Rhincodon typus isolate 14 chromosome 13, 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\nCM038810.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase MECOM
uncharacterized LOC125484729, transcript variant X3
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized LOC125484729, transcript variant X1
uncharacterized LOC125484729, transcript variant X2
histone-lysine N-methyltransferase MECOM-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60% coverage of the annotated genomic feature by RNAseq alignments
EEF1A lysine methyltransferase 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
EEF1A lysine methyltransferase 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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
EEF1A lysine methyltransferase 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
EEF1A lysine methyltransferase 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 2 isoform X1
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adaptor 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
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
39S ribosomal protein L44, mitochondrial
arf-GAP domain and FG repeat-containing protein 1-like, 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
arf-GAP domain and FG repeat-containing protein 1-like, 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 16 samples with support for all annotated introns
arf-GAP domain and FG repeat-containing protein 1-like isoform X1
arf-GAP domain and FG repeat-containing protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 22 Proteins, and 99% 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: 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: 21 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
replication factor C (activator 1) 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
replication factor C (activator 1) 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 20 Proteins, 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: 97% 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
transmembrane protein 255B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 255B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: 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: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ras GTPase-activating protein 2
zinc finger and BTB domain containing 38, transcript variant X2
zinc finger and BTB domain containing 38, transcript variant X1
zinc finger and BTB domain containing 38, transcript variant X3
zinc finger and BTB domain-containing protein 38 isoform X1
zinc finger and BTB domain-containing protein 38 isoform X2
zinc finger and BTB domain containing 38, 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 6 samples with support for all annotated introns
zinc finger and BTB domain containing 38, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
F-box only protein 36, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
F-box only protein 36, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 15 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
F-box only protein 36, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIP12-like, transcript variant X1
E3 ubiquitin-protein ligase TRIP12-like, transcript variant X2
E3 ubiquitin-protein ligase TRIP12-like isoform X1
E3 ubiquitin-protein ligase TRIP12-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins
phosphotyrosine interaction domain containing 1
PTB-containing, cubilin and LRP1-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium-transporting ATPase subunit beta-3-like
transcription factor Dp-2, transcript variant X3
transcription factor Dp-2, transcript variant X5
transcription factor Dp-2, transcript variant X2
transcription factor Dp-2, transcript variant X1
transcription factor Dp-2, transcript variant X9
transcription factor Dp-2, transcript variant X6
transcription factor Dp-2, transcript variant X7
transcription factor Dp-2, transcript variant X4
transcription factor Dp-2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
serine/threonine-protein kinase ATR-like, transcript variant X1
serine/threonine-protein kinase ATR-like isoform X1
serine/threonine-protein kinase ATR-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase ATR-like isoform X2
progestin and adipoQ receptor family member 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel, subfamily C, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
short transient receptor potential channel 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 23 Proteins, and 98% 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: procollagen C-endopeptidase enhancer 2b
uncharacterized LOC125484661, transcript variant X1
uncharacterized LOC125484661, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins
U2 snRNP-associated SURP domain containing, transcript variant X1
U2 snRNP-associated SURP domain containing, transcript variant X2
U2 snRNP-associated SURP motif-containing protein isoform X1
U2 snRNP-associated SURP domain containing, transcript variant X3
U2 snRNP-associated SURP motif-containing protein isoform X2
carbohydrate (N-acetylglucosamine-6-O) sulfotransferase 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 80% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125484685, transcript variant X2
uncharacterized LOC125484685, transcript variant X1
divergent protein kinase domain 2Ab, transcript variant X1
divergent protein kinase domain 2Ab, transcript variant X5
divergent protein kinase domain 2Ab, transcript variant X3
divergent protein kinase domain 2Ab, transcript variant X2
divergent protein kinase domain 2Ab, transcript variant X4
divergent protein kinase domain 2Ab isoform X1
divergent protein kinase domain 2Ab isoform X2
divergent protein kinase domain 2Ab isoform X3
procollagen-lysine,2-oxoglutarate 5-dioxygenase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins
zic family member 1 (odd-paired homolog, Drosophila)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 81% 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: 53 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
carboxypeptidase B1 (tissue), transcript variant X1
carboxypeptidase B1 (tissue), transcript variant X2
carboxypeptidase B-like, transcript variant X2
carboxypeptidase B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 56 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: 38 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: carboxypeptidase B-like
transmembrane protein 145, 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
transmembrane protein 145, transcript variant X3
transmembrane protein 145, 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
HPS3 biogenesis of lysosomal organelles complex 2 subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane 4 L six family member 18, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane 4 L six family member 18, transcript variant X1
transmembrane 4 L6 family member 18 isoform X1
transmembrane 4 L6 family member 18 isoform X2
glutathione hydrolase-like YwrD proenzyme
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 85% 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 92% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
WW domain containing transcription regulator 1
WW domain-containing transcription regulator protein 1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TSC22 domain family 2, transcript variant X1
TSC22 domain family 2, transcript variant X2
TSC22 domain family protein 2 isoform X1
TSC22 domain family protein 2 isoform X2
stress-associated endoplasmic reticulum protein 1, transcript variant X3
stress-associated endoplasmic reticulum protein 1, transcript variant X4
stress-associated endoplasmic reticulum protein 1, transcript variant X2
stress-associated endoplasmic reticulum protein 1, transcript variant X1
stress-associated endoplasmic reticulum protein 1, transcript variant X5
stress-associated endoplasmic reticulum protein 1 isoform X1
stress-associated endoplasmic reticulum protein 1 isoform X2
eukaryotic translation initiation factor 2A, transcript variant X1
eukaryotic translation initiation factor 2A isoform X1
eukaryotic translation initiation factor 2A, transcript variant X2
eukaryotic translation initiation factor 2A isoform X2
eukaryotic translation initiation factor 2A, transcript variant X3
eukaryotic translation initiation factor 2A isoform X3
thioredoxin reductase-like selenoprotein T
MINDY family member 4B, 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 1 sample with support for all annotated introns
MINDY family member 4B, transcript variant X1
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
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B isoform X2
inactive ubiquitin carboxyl-terminal hydrolase MINDY-4B isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 12-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
P2Y purinoceptor 14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 20 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
P2Y purinoceptor 14-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 3 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, 4 Proteins, and 95% 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: 8 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: 23 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: P2Y purinoceptor 14-like
purinergic receptor P2Y13, transcript variant X1
purinergic receptor P2Y13, transcript variant X2
purinergic receptor P2Y12, transcript variant X2
purinergic receptor P2Y12, transcript variant X7
purinergic receptor P2Y12, transcript variant X1
purinergic receptor P2Y12, transcript variant X4
purinergic receptor P2Y12, transcript variant X3
purinergic receptor P2Y12, transcript variant X6
purinergic receptor P2Y12, transcript variant X5
purinergic receptor P2Y12, transcript variant X11
purinergic receptor P2Y12, transcript variant X8
purinergic receptor P2Y12, transcript variant X10
purinergic receptor P2Y12, transcript variant X9
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: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125484732, transcript variant X1
uncharacterized LOC125484732, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
succinate receptor 1-like, transcript variant X2
succinate receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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: 13 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
succinate receptor 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125484672, 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 2 samples with support for all annotated introns
uncharacterized LOC125484672, 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 3 samples with support for all annotated introns
muscleblind-like splicing regulator 1, transcript variant X3
muscleblind-like splicing regulator 1, transcript variant X1
muscleblind-like splicing regulator 1, transcript variant X2
muscleblind-like splicing regulator 1, transcript variant X4
muscleblind-like splicing regulator 1, transcript variant X5
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 10 samples with support for all annotated introns
P2Y purinoceptor 1-like, transcript variant X1
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 7 samples with support for all annotated introns
P2Y purinoceptor 1-like, transcript variant X2
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 2 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
rho guanine nucleotide exchange factor 26
DEAH (Asp-Glu-Ala-His) box polypeptide 36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
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
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
extracellular calcium-sensing receptor-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: extracellular calcium-sensing receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 190 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 165 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 153 Proteins
extracellular calcium-sensing receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
extracellular calcium-sensing receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
extracellular calcium-sensing receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 143 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
extracellular calcium-sensing receptor-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 153 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
extracellular calcium-sensing receptor-like isoform X1
extracellular calcium-sensing receptor-like isoform X2
extracellular calcium-sensing receptor-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
probable G-protein coupled receptor 160, transcript variant X1
probable G-protein coupled receptor 160, transcript variant X2
probable G-protein coupled receptor 160, transcript variant X5
probable G-protein coupled receptor 160, transcript variant X3
probable G-protein coupled receptor 160, transcript variant X4
uncharacterized protein LOC795037 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
SKI-like proto-oncogene a, transcript variant X1
SKI-like proto-oncogene a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 39% 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 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 175 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
SEC62 homolog, preprotein translocation factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 100% coverage of the annotated genomic feature by RNAseq alignments
sterile alpha motif domain-containing protein 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 167 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 164 Proteins
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins
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; substituted 1 base at 1 genomic stop 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: 16 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 168 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 174 Proteins
membrane-spanning 4-domains subfamily A member 4A-like, transcript variant X1
membrane-spanning 4-domains subfamily A member 4A-like, transcript variant X2
membrane-spanning 4-domains subfamily A member 4A-like isoform X1
uncharacterized protein LOC109928481 isoform X2
membrane-spanning 4-domains subfamily A member 8-like
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: 149 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
segment polarity protein dishevelled homolog DVL-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
translation initiation factor eIF-2B subunit epsilon
translation initiation factor eIF-2B subunit epsilon-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% 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: 2 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
interleukin-1 receptor accessory protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
fibroblast growth factor 12, transcript variant X2
fibroblast growth factor 12, transcript variant X1
interleukin-1 receptor accessory protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nucleotidyltransferase MB21D2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dynein light chain Tctex-type protein 2B
choline-phosphate cytidylyltransferase A
organic solute transporter subunit alpha-like
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
tumor necrosis factor ligand superfamily member 10-like, transcript variant X2
tumor necrosis factor ligand superfamily member 10-like, transcript variant X1
tumor necrosis factor ligand superfamily member 10-like isoform X1
tumor necrosis factor ligand superfamily member 10-like isoform X2
growth hormone secretagogue receptor a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
growth hormone secretagogue receptor a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fibronectin type III domain containing 3Ba
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 4 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 2 member 2, transcript variant X2
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 2 samples with support for all annotated introns
solute carrier family 2 member 2, transcript variant X1
solute carrier family 2, facilitated glucose transporter member 2 isoform X2
solute carrier family 2, facilitated glucose transporter member 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
eukaryotic translation initiation factor 5A-1, transcript variant X1
eukaryotic translation initiation factor 5A-1, transcript variant X2
eukaryotic translation initiation factor 5A-1, transcript variant X4
eukaryotic translation initiation factor 5A-1, transcript variant X3
eukaryotic translation initiation factor 5A-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
probable cationic amino acid transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
scavenger receptor cysteine-rich type 1 protein M130-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
scavenger receptor cysteine-rich type 1 protein M130-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 1 sample with support for all annotated introns
scavenger receptor cysteine-rich type 1 protein M130-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 2 samples with support for all annotated introns
deleted in malignant brain tumors 1 protein-like isoform X2
scavenger receptor cysteine-rich type 1 protein M130-like isoform X1
deleted in malignant brain tumors 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 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, 7 Proteins, and 62% 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
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 140 Proteins
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; 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: 61 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 146 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC109911545, transcript variant X1
uncharacterized LOC109911545, transcript variant X2
uncharacterized LOC109911545, transcript variant X3
ATP-binding cassette, sub-family F (GCN20), member 3, transcript variant X2
ATP-binding cassette, sub-family F (GCN20), member 3, transcript variant X1
ATP-binding cassette sub-family F member 3 isoform X2
ATP-binding cassette sub-family F member 3 isoform X1
coiled-coil domain containing 50a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
coiled-coil domain-containing protein 50 isoform X2
coiled-coil domain containing 50a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain containing 50a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
coiled-coil domain-containing protein 50 isoform X3
coiled-coil domain containing 50a, transcript variant X1
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
coiled-coil domain-containing protein 50 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 65% 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: 15 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
prolyl 3-hydroxylase 2, 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 10 samples with support for all annotated introns
prolyl 3-hydroxylase 2, transcript variant X4
prolyl 3-hydroxylase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
prolyl 3-hydroxylase 2, 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
tumor protein p63, transcript variant X1
tumor protein p63, transcript variant X2
tumor protein p63, transcript variant X3
tumor protein p63, transcript variant X5
tumor protein p63, transcript variant X4
tumor protein p63, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor protein p63-regulated gene 1-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC109915896, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC109915896, transcript variant X2
uncharacterized LOC109915896, transcript variant X3
uncharacterized LOC109915896, 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 10 samples with support for all annotated introns
lipoma-preferred partner homolog, transcript variant X2
lipoma-preferred partner homolog, transcript variant X1
lipoma-preferred partner homolog, transcript variant X3
B-cell lymphoma 6 protein homolog, transcript variant X1
B-cell lymphoma 6 protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
mannan-binding lectin serine protease 1-like, transcript variant X3
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
mannan-binding lectin serine protease 1-like, transcript variant X4
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
mannan-binding lectin serine protease 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mannan-binding lectin serine protease 1-like, transcript variant X2
mannan-binding lectin serine protease 1-like isoform X1
transmembrane protease serine 11G-like isoform X2
mannan-binding lectin serine protease 1-like isoform X3
leucine rich repeat containing 34, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine rich repeat containing 34, transcript variant X2
leucine-rich repeat-containing protein 34 isoform X1
leucine-rich repeat-containing protein 34 isoform X2
leucine-rich repeat and IQ domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 31
multiple epidermal growth factor-like domains protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, 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: 9 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
very long-chain specific acyl-CoA dehydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich alpha-2-glycoprotein-like, transcript variant X1
leucine-rich alpha-2-glycoprotein-like, transcript variant X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like
disks large homolog 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
disks large homolog 1-like, transcript variant X2
disks large homolog 1-like, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
GPI mannosyltransferase 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GPI mannosyltransferase 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
GPI mannosyltransferase 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear cap binding protein subunit 2, transcript variant X1
nuclear cap binding protein subunit 2, transcript variant X2
nuclear cap-binding protein subunit 2 isoform X1
nuclear cap-binding protein subunit 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 65% 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 60% 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 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
dynein assembly factor with WDR repeat domains 1
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
SPHK1 interactor, AKAP domain containing
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain-containing protein 5B1-like, transcript variant X2
von Willebrand factor A domain-containing protein 5B1-like, transcript variant X1
von Willebrand factor A domain-containing protein 5B1-like isoform X1
von Willebrand factor A domain-containing protein 5B1-like isoform X2
dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase
calcium/calmodulin-dependent protein kinase II inhibitor 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
mitochondrial E3 ubiquitin protein ligase 1a, transcript variant X5
mitochondrial E3 ubiquitin protein ligase 1a, transcript variant X1
mitochondrial E3 ubiquitin protein ligase 1a, transcript variant X3
mitochondrial E3 ubiquitin protein ligase 1a, transcript variant X2
mitochondrial E3 ubiquitin protein ligase 1a, transcript variant X4
mitochondrial ubiquitin ligase activator of nfkb 1-A isoform X2
mitochondrial ubiquitin ligase activator of nfkb 1-A isoform X1
receptor-transporting protein 3-like, transcript variant X2
receptor-transporting protein 3-like, transcript variant X1
receptor-transporting protein 3-like isoform X2
receptor-transporting protein 3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tyrosine kinase, non-receptor, 2b, transcript variant X1
tyrosine kinase, non-receptor, 2b, transcript variant X2
tyrosine kinase, non-receptor, 2b, transcript variant X5
tyrosine kinase, non-receptor, 2b isoform X4
tyrosine kinase, non-receptor, 2b, transcript variant X3
tyrosine kinase, non-receptor, 2b, transcript variant X4
tyrosine kinase, non-receptor, 2b isoform X1
tyrosine kinase, non-receptor, 2b isoform X2
tyrosine kinase, non-receptor, 2b isoform X3
latent-transforming growth factor beta-binding protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, 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: 14 Proteins
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
rubicon autophagy regulator, transcript variant X4
rubicon autophagy regulator, transcript variant X2
rubicon autophagy regulator, transcript variant X1
rubicon autophagy regulator, transcript variant X3
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X4
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X2
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X1
run domain Beclin-1-interacting and cysteine-rich domain-containing protein isoform X3
DISP complex protein LRCH3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DISP complex protein LRCH3-like, 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 1 sample with support for all annotated introns
DISP complex protein LRCH3-like isoform X1
DISP complex protein LRCH3-like isoform X2
IQ motif containing G, transcript variant X2
IQ motif containing G, transcript variant X1
IQ motif containing G, transcript variant X3
dynein regulatory complex protein 9 isoform X2
dynein regulatory complex protein 9 isoform X1
dynein regulatory complex protein 9 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 1
5-hydroxytryptamine (serotonin) receptor 2B, G protein-coupled
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
cholinergic receptor, nicotinic, delta (muscle)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 4E family member 2, 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 2 samples with support for all annotated introns
eukaryotic translation initiation factor 4E family member 2, transcript variant X1
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
eukaryotic translation initiation factor 4E family member 2, transcript variant X4
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 9 samples with support for all annotated introns
eukaryotic translation initiation factor 4E family member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
eukaryotic translation initiation factor 4E type 2 isoform X3
eukaryotic translation initiation factor 4E type 2 isoform X1
eukaryotic translation initiation factor 4E type 2 isoform X4
eukaryotic translation initiation factor 4E type 2 isoform X2
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X7
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X4
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X3
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X5
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X1
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X6
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X2
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X8
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X9
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X11
ATP-binding cassette, sub-family C (CFTR/MRP), member 5, transcript variant X10
multidrug resistance-associated protein 5 isoform X1
multidrug resistance-associated protein 5 isoform X2
multidrug resistance-associated protein 5 isoform X3
multidrug resistance-associated protein 5 isoform X5
multidrug resistance-associated protein 5 isoform X4
tetratricopeptide repeat domain 14, transcript variant X1
tetratricopeptide repeat domain 14, transcript variant X2
tetratricopeptide repeat domain 14, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tetratricopeptide repeat domain 14, transcript variant X4
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
tetratricopeptide repeat protein 14 isoform X1
tetratricopeptide repeat protein 14 isoform X2
coiled-coil domain-containing protein 39
FMR1 autosomal homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 16 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
FMR1 autosomal homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 17 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
FMR1 autosomal homolog 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 14 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
FMR1 autosomal homolog 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 14 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
FMR1 autosomal homolog 1, transcript variant X5
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 8 samples with support for all annotated introns
fragile X mental retardation syndrome-related protein 1 isoform X1
fragile X mental retardation syndrome-related protein 1 isoform X2
fragile X mental retardation syndrome-related protein 1 isoform X3
fragile X mental retardation syndrome-related protein 1 isoform X4
fragile X mental retardation syndrome-related protein 1 isoform X5
DnaJ (Hsp40) homolog, subfamily C, member 19, transcript variant X1
DnaJ (Hsp40) homolog, subfamily C, member 19, transcript variant X2
mitochondrial import inner membrane translocase subunit TIM14 isoform X1
mitochondrial import inner membrane translocase subunit TIM14 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 113 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: 98 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial
uncharacterized LOC109934888, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC109934888 isoform X1
uncharacterized LOC109934888, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC109934888 isoform 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 4 samples with support for all annotated introns
ATPase phospholipid transporting 11B (putative)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
lysosome-associated membrane glycoprotein 3, transcript variant X2
lysosome-associated membrane glycoprotein 3 isoform X2
lysosome-associated membrane glycoprotein 3, transcript variant X1
lysosome-associated membrane glycoprotein 3 isoform X1
MCF.2 cell line derived transforming sequence-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase A
endothelin-converting enzyme 2-like, transcript variant X1
endothelin-converting enzyme 2-like, transcript variant X3
endothelin-converting enzyme 2-like, transcript variant X2
endothelin-converting enzyme 2-like isoform X1
endothelin-converting enzyme 2-like isoform X2
endothelin-converting enzyme 2-like isoform X3
proteasome 26S subunit ubiquitin receptor, non-ATPase 2
26S proteasome non-ATPase regulatory subunit 2
uncharacterized LOC125484673, 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 11 samples with support for all annotated introns
uncharacterized LOC125484673, 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 16 samples with support for all annotated introns
eukaryotic translation initiation factor 4 gamma, 1a
eukaryotic translation initiation factor 4 gamma 1a
family with sequence similarity 131 member Ab
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
heat shock protein beta-7-like, transcript variant X1
heat shock protein beta-7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49% coverage of the annotated genomic feature by RNAseq alignments
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
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00158
COORDINATES: nucleotide motif:Rfam:12.0:RF00217
uncharacterized LOC125484676, transcript variant X2
uncharacterized LOC125484676, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: lisH domain-containing protein ARMC9
uncharacterized protein LOC767698 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC767698 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC767698 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC767698 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 12 member 9 isoform X4
solute carrier family 12 member 9 isoform X3
solute carrier family 12 member 9 isoform X2
solute carrier family 12 member 9 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, including 1 sample with support for all annotated introns
COP9 constitutive photomorphogenic homolog subunit 7A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 22 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COP9 constitutive photomorphogenic homolog subunit 7A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125484662, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125484662, 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 4 samples with support for all annotated introns
protein phosphatase 1, regulatory (inhibitor) subunit 2
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
BAR_ACAPs and ArfGap_ACAP domain-containing protein, transcript variant X5
BAR_ACAPs and ArfGap_ACAP domain-containing protein, transcript variant 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, including 4 samples with support for all annotated introns
BAR_ACAPs and ArfGap_ACAP domain-containing protein, transcript variant X2
BAR_ACAPs and ArfGap_ACAP domain-containing protein, transcript variant X3
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 5 samples with support for all annotated introns
BAR_ACAPs and ArfGap_ACAP domain-containing protein, transcript variant X4
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 9 samples with support for all annotated introns
BAR_ACAPs and ArfGap_ACAP domain-containing protein, 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 4 samples with support for all annotated introns
BAR_ACAPs and ArfGap_ACAP domain-containing protein isoform X1
BAR_ACAPs and ArfGap_ACAP domain-containing protein isoform X3
BAR_ACAPs and ArfGap_ACAP domain-containing protein isoform X2
BAR_ACAPs and ArfGap_ACAP domain-containing protein isoform X4
BAR_ACAPs and ArfGap_ACAP domain-containing protein isoform X5
BAR_ACAPs and ArfGap_ACAP domain-containing protein isoform X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
xyloside xylosyltransferase 1, transcript variant X1
xyloside xylosyltransferase 1, transcript variant X2
xyloside xylosyltransferase 1 isoform X1
xyloside xylosyltransferase 1 isoform X2
family with sequence similarity 43 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
large 60S subunit nuclear export GTPase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
transmembrane protein 44, transcript variant X1
transmembrane protein 44, transcript variant X2
transmembrane protein 44, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 13 Proteins, 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: 9 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
polyamine-transporting ATPase 13A3 isoform X1
polyamine-transporting ATPase 13A3 isoform X2
polyamine-transporting ATPase 13A3 isoform X3
leucine-rich repeat-containing protein 15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125484675, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 63% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125484675, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125484675, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125484675, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dynamin-like 120 kDa protein, mitochondrial
phospholipase A and acyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipase A and acyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
phospholipase A and acyltransferase 1 isoform X1
phospholipase A and acyltransferase 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 25 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
DNA-directed RNA polymerases I, II, and III subunit RPABC3
major facilitator superfamily domain containing 8-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 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: 3 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
ephrin type-B receptor 3, transcript variant X4
ephrin type-B receptor 3, transcript variant X2
ephrin type-B receptor 3, transcript variant X3
ephrin type-B receptor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins
uncharacterized LOC125484686, transcript variant X2
uncharacterized LOC125484686, transcript variant X1
phosphodiesterase 6D, cGMP-specific, rod, delta
retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 13
NADH:ubiquinone oxidoreductase subunit B5
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 86% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 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: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125484689, transcript variant X1
uncharacterized LOC125484689, 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 5 samples with support for all annotated introns
uncharacterized LOC125484689, transcript variant X6
uncharacterized LOC125484689, 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 14 samples with support for all annotated introns
uncharacterized LOC125484689, 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 13 samples with support for all annotated introns
uncharacterized LOC125484689, transcript variant X5
calcium-activated potassium channel subunit beta-2, 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, including 1 sample with support for all annotated introns
calcium-activated potassium channel subunit beta-2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium-activated potassium channel subunit beta-2, transcript variant X4
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 5 samples with support for all annotated introns
calcium-activated potassium channel subunit beta-2, 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 2 samples with support for all annotated introns
calcium-activated potassium channel subunit beta-2 isoform X1
calcium-activated potassium channel subunit beta-2 isoform X7
calcium-activated potassium channel subunit beta-2 isoform X4
calcium-activated potassium channel subunit beta-2 isoform X2
calcium-activated potassium channel subunit beta-2, transcript variant X3
calcium-activated potassium channel subunit beta-2, transcript variant X8
calcium-activated potassium channel subunit beta-2, transcript variant X5
calcium-activated potassium channel subunit beta-2, transcript variant X6
calcium-activated potassium channel subunit beta-2 isoform X3
calcium-activated potassium channel subunit beta-2 isoform X8
calcium-activated potassium channel subunit beta-2 isoform X5
calcium-activated potassium channel subunit beta-2 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
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
inactive N-acetylated-alpha-linked acidic dipeptidase-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 49% 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 46% 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, 3 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
THAP domain-containing protein 5-like, transcript variant X3
THAP domain-containing protein 5-like, transcript variant X1
THAP domain-containing protein 5-like, transcript variant X2
THAP domain-containing protein 5-like isoform X2
THAP domain-containing protein 5-like isoform X1
THAP domain-containing protein 5-like isoform X3
coiled-coil domain-containing protein 150, transcript variant X6
coiled-coil domain-containing protein 150, transcript variant X4
coiled-coil domain-containing protein 150, transcript variant X5
coiled-coil domain-containing protein 150, transcript variant X8
coiled-coil domain-containing protein 150, transcript variant X2
coiled-coil domain-containing protein 150, transcript variant X1
coiled-coil domain-containing protein 150, transcript variant X3
coiled-coil domain-containing protein 150, transcript variant X11
coiled-coil domain-containing protein 150 isoform X3
coiled-coil domain-containing protein 150 isoform X1
coiled-coil domain-containing protein 150 isoform X5
coiled-coil domain-containing protein 150, transcript variant X7
coiled-coil domain-containing protein 150 isoform X2
coiled-coil domain-containing protein 150, transcript variant X10
coiled-coil domain-containing protein 150, transcript variant X9
coiled-coil domain-containing protein 150 isoform X4
coiled-coil domain-containing protein 150, transcript variant X12
coiled-coil domain-containing protein 150 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
c18h3orf33 homolog (H. sapiens), transcript variant X1
c18h3orf33 homolog (H. sapiens), transcript variant X2
c18h3orf33 homolog (H. sapiens), transcript variant X3
guanine monophosphate synthase, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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
guanine monophosphate synthase, transcript variant X1
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 1 sample with support for all annotated introns
guanine monophosphate synthase, 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 3 samples with support for all annotated introns
guanine monophosphate synthase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
guanine monophosphate synthase, transcript variant X5
GMP synthase [glutamine-hydrolyzing] isoform X1
GMP synthase [glutamine-hydrolyzing] isoform X3
GMP synthase [glutamine-hydrolyzing] isoform X2
solute carrier family 33 member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
solute carrier family 33 member 1, transcript variant X2
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 3 samples with support for all annotated introns
acetyl-coenzyme A transporter 1 isoform X1
solute carrier family 33 member 1, transcript variant X3
acetyl-coenzyme A transporter 1 isoform X2
guanine monophosphate synthase, transcript variant X4
GMP synthase [glutamine-hydrolyzing] isoform X4
guanine monophosphate synthase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
GMP synthase [glutamine-hydrolyzing] isoform X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: vomeronasal type-2 receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
potassium voltage-gated channel subfamily A regulatory beta subunit 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 24 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A regulatory beta subunit 1a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
voltage-gated potassium channel subunit beta-1a isoform X1
voltage-gated potassium channel subunit beta-1a isoform X3
potassium voltage-gated channel subfamily A regulatory beta subunit 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 37 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A regulatory beta subunit 1a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 2 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
voltage-gated potassium channel subunit beta-1a isoform X2
voltage-gated potassium channel subunit beta-1a isoform X4
translocon-associated protein subunit gamma
TCDD-inducible poly(ADP-ribose) polymerase, transcript variant X1
TCDD-inducible poly(ADP-ribose) polymerase, transcript variant X4
TCDD-inducible poly(ADP-ribose) polymerase, transcript variant X2
TCDD-inducible poly(ADP-ribose) polymerase, transcript variant X3
protein mono-ADP-ribosyltransferase TIPARP
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 14 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, including 4 samples with support for all annotated introns
ankyrin repeat, PH and SEC7 domain containing protein secG-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
ventricular zone expressed PH domain-containing 1, 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
ventricular zone expressed PH domain-containing 1, transcript variant X2
ventricular zone-expressed PH domain-containing protein
lysosomal amino acid transporter 1 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lysosomal amino acid transporter 1 homolog isoform X2
lysosomal amino acid transporter 1 homolog, transcript variant X1
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
lysosomal amino acid transporter 1 homolog isoform X1
transient receptor potential cation channel subfamily V member 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily V member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
serpin peptidase inhibitor, clade I (neuroserpin), member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 long SRA reads, 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
serpin peptidase inhibitor, clade I (neuroserpin), member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 31 Proteins, and 99% 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: 172 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
WD repeat-containing protein 49, 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
WD repeat-containing protein 49, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger B-box domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
acetylcholinesterase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acetylcholinesterase, transcript variant X3
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
acetylcholinesterase, transcript variant X2
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 8 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
serine palmitoyltransferase, small subunit B, transcript variant X3
serine palmitoyltransferase, small subunit B, transcript variant X2
serine palmitoyltransferase, small subunit B, transcript variant X4
serine palmitoyltransferase, small subunit B, transcript variant X5
serine palmitoyltransferase, small subunit B, transcript variant X1
serine palmitoyltransferase small subunit B isoform X1
serine palmitoyltransferase small subunit B isoform X2
NMD3 ribosome export adaptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
NMD3 ribosome export adaptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
60S ribosomal export protein NMD3 isoform X1
60S ribosomal export protein NMD3 isoform X2
protein phosphatase, Mg2+/Mn2+ dependent, 1Lb, transcript variant X1
protein phosphatase, Mg2+/Mn2+ dependent, 1Lb isoform X1
protein phosphatase, Mg2+/Mn2+ dependent, 1Lb, transcript variant X2
protein phosphatase, Mg2+/Mn2+ dependent, 1Lb isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF01295
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 11 samples with support for all annotated introns
structural maintenance of chromosomes protein 4
LOW QUALITY PROTEIN: structural maintenance of chromosomes protein 4
structural maintenance of chromosomes protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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
intraflagellar transport 80 homolog (Chlamydomonas), 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 12 samples with support for all annotated introns
intraflagellar transport 80 homolog (Chlamydomonas), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
intraflagellar transport protein 80 homolog isoform X1
intraflagellar transport protein 80 homolog isoform X2
intraflagellar transport 80 homolog (Chlamydomonas), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
intraflagellar transport protein 80 homolog isoform X3
uncharacterized protein si:dkeyp-97b10.3
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% 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: 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: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
major facilitator superfamily domain containing 1, transcript variant X4
major facilitator superfamily domain containing 1, transcript variant X3
major facilitator superfamily domain containing 1, transcript variant X1
major facilitator superfamily domain-containing protein 1 isoform X4
major facilitator superfamily domain-containing protein 1 isoform X3
major facilitator superfamily domain-containing protein 1 isoform X1
major facilitator superfamily domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myeloid leukemia factor 1, transcript variant X2
myeloid leukemia factor 1, 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
arginine/serine-rich coiled-coil 1, transcript variant X2
arginine/serine-rich coiled-coil 1, transcript variant X4
arginine/serine-rich coiled-coil 1, transcript variant X5
arginine/serine-rich coiled-coil 1, transcript variant X3
arginine/serine-rich coiled-coil 1, transcript variant X1
serine/Arginine-related protein 53 isoform X2
serine/Arginine-related protein 53 isoform 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, including 3 samples with support for all annotated introns
dedicator of cytokinesis 10, transcript variant X1
dedicator of cytokinesis 10, transcript variant X6
dedicator of cytokinesis 10, transcript variant X2
dedicator of cytokinesis 10, transcript variant X9
dedicator of cytokinesis 10, transcript variant X10
dedicator of cytokinesis 10, transcript variant X3
dedicator of cytokinesis 10, transcript variant X5
dedicator of cytokinesis 10, transcript variant X4
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 1 sample with support for all annotated introns
dedicator of cytokinesis 10, transcript variant X7
dedicator of cytokinesis protein 10 isoform X6
dedicator of cytokinesis protein 10 isoform X7
dedicator of cytokinesis protein 10 isoform X1
dedicator of cytokinesis protein 10 isoform X2
dedicator of cytokinesis protein 10 isoform X9
dedicator of cytokinesis protein 10 isoform X10
dedicator of cytokinesis protein 10 isoform X3
dedicator of cytokinesis protein 10 isoform X5
dedicator of cytokinesis protein 10 isoform X4
dedicator of cytokinesis 10, transcript variant X8
dedicator of cytokinesis protein 10 isoform X8
putative coiled-coil domain-containing protein 195
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
guanylate cyclase soluble subunit beta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, 12 Proteins, and 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: 8 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: thymus-specific serine protease
serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2
WD repeat and FYVE domain-containing protein 1
adaptor related protein complex 1 subunit sigma 3a, transcript variant X2
adaptor related protein complex 1 subunit sigma 3a, transcript variant X1
AP-1 complex subunit sigma-3a isoform X1
AP-1 complex subunit sigma-3a isoform X2
potassium voltage-gated channel, Isk-related family, member 4
potassium voltage-gated channel subfamily E member 4
acyl-CoA synthetase long chain family member 3a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
acyl-CoA synthetase long chain family member 3a, transcript variant X1
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 4 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase 3a isoform X2
long-chain-fatty-acid--CoA ligase 3a isoform X1
2-acylglycerol O-acyltransferase 1, transcript variant X1
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 4 samples with support for all annotated introns
2-acylglycerol O-acyltransferase 1 isoform X1
2-acylglycerol O-acyltransferase 1, transcript variant X2
2-acylglycerol O-acyltransferase 1 isoform X2
phenylalanyl-tRNA synthetase subunit beta
sphingosine-1-phosphate phosphatase 2, transcript variant X2
sphingosine-1-phosphate phosphatase 2, transcript variant X1
sphingosine-1-phosphate phosphatase 2, transcript variant X3
sphingosine-1-phosphate phosphatase 2 isoform X2
sphingosine-1-phosphate phosphatase 2 isoform X1
sphingosine-1-phosphate phosphatase 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 61% 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 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 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: 13 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: 14 Proteins, and 73% 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 Proteins, and 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: 26 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 72% 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, 14 Proteins, 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: 81 long SRA reads, 23 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
SPRY domain-containing SOCS box protein 1, transcript variant X9
SPRY domain-containing SOCS box protein 1, transcript variant X2
SPRY domain-containing SOCS box protein 1, transcript variant X1
SPRY domain-containing SOCS box protein 1, transcript variant X4
SPRY domain-containing SOCS box protein 1, transcript variant X5
SPRY domain-containing SOCS box protein 1, transcript variant X3
SPRY domain-containing SOCS box protein 1, transcript variant X6
SPRY domain-containing SOCS box protein 1, transcript variant X7
SPRY domain-containing SOCS box protein 1, transcript variant X8
SPRY domain-containing SOCS box protein 1 isoform X1
SPRY domain-containing SOCS box protein 1 isoform X2
tripartite motif-containing protein 42-like
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform-like
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
mitochondrial ribosomal protein S22, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 146 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
mitochondrial ribosomal protein S22, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mitochondrial ribosomal protein S22, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 145 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
mitochondrial ribosomal protein S22, transcript variant X4
28S ribosomal protein S22, mitochondrial isoform X1
28S ribosomal protein S22, mitochondrial isoform X3
28S ribosomal protein S22, mitochondrial isoform X2
28S ribosomal protein S22, mitochondrial isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 211 long SRA reads, 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
nicotinamide nucleotide adenylyltransferase 3, transcript variant X11
nicotinamide nucleotide adenylyltransferase 3, transcript variant X8
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X5
nicotinamide nucleotide adenylyltransferase 3, transcript variant X6
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 5 samples with support for all annotated introns
nicotinamide nucleotide adenylyltransferase 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nicotinamide nucleotide adenylyltransferase 3, transcript variant X5
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
nicotinamide nucleotide adenylyltransferase 3, transcript variant X7
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 4 samples with support for all annotated introns
nicotinamide nucleotide adenylyltransferase 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nicotinamide nucleotide adenylyltransferase 3, transcript variant X3
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
nicotinamide nucleotide adenylyltransferase 3, transcript variant X1
nicotinamide nucleotide adenylyltransferase 3, 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 11 samples with support for all annotated introns
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X2
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X1
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X4
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1 isoform X3
nicotinamide nucleotide adenylyltransferase 3, transcript variant X9
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X7
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
vesicle-associated membrane protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vesicle-associated membrane protein 2, transcript variant X2
transcription cofactor HES-6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 15 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription cofactor HES-6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcription cofactor HES-6-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium-binding protein 39, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
calcium-binding protein 39, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
integral membrane protein 2C, transcript variant X2
integral membrane protein 2C, transcript variant X3
integral membrane protein 2C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
G-protein coupled receptor 55-like, transcript variant X2
G-protein coupled receptor 55-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
golgin subfamily A member 6-like protein 22
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, including 1 sample with support for all annotated introns
uncharacterized protein DDB_G0292642-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 606 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein DDB_G0292642-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 636 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized protein DDB_G0292642-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 436 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein DDB_G0292642-like isoform X2
uncharacterized protein DDB_G0292642-like isoform X1
uncharacterized protein LOC109911076 isoform X3
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 47-like isoform X4
ubiquitin carboxyl-terminal hydrolase 47-like isoform X1
ubiquitin carboxyl-terminal hydrolase 47-like isoform X5
ubiquitin carboxyl-terminal hydrolase 47-like isoform X3
ubiquitin carboxyl-terminal hydrolase 47-like isoform X2
uncharacterized protein DDB_G0292642-like
uncharacterized protein LOC794380 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 251 long SRA reads, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109911079, transcript variant X2
uncharacterized LOC109911079, transcript variant X3
uncharacterized LOC109911079, transcript variant X5
uncharacterized LOC109911079, transcript variant X4
uncharacterized LOC109911079, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00277
COORDINATES: nucleotide motif:Rfam:12.0:RF00571
uncharacterized protein LOC109911079 isoform X1
uncharacterized protein LOC109911079 isoform 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 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, and 95% 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.
G-protein coupled receptor 35-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
G-protein coupled receptor 35-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 66% 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: 286 Proteins
beta-galactoside alpha-2,6-sialyltransferase 1, transcript variant X2
beta-galactoside alpha-2,6-sialyltransferase 1, transcript variant X1
beta-galactoside alpha-2,6-sialyltransferase 1, transcript variant X4
beta-galactoside alpha-2,6-sialyltransferase 1, transcript variant X3
beta-galactoside alpha-2,6-sialyltransferase 1, transcript variant X5
beta-galactoside alpha-2,6-sialyltransferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SLAM family member 5-like, transcript variant X3
SLAM family member 5-like, transcript variant X2
SLAM family member 5-like, transcript variant X1
SLAM family member 5-like, transcript variant X4
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 4 samples with support for all annotated introns
uncharacterized LOC109917759, transcript variant X1
uncharacterized LOC109917759, transcript variant X2
uncharacterized protein LOC109917759 isoform X2
uncharacterized protein LOC109917759 isoform X1
carcinoembryonic antigen-related cell adhesion molecule 1-like, transcript variant X1
carcinoembryonic antigen-related cell adhesion molecule 1-like, transcript variant X2
hepatocyte cell adhesion molecule-like isoform X1
carcinoembryonic antigen-related cell adhesion molecule 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 10 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: 5 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NCK adaptor protein 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NCK adaptor protein 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
solute carrier family 35 member G2, transcript variant X4
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 7 samples with support for all annotated introns
solute carrier family 35 member G2, transcript variant X6
solute carrier family 35 member G2, 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 2 samples with support for all annotated introns
solute carrier family 35 member G2 isoform X2
solute carrier family 35 member G2, transcript variant X1
solute carrier family 35 member G2, transcript variant X7
solute carrier family 35 member G2 isoform X1
solute carrier family 35 member G2, transcript variant X5
solute carrier family 35 member G2, transcript variant X3
solute carrier family 35 member G2 isoform X3
cohesin subunit SA-1, transcript variant X1
cohesin subunit SA-1, transcript variant X5
cohesin subunit SA-1, transcript variant X4
cohesin subunit SA-1, transcript variant X2
cohesin subunit SA-1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 221 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit beta, transcript variant X2
propionyl-CoA carboxylase subunit beta, transcript variant X1
propionyl-CoA carboxylase beta chain, mitochondrial isoform X2
propionyl-CoA carboxylase beta chain, mitochondrial isoform X1
MSL complex subunit 2, transcript variant X1
E3 ubiquitin-protein ligase MSL2 isoform X1
MSL complex subunit 2, transcript variant X2
E3 ubiquitin-protein ligase MSL2 isoform X2
MSL complex subunit 2, transcript variant X3
E3 ubiquitin-protein ligase MSL2 isoform X3
protein phosphatase 2, regulatory subunit B'', alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 2, regulatory subunit B'', alpha, 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
protein phosphatase 2, regulatory subunit B'', alpha, transcript variant X3
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit alpha isoform X1
serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit alpha isoform 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 4 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 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 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
C-C motif chemokine 20-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
C-C motif chemokine 20-like, transcript variant X2
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
potassium channel regulatory protein-like
UDP-glucose glycoprotein glucosyltransferase 1, transcript variant X4
UDP-glucose glycoprotein glucosyltransferase 1, transcript variant X2
UDP-glucose glycoprotein glucosyltransferase 1, transcript variant X3
UDP-glucose glycoprotein glucosyltransferase 1, transcript variant X1
UDP-glucose:glycoprotein glucosyltransferase 1 isoform X4
UDP-glucose:glycoprotein glucosyltransferase 1 isoform X2
UDP-glucose:glycoprotein glucosyltransferase 1 isoform X3
UDP-glucose:glycoprotein glucosyltransferase 1 isoform X1
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X2
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X8
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X7
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X6
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X3
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X1
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X4
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X5
heparan-sulfate 6-O-sulfotransferase 1-like isoform X2
heparan-sulfate 6-O-sulfotransferase 1-like isoform X3
heparan-sulfate 6-O-sulfotransferase 1-like isoform X1
heparan-sulfate 6-O-sulfotransferase 1-like isoform X4
heparan-sulfate 6-O-sulfotransferase 1-like isoform X5
heparan-sulfate 6-O-sulfotransferase 1-like isoform X6
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X9
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 3 samples with support for all annotated introns
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X11
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
heparan-sulfate 6-O-sulfotransferase 1-like, transcript variant X10
transfer RNA glycine (anticodon ACC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
pleckstrin homology domain containing, family B (evectins) member 2, transcript variant X1
pleckstrin homology domain containing, family B (evectins) member 2, transcript variant X5
pleckstrin homology domain containing, family B (evectins) member 2, transcript variant X3
pleckstrin homology domain containing, family B (evectins) member 2, transcript variant X4
pleckstrin homology domain containing, family B (evectins) member 2, transcript variant X2
pleckstrin homology domain-containing family B member 2
family with sequence similarity 168 member B
myelin-associated neurite-outgrowth inhibitor
rho guanine nucleotide exchange factor 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins
rho guanine nucleotide exchange factor 4
signal recognition particle receptor subunit beta
diacylglycerol kinase delta, transcript variant X2
diacylglycerol kinase delta, transcript variant X1
uncharacterized LOC125484680, transcript variant X1
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 1 sample with support for all annotated introns
uncharacterized LOC125484680, transcript variant X2
coagulation factor IX-like, transcript variant X2
coagulation factor IX-like, transcript variant X1
coagulation factor IX-like, transcript variant X3
coagulation factor IX-like, transcript variant X4
vitamin K-dependent protein C-like, transcript variant X1
vitamin K-dependent protein C-like, transcript variant X3
vitamin K-dependent protein C-like, transcript variant X2
interacts with SUPT6H, CTD assembly factor 1
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, including 20 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 89% coverage of the annotated genomic feature by RNAseq alignments
nuclear body protein SP140-like protein, transcript variant X3
nuclear body protein SP140-like protein, transcript variant X1
nuclear body protein SP140-like protein, transcript variant X2
nuclear body protein SP140-like protein isoform X1
nuclear body protein SP140-like protein isoform X2
nuclear body protein SP140-like protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nuclear body protein SP140-like protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1
uncharacterized LOC109914975, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized protein LOC109914975 isoform X1
uncharacterized LOC109914975, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC109914975 isoform X2
autophagy-related protein 16-1-like, transcript variant X2
autophagy-related protein 16-1-like, transcript variant X1
autophagy-related protein 16-1-like isoform X1
autophagy-related protein 16-1-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00478
phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 55% 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, 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: G-protein coupled receptor 55-like
YEATS domain-containing protein 2, transcript variant X3
YEATS domain-containing protein 2, transcript variant X2
YEATS domain-containing protein 2, transcript variant X4
YEATS domain-containing protein 2, transcript variant X1
YEATS domain-containing protein 2 isoform X1
YEATS domain-containing protein 2 isoform X2
YEATS domain-containing protein 2 isoform X4
YEATS domain-containing protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 23 Proteins, and 98% 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: 2 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
presenilins-associated rhomboid-like protein, mitochondrial
WD repeat domain 53, transcript variant X1
WD repeat domain 53, transcript variant X3
WD repeat domain 53, transcript variant X2
erythroferrone-like, transcript variant X2
erythroferrone-like, transcript variant X1
integrin-linked kinase-associated serine/threonine phosphatase, transcript variant X2
integrin-linked kinase-associated serine/threonine phosphatase, transcript variant X1
integrin-linked kinase-associated serine/threonine phosphatase, transcript variant X3
integrin-linked kinase-associated serine/threonine phosphatase 2C isoform X2
integrin-linked kinase-associated serine/threonine phosphatase 2C isoform X1
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 2 samples with support for all annotated introns
cytochrome c oxidase assembly protein COX18, mitochondrial
LOW QUALITY PROTEIN: cytochrome c oxidase assembly protein COX18, mitochondrial
uncharacterized LOC125484683, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC125484683, transcript variant X2
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 13 samples with support for all annotated introns
uncharacterized LOC125484683, transcript variant X3
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 4 samples with support for all annotated introns
uncharacterized LOC125484683, transcript variant X4
alanine--glyoxylate and serine--pyruvate aminotransferase a
selenocysteine lyase, transcript variant X3
selenocysteine lyase, transcript variant X1
selenocysteine lyase, transcript variant X2
selenocysteine lyase, transcript variant X4
ciliary rootlet coiled-coil, rootletin family member 2
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
sushi, nidogen and EGF-like domain-containing protein 1
uncharacterized LOC125484740, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125484740, 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 6 samples with support for all annotated introns
uncharacterized LOC125484740, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and MYND domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and MYND domain-containing protein 1
dual specificity phosphatase 28, transcript variant X1
dual specificity phosphatase 28, transcript variant X2
dual specificity phosphatase 28 isoform X1
dual specificity phosphatase 28 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 162 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
maestro heat-like repeat-containing protein family member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 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: substituted 6 bases at 6 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: UBX domain-containing protein 7
single-pass membrane and coiled-coil domain-containing protein 1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase PAK 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
WD repeat domain 33, transcript variant X1
WD repeat domain 33, transcript variant X2
pre-mRNA 3' end processing protein WDR33 isoform X1
WD repeat domain 33, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 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
pre-mRNA 3' end processing protein WDR33 isoform X2
DNA-directed RNA polymerase II subunit RPB4
LIM and senescent cell antigen-like-containing domain protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 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: 14 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
AMMECR nuclear protein 1, transcript variant X2
AMMECR nuclear protein 1, transcript variant X1
AMMECR nuclear protein 1, transcript variant X4
AMMECR nuclear protein 1, transcript variant X5
AMMECR nuclear protein 1, transcript variant X3
AMME syndrome candidate gene 1 protein isoform X2
AMME syndrome candidate gene 1 protein isoform X1
AMME syndrome candidate gene 1 protein isoform X3
histone deacetylase complex subunit SAP130-like
BEN domain-containing protein 5-like, transcript variant X3
BEN domain-containing protein 5-like, transcript variant X1
BEN domain-containing protein 5-like, transcript variant X2
BEN domain-containing protein 5-like isoform X2
BEN domain-containing protein 5-like isoform X1
mitochondrial transcription termination factor 4
transcription termination factor 4, mitochondrial
PAS domain containing serine/threonine kinase, transcript variant X2
PAS domain containing serine/threonine kinase, transcript variant X1
PAS domain-containing serine/threonine-protein kinase isoform X2
PAS domain-containing serine/threonine-protein kinase isoform X1
protein phosphatase 1, regulatory (inhibitor) subunit 7
protein phosphatase 1 regulatory subunit 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 14 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: 29 Proteins
high density lipoprotein binding protein a, transcript variant X3
high density lipoprotein binding protein a, transcript variant X1
high density lipoprotein binding protein a, transcript variant X2
high density lipoprotein binding protein a
centrosomal protein 19, transcript variant X2
centrosomal protein 19, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis, class X, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis, class X, 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 84% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphatidylinositol-glycan biosynthesis class X protein
bcl-2-related ovarian killer protein homolog A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, 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: 1 long SRA read, 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
autophagy related 4B, cysteine peptidase, transcript variant X2
autophagy related 4B, cysteine peptidase, transcript variant X1
autophagy related 4B, cysteine peptidase, transcript variant X4
autophagy related 4B, cysteine peptidase, transcript variant X3
deoxythymidylate kinase (thymidylate kinase)
inhibitor of growth family, member 5a, transcript variant X1
inhibitor of growth family, member 5a, transcript variant X2
inhibitor of growth protein 5a isoform X1
inhibitor of growth family, member 5a, transcript variant X3
inhibitor of growth protein 5a isoform X2
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 3 samples with support for all annotated introns
D-2-hydroxyglutarate dehydrogenase, transcript variant X4
D-2-hydroxyglutarate dehydrogenase, transcript variant X5
D-2-hydroxyglutarate dehydrogenase, transcript variant X1
D-2-hydroxyglutarate dehydrogenase, transcript variant X6
D-2-hydroxyglutarate dehydrogenase, transcript variant X2
D-2-hydroxyglutarate dehydrogenase, transcript variant X3
D-2-hydroxyglutarate dehydrogenase, mitochondrial isoform X1
D-2-hydroxyglutarate dehydrogenase, mitochondrial isoform X2
D-2-hydroxyglutarate dehydrogenase, transcript variant X7
D-2-hydroxyglutarate dehydrogenase, mitochondrial isoform X3
transforming growth factor beta activator LRRC33-like
FERM, RhoGEF and pleckstrin domain protein 2, transcript variant X1
FERM, RhoGEF and pleckstrin domain protein 2, transcript variant X2
FERM, RhoGEF and pleckstrin domain protein 2, 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 3 samples with support for all annotated introns
FERM, RhoGEF and pleckstrin domain protein 2, transcript variant X3
FERM, ARHGEF and pleckstrin domain-containing protein 2 isoform X1
FERM, ARHGEF and pleckstrin domain-containing protein 2 isoform X2
FERM, ARHGEF and pleckstrin domain-containing protein 2 isoform X4
FERM, ARHGEF and pleckstrin domain-containing protein 2 isoform X3
FERM, RhoGEF and pleckstrin domain protein 2, transcript variant X5
FERM, ARHGEF and pleckstrin domain-containing protein 2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
alpha-1,4-N-acetylglucosaminyltransferase-like, transcript variant X2
alpha-1,4-N-acetylglucosaminyltransferase-like, transcript variant X1
alpha-1,4-N-acetylglucosaminyltransferase-like isoform X2
alpha-1,4-N-acetylglucosaminyltransferase-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lactosylceramide 4-alpha-galactosyltransferase-like
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ephrin type-B receptor 1, transcript variant X2
ephrin type-B receptor 1, transcript variant X1
centrosomal protein 63, transcript variant X7
centrosomal protein 63, transcript variant X3
centrosomal protein 63, transcript variant X8
centrosomal protein 63, transcript variant X6
centrosomal protein 63, transcript variant X5
centrosomal protein 63, transcript variant X4
centrosomal protein 63, transcript variant X1
centrosomal protein 63, transcript variant X2
centrosomal protein of 63 kDa isoform X6
centrosomal protein of 63 kDa isoform X2
centrosomal protein of 63 kDa isoform X7
centrosomal protein of 63 kDa isoform X5
centrosomal protein of 63 kDa isoform X4
centrosomal protein of 63 kDa isoform X3
centrosomal protein of 63 kDa isoform X1
angiomotin like 2a, transcript variant X4
angiomotin like 2a, transcript variant X1
angiomotin like 2a, transcript variant X3
angiomotin like 2a, transcript variant X2
receptor like tyrosine kinase, transcript variant X7
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 1 sample with support for all annotated introns
receptor like tyrosine kinase, transcript variant X8
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 6 samples with support for all annotated introns
receptor like tyrosine kinase, transcript variant X1
receptor like tyrosine kinase, transcript variant X3
receptor like tyrosine kinase, transcript variant X2
receptor like tyrosine kinase, transcript variant X5
receptor like tyrosine kinase, transcript variant X4
receptor like tyrosine kinase, transcript variant X6
solute carrier organic anion transporter family member 2A1-like, transcript variant X1
solute carrier organic anion transporter family member 2A1-like isoform X1
solute carrier organic anion transporter family member 2A1-like, transcript variant X2
solute carrier organic anion transporter family member 2A1-like isoform X2
gastrula zinc finger protein XlCGF8.2DB-like, transcript variant X1
gastrula zinc finger protein XlCGF8.2DB-like, transcript variant X2
gastrula zinc finger protein XlCGF8.2DB-like