Nek9-like, transcript variant X2
serine/threonine-protein kinase Nek9-like, transcript variant X1
serine/threonine-protein kinase Nek9-like isoform X2
serine/threonine-protein kinase Nek9-like isoform X1
G patch domain-containing protein 2-like, transcript variant X1
G patch domain-containing protein 2-like, transcript variant X3
G patch domain-containing protein 2-like, transcript variant X2
G patch domain-containing protein 2-like, transcript variant X4
G patch domain-containing protein 2-like isoform X1
G patch domain-containing protein 2-like isoform X2
G patch domain-containing protein 2-like isoform X3
G patch domain-containing protein 2-like isoform X4
intraflagellar transport protein 43 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% 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, 1 Protein, 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: 21 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: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
gsk3b interacting protein, transcript variant X1
gsk3b interacting protein, transcript variant X2
gsk3b interacting protein, transcript variant X4
gsk3b interacting protein, transcript variant X3
autophagy-related protein 2 homolog B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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
autophagy-related protein 2 homolog B, 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
autophagy-related protein 2 homolog B, 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 1 sample with support for all annotated introns
autophagy-related protein 2 homolog B, transcript variant X1
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 2 samples with support for all annotated introns
autophagy-related protein 2 homolog B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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
autophagy-related protein 2 homolog B, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
autophagy-related protein 2 homolog B, transcript variant X6
autophagy-related protein 2 homolog B isoform X1
autophagy-related protein 2 homolog B isoform X4
autophagy-related protein 2 homolog B isoform X3
autophagy-related protein 2 homolog B isoform X2
autophagy-related protein 2 homolog B isoform X8
autophagy-related protein 2 homolog B isoform X5
autophagy-related protein 2 homolog B isoform X6
autophagy-related protein 2 homolog B, transcript variant X7
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
autophagy-related protein 2 homolog B isoform X7
NADP-dependent oxidoreductase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 3 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NADP-dependent oxidoreductase domain-containing protein 1
sterile alpha motif domain-containing protein 15
uncharacterized protein LOC100038766 homolog
glutathione S-transferase zeta 1, transcript variant X3
glutathione S-transferase zeta 1, transcript variant X1
glutathione S-transferase zeta 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00231
glutaredoxin-related protein 5, mitochondrial
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, including 1 sample with support for all annotated introns
autophagy-related protein 2 homolog B-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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence, mRNA (same species):INSD:AB551716.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 329 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 329 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1b
C-1-tetrahydrofolate synthase, cytoplasmic
zinc finger and BTB domain-containing protein 1
heat shock-related 70 kDa protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 547 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription factor IIIB 90 kDa subunit-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
BTB (POZ) domain containing 6b, transcript variant X2
BTB (POZ) domain containing 6b, transcript variant X1
BTB/POZ domain-containing protein 6-B isoform X1
BTB/POZ domain-containing protein 6-B isoform X2
nudix (nucleoside diphosphate linked moiety X)-type motif 14, transcript variant X1
uridine diphosphate glucose pyrophosphatase NUDT14 isoform X1
nudix (nucleoside diphosphate linked moiety X)-type motif 14, transcript variant X2
nudix (nucleoside diphosphate linked moiety X)-type motif 14, transcript variant X3
uridine diphosphate glucose pyrophosphatase NUDT14 isoform X2
nudix (nucleoside diphosphate linked moiety X)-type motif 14, transcript variant X4
uridine diphosphate glucose pyrophosphatase NUDT14 isoform X3
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: 28 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor 132, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor 132, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable G-protein coupled receptor 132, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ovarian cancer G-protein coupled receptor 1-like
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 14 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: 2 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: 17 Proteins, and 33% 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, 1 Protein, and 98% 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); 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: 18 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein angel homolog 1-like, transcript variant X2
protein angel homolog 1-like, transcript variant X1
leucine-rich repeat-containing protein 74A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
SMEK homolog 1, suppressor of mek1 (Dictyostelium), transcript variant X1
SMEK homolog 1, suppressor of mek1 (Dictyostelium), transcript variant X2
SMEK homolog 1, suppressor of mek1 (Dictyostelium), transcript variant X3
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 8 samples with support for all annotated introns
serine/threonine-protein phosphatase 4 regulatory subunit 3 isoform X1
serine/threonine-protein phosphatase 4 regulatory subunit 3 isoform X2
serine/threonine-protein phosphatase 4 regulatory subunit 3 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
ovarian cancer G-protein coupled receptor 1, transcript variant X1
ovarian cancer G-protein coupled receptor 1, transcript variant X2
ovarian cancer G-protein coupled receptor 1
ovarian cancer G-protein coupled receptor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ovarian cancer G-protein coupled receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 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: 18 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein S6 kinase alpha-5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ribosomal protein S6 kinase alpha-5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ribosomal protein S6 kinase alpha-5-like isoform X2
ribosomal protein S6 kinase alpha-5-like 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 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: 1 long SRA read, and 72% 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: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
NRDE-2, necessary for RNA interference, domain containing
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
potassium channel, subfamily K, member 13a
potassium channel subfamily K member 13a
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: 2 long SRA reads, 18 Proteins, and 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: 23 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
EF-hand calcium-binding domain-containing protein 11
general transcription factor IIA, 1, transcript variant X1
general transcription factor IIA, 1, transcript variant X2
transcription initiation factor IIA subunit 1 isoform X1
transcription initiation factor IIA subunit 1 isoform X2
general transcription factor IIA, 1, transcript variant X3
transcription initiation factor IIA subunit 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 157 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
centrosomal protein of 128 kDa, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
centrosomal protein of 128 kDa, 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
centrosomal protein of 128 kDa, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
centrosomal protein of 128 kDa, 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 3 samples with support for all annotated introns
centrosomal protein of 128 kDa, transcript variant X5
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 1 sample with support for all annotated introns
centrosomal protein of 128 kDa isoform X1
centrosomal protein of 128 kDa isoform X2
centrosomal protein of 128 kDa isoform X4
centrosomal protein of 128 kDa isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 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 Proteins, and 13% 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 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
aarF domain-containing protein kinase 1-like
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
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
SRA stem-loop interacting RNA binding protein
SRA stem-loop-interacting RNA-binding protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
poly(A) polymerase type 3, transcript variant X4
poly(A) polymerase type 3, transcript variant X3
poly(A) polymerase type 3, transcript variant X1
poly(A) polymerase type 3, transcript variant X2
poly(A) polymerase type 3, transcript variant X5
poly(A) polymerase type 3, transcript variant X6
poly(A) polymerase type 3, transcript variant X8
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
poly(A) polymerase type 3, transcript variant X7
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 3 samples with support for all annotated introns
serine palmitoyltransferase, long chain base subunit 2a, transcript variant X1
serine palmitoyltransferase, long chain base subunit 2a, transcript variant X2
serine palmitoyltransferase 2 isoform X2
serine palmitoyltransferase 2 isoform X1
serine palmitoyltransferase, long chain base subunit 2a, transcript variant X3
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 3 samples with support for all annotated introns
serine palmitoyltransferase 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 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
AHA1, activator of heat shock protein ATPase homolog 1b, transcript variant X1
AHA1, activator of heat shock protein ATPase homolog 1b, transcript variant X2
activator of 90 kDa heat shock protein ATPase homolog 1b isoform X1
activator of 90 kDa heat shock protein ATPase homolog 1b isoform 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
VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog, transcript variant X3
VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog, transcript variant X1
VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog, transcript variant X2
VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog, transcript variant X4
spermatogenesis-defective protein 39 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 410, transcript variant X1
zinc finger protein 410, transcript variant X2
ubiquinone biosynthesis monooxygenase COQ6, mitochondrial
ectonucleoside triphosphate diphosphohydrolase 5a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 24 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ectonucleoside triphosphate diphosphohydrolase 5
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 2 samples with support for all annotated introns
aldehyde dehydrogenase 6 family, member A1, transcript variant X1
aldehyde dehydrogenase 6 family, member A1, transcript variant X2
methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X1
methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X2
lin-52 DREAM MuvB core complex component, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 19 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
lin-52 DREAM MuvB core complex component, transcript variant X3
lin-52 DREAM MuvB core complex component, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
lin-52 DREAM MuvB core complex component, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 19 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
lin-52 DREAM MuvB core complex component, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
lin-52 DREAM MuvB core complex component, transcript variant X4
lin-52 DREAM MuvB core complex component, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
acetyl-coenzyme A synthetase 2-like, mitochondrial
ATP-binding cassette, sub-family D (ALD), member 4, transcript variant X1
ATP-binding cassette, sub-family D (ALD), member 4, transcript variant X2
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
ATP-binding cassette sub-family D member 4
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
synapse differentiation-inducing gene protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
NPC intracellular cholesterol transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
lysosomal cobalamin transporter ABCD4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 11 Proteins
iron-sulfur cluster assembly 2, transcript variant X2
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 3 samples with support for all annotated introns
iron-sulfur cluster assembly 2, transcript variant X1
iron-sulfur cluster assembly 2 homolog, mitochondrial
NPC intracellular cholesterol transporter 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NPC intracellular cholesterol transporter 2-like, transcript variant X3
NPC intracellular cholesterol transporter 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 35 Proteins, and 99% 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: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
latent-transforming growth factor beta-binding protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
latent-transforming growth factor beta-binding protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
apoptosis-resistant E3 ubiquitin protein ligase 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: apoptosis-resistant E3 ubiquitin protein ligase 1
FCF1 rRNA-processing protein, transcript variant X1
rRNA-processing protein FCF1 homolog isoform X1
FCF1 rRNA-processing protein, transcript variant X2
rRNA-processing protein FCF1 homolog isoform X2
uncharacterized LOC109910782, transcript variant X1
uncharacterized LOC109910782, 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 8 samples with support for all annotated introns
uncharacterized LOC109910782, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 92% 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: 13 Proteins, and 81% 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 18 samples with support for all annotated introns
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial
ribosomal protein S6 kinase-like 1, transcript variant X3
ribosomal protein S6 kinase-like 1, transcript variant X4
ribosomal protein S6 kinase-like 1, transcript variant X1
ribosomal protein S6 kinase-like 1, transcript variant X2
uncharacterized protein rps6kl1 isoform X2
uncharacterized protein rps6kl1 isoform 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 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: 36 Proteins, and 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: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 85C-A
SET domain containing 3, actin histidine methyltransferase
BAF chromatin remodeling complex subunit BCL11B a, transcript variant X2
BAF chromatin remodeling complex subunit BCL11B a, transcript variant X3
BAF chromatin remodeling complex subunit BCL11B a, transcript variant X4
BAF chromatin remodeling complex subunit BCL11B a, transcript variant X1
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 7 samples with support for all annotated introns
BAF chromatin remodeling complex subunit BCL11B a, transcript variant X5
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
uncharacterized LOC125483754, transcript variant X2
uncharacterized LOC125483754, transcript variant X1
uncharacterized LOC125483733, transcript variant X1
uncharacterized LOC125483733, transcript variant X2
VRK serine/threonine kinase 1, transcript variant X3
VRK serine/threonine kinase 1, transcript variant X1
VRK serine/threonine kinase 1, transcript variant X2
protein phosphatase 1 regulatory subunit 37-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
SEL1L adaptor subunit of ERAD E3 ubiquitin ligase
LOW QUALITY PROTEIN: UPF0547 protein C16orf87 homolog
leucine-rich repeat transmembrane protein FLRT2, transcript variant X1
leucine-rich repeat transmembrane protein FLRT2, 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 14 samples with support for all annotated introns
leucine-rich repeat transmembrane protein FLRT2
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
galactocerebrosidase-like, transcript variant X1
galactocerebrosidase-like, transcript variant X2
alpha-1-antitrypsin-like protein GS55-MS, transcript variant X1
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
alpha-1-antitrypsin-like protein GS55-MS, transcript variant X2
alpha-1-antitrypsin-like protein GS55-MS
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10b
protein phosphatase 4, regulatory subunit 4
serine/threonine-protein phosphatase 4 regulatory subunit 4
ubiquitin thioesterase OTUB2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ubiquitin thioesterase OTUB2-like, transcript variant X4
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 4 samples with support for all annotated introns
ubiquitin thioesterase OTUB2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ubiquitin thioesterase OTUB2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin thioesterase OTUB2-like isoform X4
ubiquitin thioesterase OTUB2-like isoform X2
ubiquitin thioesterase OTUB2-like isoform X1
ubiquitin thioesterase OTUB2-like isoform X3
uncharacterized LOC125483724, 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
uncharacterized LOC125483724, 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 3 samples with support for all annotated introns
coiled-coil domain-containing protein 42 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and SOCS box containing 2a, tandem duplicate 1, 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 2 samples with support for all annotated introns
ankyrin repeat and SOCS box containing 2a, tandem duplicate 1, 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 4 samples with support for all annotated introns
ankyrin repeat and SOCS box protein 2 isoform X1
ankyrin repeat and SOCS box protein 2 isoform X2
proline rich membrane anchor 1, transcript variant X4
proline rich membrane anchor 1, transcript variant X3
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
proline rich membrane anchor 1, transcript variant X1
proline rich membrane anchor 1, transcript variant X2
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 2 samples with support for all annotated introns
proline-rich membrane anchor 1 isoform X4
proline-rich membrane anchor 1 isoform X3
proline-rich membrane anchor 1 isoform X1
proline-rich membrane anchor 1 isoform X2
unc-79 homolog, NALCN channel complex subunit, transcript variant X2
unc-79 homolog, NALCN channel complex subunit, transcript variant X1
BTB (POZ) domain containing 7, transcript variant X1
BTB (POZ) domain containing 7, transcript variant X4
BTB (POZ) domain containing 7, transcript variant X2
BTB (POZ) domain containing 7, transcript variant X3
BTB/POZ domain-containing protein 7 isoform X4
BTB/POZ domain-containing protein 7 isoform X1
BTB/POZ domain-containing protein 7 isoform X2
BTB/POZ domain-containing protein 7 isoform X3
ubiquitin protein ligase E3 component n-recognin 7
putative E3 ubiquitin-protein ligase UBR7
uncharacterized protein LOC568418 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 long SRA reads, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized protein LOC568418 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 116 long SRA reads, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized protein LOC568418 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 2 samples with support for all annotated introns
uncharacterized protein si:dkeyp-55f12.3 isoform X1
uncharacterized protein si:dkeyp-55f12.3 isoform X2
transmembrane protein 251, transcript variant X2
transmembrane protein 251, transcript variant X3
transmembrane protein 251, 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 7 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 long SRA reads, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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, 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium/potassium/calcium exchanger 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
cleavage and polyadenylation specific factor 2
cleavage and polyadenylation specificity factor subunit 2
WD repeat domain 89, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
WD repeat domain 89, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 1, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 1, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 1
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 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: 127 long SRA reads, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
glycoprotein hormone subunit beta 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
glycoprotein hormone subunit beta 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily H member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109916454, transcript variant X2
uncharacterized LOC109916454, transcript variant X1
synaptotagmin-16-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
synaptotagmin-16-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
small nuclear RNA activating complex, polypeptide 1b, transcript variant X2
small nuclear RNA activating complex, polypeptide 1b, transcript variant X1
small nuclear RNA activating complex, polypeptide 1b, transcript variant X3
small nuclear RNA activating complex, polypeptide 1b, transcript variant X4
small nuclear RNA activating complex, polypeptide 1b, transcript variant X5
snRNA-activating protein complex subunit 1b isoform X1
snRNA-activating protein complex subunit 1b isoform X2
snRNA-activating protein complex subunit 1b isoform X3
hypoxia inducible factor 1 subunit alpha a, transcript variant X5
hypoxia inducible factor 1 subunit alpha a, transcript variant X2
hypoxia inducible factor 1 subunit alpha a, transcript variant X3
hypoxia inducible factor 1 subunit alpha a, transcript variant X1
hypoxia inducible factor 1 subunit alpha a, transcript variant X4
hypoxia inducible factor 1 subunit alpha a isoform X2
hypoxia inducible factor 1 subunit alpha a isoform X3
hypoxia inducible factor 1 subunit alpha a isoform X1
hypoxia inducible factor 1 subunit alpha a isoform X4
hypoxia inducible factor 1 subunit alpha a isoform X5
protein kinase C, eta, a, transcript variant X1
protein kinase C, eta, a, transcript variant X3
protein kinase C, eta, a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, and 98% 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: 52 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
MNAT1 component of CDK activating kinase, 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
MNAT1 component of CDK activating kinase, transcript variant X1
CDK-activating kinase assembly factor MAT1 isoform X1
CDK-activating kinase assembly factor MAT1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 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: 63 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: 90% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase, Mg2+/Mn2+ dependent, 1Aa, transcript variant X5
protein phosphatase, Mg2+/Mn2+ dependent, 1Aa, transcript variant X2
protein phosphatase, Mg2+/Mn2+ dependent, 1Aa, transcript variant X1
protein phosphatase, Mg2+/Mn2+ dependent, 1Aa, transcript variant X3
protein phosphatase, Mg2+/Mn2+ dependent, 1Aa, transcript variant X4
protein phosphatase, Mg2+/Mn2+ dependent, 1Aa, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dehydrogenase/reductase (SDR family) member 7, transcript variant X4
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
dehydrogenase/reductase SDR family member 7 isoform X3
dehydrogenase/reductase (SDR family) member 7, 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
dehydrogenase/reductase (SDR family) member 7, transcript variant X3
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
dehydrogenase/reductase (SDR family) member 7, 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
dehydrogenase/reductase SDR family member 7 isoform X1
dehydrogenase/reductase SDR family member 7 isoform X2
leucine rich repeat containing 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat containing 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat-containing protein 9 isoform X1
leucine-rich repeat-containing protein 9 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
echinoderm microtubule-associated protein-like 5
zinc finger CCCH domain-containing protein 14
protein tyrosine phosphatase non-receptor type 21, transcript variant X1
protein tyrosine phosphatase non-receptor type 21, transcript variant X2
tyrosine-protein phosphatase non-receptor type 21 isoform X1
tyrosine-protein phosphatase non-receptor type 21 isoform X2
spermatogenesis-associated protein 7 homolog
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
kelch-like protein 28, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 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 28, transcript variant X4
chromosome 8 C14orf28 homolog, transcript variant X3
chromosome 8 C14orf28 homolog, transcript variant X1
chromosome 8 C14orf28 homolog, transcript variant X4
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 2 samples with support for all annotated introns
chromosome 8 C14orf28 homolog, 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 6 samples with support for all annotated introns
uncharacterized protein C14orf28 homolog isoform X2
uncharacterized protein C14orf28 homolog isoform X3
uncharacterized protein C14orf28 homolog isoform X1
kelch-like protein 28, transcript variant X1
kelch-like protein 28, transcript variant X3
kelch-like protein 28, transcript variant X2
TOG array regulator of axonemal microtubules protein 1, 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
TOG array regulator of axonemal microtubules protein 1, 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 4 samples with support for all annotated introns
TOG array regulator of axonemal microtubules protein 1, 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 9 samples with support for all annotated introns
TOG array regulator of axonemal microtubules protein 1, transcript variant X4
TOG array regulator of axonemal microtubules protein 1, transcript variant X7
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
TOG array regulator of axonemal microtubules protein 1, transcript variant X6
TOG array regulator of axonemal microtubules protein 1, transcript variant X5
TOG array regulator of axonemal microtubules protein 1 isoform X1
TOG array regulator of axonemal microtubules protein 1 isoform X2
TOG array regulator of axonemal microtubules protein 1 isoform X3
TOG array regulator of axonemal microtubules protein 1 isoform X4
TOG array regulator of axonemal microtubules protein 1 isoform X5
TOG array regulator of axonemal microtubules protein 1 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
PRP39 pre-mRNA processing factor 39 homolog (yeast), transcript variant X1
PRP39 pre-mRNA processing factor 39 homolog (yeast), transcript variant X2
PRP39 pre-mRNA processing factor 39 homolog (yeast), transcript variant X3
pre-mRNA-processing factor 39 isoform X1
pre-mRNA-processing factor 39 isoform X2
pre-mRNA-processing factor 39 isoform X3
FAU ubiquitin-like and ribosomal protein S30
peptidyl-prolyl cis-trans isomerase FKBP3
Fanconi anemia group M protein-like, transcript variant X1
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
Fanconi anemia group M protein-like isoform X1
Fanconi anemia group M protein-like, transcript variant X2
Fanconi anemia group M protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 1 Protein, 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: 2 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized im:7136021, transcript variant X2
uncharacterized im:7136021, transcript variant X3
uncharacterized im:7136021, transcript variant X1
uncharacterized im:7136021, transcript variant X4
MAM domain containing glycosylphosphatidylinositol anchor 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
MAM domain-containing glycosylphosphatidylinositol anchor protein 2
transfer RNA tyrosine (anticodon GUA); 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: 1 Protein, and 86% 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, 9 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
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
kelch domain-containing protein 1, transcript variant X1
kelch domain-containing protein 1, transcript variant X3
kelch domain-containing protein 1 isoform X3
kelch domain-containing protein 1 isoform X1
kelch domain-containing protein 1, transcript variant X2
kelch domain-containing protein 1 isoform X2
uncharacterized LOC125483747, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 39% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125483747, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 60% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kelch domain containing 2, transcript variant X1
kelch domain containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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
kelch domain containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
kelch domain containing 2, transcript variant X2
kelch domain containing 2, transcript variant X3
kelch domain-containing protein 2 isoform X1
kelch domain-containing protein 2 isoform X2
kelch domain-containing protein 2 isoform X3
ribosome quality control complex subunit NEMF-like
MAPK/MAK/MRK overlapping kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MAPK/MAK/MRK overlapping kinase, transcript variant X3
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, including 1 sample with support for all annotated introns
MAPK/MAK/MRK overlapping kinase, transcript variant X2
MAPK/MAK/MRK overlapping kinase, transcript variant X4
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
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 2, regulatory subunit B', gamma a, transcript variant X1
protein phosphatase 2, regulatory subunit B', gamma a, transcript variant X2
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform isoform X1
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform isoform X2
dynein, cytoplasmic 1, heavy chain 1, transcript variant X2
dynein, cytoplasmic 1, heavy chain 1, transcript variant X1
cytoplasmic dynein 1 heavy chain 1 isoform X2
cytoplasmic dynein 1 heavy chain 1 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125483637, transcript variant X2
uncharacterized LOC125483637, transcript variant X1
uncharacterized protein LOC125483637 isoform X2
uncharacterized protein LOC125483637 isoform X1
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
brain-enriched guanylate kinase-associated protein-like
WD repeat domain 25, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 long SRA reads, 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
WD repeat domain 25, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
WD repeat domain 25, transcript variant X3
WD repeat domain 25, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tryptophanyl-tRNA synthetase 1, transcript variant X2
tryptophanyl-tRNA synthetase 1, transcript variant X3
tryptophanyl-tRNA synthetase 1, transcript variant X1
tryptophanyl-tRNA synthetase 1, transcript variant X6
tryptophanyl-tRNA synthetase 1, transcript variant X5
tryptophanyl-tRNA synthetase 1, transcript variant X4
tryptophan--tRNA ligase, cytoplasmic isoform X1
tryptophan--tRNA ligase, cytoplasmic isoform X2
solute carrier family 25 member 47b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 25 member 47b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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
solute carrier family 25 member 47b, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 25 member 47b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
solute carrier family 25 member 47b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 25 member 47b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 25 member 47b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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
solute carrier family 25 member 47-B isoform X1
solute carrier family 25 member 47-B isoform X5
solute carrier family 25 member 47-B isoform X2
solute carrier family 25 member 47-B isoform X6
solute carrier family 25 member 47-B isoform X3
solute carrier family 25 member 47-B isoform X4
mitochondrial basic amino acids transporter, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mitochondrial basic amino acids transporter, transcript variant X1
mitochondrial basic amino acids transporter, transcript variant X3
mitochondrial basic amino acids transporter
transcriptional repressor protein YY1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sphingolipid delta(4)-desaturase/C4-monooxygenase DES2
LOW QUALITY PROTEIN: ena/VASP-like protein
echinoderm microtubule-associated protein-like 1 isoform X2
echinoderm microtubule-associated protein-like 1 isoform X1
echinoderm microtubule-associated protein-like 1 isoform X3
echinoderm microtubule-associated protein-like 1 isoform X5
echinoderm microtubule-associated protein-like 1 isoform X4
extracellular tyrosine-protein kinase PKDCC-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 839, transcript variant X1
zinc finger protein 839, transcript variant X2
cyclin-dependent kinase 2 interacting protein
cyclin-dependent kinase 2-interacting protein
tectonin beta-propeller repeat containing 2, transcript variant X2
tectonin beta-propeller repeat containing 2, transcript variant X1
tectonin beta-propeller repeat containing 2, transcript variant X3
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
tectonin beta-propeller repeat-containing protein 2 isoform X1
tectonin beta-propeller repeat-containing protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, and 55% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ankyrin repeat domain-containing protein 9
REST corepressor 1, transcript variant X1
REST corepressor 1, transcript variant X2
TNF receptor-associated factor 3, transcript variant X4
TNF receptor-associated factor 3, transcript variant X2
TNF receptor-associated factor 3, transcript variant X3
TNF receptor-associated factor 3, transcript variant X1
TNF receptor-associated factor 3 isoform X1
TNF receptor-associated factor 3, transcript variant X5
TNF receptor-associated factor 3 isoform X2
CDC42 binding protein kinase beta (DMPK-like), transcript variant X2
CDC42 binding protein kinase beta (DMPK-like), transcript variant X8
CDC42 binding protein kinase beta (DMPK-like), transcript variant X7
CDC42 binding protein kinase beta (DMPK-like), transcript variant X6
CDC42 binding protein kinase beta (DMPK-like), transcript variant X5
CDC42 binding protein kinase beta (DMPK-like), transcript variant X4
CDC42 binding protein kinase beta (DMPK-like), transcript variant X3
CDC42 binding protein kinase beta (DMPK-like), transcript variant X1
serine/threonine-protein kinase MRCK beta isoform X7
serine/threonine-protein kinase MRCK beta isoform X6
serine/threonine-protein kinase MRCK beta isoform X5
serine/threonine-protein kinase MRCK beta isoform X4
serine/threonine-protein kinase MRCK beta isoform X3
serine/threonine-protein kinase MRCK beta isoform X2
serine/threonine-protein kinase MRCK beta isoform X1
serine/threonine-protein kinase MRCK beta isoform X8
uncharacterized protein LOC799956 homolog
exocyst complex component 3-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% 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 58% 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: 25 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
eukaryotic translation initiation factor 5, transcript variant X1
eukaryotic translation initiation factor 5, transcript variant X3
eukaryotic translation initiation factor 5, transcript variant X2
eukaryotic translation initiation factor 5
MAP/microtubule affinity-regulating kinase 3a, transcript variant X1
MAP/microtubule affinity-regulating kinase 3a, transcript variant X5
MAP/microtubule affinity-regulating kinase 3a, transcript variant X2
MAP/microtubule affinity-regulating kinase 3a, transcript variant X4
MAP/microtubule affinity-regulating kinase 3a, transcript variant X7
MAP/microtubule affinity-regulating kinase 3a, transcript variant X8
MAP/microtubule affinity-regulating kinase 3a, transcript variant X10
MAP/microtubule affinity-regulating kinase 3a, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
MAP/microtubule affinity-regulating kinase 3a, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
MAP/microtubule affinity-regulating kinase 3a, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MAP/microtubule affinity-regulating kinase 3a, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
MAP/microtubule affinity-regulating kinase 3a, transcript variant X18
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 7 samples with support for all annotated introns
MAP/microtubule affinity-regulating kinase 3a, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
MAP/microtubule affinity-regulating kinase 3a, transcript variant X12
MAP/microtubule affinity-regulating kinase 3a, transcript variant X3
MAP/microtubule affinity-regulating kinase 3a, transcript variant X9
MAP/microtubule affinity-regulating kinase 3a, transcript variant X6
MAP/microtubule affinity-regulating kinase 3a isoform X1
MAP/microtubule affinity-regulating kinase 3a isoform X5
MAP/microtubule affinity-regulating kinase 3a isoform X3
MAP/microtubule affinity-regulating kinase 3a isoform X6
MAP/microtubule affinity-regulating kinase 3a isoform X2
MAP/microtubule affinity-regulating kinase 3a isoform X4
MAP/microtubule affinity-regulating kinase 3a isoform X7
MAP/microtubule affinity-regulating kinase 3a isoform X8
MAP/microtubule affinity-regulating kinase 3a isoform X9
MAP/microtubule affinity-regulating kinase 3a isoform X10
MAP/microtubule affinity-regulating kinase 3a isoform X13
MAP/microtubule affinity-regulating kinase 3a isoform X12
MAP/microtubule affinity-regulating kinase 3a isoform X14
MAP/microtubule affinity-regulating kinase 3a isoform X15
MAP/microtubule affinity-regulating kinase 3a isoform X16
MAP/microtubule affinity-regulating kinase 3a, transcript variant X13
MAP/microtubule affinity-regulating kinase 3a, transcript variant X11
MAP/microtubule affinity-regulating kinase 3a isoform X11
tRNA methyltransferase 61A, transcript variant X1
tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61A isoform X1
tRNA methyltransferase 61A, transcript variant X2
tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61A isoform X2
uncharacterized LOC125483650, transcript variant X2
uncharacterized LOC125483650, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
BAG family molecular chaperone regulator 5
kinesin light chain 1a, transcript variant X2
kinesin light chain 1a, transcript variant X3
kinesin light chain 1a, transcript variant X1
kinesin light chain 1a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein phosphatase 1, regulatory subunit 13Bb
zinc finger, FYVE domain containing 21, transcript variant X1
zinc finger, FYVE domain containing 21, transcript variant X2
zinc finger FYVE domain-containing protein 21 isoform X2
zinc finger FYVE domain-containing protein 21 isoform X1
zinc finger, FYVE domain containing 21, transcript variant X3
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 6 samples with support for all annotated introns
apoptosis-stimulating of p53 protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
X-ray repair complementing defective repair in Chinese hamster cells 3, transcript variant X1
X-ray repair complementing defective repair in Chinese hamster cells 3, transcript variant X3
X-ray repair complementing defective repair in Chinese hamster cells 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: 60 kDa lysophospholipase-like
probable ATP-dependent RNA helicase spindle-E
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 6 long SRA reads, 4 Proteins, and 96% 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 91% 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 94% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125483753, transcript variant X2
uncharacterized LOC125483753, transcript variant X3
uncharacterized LOC125483753, transcript variant X1
uncharacterized LOC125483753, transcript variant X4
uncharacterized protein LOC125483753 isoform X1
uncharacterized protein LOC125483753 isoform X3
uncharacterized protein LOC125483753 isoform 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 9 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 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, 1 Protein, and 95% 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: 3 long SRA reads, 11 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
adenylosuccinate synthase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
adenylosuccinate synthetase isozyme 1 A isoform X1
adenylosuccinate synthase 1, transcript variant X2
adenylosuccinate synthetase isozyme 1 A isoform X2
RAC-alpha serine/threonine-protein kinase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger and BTB domain containing 42, transcript variant X8
zinc finger and BTB domain containing 42, transcript variant X9
zinc finger and BTB domain containing 42, transcript variant X1
zinc finger and BTB domain containing 42, transcript variant X2
zinc finger and BTB domain-containing protein 18.2 isoform X1
zinc finger and BTB domain-containing protein 18.2 isoform X2
zinc finger and BTB domain containing 42, transcript variant X3
zinc finger and BTB domain containing 42, transcript variant X5
zinc finger and BTB domain containing 42, transcript variant X4
zinc finger and BTB domain containing 42, transcript variant X6
zinc finger and BTB domain containing 42, transcript variant X7
zinc finger and BTB domain-containing protein 18.2 isoform X3
centrosomal protein 170Bb, transcript variant X1
centrosomal protein 170Bb, transcript variant X2
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 1 sample with support for all annotated introns
centrosomal protein 170Bb, transcript variant X8
centrosomal protein 170Bb, transcript variant X7
centrosomal protein of 170 kDa protein B isoform X1
centrosomal protein of 170 kDa protein B isoform X2
centrosomal protein of 170 kDa protein B isoform X5
centrosomal protein of 170 kDa protein B isoform X4
centrosomal protein 170Bb, transcript variant X4
centrosomal protein 170Bb, transcript variant X3
centrosomal protein 170Bb, transcript variant X6
centrosomal protein 170Bb, transcript variant X5
centrosomal protein of 170 kDa protein B isoform X3
5'-3' exonuclease PLD3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 15 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
5'-3' exonuclease PLD3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein AHNAK2-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
protein AHNAK2-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
SERTA domain-containing protein 2-like, 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 6 samples with support for all annotated introns
SERTA domain-containing protein 2-like, transcript variant X2
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 4 samples with support for all annotated introns
cell division cycle associated 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 116 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
cell division cycle associated 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
cell division cycle associated 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cell division cycle-associated protein 4 isoform X3
cell division cycle-associated protein 4 isoform X1
cell division cycle-associated protein 4 isoform X2
valosin containing protein lysine (K) methyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 17 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein-lysine methyltransferase METTL21D
L-2-hydroxyglutarate dehydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
distal membrane arm assembly component 2 like, transcript variant X2
distal membrane arm assembly component 2 like, transcript variant X3
distal membrane arm assembly component 2 like, transcript variant X1
L-2-hydroxyglutarate dehydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 91% 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, 41 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 long SRA reads, 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
cyclin-dependent kinase-like 1 (CDC2-related kinase)
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 1 sample with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 5 isoform X2
mitogen-activated protein kinase kinase kinase kinase 5 isoform X1
salvador family WW domain containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
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
phosphorylase, glycogen, liver, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 87 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
phosphorylase, glycogen, liver, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
phosphorylase, glycogen, liver, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
glycogen phosphorylase, liver form isoform X3
glycogen phosphorylase, liver form isoform X2
glycogen phosphorylase, liver form isoform X1
uncharacterized LOC125483726, transcript variant X2
uncharacterized LOC125483726, transcript variant X1
uncharacterized LOC125483726, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin-related transmembrane protein 1, transcript variant X2
thioredoxin-related transmembrane protein 1, transcript variant X1
thioredoxin-related transmembrane protein 1 isoform X2
thioredoxin-related transmembrane protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 14 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, transcript variant X2
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, transcript variant X1
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2
RNA transcription, translation and transport factor
RNA transcription, translation and transport factor protein
nidogen 2a (osteonidogen), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nidogen 2a (osteonidogen), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nidogen 2a (osteonidogen), 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
nidogen 2a (osteonidogen), transcript variant X5
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 5 samples with support for all annotated introns
nidogen 2a (osteonidogen), transcript variant X2
nidogen 2a (osteonidogen), transcript variant X1
uncharacterized protein nid2a isoform X2
uncharacterized protein nid2a isoform X1
prostaglandin E receptor 2a (subtype EP2)
thioredoxin domain-containing protein 16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 54% 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: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin domain-containing protein 16
glucosamine-phosphate N-acetyltransferase 1, transcript variant X1
glucosamine 6-phosphate N-acetyltransferase isoform X1
glucosamine-phosphate N-acetyltransferase 1, transcript variant X2
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 10 samples with support for all annotated introns
glucosamine 6-phosphate N-acetyltransferase 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 17 samples with support for all annotated introns
serine/threonine/tyrosine interacting protein, 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 6 samples with support for all annotated introns
serine/threonine/tyrosine-interacting protein isoform X2
serine/threonine/tyrosine interacting protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
serine/threonine/tyrosine-interacting protein isoform X1
serine/threonine/tyrosine interacting protein, transcript variant X3
serine/threonine/tyrosine interacting protein, transcript variant X5
serine/threonine/tyrosine interacting protein, 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 6 samples with support for all annotated introns
serine/threonine/tyrosine-interacting protein isoform X3
G protein-coupled receptor 137c, transcript variant X1
G protein-coupled receptor 137c, transcript variant X2
integral membrane protein GPR137C isoform X2
integral membrane protein GPR137C isoform X1
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 8 samples with support for all annotated introns
FERM domain containing kindlin 2, transcript variant X5
FERM domain containing kindlin 2, transcript variant X4
FERM domain containing kindlin 2, transcript variant X3
FERM domain containing kindlin 2, transcript variant X1
FERM domain containing kindlin 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125483629, transcript variant X1
uncharacterized LOC125483629, transcript variant X2
bone morphogenetic protein 4, 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 6 samples with support for all annotated introns
bone morphogenetic protein 4, transcript variant X3
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 2 samples with support for all annotated introns
bone morphogenetic protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
cyclin-dependent kinase inhibitor 3, transcript variant X2
cyclin-dependent kinase inhibitor 3, transcript variant X1
cyclin-dependent kinase inhibitor 3 isoform X1
cyclin-dependent kinase inhibitor 3 isoform X2
cornichon family AMPA receptor auxiliary protein 1
sterile alpha motif domain containing 4A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 17 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: 9 long SRA reads, 56 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
WD repeat and HMG-box DNA-binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
WD repeat and HMG-box DNA-binding protein 1-like, transcript variant X1
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 4 samples with support for all annotated introns
WD repeat and HMG-box DNA-binding protein 1-like, transcript variant X2
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 7 samples with support for all annotated introns
WD repeat and HMG-box DNA-binding protein 1-like isoform X1
WD repeat and HMG-box DNA-binding protein 1-like isoform X2
glia maturation factor beta, transcript variant X3
glia maturation factor beta, transcript variant X1
glia maturation factor beta, transcript variant X2
glia maturation factor beta, transcript variant X4
cell growth regulator with ring finger domain 1
cell growth regulator with RING finger domain protein 1
organic solute transporter subunit alpha-like
lectin, galactoside binding soluble 3b, transcript variant X2
lectin, galactoside binding soluble 3b, transcript variant X1
lectin, galactoside binding soluble 3b, transcript variant X3
F-box only protein 34, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
F-box only protein 34, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
F-box only protein 34, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 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
F-box only protein 34, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
F-box only protein 34, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 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
F-box only protein 34, transcript variant X2
F-box only protein 34, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125483657, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125483657, transcript variant X2
beclin 1-associated autophagy-related key regulator
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 5 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, 3 Proteins, and 100% 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: 5 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
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 17 samples with support for all annotated introns
E3 ubiquitin-protein ligase pellino homolog 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
adaptor related protein complex 5 subunit mu 1, transcript variant X1
adaptor related protein complex 5 subunit mu 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 30, NatC catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 19 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
armadillo like helical domain containing 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
armadillo-like helical domain-containing protein 4
F-box/WD repeat-containing protein 7-like
uncharacterized LOC125483761, transcript variant X4
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 LOC125483761, transcript variant X5
uncharacterized LOC125483761, transcript variant X6
uncharacterized LOC125483761, transcript variant X3
uncharacterized LOC125483761, transcript variant X1
uncharacterized LOC125483761, transcript variant X2
AT rich interactive domain 4A (RBP1-like), transcript variant X1
AT rich interactive domain 4A (RBP1-like), transcript variant X2
AT-rich interactive domain-containing protein 4A
mitochondrial import receptor subunit TOM20 homolog
translocase of inner mitochondrial membrane 9 homolog, transcript variant X3
translocase of inner mitochondrial membrane 9 homolog, transcript variant X1
translocase of inner mitochondrial membrane 9 homolog, transcript variant X2
mitochondrial import inner membrane translocase subunit Tim9
protein TALPID3-like, 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
protein TALPID3-like, transcript variant X3
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
protein TALPID3-like, 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 11 samples with support for all annotated introns
protein TALPID3-like, 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 7 samples with support for all annotated introns
protein TALPID3-like, transcript variant X2
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 11 samples with support for all annotated introns
interferon regulatory factor 2 binding protein-like
probable E3 ubiquitin-protein ligase IRF2BPL
KIAA0586 ortholog, transcript variant X2
KIAA0586 ortholog, transcript variant X3
KIAA0586 ortholog, transcript variant X1
KIAA0586 ortholog, transcript variant X4
KIAA0586 ortholog, transcript variant X5
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
dishevelled-binding antagonist of beta-catenin 1
potassium channel subfamily K member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
dishevelled associated activator of morphogenesis 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 15 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
disheveled-associated activator of morphogenesis 1
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
trans-L-3-hydroxyproline dehydratase, transcript variant X1
trans-L-3-hydroxyproline dehydratase, transcript variant X2
trans-L-3-hydroxyproline dehydratase isoform X1
trans-L-3-hydroxyproline dehydratase isoform X2
jnk1/mapk8 associated membrane protein, transcript variant X2
JNK1/MAPK8-associated membrane protein isoform X2
jnk1/mapk8 associated membrane protein, transcript variant X1
JNK1/MAPK8-associated membrane protein isoform X1
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
coiled-coil domain-containing protein 175
leucine rich repeat and fibronectin type III domain containing 5a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat and fibronectin type-III domain-containing protein 5
gem (nuclear organelle) associated protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
gem (nuclear organelle) associated protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
gem (nuclear organelle) associated protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
trafficking protein particle complex subunit 6B, transcript variant X4
trafficking protein particle complex subunit 6B, transcript variant X1
trafficking protein particle complex subunit 6B, transcript variant X2
trafficking protein particle complex subunit 6B, 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 4 samples with support for all annotated introns
trafficking protein particle complex subunit 6b isoform X1
trafficking protein particle complex subunit 6b isoform X4
trafficking protein particle complex subunit 6b isoform X2
trafficking protein particle complex subunit 6b isoform X3
F-box only protein 33, transcript variant X1
F-box only protein 33, transcript variant X2
CTAGE family, member 5, transcript variant X1
CTAGE family, member 5, transcript variant X2
transport and Golgi organization protein 1 homolog
family with sequence similarity 177 member A1
protein phosphatase 2, regulatory subunit B'', gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit gamma
mitochondrial ribonuclease P catalytic subunit
proteasome 20S subunit alpha 6a, transcript variant X2
proteasome 20S subunit alpha 6a, transcript variant X1
proteasome subunit alpha type-6a isoform X1
proteasome subunit alpha type-6a isoform X2
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha b
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
ral GTPase-activating protein subunit alpha-1-like, transcript variant X1
ral GTPase-activating protein subunit alpha-1-like isoform X1
ral GTPase-activating protein subunit alpha-1-like, transcript variant X4
ral GTPase-activating protein subunit alpha-1-like, transcript variant X3
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 11 samples with support for all annotated introns
ral GTPase-activating protein subunit alpha-1-like, 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 3 samples with support for all annotated introns
ral GTPase-activating protein subunit alpha-1-like, transcript variant X2
ral GTPase-activating protein subunit alpha-1-like isoform X2
ral GTPase-activating protein subunit alpha-1-like, transcript variant X6
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 6 samples with support for all annotated introns
ral GTPase-activating protein subunit alpha-1-like isoform X3
ral GTPase-activating protein subunit alpha-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments
breast cancer metastasis-suppressor 1-like protein-A
MAP3K12 binding inhibitory protein 1, transcript variant X2
MAP3K12 binding inhibitory protein 1, transcript variant X1
MAP3K12 binding inhibitory protein 1, transcript variant X3
MAP3K12-binding inhibitory protein 1 isoform X2
MAP3K12-binding inhibitory protein 1 isoform X3
MAP3K12-binding inhibitory protein 1 isoform X1
uncharacterized LOC125483644, transcript variant X2
uncharacterized LOC125483644, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NK2 transcription factor related, locus 9 (Drosophila)
NK2 transcription factor related, locus 9
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 25 member 21, transcript variant X1
solute carrier family 25 member 21, transcript variant X2
mitochondrial 2-oxodicarboxylate carrier isoform X2
mitochondrial 2-oxodicarboxylate carrier isoform X1
mirror-image polydactyly 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mirror-image polydactyly 1, 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 1 sample with support for all annotated introns
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
hepatocyte nuclear factor 3-alpha isoform X2
hepatocyte nuclear factor 3-alpha isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 201-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Sec23 homolog A, coat complex II component
signal recognition particle 54, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 long SRA reads, 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
signal recognition particle 54, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 long SRA reads, 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
signal recognition particle 54 kDa protein
bromodomain adjacent to zinc finger domain protein 1A-like
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 11 samples with support for all annotated introns
bromodomain adjacent to zinc finger domain, 1A
bromodomain adjacent to zinc finger domain protein 1A
cofilin 2 (muscle), transcript variant X1
cofilin 2 (muscle), transcript variant X2
serine palmitoyltransferase, small subunit A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
serine palmitoyltransferase small subunit A
egl-9 family hypoxia-inducible factor 3, transcript variant X1
egl-9 family hypoxia-inducible factor 3, transcript variant X2
egl-9 family hypoxia-inducible factor 3, transcript variant X3
neuronal PAS domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% 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 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 15 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
HEAT repeat-containing protein 5A-like, transcript variant X5
HEAT repeat-containing protein 5A-like, transcript variant X2
HEAT repeat-containing protein 5A-like, transcript variant X4
HEAT repeat-containing protein 5A-like, transcript variant X1
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 9 samples with support for all annotated introns
HEAT repeat-containing protein 5A-like, transcript variant X6
HEAT repeat-containing protein 5A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
trihelix transcription factor GT-3a-like
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 11 samples with support for all annotated introns
nucleotide binding protein-like, transcript variant X2
nucleotide binding protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 76% 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 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
adaptor related protein complex 4 subunit sigma 1, transcript variant X1
adaptor related protein complex 4 subunit sigma 1, transcript variant X2
striatin, calmodulin binding protein 3, transcript variant X3
striatin, calmodulin binding protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
striatin, calmodulin binding protein 3, transcript variant X4
striatin, calmodulin binding protein 3, transcript variant X1
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 4 samples with support for all annotated introns
striatin, calmodulin binding protein 3, 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 4 samples with support for all annotated introns
striatin, calmodulin binding protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
striatin, calmodulin binding protein 3, transcript variant X6
coagulation factor C homolog, cochlin (Limulus polyphemus), transcript variant X2
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 1 sample with support for all annotated introns
coagulation factor C homolog, cochlin (Limulus polyphemus), 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 29 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
G2/M-phase specific E3 ubiquitin protein ligase, transcript variant X2
G2/M-phase specific E3 ubiquitin protein ligase, transcript variant X1
G2/M-phase specific E3 ubiquitin protein ligase, transcript variant X3
G2/M-phase specific E3 ubiquitin protein ligase, transcript variant X4
G2/M phase-specific E3 ubiquitin-protein ligase isoform X2
G2/M phase-specific E3 ubiquitin-protein ligase isoform X1
G2/M phase-specific E3 ubiquitin-protein ligase isoform X3
protein kinase D1, transcript variant X1
protein kinase D1, transcript variant X2
serine/threonine-protein kinase D1 isoform X1
serine/threonine-protein kinase D1 isoform X2
protein kinase D1, transcript variant X3
serine/threonine-protein kinase D1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
RNA-binding protein Nova-1, transcript variant X3
RNA-binding protein Nova-1, transcript variant X4
RNA-binding protein Nova-1, transcript variant X2
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
RNA-binding protein Nova-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
actin, alpha cardiac muscle 1-like, transcript variant X2
actin, alpha cardiac muscle 1-like, transcript variant X1
aquarius intron-binding spliceosomal factor
diphthamine biosynthesis 6, transcript variant X1
diphthamine biosynthesis 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 95% 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: 1 long SRA read, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125483620, transcript variant X2
uncharacterized LOC125483620, transcript variant X3
uncharacterized LOC125483620, transcript variant X1
CDAN1 interacting nuclease 1, transcript variant X1
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 6 samples with support for all annotated introns
CDAN1 interacting nuclease 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 5 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: 5 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
sprouty related EVH1 domain containing 1
sprouty-related, EVH1 domain-containing protein 1
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
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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 39 Proteins, 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: 6 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 92% 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: 87 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 64% 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 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: 50 Proteins
uncharacterized protein LOC571819 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ER membrane protein complex subunit 7b, transcript variant X2
ER membrane protein complex subunit 7b, transcript variant X1
ER membrane protein complex subunit 7 isoform X2
ER membrane protein complex subunit 7 isoform X1
katanin p80 subunit B-like 1, transcript variant X3
katanin p80 subunit B-like 1, transcript variant X6
katanin p80 subunit B-like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
katanin p80 subunit B-like 1, transcript variant X2
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
katanin p80 subunit B-like 1, transcript variant X4
katanin p80 subunit B-like 1, transcript variant X5
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 4 samples with support for all annotated introns
fibrous sheath interacting protein 1, transcript variant X9
fibrous sheath interacting protein 1, transcript variant X4
fibrous sheath interacting protein 1, transcript variant X8
fibrous sheath interacting protein 1, transcript variant X3
fibrous sheath interacting protein 1, transcript variant X2
fibrous sheath interacting protein 1, 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 4 samples with support for all annotated introns
fibrous sheath interacting protein 1, transcript variant X5
fibrous sheath-interacting protein 1 isoform X2
fibrous sheath-interacting protein 1 isoform X1
fibrous sheath-interacting protein 1 isoform X5
fibrous sheath interacting protein 1, transcript variant X7
fibrous sheath-interacting protein 1 isoform X4
fibrous sheath interacting protein 1, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
fibrous sheath interacting protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fibrous sheath interacting protein 1, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibrous sheath-interacting protein 1 isoform X6
fibrous sheath-interacting protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, 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: 13 Proteins
eukaryotic translation initiation factor 2, subunit 1 alpha b
eukaryotic translation initiation factor 2 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger FYVE domain-containing protein 26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
vesicle transport through interaction with t-SNAREs 1B
vesicle transport through interaction with t-SNAREs homolog 1B
protein associated with LIN7 1, MAGUK p55 family member a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% 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: 5 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC109917769, transcript variant X1
uncharacterized LOC109917769, 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 5 samples with support for all annotated introns
myc associated factor X, transcript variant X1
myc associated factor X, transcript variant X2
farnesyltransferase, CAAX box, beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 long SRA reads, 17 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
farnesyltransferase, CAAX box, beta, transcript variant X1
protein farnesyltransferase subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 30 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
spectrin beta chain, non-erythrocytic 1-like
cysteine-rich motor neuron 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 long SRA reads, 43 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125481054, transcript variant X4
uncharacterized LOC125481054, transcript variant X3
uncharacterized LOC125481054, transcript variant X2
uncharacterized LOC125481054, transcript variant X1
serine/arginine-rich splicing factor 5-like, transcript variant X2
serine/arginine-rich splicing factor 5-like, transcript variant X1
serine/arginine-rich splicing factor 5-like
serine/arginine-rich splicing factor 5-like isoform X1
serine/arginine-rich splicing factor 5-like, transcript variant X3
serine/arginine-rich splicing factor 5-like isoform X2
serine/arginine-rich splicing factor 5, transcript variant X4
serine/arginine-rich splicing factor 5, transcript variant X2
serine/arginine-rich splicing factor 5, transcript variant X3
serine/arginine-rich splicing factor 5, transcript variant X1
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
SPARC related modular calcium binding 1, transcript variant X1
SPARC related modular calcium binding 1, transcript variant X2
SPARC related modular calcium binding 1, transcript variant X4
SPARC related modular calcium binding 1, transcript variant X3
SPARC related modular calcium binding 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
SPARC-related modular calcium-binding protein 1 isoform X1
SPARC-related modular calcium-binding protein 1 isoform X2
SPARC-related modular calcium-binding protein 1 isoform X4
SPARC-related modular calcium-binding protein 1 isoform X3
SPARC-related modular calcium-binding protein 1 isoform X5
transfer RNA glutamine (anticodon CUG); 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: 17 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
peroxisomal N(1)-acetyl-spermine/spermidine oxidase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 6
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 9 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 28 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 28 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 28 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 28 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 11-like
signal-induced proliferation-associated 1 like 1, transcript variant X4
signal-induced proliferation-associated 1 like 1, transcript variant X2
signal-induced proliferation-associated 1 like 1, transcript variant X7
signal-induced proliferation-associated 1 like 1, transcript variant X6
signal-induced proliferation-associated 1 like 1, transcript variant X5
signal-induced proliferation-associated 1 like 1, transcript variant X1
signal-induced proliferation-associated 1 like 1, transcript variant X10
signal-induced proliferation-associated 1 like 1, transcript variant X8
signal-induced proliferation-associated 1 like 1, transcript variant X3
signal-induced proliferation-associated 1 like 1, transcript variant X9
signal-induced proliferation-associated 1-like protein 1 isoform X1
signal-induced proliferation-associated 1-like protein 1 isoform X2
regulator of G-protein signaling 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
regulator of G-protein signaling 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
regulator of G-protein signaling 6-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
regulator of G-protein signaling 6-like isoform X2
regulator of G-protein signaling 6-like isoform X1
regulator of G-protein signaling 6-like isoform X3
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
C-type lectin domain family 18 member A-like
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
protein phosphatase 1 regulatory inhibitor subunit 14D
protein phosphatase 1 regulatory subunit 14C
kunitz-type protease inhibitor 1, 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 10 samples with support for all annotated introns
kunitz-type protease inhibitor 1, transcript variant X1
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, including 10 samples with support for all annotated introns
kunitz-type protease inhibitor 1 isoform X1
kunitz-type protease inhibitor 1 isoform X2
signal recognition particle 14 kDa protein
pleckstrin homology domain-containing family G member 3-like
BUB1 mitotic checkpoint serine/threonine kinase Bb
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, including 5 samples with support for all annotated introns
mitotic checkpoint serine/threonine-protein kinase BUB1 beta
BUB1 mitotic checkpoint serine/threonine kinase Ba
coiled-coil domain-containing protein 177
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
exonuclease 3'-5' domain containing 2, transcript variant X2
exonuclease 3'-5' domain containing 2, transcript variant X4
exonuclease 3'-5' domain containing 2, transcript variant X3
exonuclease 3'-5' domain containing 2, transcript variant X5
exonuclease 3'-5' domain containing 2, transcript variant X1
exonuclease 3'-5' domain-containing protein 2 isoform X2
exonuclease 3'-5' domain-containing protein 2 isoform X1
uncharacterized LOC125483691, transcript variant X2
uncharacterized LOC125483691, transcript variant X1
phosphofurin acidic cluster sorting protein 2
homeodomain-interacting protein kinase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
phosphofurin acidic cluster sorting protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% 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: 2 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
RNA polymerase II associated protein 1, transcript variant X3
RNA polymerase II associated protein 1, transcript variant X5
RNA polymerase II associated protein 1, transcript variant X2
RNA polymerase II associated protein 1, transcript variant X1
RNA polymerase II associated protein 1, transcript variant X4
RNA polymerase II-associated protein 1 isoform X1
RNA polymerase II-associated protein 1 isoform X3
RNA polymerase II-associated protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
bromo adjacent homology domain containing 1, transcript variant X3
bromo adjacent homology domain containing 1, transcript variant X5
bromo adjacent homology domain containing 1, transcript variant X1
bromo adjacent homology domain containing 1, transcript variant X6
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 5 samples with support for all annotated introns
bromo adjacent homology domain containing 1, transcript variant X2
bromo adjacent homology domain containing 1, transcript variant X4
bromo adjacent homology domain-containing 1 protein isoform X1
bromo adjacent homology domain-containing 1 protein isoform X2
bromo adjacent homology domain-containing 1 protein isoform X3
uncharacterized LOC125483703, transcript variant X2
uncharacterized LOC125483703, transcript variant X1
MAX dimerization protein MGA a, transcript variant X1
MAX dimerization protein MGA a, transcript variant X4
MAX dimerization protein MGA a, transcript variant X3
MAX dimerization protein MGA a, transcript variant X2
MAX dimerization protein MGA a isoform X1
MAX dimerization protein MGA a isoform X3
MAX dimerization protein MGA a isoform X2
mitogen-activated protein kinase binding protein 1
mitogen-activated protein kinase-binding protein 1
bifunctional peptidase and (3S)-lysyl hydroxylase JMJD7
isovaleryl-CoA dehydrogenase, transcript variant X1
isovaleryl-CoA dehydrogenase, mitochondrial isoform X1
isovaleryl-CoA dehydrogenase, transcript variant X3
isovaleryl-CoA dehydrogenase, transcript variant X2
isovaleryl-CoA dehydrogenase, mitochondrial isoform X2
isovaleryl-CoA dehydrogenase, mitochondrial isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol glycan anchor biosynthesis, class H, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis, class H, transcript variant X2
phosphatidylinositol N-acetylglucosaminyltransferase subunit H isoform X1
phosphatidylinositol N-acetylglucosaminyltransferase subunit H isoform X2
pleckstrin homology domain containing, family H (with MyTH4 domain) member 1
pleckstrin homology domain-containing family H member 1
zinc finger protein 36, C3H type-like 1a, transcript variant X3
zinc finger protein 36, C3H type-like 1a, transcript variant X1
mRNA decay activator protein ZFP36L1a isoform X1
zinc finger protein 36, C3H type-like 1a, transcript variant X2
mRNA decay activator protein ZFP36L1a isoform X2
mRNA decay activator protein ZFP36L1a isoform X3
DNA repair protein RAD51 homolog 2 isoform X1
DNA repair protein RAD51 homolog 2 isoform X4
DNA repair protein RAD51 homolog 2 isoform X3
DNA repair protein RAD51 homolog 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
metastasis-associated protein MTA1-like, transcript variant X1
metastasis-associated protein MTA1-like isoform X1
metastasis-associated protein MTA1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
metastasis-associated protein MTA1-like isoform X3
metastasis-associated protein MTA1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
metastasis-associated protein MTA1-like isoform X4
metastasis-associated protein MTA1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
metastasis-associated protein MTA1-like isoform X2
coiled-coil domain containing 135, transcript variant X1
coiled-coil domain containing 135, transcript variant X2
coiled-coil domain containing 135, transcript variant X3
dynein regulatory complex subunit 7 isoform X1
dynein regulatory complex subunit 7 isoform X2
dynein regulatory complex subunit 7 isoform X3
kinetochore localized astrin (SPAG5) binding protein, transcript variant X1
kinetochore localized astrin (SPAG5) binding protein, transcript variant X2
kinetochore localized astrin (SPAG5) binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 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
DnaJ (Hsp40) homolog, subfamily C, member 17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 8 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109912712, transcript variant X1
uncharacterized LOC109912712, transcript variant X2
regulator of microtubule dynamics protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
abscission/NoCut checkpoint regulator-like, transcript variant X1
abscission/NoCut checkpoint regulator-like, transcript variant X2
abscission/NoCut checkpoint regulator-like isoform X1
abscission/NoCut checkpoint regulator-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
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: 7 Proteins
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
neutral alpha-glucosidase C-like, transcript variant X3
neutral alpha-glucosidase C-like, transcript variant X2
neutral alpha-glucosidase C-like, transcript variant X1
neutral alpha-glucosidase C-like, transcript variant X4
neutral alpha-glucosidase C-like, transcript variant X5
neutral alpha-glucosidase C-like isoform X1
neutral alpha-glucosidase C-like isoform X2
neutral alpha-glucosidase C-like isoform X3
neutral alpha-glucosidase C-like, 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 5 samples with support for all annotated introns
neutral alpha-glucosidase C-like isoform X4
transmembrane protein 87A, transcript variant X1
transmembrane protein 87A, transcript variant X2
transmembrane protein 87A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 172 long SRA reads, 5 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: 7 long SRA reads, 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 2 alpha kinase 4
RNA pseudouridine synthase domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
RNA pseudouridylate synthase domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
coiled-coil domain-containing protein 32
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ChaC, cation transport regulator homolog 1 (E. coli)
glutathione-specific gamma-glutamylcyclotransferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase PAK 4-like, transcript variant X1
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 3 samples with support for all annotated introns
serine/threonine-protein kinase PAK 4-like, transcript variant X2
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
serine/threonine-protein kinase PAK 4-like isoform X1
serine/threonine-protein kinase PAK 4-like isoform X2
opa interacting protein 5, transcript variant X3
opa interacting protein 5, transcript variant X2
opa interacting protein 5, transcript variant X1
nucleolar and spindle associated protein 1
nucleolar and spindle-associated protein 1
NADH:ubiquinone oxidoreductase complex assembly factor 1
complex I intermediate-associated protein 30, mitochondrial
RTF1 homolog, Paf1/RNA polymerase II complex component
RNA polymerase-associated protein RTF1 homolog
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
synaptosomal-associated protein 23-like, transcript variant X1
synaptosomal-associated protein 23-like isoform X1
synaptosomal-associated protein 23-like, transcript variant X2
synaptosomal-associated protein 23-like isoform X2
leucine rich repeat containing 57, transcript variant X1
leucine rich repeat containing 57, transcript variant X2
leucine-rich repeat-containing protein 57
HAUS augmin like complex subunit 2, transcript variant X2
HAUS augmin like complex subunit 2, transcript variant X1
VPS18 core subunit of CORVET and HOPS complexes
vacuolar protein sorting-associated protein 18 homolog
cysteine-rich protein 2-like, transcript variant X2
cysteine-rich protein 2-like, transcript variant X3
cysteine-rich protein 2-like, transcript variant X1
coiled-coil domain-containing protein 9-like, transcript variant X2
coiled-coil domain-containing protein 9-like, transcript variant X1
coiled-coil domain-containing protein 9-like isoform X2
coiled-coil domain-containing protein 9-like isoform X1
coiled-coil domain-containing protein 9B-like
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
pleckstrin homology domain containing, family D (with coiled-coil domains) member 1
pleckstrin homology domain-containing family D member 1
polypeptide N-acetylgalactosaminyltransferase 16-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 16-like isoform X1
polypeptide N-acetylgalactosaminyltransferase 16-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 16-like isoform X2
dynein, axonemal, light chain 1, transcript variant X2
dynein, axonemal, light chain 1, transcript variant X1
dynein axonemal light chain 1 isoform X2
dynein axonemal light chain 1 isoform X1
mitotic deacetylase associated SANT domain protein b, transcript variant X3
mitotic deacetylase associated SANT domain protein b, transcript variant X1
mitotic deacetylase associated SANT domain protein b, transcript variant X2
mitotic deacetylase-associated SANT domain protein isoform X2
mitotic deacetylase-associated SANT domain protein isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
prostaglandin reductase 2, transcript variant X2
prostaglandin reductase 2, transcript variant X5
prostaglandin reductase 2, transcript variant X8
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 8 samples with support for all annotated introns
prostaglandin reductase 2, transcript variant X1
prostaglandin reductase 2, transcript variant X4
prostaglandin reductase 2, transcript variant X3
prostaglandin reductase 2, transcript variant X6
prostaglandin reductase 2, transcript variant X7
ubiquitin protein ligase E3 component n-recognin 1
photoreceptor outer segment membrane glycoprotein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 3 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: 14 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
StAR-related lipid transfer (START) domain containing 9
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
BRD4-interacting chromatin-remodeling complex-associated protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
BRD4-interacting chromatin-remodeling complex-associated protein-like isoform X1
BRD4-interacting chromatin-remodeling complex-associated protein-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 3 samples with support for all annotated introns
BRD4-interacting chromatin-remodeling complex-associated protein-like isoform X2
NUMB endocytic adaptor protein, transcript variant X2
NUMB endocytic adaptor protein, transcript variant X6
NUMB endocytic adaptor protein, transcript variant X1
NUMB endocytic adaptor protein, transcript variant X4
NUMB endocytic adaptor protein, transcript variant X3
NUMB endocytic adaptor protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 80% 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 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
double PHD fingers 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
double PHD fingers 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
double PHD fingers 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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
WD repeat domain 21, transcript variant X1
WD repeat domain 21, transcript variant X7
WD repeat domain 21, transcript variant X8
WD repeat domain 21, transcript variant X6
WD repeat domain 21, transcript variant X3
WD repeat domain 21, transcript variant X2
WD repeat domain 21, transcript variant X5
WD repeat domain 21, transcript variant X4
zinc finger FYVE domain-containing protein 1
RNA binding motif protein 25b, transcript variant X1
RNA binding motif protein 25b, transcript variant X2
RNA binding motif protein 25b, transcript variant X3
zinc finger FYVE domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 436-like, transcript variant X2
zinc finger protein 436-like, transcript variant X1
gastrula zinc finger protein XlCGF17.1-like, transcript variant X4
gastrula zinc finger protein XlCGF17.1-like, transcript variant X1
gastrula zinc finger protein XlCGF17.1-like, transcript variant X2
gastrula zinc finger protein XlCGF17.1-like, transcript variant X3
gastrula zinc finger protein XlCGF17.1-like
zinc finger protein 239-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger protein 239-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
gastrula zinc finger protein XlCGF7.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125483651, transcript variant X2
uncharacterized LOC125483651, transcript variant X1
transfer RNA alanine (anticodon UGC); 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
zinc finger protein 239-like, 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 5 samples with support for all annotated introns
zinc finger protein 239-like, transcript variant X3
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 6 samples with support for all annotated introns
zinc finger protein 239-like, 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 6 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 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
transfer RNA valine (anticodon GAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
gastrula zinc finger protein XlCGF71.1-like
transfer RNA asparagine (anticodon AUU); 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 Proteins, and 16% 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 20 samples with support for all annotated introns
uncharacterized LOC109929207, transcript variant X1
uncharacterized LOC109929207, transcript variant X3
uncharacterized LOC109929207, transcript variant X2
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 10 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, and 77% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC109928957, transcript variant X1
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 19 samples with support for all annotated introns
uncharacterized LOC109928957, transcript variant X2
uncharacterized LOC109928957, 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 2 samples with support for all annotated introns
uncharacterized LOC109928957, transcript variant X4
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 4 samples with support for all annotated introns
zinc finger protein 664-like, transcript variant X3
zinc finger protein 664-like, transcript variant X1
zinc finger protein 664-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125483681, transcript variant X3
uncharacterized LOC125483681, 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 12 samples with support for all annotated introns
uncharacterized LOC125483681, transcript variant X2
transfer RNA cysteine (anticodon ACA); 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: 1 long SRA read, and 33% 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: 1 Protein, and 14% 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 Protein, and 16% 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 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
oocyte zinc finger protein XlCOF6.1-like
LOW QUALITY PROTEIN: probable G-protein coupled receptor 139
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
putative zinc finger protein 66, transcript variant X3
putative zinc finger protein 66, transcript variant X2
putative zinc finger protein 66, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 623-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zinc finger protein 623-like, transcript variant X5
zinc finger protein 623-like, transcript variant X4
zinc finger protein 623-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 623-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
prolactin-releasing peptide receptor-like
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 15 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 77% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon ACU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125483842, 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 14 samples with support for all annotated introns
uncharacterized LOC125483849, transcript variant X4
uncharacterized LOC125483849, transcript variant X5
uncharacterized LOC125483849, transcript variant X2
uncharacterized LOC125483849, transcript variant X3
uncharacterized LOC125483849, transcript variant X1
uncharacterized LOC125483842, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC125483848, 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 20 samples with support for all annotated introns
uncharacterized LOC125483848, 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 10 samples with support for all annotated introns
uncharacterized LOC125483850, 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 13 samples with support for all annotated introns
uncharacterized LOC125483850, transcript variant X3
uncharacterized LOC125483850, transcript variant X1
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125483851, transcript variant X1
uncharacterized LOC125483851, transcript variant X2
uncharacterized LOC125483853, transcript variant X5
uncharacterized LOC125483853, transcript variant X2
uncharacterized LOC125483853, transcript variant X3
uncharacterized LOC125483853, transcript variant X1
uncharacterized LOC125483853, transcript variant X4
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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125483837, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC125483837, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC125483837, transcript variant X2
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 5 samples with support for all annotated introns
transfer RNA proline (anticodon AGG); 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: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
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 2 samples with support for all annotated introns
uncharacterized LOC125483860, transcript variant X2
uncharacterized LOC125483860, 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 11 samples with support for all annotated introns
transfer RNA tryptophan (anticodon CCA); 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: 96% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
gastrula zinc finger protein XlCGF7.1-like, transcript variant X2
gastrula zinc finger protein XlCGF7.1-like, transcript variant X3
gastrula zinc finger protein XlCGF7.1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125483852, transcript variant X1
uncharacterized LOC125483852, transcript variant X2
uncharacterized LOC125483861, transcript variant X2
uncharacterized LOC125483861, transcript variant X1
uncharacterized LOC125483867, transcript variant X2
uncharacterized LOC125483867, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 83% 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: 29 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA opal suppressor (anticodon UCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC125483838, 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 8 samples with support for all annotated introns
uncharacterized LOC125483838, transcript variant X1
uncharacterized LOC125483838, transcript variant X4
uncharacterized LOC125483838, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 41% 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 16 samples with support for all annotated introns
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.