Stegostoma fasciatum isolate 6-17 chromosome 14, sSteFas1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Stegostomatidae; Stegostoma.
REFSEQ INFORMATION: The reference sequence is identical to\nCM039240.1.\nAssembly name: sSteFas1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/17. The\noriginal whole-genome shotgun project has the accession\nJAFIRC000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Platanus v. 1.2.4; P_RNA_scaffolder v.\n commit 7941e0f on May 30, at github;\n 3D-DNA v. 180922\nAssembly Name :: sSteFas1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 95.8x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Stegostoma fasciatum Annotation\n Release 100\nAnnotation Version :: 100\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.
COORDINATES: polyA evidence [ECO:0006239]
coiled-coil domain containing 160, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
coiled-coil domain containing 160, 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 23 samples with support for all annotated introns
coiled-coil domain-containing protein 160
PHD finger protein 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
PHD finger protein 6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
PHD finger protein 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PHD finger protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
PHD finger protein 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PHD finger protein 6, transcript variant X4
hypoxanthine phosphoribosyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
hypoxanthine phosphoribosyltransferase 1, 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 1 sample with support for all annotated introns
hypoxanthine-guanine phosphoribosyltransferase isoform X2
hypoxanthine-guanine phosphoribosyltransferase isoform X1
motile sperm domain containing 1, transcript variant X6
motile sperm domain containing 1, transcript variant X1
motile sperm domain containing 1, transcript variant X2
motile sperm domain containing 1, transcript variant X3
motile sperm domain containing 1, transcript variant X4
motile sperm domain containing 1, transcript variant X5
motile sperm domain-containing protein 1 isoform X2
motile sperm domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
MAP7 domain containing 3, transcript variant X7
MAP7 domain containing 3, transcript variant X4
MAP7 domain containing 3, transcript variant X6
MAP7 domain containing 3, transcript variant X5
MAP7 domain containing 3, transcript variant X3
MAP7 domain containing 3, transcript variant X2
MAP7 domain containing 3, transcript variant X1
MAP7 domain-containing protein 2 isoform X7
MAP7 domain-containing protein 2 isoform X6
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
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
transcription cofactor vestigial-like protein 1, 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 5 samples with support for all annotated introns
transcription cofactor vestigial-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transcription cofactor vestigial-like protein 1 isoform X2
transcription cofactor vestigial-like protein 1 isoform X1
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6, transcript variant X2
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6, transcript variant X3
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6, transcript variant X1
rho guanine nucleotide exchange factor 6 isoform X2
rho guanine nucleotide exchange factor 6 isoform X3
rho guanine nucleotide exchange factor 6 isoform X1
RNA binding motif protein X-linked, transcript variant X5
RNA binding motif protein X-linked, transcript variant X2
RNA binding motif protein X-linked, transcript variant X4
RNA binding motif protein X-linked, transcript variant X1
RNA binding motif protein X-linked, transcript variant X3
RNA-binding motif protein, X chromosome isoform X2
RNA-binding motif protein, X chromosome isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00270
transmembrane 9 superfamily member 2-like, transcript variant X1
transmembrane 9 superfamily member 2-like isoform X1
transmembrane 9 superfamily member 2-like, transcript variant X2
transmembrane 9 superfamily member 2-like isoform X2
zinc finger protein ZIC 1-like, 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 8 samples with support for all annotated introns
zinc finger protein ZIC 1-like, transcript variant X2
zic family member 3 heterotaxy 1 (odd-paired homolog, Drosophila)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
fibroblast growth factor 13a, transcript variant X2
fibroblast growth factor 13a, transcript variant X3
fibroblast growth factor 13a, transcript variant X1
fat storage-inducing transmembrane protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
MCF.2 cell line derived transforming sequence a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
phospholipid-transporting ATPase IG-like
flocculation protein FLO11-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
flocculation protein FLO11-like, transcript variant X3
flocculation protein FLO11-like, transcript variant X1
flocculation protein FLO11-like, transcript variant X2
flocculation protein FLO11-like isoform X2
flocculation protein FLO11-like isoform X4
flocculation protein FLO11-like isoform X3
flocculation protein FLO11-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SRY-box transcription factor 3, transcript variant X2
SRY-box transcription factor 3, transcript variant X1
SRY-box transcription factor 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
SLIT and NTRK-like family, member 4, transcript variant X1
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 2 samples with support for all annotated introns
SLIT and NTRK-like family, member 4, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
fragile X messenger ribonucleoprotein 1, transcript variant X1
fragile X messenger ribonucleoprotein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
fragile X messenger ribonucleoprotein 1, transcript variant X4
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 24 samples with support for all annotated introns
fragile X messenger ribonucleoprotein 1, transcript variant X2
synaptic functional regulator FMR1 isoform X1
synaptic functional regulator FMR1 isoform X2
synaptic functional regulator FMR1 isoform X3
synaptic functional regulator FMR1 isoform X4
uncharacterized LOC125458949, transcript variant X2
uncharacterized LOC125458949, transcript variant X1
uncharacterized LOC125458949, transcript variant X4
uncharacterized LOC125458949, transcript variant X3
uncharacterized protein LOC125458949 isoform X1
uncharacterized protein LOC125458949 isoform X2
AF4/FMR2 family, member 2, 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 2 samples with support for all annotated introns
AF4/FMR2 family, member 2, transcript variant X2
uncharacterized protein LOC321250 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein LOC321250 homolog, transcript variant X1
LON peptidase N-terminal domain and RING finger protein 3-like
family with sequence similarity 199, X-linked, 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, including 6 samples with support for all annotated introns
family with sequence similarity 199, X-linked, 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 24 samples with support for all annotated introns
family with sequence similarity 199, X-linked, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
aristaless-related homeobox protein-like, transcript variant X1
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
aristaless-related homeobox protein-like isoform X1
aristaless-related homeobox protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
aristaless-related homeobox protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aristaless-related homeobox protein-like isoform X2
interleukin 1 receptor accessory protein-like 2, transcript variant X1
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 1 sample with support for all annotated introns
X-linked interleukin-1 receptor accessory protein-like 2 isoform X1
interleukin 1 receptor accessory protein-like 2, 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 1 sample with support for all annotated introns
X-linked interleukin-1 receptor accessory protein-like 2 isoform X2
mitogen-activated protein kinase kinase kinase kinase 4
RPA1 related single stranded DNA binding protein
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 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF128, transcript variant X2
E3 ubiquitin-protein ligase RNF128 isoform X2
E3 ubiquitin-protein ligase RNF128, transcript variant X3
E3 ubiquitin-protein ligase RNF128, transcript variant X1
E3 ubiquitin-protein ligase RNF128 isoform X1
E3 ubiquitin-protein ligase RNF128 isoform X3
TBC1 domain family member 8B, transcript variant X1
TBC1 domain family member 8B, transcript variant X2
TBC1 domain family member 8B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
neuronal PAS domain-containing protein 2
vacuolar ATPase assembly integral membrane protein vma21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
high mobility group protein B3-like, transcript variant X2
high mobility group protein B3-like, transcript variant X1
high mobility group protein B3-like, transcript variant X3
high mobility group protein B3-like isoform X1
high mobility group protein B3-like isoform X2
CD99 molecule-like 2, 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 17 samples with support for all annotated introns
CD99 molecule-like 2, 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
CD99 molecule-like 2, 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 20 samples with support for all annotated introns
CD99 molecule-like 2, 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 15 samples with support for all annotated introns
myotubularin related protein 1b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myotubularin related protein 1b, transcript variant X2
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 1 sample with support for all annotated introns
myotubularin-related protein 1b isoform X2
myotubularin related protein 1b, transcript variant X9
myotubularin related protein 1b, transcript variant X7
myotubularin related protein 1b, transcript variant X4
myotubularin related protein 1b, transcript variant X6
myotubularin related protein 1b, transcript variant X1
myotubularin related protein 1b, transcript variant X5
myotubularin related protein 1b, transcript variant X10
myotubularin related protein 1b, transcript variant X8
myotubularin-related protein 1b isoform X6
myotubularin-related protein 1b isoform X3
myotubularin-related protein 1b isoform X5
myotubularin-related protein 1b isoform X8
myotubularin-related protein 1b isoform X1
myotubularin-related protein 1b isoform X4
myotubularin-related protein 1b isoform X7
myotubularin-related protein 1b isoform X9
mastermind-like protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mastermind-like protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mastermind-like protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mastermind-like protein 2, 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 20 samples with support for all annotated introns
mastermind-like protein 2, transcript variant X3
uncharacterized protein LOC550336 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized protein LOC550336 homolog, 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 17 samples with support for all annotated introns
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
heat shock transcription factor, Y-linked-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
ankyrin repeat domain-containing protein 46, transcript variant X1
ankyrin repeat domain-containing protein 46, transcript variant X2
ankyrin repeat domain-containing protein 46 isoform X2
ankyrin repeat domain-containing protein 46 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
membrane-associated progesterone receptor component 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
uncharacterized si:rp71-46j2.7, 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 6 samples with support for all annotated introns
uncharacterized si:rp71-46j2.7, 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 7 samples with support for all annotated introns
uncharacterized si:rp71-46j2.7, transcript variant X3
uncharacterized protein si:rp71-46j2.7 isoform X1
uncharacterized protein si:rp71-46j2.7 isoform X2
uncharacterized protein si:rp71-46j2.7 isoform X3
ubiquitin-conjugating enzyme E2A (RAD6 homolog), transcript variant X2
ubiquitin-conjugating enzyme E2A (RAD6 homolog), transcript variant X1
ubiquitin-conjugating enzyme E2 A isoform X1
ubiquitin-conjugating enzyme E2 A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
sosondowah ankyrin repeat domain family d
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
ankyrin repeat domain-containing protein SOWAHC
UPF3B regulator of nonsense mediated mRNA decay
NADH:ubiquinone oxidoreductase subunit A1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 1
A-kinase anchoring protein 14, transcript variant X3
A-kinase anchoring protein 14, transcript variant X2
A-kinase anchoring protein 14, transcript variant X1
A-kinase anchoring protein 14, transcript variant X4
NFKB activating protein, transcript variant X2
NFKB activating protein, transcript variant X1
zinc finger and BTB domain containing 33, transcript variant X2
zinc finger and BTB domain containing 33, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger and BTB domain containing 33, 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 23 samples with support for all annotated introns
zinc finger and BTB domain containing 33, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 255A, transcript variant X2
transmembrane protein 255A, transcript variant X3
transmembrane protein 255A, transcript variant X1
protein ATP1B4-like, transcript variant X2
protein ATP1B4-like, transcript variant X1
transcription factor Dp-1-like, transcript variant X3
transcription factor Dp-1-like, transcript variant X1
transcription factor Dp-1-like, transcript variant X2
transcription factor Dp-1-like isoform X1
transcription factor Dp-1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 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: 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
STING1 ER exit protein 1, transcript variant X1
STING1 ER exit protein 1, transcript variant X2
uncharacterized LOC125458716, transcript variant X2
uncharacterized LOC125458716, transcript variant X1
uncharacterized LOC125458716, 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 19 samples with support for all annotated introns
uncharacterized protein LOC125458716 isoform X3
uncharacterized protein LOC125458716 isoform X2
uncharacterized protein LOC125458716 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
androgen receptor, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
androgen receptor, transcript variant X5
androgen receptor, transcript variant X3
androgen receptor, transcript variant X4
androgen receptor, transcript variant X2
androgen receptor, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
androgen receptor, transcript variant X7
androgen receptor, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
androgen receptor, transcript variant X10
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 1 sample with support for all annotated introns
androgen receptor, transcript variant X1
androgen receptor, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
androgen receptor, transcript variant X12
tumor necrosis factor receptor superfamily member 27
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 3 samples with support for all annotated introns
phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 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: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
collagen, type IV, alpha 6, transcript variant X5
collagen, type IV, alpha 6, transcript variant X3
collagen, type IV, alpha 6, transcript variant X1
collagen, type IV, alpha 6, transcript variant X4
collagen, type IV, alpha 6, transcript variant X2
collagen, type IV, alpha 5 (Alport syndrome)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X2
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13B-like isoform X2
tumor necrosis factor ligand superfamily member 13B-like isoform X1
autophagy related 4A, cysteine peptidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
autophagy related 4A, cysteine peptidase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 10
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 14 samples with support for all annotated introns
cytokine receptor common subunit gamma-like, transcript variant X4
cytokine receptor common subunit gamma-like, 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 16 samples with support for all annotated introns
cytokine receptor common subunit gamma-like, transcript variant X1
cytokine receptor common subunit gamma-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 24 samples with support for all annotated introns
cytokine receptor common subunit gamma-like isoform X2
cytokine receptor common subunit gamma-like isoform X3
cytokine receptor common subunit gamma-like isoform X1
cytokine receptor common subunit gamma-like isoform 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
forkhead box protein O1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
forkhead box protein O1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ring finger protein, LIM domain interacting, transcript variant X1
ring finger protein, LIM domain interacting, transcript variant X2
E3 ubiquitin-protein ligase RLIM isoform X1
E3 ubiquitin-protein ligase RNF12-A isoform X2
neurite extension and migration factor b, transcript variant X4
neurite extension and migration factor b, transcript variant X3
neurite extension and migration factor b, transcript variant X1
neurite extension and migration factor b, 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
neurite extension and migration factor isoform X3
neurite extension and migration factor isoform X2
neurite extension and migration factor isoform X1
ATP-binding cassette, sub-family B (MDR/TAP), member 7
iron-sulfur clusters transporter ABCB7, mitochondrial
uracil phosphoribosyltransferase (FUR1) homolog (S. cerevisiae), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uracil phosphoribosyltransferase (FUR1) homolog (S. cerevisiae), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uracil phosphoribosyltransferase homolog isoform X1
uracil phosphoribosyltransferase homolog isoform X2
zinc finger DHHC-type palmitoyltransferase 15b, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 15b, transcript variant X2
palmitoyltransferase ZDHHC15B isoform X1
palmitoyltransferase ZDHHC15B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ATRX chromatin remodeler, transcript variant X3
ATRX chromatin remodeler, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
ATRX chromatin remodeler, 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 5 samples with support for all annotated introns
transcriptional regulator ATRX isoform X1
transcriptional regulator ATRX isoform X3
transcriptional regulator ATRX isoform X2
ATRX chromatin remodeler, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transcriptional regulator ATRX isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transforming growth factor beta activator LRRC33-like, transcript variant X3
transforming growth factor beta activator LRRC33-like, transcript variant X2
transforming growth factor beta activator LRRC33-like, transcript variant X1
transforming growth factor beta activator LRRC33-like
transforming growth factor beta activator LRRC33-like, transcript variant X4
transforming growth factor beta activator LRRC33-like, transcript variant X5
retinal guanylyl cyclase 2-like, transcript variant X7
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
retinal guanylyl cyclase 2-like, transcript variant X6
retinal guanylyl cyclase 2-like, transcript variant X5
retinal guanylyl cyclase 2-like, transcript variant X3
retinal guanylyl cyclase 2-like, 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 1 sample with support for all annotated introns
retinal guanylyl cyclase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retinal guanylyl cyclase 2-like isoform X3
retinal guanylyl cyclase 2-like isoform X2
retinal guanylyl cyclase 2-like isoform X1
retinal guanylyl cyclase 2-like isoform X5
retinal guanylyl cyclase 2-like isoform X6
retinal guanylyl cyclase 2-like isoform X7
retinal guanylyl cyclase 2-like, transcript variant X4
retinal guanylyl cyclase 2-like isoform X4
nuclear transport factor 2-like export factor 2
acyl-CoA synthetase long chain family member 4a, transcript variant X2
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 11 samples with support for all annotated introns
acyl-CoA synthetase long chain family member 4a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase 4 isoform X1
long-chain-fatty-acid--CoA ligase 4 isoform X2
transmembrane protein 164-like, 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 14 samples with support for all annotated introns
transmembrane protein 164-like, transcript variant X2
transmembrane protein 164-like isoform X1
transmembrane protein 164-like isoform X2
AMME syndrome candidate gene 1 protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
AMME syndrome candidate gene 1 protein homolog, transcript variant X2
AMME syndrome candidate gene 1 protein homolog isoform X1
AMME syndrome candidate gene 1 protein homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase PAK 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
serine/threonine-protein kinase PAK 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
serine/threonine-protein kinase PAK 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
serine/threonine-protein kinase PAK 3, transcript variant X5
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 16 samples with support for all annotated introns
serine/threonine-protein kinase PAK 3, transcript variant X2
serine/threonine-protein kinase PAK 3 isoform X1
serine/threonine-protein kinase PAK 3 isoform X2
serine/threonine-protein kinase PAK 3 isoform X3
serine/threonine-protein kinase PAK 3 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal migration protein doublecortin-like, transcript variant X1
neuronal migration protein doublecortin-like, transcript variant X3
neuronal migration protein doublecortin-like, transcript variant X2
neuronal migration protein doublecortin-like isoform X2
neuronal migration protein doublecortin-like isoform X1
neuronal migration protein doublecortin-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 15 samples with support for all annotated introns
neuronal migration protein doublecortin-like isoform X3
ALG13 UDP-N-acetylglucosaminyltransferase subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
putative bifunctional UDP-N-acetylglucosamine transferase and deubiquitinase ALG13
short transient receptor potential channel 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
short transient receptor potential channel 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
short transient receptor potential channel 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ATPase copper transporting alpha, transcript variant X2
ATPase copper transporting alpha, transcript variant X4
ATPase copper transporting alpha, transcript variant X1
ATPase copper transporting alpha, transcript variant X3
cytochrome c oxidase subunit 7B, mitochondrial
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger MYM-type protein 3-like, transcript variant X1
zinc finger MYM-type protein 3-like, transcript variant X2
zinc finger MYM-type protein 3-like isoform X1
zinc finger MYM-type protein 3-like isoform X2
gap junction alpha-3 protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gap junction alpha-3 protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction alpha-3 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gap junction alpha-3 protein-like, transcript variant X3
gap junction alpha-3 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 113 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin (CD79A) binding protein 1
wiskott-Aldrich syndrome protein family member 3-like, transcript variant X2
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 4 samples with support for all annotated introns
wiskott-Aldrich syndrome protein family member 3-like, transcript variant X3
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 1 sample with support for all annotated introns
wiskott-Aldrich syndrome protein family member 3-like, transcript variant X1
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 8 samples with support for all annotated introns
wiskott-Aldrich syndrome protein family member 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
wiskott-Aldrich syndrome protein family member 3-like isoform X1
wiskott-Aldrich syndrome protein family member 3-like isoform X2
G-protein coupled receptor 12-like, transcript variant X1
G-protein coupled receptor 12-like, transcript variant X2
G-protein coupled receptor 12-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 12-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RAS-like, family 11, member A, transcript variant X1
ras-like protein family member 11A-like isoform X1
RAS-like, family 11, member A, transcript variant X2
ras-like protein family member 11A-like isoform X2
ligand of numb-protein X 2b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ligand of numb-protein X 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ligand of numb-protein X 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ligand of numb-protein X 2b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pre-mRNA 3'-end-processing factor FIP1-like, transcript variant X2
pre-mRNA 3'-end-processing factor FIP1-like, transcript variant X3
pre-mRNA 3'-end-processing factor FIP1-like, transcript variant X1
pre-mRNA 3'-end-processing factor FIP1-like isoform X3
pre-mRNA 3'-end-processing factor FIP1-like isoform X2
pre-mRNA 3'-end-processing factor FIP1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
cysteine-rich hydrophobic domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 79% 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
vascular endothelial growth factor receptor kdr-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00288
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
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 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase XIAP-like, transcript variant X6
E3 ubiquitin-protein ligase XIAP-like, transcript variant X4
E3 ubiquitin-protein ligase XIAP-like, transcript variant X1
E3 ubiquitin-protein ligase XIAP-like, transcript variant X5
E3 ubiquitin-protein ligase XIAP-like, transcript variant X2
E3 ubiquitin-protein ligase XIAP-like, transcript variant X3
E3 ubiquitin-protein ligase XIAP-like isoform X1
E3 ubiquitin-protein ligase XIAP-like isoform X2
stromal antigen 2b, transcript variant X1
stromal antigen 2b, transcript variant X5
stromal antigen 2b, transcript variant X6
stromal antigen 2b, transcript variant X2
stromal antigen 2b, transcript variant X4
stromal antigen 2b, transcript variant X3
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 6 samples with support for all annotated introns
teneurin transmembrane protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
teneurin transmembrane protein 1, transcript variant X4
teneurin transmembrane protein 1, transcript variant X3
teneurin transmembrane protein 1, transcript variant X7
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 6 samples with support for all annotated introns
teneurin transmembrane protein 1, 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 6 samples with support for all annotated introns
teneurin transmembrane protein 1, transcript variant X1
teneurin transmembrane protein 1, transcript variant X5
teneurin transmembrane protein 1, transcript variant X8
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
teneurin transmembrane protein 1, transcript variant X9
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 2 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X1
probable global transcription activator SNF2L1 isoform X2
probable global transcription activator SNF2L1 isoform X3
probable global transcription activator SNF2L1 isoform X1
GRB2 associated binding protein 3, transcript variant X2
GRB2 associated binding protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
GRB2-associated-binding protein 3 isoform X1
GRB2 associated binding protein 3, transcript variant X3
GRB2-associated-binding protein 3 isoform X2
Cdc42 guanine nucleotide exchange factor (GEF) 9a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Cdc42 guanine nucleotide exchange factor (GEF) 9a, transcript variant X1
Cdc42 guanine nucleotide exchange factor (GEF) 9a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor (GEF) 9a, transcript variant X3
Cdc42 guanine nucleotide exchange factor (GEF) 9a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor (GEF) 9a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
spermatogenesis-associated protein 13 isoform X1
rho guanine nucleotide exchange factor 9 isoform X3
rho guanine nucleotide exchange factor 9 isoform X4
rho guanine nucleotide exchange factor 9 isoform X2
rho guanine nucleotide exchange factor 9 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
ankyrin repeat and SOCS box-containing 12a
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein C8orf48-like, 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
uncharacterized protein C8orf48-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein C8orf48-like, transcript variant X3
uncharacterized protein C8orf48-like isoform X2
uncharacterized protein C8orf48-like isoform X1
uncharacterized protein C8orf48-like isoform X3
zinc finger C4H2 domain-containing protein
zinc finger CCCH-type containing 12B, transcript variant X1
probable ribonuclease ZC3H12B isoform X1
zinc finger CCCH-type containing 12B, transcript variant X3
zinc finger CCCH-type containing 12B, transcript variant X2
probable ribonuclease ZC3H12B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Rho GTPase activating protein 20b, transcript variant X3
Rho GTPase activating protein 20b, transcript variant X1
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 5 samples with support for all annotated introns
Rho GTPase activating protein 20b, transcript variant X2
Rho GTPase activating protein 20b, 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 1 sample with support for all annotated introns
rho GTPase-activating protein 20 isoform X1
rho GTPase-activating protein 20 isoform X2
rho GTPase-activating protein 20 isoform X3
V-set and immunoglobulin domain-containing protein 4-like, transcript variant X3
V-set and immunoglobulin domain-containing protein 4-like, transcript variant X4
V-set and immunoglobulin domain-containing protein 4-like, 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 18 samples with support for all annotated introns
V-set and immunoglobulin domain-containing protein 4-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 12 samples with support for all annotated introns
V-set and immunoglobulin domain-containing protein 4-like isoform X1
V-set and immunoglobulin domain-containing protein 4-like isoform X2
non-POU domain-containing octamer-binding protein-like, transcript variant X1
non-POU domain-containing octamer-binding protein-like, transcript variant X2
non-POU domain-containing octamer-binding protein-like isoform X1
non-POU domain-containing octamer-binding protein-like, transcript variant X3
non-POU domain-containing octamer-binding protein-like isoform X2
C1GALT1-specific chaperone 1, transcript variant X3
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 21 samples with support for all annotated introns
C1GALT1-specific chaperone 1, transcript variant X1
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 9 samples with support for all annotated introns
C1GALT1-specific chaperone 1, 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 2 samples with support for all annotated introns
lysosomal-associated membrane protein 2, transcript variant X1
lysosomal-associated membrane protein 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 19 samples with support for all annotated introns
lysosomal-associated membrane protein 2, 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 19 samples with support for all annotated introns
lysosomal-associated membrane protein 2, transcript variant X4
lysosomal-associated membrane protein 2, transcript variant X5
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 23 samples with support for all annotated introns
lysosome-associated membrane glycoprotein 2 isoform X1
lysosome-associated membrane glycoprotein 2 isoform X4
lysosome-associated membrane glycoprotein 2 isoform X3
lysosome-associated membrane glycoprotein 2 isoform X5
lysosome-associated membrane glycoprotein 2 isoform X2
heat shock factor protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
heat shock factor protein 1-like isoform X4
heat shock factor protein 1-like, transcript variant X2
heat shock factor protein 1-like, transcript variant X3
heat shock factor protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heat shock factor protein 1-like isoform X3
heat shock factor protein 1-like isoform X2
heat shock factor protein 1-like isoform X1
uncharacterized protein C21orf140 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
synaptotagmin-like protein 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
synaptotagmin-like protein 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 12 samples with support for all annotated introns
synaptotagmin-like protein 2, transcript variant X3
synaptotagmin-like protein 2, transcript variant X4
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
synaptotagmin-like protein 2, transcript variant X5
synaptotagmin-like protein 2, transcript variant X6
ras-related protein Rab-39B, transcript variant X2
ras-related protein Rab-39B, transcript variant X1
ras-related protein Rab-39B, transcript variant X3
ras-related protein Rab-39B, transcript variant X4
von Hippel-Lindau binding protein 1, transcript variant X2
von Hippel-Lindau binding protein 1, transcript variant X1
phosphatidylinositol-binding clathrin assembly protein, transcript variant X1
phosphatidylinositol-binding clathrin assembly protein, transcript variant X2
phosphatidylinositol-binding clathrin assembly protein, transcript variant X5
phosphatidylinositol-binding clathrin assembly protein, transcript variant X8
phosphatidylinositol-binding clathrin assembly protein, transcript variant X6
phosphatidylinositol-binding clathrin assembly protein, transcript variant X3
phosphatidylinositol-binding clathrin assembly protein, transcript variant X7
phosphatidylinositol-binding clathrin assembly protein, transcript variant X4
phosphatidylinositol-binding clathrin assembly protein isoform X7
phosphatidylinositol-binding clathrin assembly protein isoform X5
phosphatidylinositol-binding clathrin assembly protein isoform X2
phosphatidylinositol-binding clathrin assembly protein isoform X4
phosphatidylinositol-binding clathrin assembly protein isoform X6
phosphatidylinositol-binding clathrin assembly protein isoform X3
phosphatidylinositol-binding clathrin assembly protein isoform X1
serine protease 23-like, transcript variant X1
serine protease 23-like, transcript variant X3
serine protease 23-like, transcript variant X2
serine protease 23-like, transcript variant X4
ras-related protein Rab-38-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ras-related protein Rab-38-like, transcript variant X2
ras-related protein Rab-38-like isoform X1
ras-related protein Rab-38-like isoform X2
uncharacterized protein LOC445063 homolog
cysteine and histidine-rich domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
small nuclear ribonucleoprotein 35 (U11/U12)
U11/U12 small nuclear ribonucleoprotein 35 kDa protein
high affinity cationic amino acid transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
StAR-related lipid transfer (START) domain containing 8, transcript variant X1
stAR-related lipid transfer protein 8 isoform X1
StAR-related lipid transfer (START) domain containing 8, 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 5 samples with support for all annotated introns
stAR-related lipid transfer protein 8 isoform X2
StAR-related lipid transfer (START) domain containing 8, transcript variant X3
stAR-related lipid transfer protein 8 isoform X3
glycerophosphoinositol inositolphosphodiesterase GDPD2-like, transcript variant X1
glycerophosphoinositol inositolphosphodiesterase GDPD2-like, transcript variant X2
glycerophosphodiester phosphodiesterase domain-containing protein 5-like isoform X1
glycerophosphoinositol inositolphosphodiesterase GDPD2-like isoform X2
PDZ domain containing 11, transcript variant X2
PDZ domain containing 11, transcript variant X1
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 19 samples with support for all annotated introns
mediator complex subunit 12, 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 6 samples with support for all annotated introns
mediator complex subunit 12, 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 16 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 12 isoform X1
mediator of RNA polymerase II transcription subunit 12 isoform X2
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 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: 32 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: 51 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: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-related protein Rab-6A-like, transcript variant X2
ras-related protein Rab-6A-like, transcript variant X1
ras-related protein Rab-6A-like isoform X2
ras-related protein Rab-6A-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
discs, large homolog 3 (Drosophila), transcript variant X4
discs, large homolog 3 (Drosophila), transcript variant X1
discs, large homolog 3 (Drosophila), transcript variant X2
discs, large homolog 3 (Drosophila), transcript variant X3
discs, large homolog 3 (Drosophila), transcript variant X6
discs, large homolog 3 (Drosophila), transcript variant X5
discs, large homolog 3 (Drosophila), transcript variant X8
discs, large homolog 3 (Drosophila), transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, transcript variant X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, transcript variant X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X1
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X3
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X2
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X1
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X4
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X6
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X5
transcription initiation factor TFIID subunit 1
rho-related GTP-binding protein RhoG-like, transcript variant X3
rho-related GTP-binding protein RhoG-like, transcript variant X1
rho-related GTP-binding protein RhoG-like, transcript variant X2
rho-related GTP-binding protein RhoG-like
FH2 domain containing 2, transcript variant X2
FH2 domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
centromere protein I, transcript variant X1
centromere protein I, transcript variant X2
XK related X-linked, transcript variant X1
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 4 samples with support for all annotated introns
XK related X-linked, transcript variant X3
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
XK related X-linked, transcript variant X5
XK related X-linked, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
XK related X-linked, 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 5 samples with support for all annotated introns
XK related X-linked, transcript variant X6
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
XK related X-linked, transcript variant X7
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 13 samples with support for all annotated introns
FERM and PDZ domain-containing protein 3
uncharacterized LOC125458620, transcript variant X2
uncharacterized LOC125458620, transcript variant X1
cytochrome c oxidase assembly protein COX11, mitochondrial, transcript variant X4
cytochrome c oxidase assembly protein COX11, mitochondrial, transcript variant X1
cytochrome c oxidase assembly protein COX11, mitochondrial, transcript variant X3
cytochrome c oxidase assembly protein COX11, mitochondrial, transcript variant X2
cytochrome c oxidase assembly protein COX11, mitochondrial
MORC family CW-type zinc finger protein 4-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
MORC family CW-type zinc finger protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MORC family CW-type zinc finger protein 4-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, including 2 samples with support for all annotated introns
MORC family CW-type zinc finger protein 4-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 3 samples with support for all annotated introns
MORC family CW-type zinc finger protein 4-like, transcript variant X5
MORC family CW-type zinc finger protein 4-like isoform X1
MORC family CW-type zinc finger protein 3-like isoform X2
MORC family CW-type zinc finger protein 3-like isoform X3
MORC family CW-type zinc finger protein 3-like isoform X4
MORC family CW-type zinc finger protein 3-like isoform X5
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 3 samples with support for all annotated introns
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 9 samples with support for all annotated introns
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 6 samples with support for all annotated introns
Rho GTPase activating protein 36, transcript variant X2
Rho GTPase activating protein 36, 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 2 samples with support for all annotated introns
rho GTPase-activating protein 36 isoform X1
rho GTPase-activating protein 36 isoform X2
Rho GTPase activating protein 36, transcript variant X3
rho GTPase-activating protein 36 isoform X3
probable E3 ubiquitin-protein ligase MID2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase MID2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase MID2, transcript variant X2
probable E3 ubiquitin-protein ligase MID2
NIMA-related kinase 12, transcript variant X2
NIMA-related kinase 12, transcript variant X3
NIMA-related kinase 12, transcript variant X1
NIMA-related kinase 12, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein Shroom4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein Shroom4-like, transcript variant X6
protein Shroom4-like, 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 3 samples with support for all annotated introns
protein Shroom4-like, transcript variant X3
protein Shroom4-like, transcript variant X5
protein Shroom4-like, transcript variant X4
chloride channel, voltage-sensitive 5b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
chloride channel, voltage-sensitive 5b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
chloride channel, voltage-sensitive 5b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
chloride channel, voltage-sensitive 5b, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chloride channel, voltage-sensitive 5b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
chloride channel, voltage-sensitive 5b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
chloride channel, voltage-sensitive 5b, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
chloride channel, voltage-sensitive 5b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
H(+)/Cl(-) exchange transporter 5 isoform X1
chloride channel, voltage-sensitive 5b, transcript variant X11
chloride channel, voltage-sensitive 5b, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
H(+)/Cl(-) exchange transporter 5 isoform X2
chloride channel, voltage-sensitive 5b, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
H(+)/Cl(-) exchange transporter 5 isoform X3
TNF superfamily member 10, like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TNF superfamily member 10, like, 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 18 samples with support for all annotated introns
TNF superfamily member 10, like isoform X2
TNF superfamily member 10, like isoform X1
TNF superfamily member 10, like, transcript variant X3
TNF superfamily member 10, like isoform X3
uncharacterized si:dkey-171c9.3, transcript variant X2
uncharacterized si:dkey-171c9.3, transcript variant X1
uncharacterized protein si:dkey-171c9.3 isoform X2
uncharacterized protein si:dkey-171c9.3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
methionyl-tRNA synthetase 2, mitochondrial, transcript variant X2
methionyl-tRNA synthetase 2, mitochondrial, transcript variant X1
methionine--tRNA ligase, mitochondrial isoform X2
methionine--tRNA ligase, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein eva-1 homolog C, transcript variant X1
protein eva-1 homolog C, transcript variant X2
OCRL inositol polyphosphate-5-phosphatase, transcript variant X2
OCRL inositol polyphosphate-5-phosphatase, transcript variant X1
inositol polyphosphate 5-phosphatase OCRL isoform X2
inositol polyphosphate 5-phosphatase OCRL isoform X1
inositol polyphosphate 5-phosphatase OCRL-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound, transcript variant X1
X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound, transcript variant X3
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 4 samples with support for all annotated introns
X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound, 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
X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound, transcript variant X4
SAM and SH3 domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
SAM and SH3 domain containing 3, 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 11 samples with support for all annotated introns
SAM and SH3 domain-containing protein 3 isoform X1
SAM and SH3 domain-containing protein 3 isoform X2
zinc finger DHHC-type palmitoyltransferase 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC553498 homolog, transcript variant X1
U3 small nucleolar RNA-associated protein 14 homolog A isoform X1
uncharacterized protein LOC553498 homolog, transcript variant X2
U3 small nucleolar RNA-associated protein 14 homolog A isoform X2
uncharacterized LOC125458654, transcript variant X2
uncharacterized LOC125458654, transcript variant X1
BCL6 corepressor-like 1, transcript variant X2
BCL6 corepressor-like 1, transcript variant X1
BCL6 corepressor-like 1, transcript variant X3
BCL-6 corepressor-like protein 1 isoform X1
BCL-6 corepressor-like protein 1 isoform X2
sushi-repeat containing protein X-linked 2, 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 13 samples with support for all annotated introns
sushi repeat-containing protein SRPX2 isoform X2
sushi-repeat containing protein X-linked 2, transcript variant X1
sushi repeat-containing protein SRPX2 isoform X1
uncharacterized protein LOC335392 homolog
uncharacterized protein si:ch211-153b23.4
uncharacterized protein LOC321177 homolog
glutamine amidotransferase-like class 1 domain-containing protein 3, mitochondrial
uncharacterized protein LOC565650 homolog
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: 3 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein zgc:174917
glyoxalase domain containing 5, transcript variant X2
glyoxalase domain containing 5, 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 1 sample with support for all annotated introns
glyoxalase domain-containing protein 5 isoform X2
glyoxalase domain-containing protein 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein si:ch211-153b23.3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
exocyst complex component 1-like, transcript variant X1
exocyst complex component 1-like isoform X1
exocyst complex component 1-like, transcript variant X2
exocyst complex component 1-like isoform X2
potassium channel tetramerisation domain containing 12b
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
BTB/POZ domain-containing protein KCTD12b
TNFAIP3-interacting protein 3, transcript variant X2
TNFAIP3-interacting protein 3, transcript variant X1
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
Kruppel-like factor 5 like, transcript variant X1
Kruppel-like factor 5 like, transcript variant X2
Krueppel-like factor 8, transcript variant X13
Krueppel-like factor 8, transcript variant X2
Krueppel-like factor 8, transcript variant X1
Krueppel-like factor 8, transcript variant X7
Krueppel-like factor 8, transcript variant X15
Krueppel-like factor 8, transcript variant X14
Krueppel-like factor 8, transcript variant X6
Krueppel-like factor 8, transcript variant X3
Krueppel-like factor 8, transcript variant X5
Krueppel-like factor 8, transcript variant X11
Krueppel-like factor 8, transcript variant X10
Krueppel-like factor 8, transcript variant X12
Krueppel-like factor 8, transcript variant X9
Krueppel-like factor 8, transcript variant X8
Krueppel-like factor 8, transcript variant X4
glucose-dependent insulinotropic receptor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
seven in absentia homolog 2 (Drosophila)-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibrous sheath-interacting protein 2-like, transcript variant X2
fibrous sheath-interacting protein 2-like isoform X2
fibrous sheath-interacting protein 2-like, transcript variant X1
fibrous sheath-interacting protein 2-like isoform X1
tumor necrosis factor ligand superfamily member 10-like
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 20 samples with support for all annotated introns
ATP-binding cassette sub-family C member 5-like, transcript variant X1
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 1 sample with support for all annotated introns
ATP-binding cassette sub-family C member 5-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette sub-family C member 5-like, transcript variant X2
ATP-binding cassette sub-family C member 5-like, transcript variant X4
ATP-binding cassette sub-family C member 5-like, transcript variant X3
ATP-binding cassette sub-family C member 5-like, transcript variant X5
ATP-binding cassette sub-family C member 5-like isoform X1
ATP-binding cassette sub-family C member 5-like isoform X5
ATP-binding cassette sub-family C member 5-like isoform X2
ATP-binding cassette sub-family C member 5-like isoform X3
ATP-binding cassette sub-family C member 5-like isoform X4
ecto-NOX disulfide-thiol exchanger 2-like
centrin, EF-hand protein, 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
centrin, EF-hand protein, 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
centrin, EF-hand protein, 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
NAD(P) dependent steroid dehydrogenase-like, 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 8 samples with support for all annotated introns
NAD(P) dependent steroid dehydrogenase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating
SLAIN motif-containing protein-like, 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 16 samples with support for all annotated introns
SLAIN motif-containing protein-like, 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 16 samples with support for all annotated introns
SLAIN motif-containing protein-like isoform X1
SLAIN motif-containing protein-like isoform X2
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 24 samples with support for all annotated introns
DNA-directed RNA polymerases I and III subunit RPAC2
endothelin receptor type B-like, transcript variant X3
endothelin receptor type B-like, transcript variant X2
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 1 sample with support for all annotated introns
endothelin receptor type B-like, transcript variant X1
endothelin receptor type B-like isoform X2
endothelin receptor type B-like isoform X1
brain-specific homeobox/POU domain protein 3-like
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
protein sprouty homolog 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
protein sprouty homolog 2, transcript variant X5
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 4 samples with support for all annotated introns
protein sprouty homolog 2, transcript variant X3
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 10 samples with support for all annotated introns
protein sprouty homolog 2, transcript variant X4
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
protein sprouty homolog 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
short coiled-coil protein B-like, transcript variant X9
short coiled-coil protein B-like, transcript variant X1
short coiled-coil protein B-like, 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 8 samples with support for all annotated introns
short coiled-coil protein B-like, transcript variant X6
short coiled-coil protein B-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
short coiled-coil protein B-like, transcript variant X3
uncharacterized protein LOC125458722 isoform X6
short coiled-coil protein B-like isoform X3
short coiled-coil protein B-like, transcript variant X2
short coiled-coil protein B-like isoform X2
short coiled-coil protein B-like isoform X1
short coiled-coil protein B-like isoform X4
short coiled-coil protein B-like, transcript variant X8
short coiled-coil protein B-like, transcript variant X7
short coiled-coil protein B-like isoform X5
trimethyllysine dioxygenase, mitochondrial
H/ACA ribonucleoprotein complex subunit DKC1
COORDINATES: nucleotide motif:Rfam:12.0:RF00567
COORDINATES: nucleotide motif:Rfam:12.0:RF00137
COORDINATES: nucleotide motif:Rfam:12.0:RF00340
55 kDa erythrocyte membrane protein-like, transcript variant X3
55 kDa erythrocyte membrane protein-like, transcript variant X1
55 kDa erythrocyte membrane protein-like, transcript variant X2
55 kDa erythrocyte membrane protein-like isoform X3
55 kDa erythrocyte membrane protein-like isoform X2
55 kDa erythrocyte membrane protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
BRCA1/BRCA2-containing complex, subunit 3
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X1
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X2
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X3
coagulation factor VIII, procoagulant component
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cleavage stimulation factor subunit 2-like, transcript variant X2
cleavage stimulation factor subunit 2-like, transcript variant X3
cleavage stimulation factor subunit 2-like, transcript variant X1
cleavage stimulation factor subunit 2-like isoform X2
cleavage stimulation factor subunit 2-like isoform X3
cleavage stimulation factor subunit 2-like isoform X1
tRNA methyltransferase 12 homolog, 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 20 samples with support for all annotated introns
tRNA methyltransferase 12 homolog, transcript variant X2
tRNA wybutosine-synthesizing protein 2 homolog
mitochondrial fission factor-like, transcript variant X5
mitochondrial fission factor-like, transcript variant X4
mitochondrial fission factor-like, transcript variant X3
mitochondrial fission factor-like, transcript variant X1
mitochondrial fission factor-like, transcript variant X2
mitochondrial fission factor-like isoform X5
mitochondrial fission factor-like isoform X4
mitochondrial fission factor-like isoform X3
mitochondrial fission factor homolog A-like isoform X1
mitochondrial fission factor homolog A-like isoform X2
transmembrane gamma-carboxyglutamic acid protein 3, transcript variant X3
transmembrane gamma-carboxyglutamic acid protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transmembrane gamma-carboxyglutamic acid protein 3, 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 14 samples with support for all annotated introns
transmembrane gamma-carboxyglutamic acid protein 3 isoform X3
transmembrane gamma-carboxyglutamic acid protein 3 isoform X2
transmembrane gamma-carboxyglutamic acid protein 3 isoform X1
phospholipase A2, group XIIA, 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 24 samples with support for all annotated introns
phospholipase A2, group XIIA, 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 6 samples with support for all annotated introns
protein (peptidylprolyl cis/trans isomerase) NIMA-interacting, 4 (parvulin)
peptidyl-prolyl cis-trans isomerase NIMA-interacting 4
phosphorylase kinase, alpha 1a (muscle), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphorylase kinase, alpha 1a (muscle), transcript variant X2
phosphorylase kinase, alpha 1a (muscle), transcript variant X3
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 3 samples with support for all annotated introns
phosphorylase kinase, alpha 1a (muscle), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
phosphorylase kinase, alpha 1a (muscle), transcript variant X5
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform isoform X1
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform isoform X2
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform isoform X4
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform isoform X3
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform isoform X5
histone deacetylase 8, 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 21 samples with support for all annotated introns
histone deacetylase 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
histone deacetylase 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
histone deacetylase 8, transcript variant X5
histone deacetylase 8, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
histone deacetylase 8, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor-like protein 13B
uncharacterized protein LOC555281 homolog
zinc finger protein 711, transcript variant X3
zinc finger protein 711, transcript variant X2
zinc finger protein 711, transcript variant X4
zinc finger protein 711, transcript variant X5
zinc finger protein 711, transcript variant X1
rab proteins geranylgeranyltransferase component A 1
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 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 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane protein 33-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
transmembrane protein 33-like, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
kelch-like protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kelch-like protein 4, transcript variant X3
kelch-like protein 4, transcript variant X1
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
protocadherin-20-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protocadherin-20-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
diaphanous-related formin 2, transcript variant X1
diaphanous-related formin 2, transcript variant X4
diaphanous-related formin 2, transcript variant X2
diaphanous-related formin 2, transcript variant X3
diaphanous-related formin 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC125458634, transcript variant X2
uncharacterized LOC125458634, transcript variant X1
E74-like ETS transcription factor 1, transcript variant X2
E74-like ETS transcription factor 1, transcript variant X4
E74-like ETS transcription factor 1, transcript variant X1
E74-like ETS transcription factor 1, transcript variant X3
E74-like ETS transcription factor 1, transcript variant X5
E74-like ETS transcription factor 1, transcript variant X6
ETS-related transcription factor Elf-1 isoform X2
ETS-related transcription factor Elf-1 isoform X1
ETS-related transcription factor Elf-1 isoform X3
ETS-related transcription factor Elf-1 isoform X4
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
apoptosis inducing factor mitochondrion associated 1, transcript variant X1
apoptosis inducing factor mitochondrion associated 1, transcript variant X2
apoptosis-inducing factor 1, mitochondrial isoform X1
apoptosis-inducing factor 1, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
interferon gamma receptor 1-like, transcript variant X1
interferon gamma receptor 1-like, transcript variant X2
interferon gamma receptor 1-like isoform X1
interferon gamma receptor 1-like isoform X2
chloride intracellular channel 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
chloride intracellular channel 2, transcript variant X3
chloride intracellular channel 2, transcript variant X4
chloride intracellular channel 2, transcript variant X2
chloride intracellular channel protein 2 isoform X1
chloride intracellular channel protein 2 isoform X2
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X1
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X5
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X2
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X4
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X3
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X1
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X5
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X2
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X3
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X4
interleukin-13 receptor subunit alpha-2-like, transcript variant X1
interleukin-13 receptor subunit alpha-2-like, transcript variant X2
interleukin-13 receptor subunit alpha-2-like, transcript variant X5
interleukin-13 receptor subunit alpha-2-like, transcript variant X3
interleukin-13 receptor subunit alpha-2-like, transcript variant X6
interleukin-13 receptor subunit alpha-2-like, transcript variant X4
interleukin-13 receptor subunit alpha-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial-like
TAF9 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 9
fibronectin type-III domain-containing protein 3A-like, 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 16 samples with support for all annotated introns
fibronectin type-III domain-containing protein 3A-like, 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 7 samples with support for all annotated introns
fibronectin type-III domain-containing protein 3A-like, transcript variant X3
fibronectin type-III domain-containing protein 3A-like isoform X1
fibronectin type-III domain-containing protein 3A-like, 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 4 samples with support for all annotated introns
fibronectin type-III domain-containing protein 3a-like isoform X2
cysteinyl leukotriene receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
cysteinyl leukotriene receptor 1-like, transcript variant X2
cysteinyl leukotriene receptor 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cysteinyl leukotriene receptor 1-like isoform X1
cysteinyl leukotriene receptor 1-like isoform X2
uncharacterized LOC125458856, transcript variant X2
uncharacterized LOC125458856, transcript variant X1
type-1 angiotensin II receptor-like, transcript variant X3
type-1 angiotensin II receptor-like, transcript variant X5
type-1 angiotensin II receptor-like, transcript variant X4
type-1 angiotensin II receptor-like, transcript variant X1
type-1 angiotensin II receptor-like, transcript variant X2
lysophosphatidic acid receptor 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
lysophosphatidic acid receptor 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
lysophosphatidic acid receptor 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable G-protein coupled receptor 174, 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
probable G-protein coupled receptor 174, transcript variant X5
probable G-protein coupled receptor 174, transcript variant X8
probable G-protein coupled receptor 174, transcript variant X1
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
probable G-protein coupled receptor 174, transcript variant X2
probable G-protein coupled receptor 174, transcript variant X9
probable G-protein coupled receptor 174, transcript variant X10
probable G-protein coupled receptor 174, transcript variant X6
probable G-protein coupled receptor 174, transcript variant X3
probable G-protein coupled receptor 174, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
2-Hydroxyacid oxidase 2-like, 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
2-Hydroxyacid oxidase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
terminal nucleotidyltransferase 5C-like, transcript variant X4
terminal nucleotidyltransferase 5C-like, transcript variant X5
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 9 samples with support for all annotated introns
terminal nucleotidyltransferase 5C-like, transcript variant X1
terminal nucleotidyltransferase 5C-like isoform X1
terminal nucleotidyltransferase 5C-like, 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 3 samples with support for all annotated introns
terminal nucleotidyltransferase 5C-like, 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 2 samples with support for all annotated introns
terminal nucleotidyltransferase 5C-like isoform X2
terminal nucleotidyltransferase 5C-like isoform X3
terminal nucleotidyltransferase 5C-like isoform X4
terminal nucleotidyltransferase 5C-like isoform X5
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
bromodomain and WD repeat domain containing 3, 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 17 samples with support for all annotated introns
bromodomain and WD repeat-containing protein 3 isoform X1
bromodomain and WD repeat domain containing 3, 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 11 samples with support for all annotated introns
bromodomain and WD repeat domain containing 3, transcript variant X3
bromodomain and WD repeat-containing protein 3 isoform X2
bromodomain and WD repeat domain containing 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
bromodomain and WD repeat-containing protein 3 isoform X3
uncharacterized LOC125458668, transcript variant X2
uncharacterized LOC125458668, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
high mobility group nucleosomal binding domain 7, transcript variant X3
high mobility group nucleosomal binding domain 7, transcript variant X1
high mobility group nucleosomal binding domain 7, transcript variant X4
high mobility group nucleosomal binding domain 7, transcript variant X2
high mobility group nucleosomal binding domain 7 isoform X3
high mobility group nucleosomal binding domain 7 isoform X1
high mobility group nucleosomal binding domain 7 isoform X4
high mobility group nucleosomal binding domain 7 isoform X2
SH3 domain binding glutamate-rich protein like, transcript variant X2
SH3 domain-binding glutamic acid-rich-like protein isoform X2
SH3 domain binding glutamate-rich protein like, transcript variant X1
SH3 domain-binding glutamic acid-rich-like protein isoform X1
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like, transcript variant X1
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like, transcript variant X2
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like isoform X1
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like, transcript variant X3
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like isoform X2
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like isoform X3
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like, transcript variant X4
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like, transcript variant X5
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like isoform X4
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like isoform X5
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like, transcript variant X6
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
U2 snRNP-associated SURP motif-containing protein-like, transcript variant X1
U2 snRNP-associated SURP motif-containing protein-like, transcript variant X3
U2 snRNP-associated SURP motif-containing protein-like, transcript variant X2
U2 snRNP-associated SURP motif-containing protein-like isoform X1
U2 snRNP-associated SURP motif-containing protein-like isoform X2
U2 snRNP-associated SURP motif-containing protein-like isoform X3
plastin 3 (T isoform), transcript variant X1
plastin 3 (T isoform), transcript variant X3
plastin 3 (T isoform), transcript variant X4
plastin 3 (T isoform), transcript variant X5
plastin 3 (T isoform), transcript variant X2
diamine acetyltransferase 1-like, transcript variant X4
diamine acetyltransferase 1-like, transcript variant X3
diamine acetyltransferase 1-like, transcript variant X7
diamine acetyltransferase 1-like, transcript variant X5
diamine acetyltransferase 1-like, transcript variant X6
diamine acetyltransferase 1-like, transcript variant X1
diamine acetyltransferase 1-like, transcript variant X2
spermidine/spermine N(1)-acetyltransferase-like protein 1 isoform X1
diamine acetyltransferase 1-like isoform X2
MICOS complex subunit MIC27-like, transcript variant X2
MICOS complex subunit MIC27-like, transcript variant X1
MICOS complex subunit MIC27-like isoform X1
MICOS complex subunit MIC27-like isoform X2
connector enhancer of kinase suppressor of ras 2, transcript variant X3
connector enhancer of kinase suppressor of ras 2, 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 5 samples with support for all annotated introns
connector enhancer of kinase suppressor of ras 2, transcript variant X2
connector enhancer of kinase suppressor of ras 2, transcript variant X4
connector enhancer of kinase suppressor of ras 2 isoform X3
connector enhancer of kinase suppressor of ras 2 isoform X1
connector enhancer of kinase suppressor of ras 2 isoform X2
connector enhancer of kinase suppressor of ras 2 isoform X4
connector enhancer of kinase suppressor of ras 2, transcript variant X5
highly divergent homeobox, transcript variant X3
highly divergent homeobox, transcript variant X6
highly divergent homeobox, transcript variant X10
highly divergent homeobox, transcript variant X9
highly divergent homeobox, transcript variant X5
highly divergent homeobox, transcript variant X4
highly divergent homeobox, transcript variant X1
highly divergent homeobox, transcript variant X8
highly divergent homeobox, transcript variant X7
highly divergent homeobox, transcript variant X2
ribosomal protein S6 kinase alpha-6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ribosomal protein S6 kinase alpha-6, transcript variant X3
ribosomal protein S6 kinase alpha-6 isoform X1
ribosomal protein S6 kinase alpha-6 isoform X3
ribosomal protein S6 kinase alpha-6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ribosomal protein S6 kinase alpha-6 isoform X2
ribosomal protein S6 kinase alpha-6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribosomal protein S6 kinase alpha-6, transcript variant X4
ribosomal protein S6 kinase alpha-6 isoform X4
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
POU domain, class 3, transcription factor 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
sodium/hydrogen exchanger 2-like, transcript variant X1
sodium/hydrogen exchanger 2-like isoform X1
sodium/hydrogen exchanger 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium/hydrogen exchanger 2-like isoform X2
sodium/hydrogen exchanger 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium/hydrogen exchanger 2-like isoform X3
nuclear receptor subfamily 0 group B member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 21% 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 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 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: 8 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
kelch-like family member 13, transcript variant X6
kelch-like family member 13, transcript variant X1
kelch-like family member 13, transcript variant X7
kelch-like family member 13, transcript variant X3
kelch-like family member 13, transcript variant X5
kelch-like family member 13, transcript variant X2
kelch-like family member 13, transcript variant X4
kelch-like family member 13, transcript variant X8
WD repeat domain 44, transcript variant X1
WD repeat-containing protein 44 isoform X1
WD repeat domain 44, transcript variant X2
WD repeat-containing protein 44 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 92% 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: tRNA (uracil-5-)-methyltransferase homolog B
muscleblind-like protein 3, transcript variant X4
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
muscleblind-like protein 3, transcript variant X3
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 6 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X5
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
muscleblind-like protein 3, transcript variant X2
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 5 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X6
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 4 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X8
muscleblind-like protein 3, transcript variant X15
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
muscleblind-like protein 3, transcript variant X1
muscleblind-like protein 3, transcript variant X11
muscleblind-like protein 3, transcript variant X7
muscleblind-like protein 3, transcript variant X13
muscleblind-like protein 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X12
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 7 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X16
muscleblind-like protein 3, transcript variant X14
interleukin-13 receptor subunit alpha-1-like
dedicator of cytokinesis protein 11-like, transcript variant X5
dedicator of cytokinesis protein 11-like, transcript variant X1
dedicator of cytokinesis protein 11-like, transcript variant X3
dedicator of cytokinesis protein 11-like, transcript variant X2
dedicator of cytokinesis protein 11-like, transcript variant X6
dedicator of cytokinesis protein 11-like, transcript variant X4
dedicator of cytokinesis protein 11-like isoform X5
dedicator of cytokinesis protein 11-like isoform X1
dedicator of cytokinesis protein 11-like isoform X3
dedicator of cytokinesis protein 11-like isoform X2
dedicator of cytokinesis protein 11-like isoform X6
dedicator of cytokinesis protein 11-like isoform X4
uncharacterized LOC125458692, transcript variant X1
uncharacterized LOC125458692, transcript variant X2
interferon-inducible GTPase 5-like, transcript variant X2
interferon-inducible GTPase 5-like, transcript variant X3
interferon-inducible GTPase 5-like, transcript variant X4
interferon-inducible GTPase 5-like, transcript variant X5
interferon-inducible GTPase 5-like, transcript variant X1
interferon-inducible GTPase 5-like, transcript variant X6
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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: interferon-inducible GTPase 1-like
diacylglycerol kinase eta, transcript variant X2
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 4 samples with support for all annotated introns
diacylglycerol kinase eta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
diacylglycerol kinase eta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: T-cell-specific guanine nucleotide triphosphate-binding protein 2-like
proteolipid protein DM alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
proteolipid protein DM alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glycine receptor, alpha 4a, transcript variant X3
glycine receptor, alpha 4a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glycine receptor, alpha 4a, transcript variant X1
glycine receptor, alpha 4a, transcript variant X4
galactosidase, alpha, transcript variant X1
galactosidase, alpha, transcript variant X2
Bruton agammaglobulinemia tyrosine kinase, transcript variant X1
Bruton agammaglobulinemia tyrosine kinase, transcript variant X3
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 8 samples with support for all annotated introns
Bruton agammaglobulinemia tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
translocase of inner mitochondrial membrane 8 homolog A (yeast)
mitochondrial import inner membrane translocase subunit Tim8 A
uncharacterized protein LOC494104 homolog, transcript variant X3
uncharacterized protein LOC494104 homolog, transcript variant X1
uncharacterized protein LOC494104 homolog, transcript variant X2
TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 7
gamma-aminobutyric acid receptor subunit gamma-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit gamma-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit gamma-4-like isoform X2
gamma-aminobutyric acid receptor subunit gamma-4-like isoform X1
gamma-aminobutyric acid receptor subunit alpha-3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit alpha-3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit alpha-3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit alpha-3-like, transcript variant X4
gamma-aminobutyric acid receptor subunit alpha-3-like isoform X1
gamma-aminobutyric acid receptor subunit alpha-3-like isoform X2
gamma-aminobutyric acid receptor subunit alpha-3-like isoform X3
gamma-aminobutyric acid receptor subunit beta-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-4-like isoform X2
gamma-aminobutyric acid receptor subunit beta-4-like, transcript variant X3
gamma-aminobutyric acid receptor subunit beta-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-4-like isoform X1
gamma-aminobutyric acid receptor subunit beta-4-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-4-like isoform X4
gamma-aminobutyric acid receptor subunit beta-4-like, transcript variant X4
gamma-aminobutyric acid receptor subunit beta-4-like isoform X3
dynein axonemal assembly factor 6, transcript variant X1
dynein axonemal assembly factor 6, transcript variant X3
dynein axonemal assembly factor 6, transcript variant X4
dynein axonemal assembly factor 6, transcript variant X2
cyclic nucleotide-gated olfactory channel-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
nitric oxide synthase, brain-like, transcript variant X1
nitric oxide synthase, brain-like, transcript variant X2
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, including 5 samples with support for all annotated introns
nitric oxide synthase, brain-like isoform X1
nitric oxide synthase, brain-like isoform X2
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, including 14 samples with support for all annotated introns
uncharacterized LOC125459039, transcript variant X2
uncharacterized LOC125459039, transcript variant X1
zinc finger protein 229-like, transcript variant X1
zinc finger protein 229-like, transcript variant X3
zinc finger protein 229-like, transcript variant X2
zinc finger protein 229-like, transcript variant X4
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X5
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X4
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X7
zinc finger protein 239-like, transcript variant X6
zinc finger protein 239-like, transcript variant X9
zinc finger protein 239-like, transcript variant X8