Stegostoma fasciatum isolate 6-17 chromosome 25, 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\nCM039251.1.\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.
scavenger receptor class B member 1-like, transcript variant X1
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 7 samples with support for all annotated introns
scavenger receptor class B member 1-like, transcript variant X4
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 21 samples with support for all annotated introns
scavenger receptor class B member 1-like, 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
scavenger receptor class B member 1-like, 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 3 samples with support for all annotated introns
scavenger receptor class B member 1-like isoform X1
scavenger receptor class B member 1-like isoform X4
scavenger receptor class B member 1-like isoform X3
scavenger receptor class B member 1-like isoform X2
scavenger receptor class B member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
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 12 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 15 samples with support for all annotated introns
coiled-coil domain containing 92, transcript variant X4
coiled-coil domain containing 92, transcript variant X2
coiled-coil domain containing 92, transcript variant X3
coiled-coil domain containing 92, transcript variant X6
coiled-coil domain containing 92, transcript variant X5
coiled-coil domain containing 92, transcript variant X1
coiled-coil domain-containing protein 92
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dynein axonemal heavy chain 10
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 21 samples with support for all annotated introns
V-type proton ATPase 116 kDa subunit a 2-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 1 sample with support for all annotated introns
V-type proton ATPase 116 kDa subunit a 2-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, including 1 sample with support for all annotated introns
V-type proton ATPase 116 kDa subunit a 2-like isoform X1
V-type proton ATPase 116 kDa subunit a 2-like isoform X2
tectonic family member 2, transcript variant X2
tectonic family member 2, transcript variant X1
uncharacterized LOC125464251, 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
uncharacterized LOC125464251, 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 2 samples with support for all annotated introns
uncharacterized protein LOC125464251 isoform X1
uncharacterized protein LOC125464251 isoform X2
general transcription factor IIH, polypeptide 3
general transcription factor IIH subunit 3
eukaryotic translation initiation factor 2B, subunit 1 alpha
translation initiation factor eIF-2B subunit alpha
DEAD (Asp-Glu-Ala-Asp) box polypeptide 55
transmembrane p24 trafficking protein 2, transcript variant X2
transmembrane p24 trafficking protein 2, transcript variant X1
transmembrane emp24 domain-containing protein 2 isoform X2
transmembrane emp24 domain-containing protein 2 isoform X1
Rab interacting lysosomal protein-like 1, transcript variant X1
Rab interacting lysosomal protein-like 1, 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 8 samples with support for all annotated introns
N-lysine methyltransferase KMT5A-like, transcript variant X2
N-lysine methyltransferase KMT5A-like, transcript variant X1
N-lysine methyltransferase KMT5A-like, transcript variant X7
N-lysine methyltransferase KMT5A-like, transcript variant X5
N-lysine methyltransferase KMT5A-like, transcript variant X3
N-lysine methyltransferase KMT5A-like, transcript variant X8
N-lysine methyltransferase KMT5A-like, transcript variant X6
N-lysine methyltransferase KMT5A-like, transcript variant X4
N-lysine methyltransferase KMT5A-like isoform X2
N-lysine methyltransferase KMT5A-like isoform X1
N-lysine methyltransferase KMT5A-like isoform X5
N-lysine methyltransferase KMT5A-like isoform X3
N-lysine methyltransferase KMT5A-like isoform X8
N-lysine methyltransferase KMT5A-like isoform X7
N-lysine methyltransferase KMT5A-like isoform X6
N-lysine methyltransferase KMT5A-like isoform X4
N-lysine methyltransferase KMT5A-like, transcript variant X9
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
N-lysine methyltransferase KMT5A-like, transcript variant X10
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
N-lysine methyltransferase KMT5A-like isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
cyclin-dependent kinase 2-associated protein 1
mitochondrial translation release factor in rescue
M-phase phosphoprotein 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
M-phase phosphoprotein 9, transcript variant X1
M-phase phosphoprotein 9, transcript variant X4
M-phase phosphoprotein 9, transcript variant X6
M-phase phosphoprotein 9, 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 2 samples with support for all annotated introns
M-phase phosphoprotein 9, 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 1 sample with support for all annotated introns
phosphatidylinositol transfer protein, beta, transcript variant X1
phosphatidylinositol transfer protein, beta, transcript variant X3
phosphatidylinositol transfer protein, beta, transcript variant X4
phosphatidylinositol transfer protein, beta, transcript variant X2
phosphatidylinositol transfer protein beta isoform
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
membrane-associated phosphatidylinositol transfer protein 2, transcript variant X1
membrane-associated phosphatidylinositol transfer protein 2, transcript variant X4
membrane-associated phosphatidylinositol transfer protein 2, transcript variant X2
membrane-associated phosphatidylinositol transfer protein 2, transcript variant X5
membrane-associated phosphatidylinositol transfer protein 2, transcript variant X3
membrane-associated phosphatidylinositol transfer protein 2 isoform X1
membrane-associated phosphatidylinositol transfer protein 2 isoform X4
membrane-associated phosphatidylinositol transfer protein 2 isoform X2
membrane-associated phosphatidylinositol transfer protein 2 isoform X5
membrane-associated phosphatidylinositol transfer protein 2 isoform X3
ADP-ribosylation factor-like 6 interacting protein 4, transcript variant X2
ADP-ribosylation factor-like protein 6-interacting protein 4 isoform X2
ADP-ribosylation factor-like 6 interacting protein 4, 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
ADP-ribosylation factor-like protein 6-interacting protein 4 isoform X1
2-oxoglutarate and iron-dependent oxygenase domain containing 2
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2
uncharacterized protein LOC503528 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 8 samples with support for all annotated introns
uncharacterized protein LOC503528 homolog, 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 16 samples with support for all annotated introns
uncharacterized protein zgc:113436 isoform X1
uncharacterized protein zgc:113436 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 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: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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 7 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 97% coverage of the annotated genomic feature by RNAseq alignments
splicing factor SWAP, transcript variant X1
splicing factor SWAP, transcript variant X4
splicing factor SWAP, transcript variant X2
splicing factor SWAP, 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 17 samples with support for all annotated introns
splicing factor, suppressor of white-apricot homolog isoform X1
splicing factor, suppressor of white-apricot homolog isoform X3
splicing factor, suppressor of white-apricot homolog isoform X2
splicing factor SWAP, transcript variant X5
splicing factor SWAP, transcript variant X6
splicing factor, suppressor of white-apricot homolog isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
unc-51 like autophagy activating kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
E1A binding protein p400, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E1A binding protein p400, transcript variant X6
E1A binding protein p400, transcript variant X5
E1A binding protein p400, transcript variant X8
E1A binding protein p400, transcript variant X2
E1A binding protein p400, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
E1A binding protein p400, transcript variant X4
E1A binding protein p400, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E1A binding protein p400, transcript variant X7
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00562
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
polypeptide N-acetylgalactosaminyltransferase 9
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
autism susceptibility gene 2 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
autism susceptibility gene 2 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
autism susceptibility gene 2 protein-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 3 samples with support for all annotated introns
autism susceptibility gene 2 protein-like
checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase, transcript variant X2
checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase, 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 20 samples with support for all annotated introns
checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase, 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 4 samples with support for all annotated introns
checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase, 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 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase CHFR isoform X2
E3 ubiquitin-protein ligase CHFR isoform X1
E3 ubiquitin-protein ligase CHFR isoform X3
E3 ubiquitin-protein ligase CHFR isoform X4
uncharacterized si:dkey-112e17.1, transcript variant X1
uncharacterized si:dkey-112e17.1, transcript variant X2
uncharacterized protein si:dkey-112e17.1 isoform X1
uncharacterized protein si:dkey-112e17.1 isoform X2
ankyrin repeat and LEM domain containing 2
ankyrin repeat and LEM domain-containing protein 2
PGAM family member 5, serine/threonine protein phosphatase, mitochondrial
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 24 samples with support for all annotated introns
serine/threonine-protein phosphatase PGAM5, mitochondrial
zinc finger DHHC-type palmitoyltransferase 8b
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 7 samples with support for all annotated introns
tRNA methyltransferase 2 homolog A, transcript variant X1
tRNA methyltransferase 2 homolog A, transcript variant X2
tRNA (uracil-5-)-methyltransferase homolog A isoform X1
tRNA (uracil-5-)-methyltransferase homolog A isoform X2
DGCR8 microprocessor complex subunit, 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 22 samples with support for all annotated introns
DGCR8 microprocessor complex subunit, 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 23 samples with support for all annotated introns
microprocessor complex subunit DGCR8 isoform X2
microprocessor complex subunit DGCR8 isoform X1
transport and golgi organization 2 homolog (Drosophila), 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 5 samples with support for all annotated introns
transport and golgi organization 2 homolog (Drosophila), transcript variant X5
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
transport and golgi organization 2 homolog (Drosophila), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transport and golgi organization 2 homolog (Drosophila), 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 2 samples with support for all annotated introns
transport and golgi organization 2 homolog (Drosophila), 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 1 sample with support for all annotated introns
transport and Golgi organization protein 2 homolog isoform X3
transport and Golgi organization protein 2 homolog isoform X1
transport and Golgi organization protein 2 homolog isoform X2
ARVCF delta catenin family member b, transcript variant X17
ARVCF delta catenin family member b, transcript variant X16
ARVCF delta catenin family member b, transcript variant X4
ARVCF delta catenin family member b, transcript variant X1
ARVCF delta catenin family member b, transcript variant X6
ARVCF delta catenin family member b, transcript variant X5
ARVCF delta catenin family member b, transcript variant X9
ARVCF delta catenin family member b, transcript variant X12
ARVCF delta catenin family member b, transcript variant X10
ARVCF delta catenin family member b, transcript variant X14
ARVCF delta catenin family member b, transcript variant X2
ARVCF delta catenin family member b, transcript variant X3
ARVCF delta catenin family member b, transcript variant X11
ARVCF delta catenin family member b isoform X3
ARVCF delta catenin family member b isoform X1
ARVCF delta catenin family member b isoform X2
ARVCF delta catenin family member b, transcript variant X15
ARVCF delta catenin family member b, transcript variant X7
ARVCF delta catenin family member b isoform X4
ARVCF delta catenin family member b, transcript variant X13
ARVCF delta catenin family member b, transcript variant X8
ARVCF delta catenin family member b isoform X5
ARVCF delta catenin family member b isoform X6
catechol-O-methyltransferase a, 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 1 sample with support for all annotated introns
catechol-O-methyltransferase a, transcript variant X1
catechol-O-methyltransferase a, transcript variant 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 6 samples with support for all annotated introns
catechol-O-methyltransferase a, transcript variant X3
catechol-O-methyltransferase a, transcript variant X6
catechol-O-methyltransferase a, transcript variant X5
catechol O-methyltransferase A isoform X2
catechol O-methyltransferase A isoform X1
catechol O-methyltransferase A isoform X3
thioredoxin reductase 2, tandem duplicate 2
guanine nucleotide binding protein (G protein), beta polypeptide 1-like, transcript variant X1
guanine nucleotide binding protein (G protein), beta polypeptide 1-like, transcript variant X2
guanine nucleotide binding protein (G protein), beta polypeptide 1-like, transcript variant X3
guanine nucleotide-binding protein subunit beta-like protein 1
T-box transcription factor 1, transcript variant X5
T-box transcription factor 1, transcript variant X6
T-box transcription factor 1, 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 2 samples with support for all annotated introns
T-box transcription factor 1, transcript variant X3
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
T-box transcription factor 1, transcript variant X1
T-box transcription factor 1, transcript variant X4
T-box transcription factor TBX1 isoform X2
T-box transcription factor TBX1 isoform X1
T-box transcription factor TBX1 isoform X4
T-box transcription factor TBX1 isoform X3
clathrin, heavy chain-like 1, transcript variant X1
clathrin, heavy chain-like 1, transcript variant X3
clathrin, heavy chain-like 1, transcript variant X4
clathrin, heavy chain-like 1, transcript variant X2
clathrin, heavy chain-like 1, transcript variant X6
clathrin, heavy chain-like 1, transcript variant X5
wiskott-Aldrich syndrome protein family member 2-like
tricarboxylate transport protein, mitochondrial
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 24 samples with support for all annotated introns
somatomedin-B and thrombospondin type-1 domain-containing protein
phosphatidylinositol 4-kinase, catalytic, alpha b
serpin peptidase inhibitor, clade D (heparin cofactor), member 1, transcript variant X2
serpin peptidase inhibitor, clade D (heparin cofactor), member 1, transcript variant X1
hypermethylated in cancer 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
hypermethylated in cancer 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
YdjC chitooligosaccharide deacetylase homolog, transcript variant X3
YdjC chitooligosaccharide deacetylase homolog, transcript variant X2
YdjC chitooligosaccharide deacetylase homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
stromal cell-derived factor 2-like protein 1
WSC domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WSC domain containing 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WSC domain containing 2, transcript variant X4
WSC domain containing 2, transcript variant X5
WSC domain containing 2, transcript variant X3
WSC domain containing 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 13 samples with support for all annotated introns
leucine rich repeat containing 74B, transcript variant X2
leucine rich repeat containing 74B, transcript variant X1
leucine rich repeat containing 74B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat-containing protein 74B isoform X1
leucine-rich repeat-containing protein 74B isoform X3
leucine-rich repeat-containing protein 74B isoform X2
solute carrier family 7 member 4, 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 1 sample with support for all annotated introns
solute carrier family 7 member 4, transcript variant X1
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 6 samples with support for all annotated introns
solute carrier family 7 member 4, transcript variant X2
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 4 samples with support for all annotated introns
DiGeorge syndrome critical region gene 6, transcript variant X3
DiGeorge syndrome critical region gene 6, transcript variant X1
DiGeorge syndrome critical region gene 6, transcript variant X2
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2, transcript variant X3
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2, transcript variant X1
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2, 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 8 samples with support for all annotated introns
Hermansky-Pudlak syndrome 4 protein isoform X2
Hermansky-Pudlak syndrome 4 protein isoform X1
aspartate beta-hydroxylase domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
aspartate beta-hydroxylase domain-containing protein 2 isoform X1
aspartate beta-hydroxylase domain containing 2, transcript variant X2
aspartate beta-hydroxylase domain-containing protein 2 isoform X2
seizure 6-like protein, 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 7 samples with support for all annotated introns
seizure 6-like protein, transcript variant X1
seizure 6-like protein, 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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
crystallin, beta B1, transcript variant X1
crystallin, beta B1, transcript variant X2
crystallin, beta A4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
crystallin, beta A4, transcript variant X2
potassium channel tetramerization domain containing 10, 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 3 samples with support for all annotated introns
potassium channel tetramerization domain containing 10, 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 22 samples with support for all annotated introns
potassium channel tetramerization domain containing 10, 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 23 samples with support for all annotated introns
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X1
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X2
OTU domain-containing protein 5-like, transcript variant X2
OTU domain-containing protein 5-like, transcript variant X1
translation initiation factor IF-2-like isoform X1
translation initiation factor IF-2-like isoform X2
OTU domain-containing protein 5-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 3 samples with support for all annotated introns
OTU domain-containing protein 5-like, transcript variant X4
OTU domain-containing protein 5-like isoform X3
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X3
small G protein signaling modulator 1a, 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
small G protein signaling modulator 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
small G protein signaling modulator 1 isoform X1
small G protein signaling modulator 1 isoform X2
ubiquitin carboxyl-terminal hydrolase 30-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
alkB homolog 2, alpha-ketoglutarate dependent dioxygenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
acetyl-CoA carboxylase beta, transcript variant X1
acetyl-CoA carboxylase beta, transcript variant X2
acetyl-CoA carboxylase beta, 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
ubiquitin protein ligase E3B, 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
ubiquitin protein ligase E3B, 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 12 samples with support for all annotated introns
ubiquitin protein ligase E3B, 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 16 samples with support for all annotated introns
ubiquitin protein ligase E3B, transcript variant 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 7 samples with support for all annotated introns
ubiquitin protein ligase E3B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 222 member Aa, 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 4 samples with support for all annotated introns
family with sequence similarity 222 member Aa, transcript variant X2
family with sequence similarity 222 member Aa, 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 2 samples with support for all annotated introns
family with sequence similarity 222 member Aa, transcript variant X7
family with sequence similarity 222 member Aa, transcript variant X5
family with sequence similarity 222 member Aa, transcript variant X6
family with sequence similarity 222 member Aa, transcript variant X8
family with sequence similarity 222 member Aa, transcript variant X4
transient receptor potential cation channel, subfamily V, member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily V member 4
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
trichoplein keratin filament-binding protein
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X13
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X4
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X3
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X5
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X2
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X1
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X10
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X7
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X12
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X11
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X9
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X6
ARF GTPase-activating protein GIT2a isoform X13
ARF GTPase-activating protein GIT2a isoform X4
ARF GTPase-activating protein GIT2a isoform X10
ARF GTPase-activating protein GIT2a isoform X7
ARF GTPase-activating protein GIT2a isoform X3
ARF GTPase-activating protein GIT2a isoform X12
ARF GTPase-activating protein GIT2a isoform X11
ARF GTPase-activating protein GIT2a isoform X9
ARF GTPase-activating protein GIT2a isoform X5
ARF GTPase-activating protein GIT2a isoform X6
ARF GTPase-activating protein GIT2a isoform X2
ARF GTPase-activating protein GIT2a isoform X1
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X8
ARF GTPase-activating protein GIT2a isoform X8
ankyrin repeat domain 13A, transcript variant X3
ankyrin repeat domain 13A, transcript variant X2
ankyrin repeat domain 13A, transcript variant 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 21 samples with support for all annotated introns
ankyrin repeat domain 13A, transcript variant X1
ankyrin repeat domain 13A, transcript variant X5
ankyrin repeat domain-containing protein 13A isoform X1
ankyrin repeat domain-containing protein 13A isoform X2
ankyrin repeat domain-containing protein 13A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
D-amino-acid oxidase-like, transcript variant X3
D-amino-acid oxidase-like, transcript variant X1
D-amino-acid oxidase-like, transcript variant X4
D-amino-acid oxidase-like, transcript variant X2
protein phosphatase Slingshot homolog 1-like, transcript variant X1
protein phosphatase Slingshot homolog 1-like, 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 10 samples with support for all annotated introns
protein phosphatase Slingshot homolog 1-like isoform X1
protein phosphatase Slingshot homolog 1-like isoform X2
protein phosphatase Slingshot homolog 1-like, transcript variant X3
uncharacterized protein LOC125464061 isoform X3
uncharacterized protein LOC125464034 isoform X1
transmembrane protein 119-like, transcript variant X2
transmembrane protein 119-like, transcript variant X1
protein tyrosine phosphatase non-receptor type 11a, 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 23 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 11a, 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 13 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 11 isoform X2
tyrosine-protein phosphatase non-receptor type 11 isoform X1
rabphilin-3A-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
rabphilin-3A-like, transcript variant X3
rabphilin-3A-like, transcript variant X1
rabphilin-3A-like, transcript variant X6
rabphilin-3A-like, transcript variant X5
rabphilin-3A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1-like, transcript variant X2
sodium- and chloride-dependent GABA transporter 1-like isoform X2
sodium- and chloride-dependent GABA transporter 1-like, transcript variant X4
sodium- and chloride-dependent GABA transporter 1-like, transcript variant X5
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
sodium- and chloride-dependent GABA transporter 1-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 5 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1-like isoform X1
sodium- and chloride-dependent GABA transporter 1-like isoform X3
sodium- and chloride-dependent GABA transporter ine-like isoform X5
sodium- and chloride-dependent GABA transporter 1-like isoform X4
uncharacterized LOC125463995, transcript variant X1
uncharacterized LOC125463995, transcript variant X2
acyl-CoA dehydrogenase family member 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized protein LOC568894 homolog, transcript variant X4
uncharacterized protein LOC568894 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 7 samples with support for all annotated introns
uncharacterized protein LOC568894 homolog, 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 15 samples with support for all annotated introns
uncharacterized protein LOC568894 homolog, transcript variant X3
MORC family CW-type zinc finger 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
MORC family CW-type zinc finger 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
MORC family CW-type zinc finger 2, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
aldehyde dehydrogenase, mitochondrial-like, transcript variant X2
aldehyde dehydrogenase, mitochondrial-like, transcript variant X1
aldehyde dehydrogenase, mitochondrial-like
MAPK activated protein kinase 5, transcript variant X1
MAP kinase-activated protein kinase 5 isoform X1
MAPK activated protein kinase 5, transcript variant X2
MAP kinase-activated protein kinase 5 isoform 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
endoplasmic reticulum resident protein 29-like
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
N-alpha-acetyltransferase 25, NatB auxiliary subunit, 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 17 samples with support for all annotated introns
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X2
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X1
TRAF-type zinc finger domain-containing protein 1-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 21 samples with support for all annotated introns
TRAF-type zinc finger domain-containing protein 1-like, transcript variant X3
TRAF-type zinc finger domain-containing protein 1-like, 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 6 samples with support for all annotated introns
TRAF-type zinc finger domain-containing protein 1-like isoform X1
TRAF-type zinc finger domain-containing protein 1-like isoform X2
probable E3 ubiquitin-protein ligase HECTD4
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
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
inositol polyphosphate-5-phosphatase Jb, 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 5 samples with support for all annotated introns
inositol polyphosphate-5-phosphatase Jb, transcript variant X4
inositol polyphosphate-5-phosphatase Jb, transcript variant X5
inositol polyphosphate-5-phosphatase Jb, 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 2 samples with support for all annotated introns
inositol polyphosphate-5-phosphatase Jb, 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 7 samples with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X1
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X4
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X5
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X2
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
purinergic receptor P2X, ligand-gated ion channel, 2
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
polymerase (DNA directed), epsilon, transcript variant X1
DNA polymerase epsilon catalytic subunit A isoform X1
polymerase (DNA directed), epsilon, transcript variant X2
DNA polymerase epsilon catalytic subunit A isoform X2
peroxisomal membrane protein 2, transcript variant X3
peroxisomal membrane protein 2, transcript variant X1
peroxisomal membrane protein 2 isoform X3
peroxisomal membrane protein 2 isoform X1
peroxisomal membrane protein 2, transcript variant X2
peroxisomal membrane protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125464051, transcript variant X1
uncharacterized LOC125464051, transcript variant X2
crystallin, beta B3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
crystallin, beta B3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 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: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein-tyrosine sulfotransferase 2-like, transcript variant X7
protein-tyrosine sulfotransferase 2-like, transcript variant X2
protein-tyrosine sulfotransferase 2-like, transcript variant X5
protein-tyrosine sulfotransferase 2-like, transcript variant X1
protein-tyrosine sulfotransferase 2-like, transcript variant X6
protein-tyrosine sulfotransferase 2-like, transcript variant X4
protein-tyrosine sulfotransferase 2-like, transcript variant X3
protein-tyrosine sulfotransferase 2-like isoform X1
protein-tyrosine sulfotransferase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
clustered mitochondria protein homolog, 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 11 samples with support for all annotated introns
clustered mitochondria protein homolog isoform X1
clustered mitochondria protein homolog, transcript variant X2
clustered mitochondria protein homolog isoform 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 19 samples with support for all annotated introns
tuftelin interacting protein 11, transcript variant X1
tuftelin interacting protein 11, transcript variant X2
tuftelin-interacting protein 11 isoform X1
tuftelin interacting protein 11, transcript variant X3
tuftelin-interacting protein 11 isoform X2
tetratricopeptide repeat domain 28, transcript variant X1
tetratricopeptide repeat domain 28, transcript variant X3
tetratricopeptide repeat domain 28, transcript variant X2
tetratricopeptide repeat domain 28, transcript variant X4
tetratricopeptide repeat protein 28 isoform X1
tetratricopeptide repeat protein 28 isoform X3
tetratricopeptide repeat protein 28 isoform X2
tetratricopeptide repeat protein 28 isoform X4
tetratricopeptide repeat domain 28, transcript variant X5
tetratricopeptide repeat protein 28 isoform X5
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
scavenger receptor class F, member 2, transcript variant X4
scavenger receptor class F, member 2, transcript variant X3
scavenger receptor class F, member 2, 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 11 samples with support for all annotated introns
scavenger receptor class F, member 2, transcript variant X1
proline dehydrogenase 1, mitochondrial-like, transcript variant X2
proline dehydrogenase 1, mitochondrial-like, transcript variant X1
proline dehydrogenase 1, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
THO complex subunit 5 homolog isoform X1
THO complex subunit 5 homolog isoform X2
uncharacterized protein LOC564476 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC564476 homolog, transcript variant X3
uncharacterized protein LOC564476 homolog, transcript variant X6
uncharacterized protein LOC564476 homolog, transcript variant X4
uncharacterized protein LOC564476 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC564476 homolog, 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 17 samples with support for all annotated introns
uncharacterized protein zgc:193801 isoform X1
uncharacterized protein zgc:193801 isoform X2
adaptor related protein complex 1 subunit beta 1, transcript variant X1
adaptor related protein complex 1 subunit beta 1, transcript variant X2
adaptor related protein complex 1 subunit beta 1, transcript variant X3
adaptor related protein complex 1 subunit beta 1, transcript variant X4
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
RNA-binding protein EWS-like, transcript variant X1
RNA-binding protein EWS-like, transcript variant X2
rhomboid domain containing 3, transcript variant X1
rhomboid domain containing 3, transcript variant X2
rhomboid domain-containing protein 3 isoform X1
rhomboid domain-containing protein 3 isoform X2
EMI domain containing 1, transcript variant X1
EMI domain containing 1, transcript variant X4
EMI domain containing 1, transcript variant X2
EMI domain-containing protein 1 isoform X1
EMI domain-containing protein 1 isoform X2
EMI domain-containing protein 1 isoform X4
EMI domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
EMI domain-containing protein 1 isoform X3
deltex 1, E3 ubiquitin ligase, transcript variant X1
E3 ubiquitin-protein ligase DTX1 isoform X1
deltex 1, E3 ubiquitin ligase, transcript variant X2
E3 ubiquitin-protein ligase DTX1 isoform X2
rasGAP-activating-like protein 1, transcript variant X2
rasGAP-activating-like protein 1, transcript variant X1
rasGAP-activating-like protein 1, transcript variant X3
rasGAP-activating-like protein 1 isoform X2
rasGAP-activating-like protein 1 isoform X1
rasGAP-activating-like protein 1 isoform X3
cytosolic arginine sensor for mTORC1 subunit 2-like
galactose-3-O-sulfotransferase 1a, transcript variant X5
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 1 sample with support for all annotated introns
galactose-3-O-sulfotransferase 1a, transcript variant X1
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 10 samples with support for all annotated introns
galactose-3-O-sulfotransferase 1a, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
galactose-3-O-sulfotransferase 1a, transcript variant X6
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 11 samples with support for all annotated introns
galactose-3-O-sulfotransferase 1a, 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 9 samples with support for all annotated introns
galactose-3-O-sulfotransferase 1a, transcript variant X4
galactose-3-O-sulfotransferase 1a, transcript variant X3
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 2 samples with support for all annotated introns
galactosylceramide sulfotransferase isoform X1
galactosylceramide sulfotransferase isoform X2
zona pellucida sperm-binding protein 3-like
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 22 samples with support for all annotated introns
SEC14-like lipid binding 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SEC14-like lipid binding 8, transcript variant X1
RING finger protein 215-like, transcript variant X2
RING finger protein 215-like, transcript variant X1
RING finger protein 215-like, transcript variant X3
coiled-coil domain containing 157, 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 2 samples with support for all annotated introns
coiled-coil domain-containing protein 157 isoform X2
coiled-coil domain containing 157, 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 9 samples with support for all annotated introns
coiled-coil domain containing 157, transcript variant X2
coiled-coil domain-containing protein 157 isoform X1
coiled-coil domain containing 157, transcript variant X4
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 14 samples with support for all annotated introns
coiled-coil domain-containing protein 157 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
BRCA1 associated protein, transcript variant X2
BRCA1 associated protein, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 1 Protein, 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
SH2B adaptor protein 3, 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 14 samples with support for all annotated introns
SH2B adaptor protein 3, transcript variant X5
SH2B adaptor protein 3, 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 4 samples with support for all annotated introns
SH2B adaptor protein 3, transcript variant X2
SH2B adaptor protein 3, transcript variant X1
PH domain containing endocytic trafficking adaptor 1
cut-like homeobox 2b, transcript variant X2
cut-like homeobox 2b, 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
cut-like homeobox 2b, transcript variant X3
cut-like homeobox 2b, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
myosin regulatory light chain 2, ventricular/cardiac muscle isoform
coiled-coil domain-containing protein 63-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 15% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase PP1-gamma catalytic subunit A
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
tectonic family member 1, transcript variant X1
tectonic family member 1, transcript variant X2
protein phosphatase PTC7 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 9 samples with support for all annotated introns
protein phosphatase PTC7 homolog, 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 21 samples with support for all annotated introns
protein phosphatase PTC7 homolog isoform X1
protein phosphatase PTC7 homolog isoform X2
VPS29 retromer complex component, transcript variant X3
VPS29 retromer complex component, transcript variant X2
vacuolar protein sorting-associated protein 29 isoform X2
vacuolar protein sorting-associated protein 29 isoform X3
VPS29 retromer complex component, transcript variant X1
vacuolar protein sorting-associated protein 29 isoform X1
actin related protein 2/3 complex, subunit 3
actin-related protein 2/3 complex subunit 3
ubiquitin-conjugating enzyme E2G 1b (UBC7 homolog, yeast)
anaphase promoting complex subunit 7, 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 8 samples with support for all annotated introns
anaphase promoting complex subunit 7, 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 4 samples with support for all annotated introns
anaphase promoting complex subunit 7, 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 21 samples with support for all annotated introns
anaphase-promoting complex subunit 7 isoform X3
anaphase-promoting complex subunit 7 isoform X1
anaphase-promoting complex subunit 7 isoform X2
anaphase promoting complex subunit 7, transcript variant X4
anaphase-promoting complex subunit 7 isoform X4
sarcoplasmic/endoplasmic reticulum calcium ATPase 2, transcript variant X1
sarcoplasmic/endoplasmic reticulum calcium ATPase 2, transcript variant X2
sarcoplasmic/endoplasmic reticulum calcium ATPase 2
intraflagellar transport 81 homolog, 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 11 samples with support for all annotated introns
intraflagellar transport 81 homolog, transcript variant X3
intraflagellar transport 81 homolog, transcript variant X5
intraflagellar transport 81 homolog, transcript variant X4
intraflagellar transport 81 homolog, transcript variant X1
intraflagellar transport protein 81 homolog isoform X1
intraflagellar transport protein 81 homolog isoform X2
intraflagellar transport 81 homolog, transcript variant X6
intraflagellar transport protein 81 homolog isoform X3
purinergic receptor P2X, ligand-gated ion channel, 4a, transcript variant X1
purinergic receptor P2X, ligand-gated ion channel, 4a, transcript variant X2
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X3
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X1
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X2
calcium/calmodulin-dependent protein kinase kinase 2-like isoform X2
calcium/calmodulin-dependent protein kinase kinase 2-like isoform 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 9 samples with support for all annotated introns
ring finger protein 34a, 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 24 samples with support for all annotated introns
ring finger protein 34a, 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 16 samples with support for all annotated introns
ring finger protein 34a, 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 24 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF34a isoform X1
E3 ubiquitin-protein ligase RNF34a isoform X2
E3 ubiquitin-protein ligase RNF34a isoform X3
lysine-specific demethylase 2B-like, transcript variant X9
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 8 samples with support for all annotated introns
lysine-specific demethylase 2B-like, transcript variant X16
lysine-specific demethylase 2B-like, transcript variant X2
lysine-specific demethylase 2B-like, transcript variant X11
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
lysine-specific demethylase 2B-like, transcript variant X10
lysine-specific demethylase 2B-like, transcript variant X13
lysine-specific demethylase 2B-like, transcript variant X12
lysine-specific demethylase 2B-like, transcript variant X7
lysine-specific demethylase 2B-like, transcript variant X6
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 11 samples with support for all annotated introns
lysine-specific demethylase 2B-like, transcript variant X4
lysine-specific demethylase 2B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
lysine-specific demethylase 2B-like, transcript variant X8
lysine-specific demethylase 2B-like, transcript variant X1
lysine-specific demethylase 2B-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
lysine-specific demethylase 2B-like, transcript variant X15
lysine-specific demethylase 2B-like, transcript variant X14
lysine-specific demethylase 2B-like, transcript variant X17
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 10 samples with support for all annotated introns
lysine-specific demethylase 2B-like, transcript variant X18
lysine-specific demethylase 2B-like isoform X2
lysine-specific demethylase 2B-like isoform X11
lysine-specific demethylase 2B-like isoform X10
lysine-specific demethylase 2B-like isoform X7
lysine-specific demethylase 2B-like isoform X6
lysine-specific demethylase 2B-like isoform X5
lysine-specific demethylase 2B-like isoform X4
lysine-specific demethylase 2B-like isoform X3
lysine-specific demethylase 2B-like isoform X8
lysine-specific demethylase 2B-like isoform X1
lysine-specific demethylase 2B-like isoform X9
lysine-specific demethylase 2B-like isoform X12
lysine-specific demethylase 2B-like isoform X13
calcium release-activated calcium channel protein 1-like, transcript variant X1
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 24 samples with support for all annotated introns
calcium release-activated calcium channel protein 1-like, transcript variant X2
calcium release-activated calcium channel protein 1-like isoform X1
calcium release-activated calcium channel protein 1-like isoform X2
MORN repeat containing 3, transcript variant X2
MORN repeat containing 3, transcript variant X1
transmembrane protein 120B, 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 3 samples with support for all annotated introns
transmembrane protein 120B, 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 3 samples with support for all annotated introns
transmembrane protein 120B, transcript variant X4
transmembrane protein 120B, transcript variant X1
ras homolog family member F, transcript variant X1
ras homolog family member F, transcript variant X2
ras homolog family member F, transcript variant X3
SET domain containing 1B, histone lysine methyltransferase a
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 9 samples with support for all annotated introns
histone-lysine N-methyltransferase SETD1B-A
proteasome 26S subunit, non-ATPase 9, transcript variant X2
proteasome 26S subunit, non-ATPase 9, transcript variant X1
26S proteasome non-ATPase regulatory subunit 9 isoform X1
26S proteasome non-ATPase regulatory subunit 9 isoform X2
cilia and flagella associated protein 251, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia and flagella associated protein 251, transcript variant X2
cilia- and flagella-associated protein 251 isoform X1
cilia- and flagella-associated protein 251 isoform X2
BAF chromatin remodeling complex subunit BCL7A
B-cell CLL/lymphoma 7 protein family member A
leucine-rich repeat-containing protein 43-like
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
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4-like
diablo IAP-binding mitochondrial protein-like
VPS33A core subunit of CORVET and HOPS complexes
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 23 samples with support for all annotated introns
vacuolar protein sorting-associated protein 33A
CAP-Gly domain-containing linker protein 1-like, transcript variant X4
CAP-Gly domain-containing linker protein 1-like, transcript variant X3
CAP-Gly domain-containing linker protein 1-like, transcript variant X2
CAP-Gly domain-containing linker protein 1-like, transcript variant X1
CAP-Gly domain-containing linker protein 1-like isoform X4
CAP-Gly domain-containing linker protein 1-like isoform X3
CAP-Gly domain-containing linker protein 1-like isoform X2
CAP-Gly domain-containing linker protein 1-like isoform X1
zinc finger CCHC domain-containing protein 8
uncharacterized protein LOC562347 homolog, 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 23 samples with support for all annotated introns
uncharacterized protein LOC562347 homolog, transcript variant X2
uncharacterized protein si:ch211-110p13.9 isoform X1
uncharacterized protein si:ch211-110p13.9 isoform X2
arginine/serine-rich coiled-coil protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
coiled-coil domain containing 62, transcript variant X1
coiled-coil domain containing 62, transcript variant X2
coiled-coil domain-containing protein 62 isoform X1
coiled-coil domain-containing protein 62 isoform X2
huntingtin-interacting protein 1-related protein-like
vacuolar protein sorting-associated protein 37B-like, transcript variant X1
vacuolar protein sorting-associated protein 37B-like, transcript variant X2
vacuolar protein sorting-associated protein 37B-like isoform X1
vacuolar protein sorting-associated protein 37B-like isoform X2
transmembrane protein 132C-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 10 samples with support for all annotated introns
transmembrane protein 132C-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 11 samples with support for all annotated introns
glycosyltransferase 1 domain containing 1, transcript variant X1
glycosyltransferase 1 domain containing 1, 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 20 samples with support for all annotated introns
glycosyltransferase 1 domain-containing protein 1 isoform X2
glycosyltransferase 1 domain-containing protein 1 isoform 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 8 samples with support for all annotated introns
transmembrane protein 132C-like isoform X1
transmembrane protein 132C-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
DEAH (Asp-Glu-Ala-His) box polypeptide 37
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 16 samples with support for all annotated introns
probable ATP-dependent RNA helicase DHX37
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
iron-sulfur cluster assembly enzyme ISCU, mitochondrial
spliceosome associated factor 3, U4/U6 recycling protein, 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 24 samples with support for all annotated introns
spliceosome associated factor 3, U4/U6 recycling protein, transcript variant X2
squamous cell carcinoma antigen recognized by T-cells 3 isoform X1
squamous cell carcinoma antigen recognized by T-cells 3 isoform X2
myotubularin related protein 3, transcript variant X12
myotubularin related protein 3, transcript variant X7
myotubularin related protein 3, transcript variant X16
myotubularin related protein 3, transcript variant X15
myotubularin related protein 3, transcript variant X11
myotubularin related protein 3, transcript variant X9
myotubularin related protein 3, transcript variant X14
myotubularin related protein 3, transcript variant X10
myotubularin related protein 3, transcript variant X1
myotubularin related protein 3, transcript variant X13
myotubularin related protein 3, transcript variant X2
myotubularin related protein 3, transcript variant X5
myotubularin related protein 3, transcript variant X8
myotubularin related protein 3, transcript variant X4
myotubularin related protein 3, transcript variant X3
myotubularin related protein 3, transcript variant X6
myotubularin-related protein 3 isoform X5
myotubularin-related protein 3 isoform X9
myotubularin-related protein 3 isoform X8
myotubularin-related protein 3 isoform X4
myotubularin-related protein 3 isoform X2
myotubularin-related protein 3 isoform X7
myotubularin-related protein 3 isoform X3
myotubularin-related protein 3 isoform X1
myotubularin-related protein 3 isoform X6
myotubularin related protein 3, transcript variant X19
myotubularin related protein 3, transcript variant X18
myotubularin related protein 3, transcript variant X17
myotubularin related protein 3, transcript variant X20
myotubularin-related protein 3 isoform X11
myotubularin-related protein 3 isoform X10
activating signal cointegrator 1 complex subunit 2, 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 20 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 2 isoform X1
activating signal cointegrator 1 complex subunit 2 isoform 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 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 22 samples with support for all annotated introns
cilia and flagella associated protein 73, transcript variant X1
cilia and flagella associated protein 73, transcript variant X3
cilia and flagella associated protein 73, transcript variant X2
coiled-coil domain-containing protein 42 homolog isoform X1
coiled-coil domain-containing protein 42 homolog isoform X3
coiled-coil domain-containing protein 42 homolog isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 54
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 21 samples with support for all annotated introns
RBPJ-interacting and tubulin-associated protein 1-like, transcript variant X2
RBPJ-interacting and tubulin-associated protein 1-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 19 samples with support for all annotated introns
RBPJ-interacting and tubulin-associated protein 1-like
two pore segment channel 1, transcript variant X1
two pore segment channel 1, transcript variant X2
solute carrier family 8 member B1, transcript variant X1
solute carrier family 8 member B1, transcript variant X3
solute carrier family 8 member B1, transcript variant X2
solute carrier family 8 member B1, 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 11 samples with support for all annotated introns
solute carrier family 8 member B1, 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 20 samples with support for all annotated introns
mitochondrial sodium/calcium exchanger protein isoform X3
mitochondrial sodium/calcium exchanger protein isoform X2
mitochondrial sodium/calcium exchanger protein isoform X1
calcineurin B homologous protein 3-like, transcript variant X3
calcineurin B homologous protein 3-like, transcript variant X1
calcineurin B homologous protein 3-like, transcript variant X2
calcineurin B homologous protein 3-like, transcript variant X4
calcineurin B homologous protein 3-like isoform X1
calcineurin B homologous protein 3-like isoform X2
calcineurin B homologous protein 3-like isoform X3
serine dehydratase-like, transcript variant X3
serine dehydratase-like, transcript variant X2
serine dehydratase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125464351, transcript variant X4
uncharacterized LOC125464351, transcript variant X3
uncharacterized LOC125464351, transcript variant X2
uncharacterized LOC125464351, transcript variant X1
RNA binding motif protein 19, 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 3 samples with support for all annotated introns
RNA binding motif protein 19, 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 20 samples with support for all annotated introns
RNA binding motif protein 19, transcript variant X3
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 11 samples with support for all annotated introns
T-box transcription factor 5b, transcript variant X5
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
T-box transcription factor 5b, transcript variant X6
T-box transcription factor 5b, transcript variant X3
T-box transcription factor 5b, transcript variant X4
T-box transcription factor 5b, 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 3 samples with support for all annotated introns
T-box transcription factor 5b, transcript variant X7
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 5 samples with support for all annotated introns
T-box transcription factor 5b, transcript variant X1
T-box transcription factor TBX5b isoform X2
T-box transcription factor TBX5b isoform X1
uncharacterized LOC125463913, transcript variant X2
uncharacterized LOC125463913, transcript variant X1
uncharacterized LOC125463913, transcript variant X3
mediator of RNA polymerase II transcription subunit 13-like, 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 15 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 13-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 15 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 13-like isoform X2
mediator of RNA polymerase II transcription subunit 13-like isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
SREBF pathway regulator in golgi 1, transcript variant X3
SREBF pathway regulator in golgi 1, transcript variant X1
SREBF pathway regulator in golgi 1, transcript variant X2
SREBP regulating gene protein isoform X3
SREBP regulating gene protein isoform X2
SREBP regulating gene protein isoform X1
ring finger protein, transmembrane 2, 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 10 samples with support for all annotated introns
ring finger protein, transmembrane 2, 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 7 samples with support for all annotated introns
RING finger and transmembrane domain-containing protein 2 isoform X1
RING finger and transmembrane domain-containing protein 2 isoform X2
F-box and WD repeat domain containing 8, 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
F-box and WD repeat domain containing 8, transcript variant X3
F-box and WD repeat domain containing 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 16 samples with support for all annotated introns
F-box/WD repeat-containing protein 8 isoform X1
F-box/WD repeat-containing protein 8 isoform X2
F-box/WD repeat-containing protein 8 isoform X3
V-set and immunoglobulin domain containing 10, transcript variant X4
V-set and immunoglobulin domain containing 10, 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 14 samples with support for all annotated introns
V-set and immunoglobulin domain containing 10, 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 10 samples with support for all annotated introns
V-set and immunoglobulin domain containing 10, transcript variant X3
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
V-set and immunoglobulin domain-containing protein 10
WD repeat and SOCS box containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
WD repeat and SOCS box containing 2, 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 16 samples with support for all annotated introns
WD repeat and SOCS box-containing protein 2 isoform X1
WD repeat and SOCS box-containing protein 2 isoform X2
replication factor C (activator 1) 5, transcript variant X2
replication factor C (activator 1) 5, transcript variant X1
replication factor C (activator 1) 5, transcript variant X3
replication factor C subunit 5 isoform X2
replication factor C subunit 5 isoform X1
replication factor C subunit 5 isoform X3
nitric oxide synthase 1 (neuronal), transcript variant X1
nitric oxide synthase 1 (neuronal), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphatidylethanolamine binding protein 1
phosphatidylethanolamine-binding protein 1
serine/threonine-protein kinase TAO3 isoform X2
serine/threonine-protein kinase TAO3 isoform X1
SDS3 homolog, SIN3A corepressor complex component
sin3 histone deacetylase corepressor complex component SDS3
serine/arginine repetitive matrix 4, transcript variant X2
serine/arginine repetitive matrix 4, transcript variant X1
serine/arginine repetitive matrix protein 4 isoform X1
serine/arginine repetitive matrix 4, transcript variant X3
serine/arginine repetitive matrix protein 4 isoform X2
coiled-coil domain-containing protein 60-like, transcript variant X1
coiled-coil domain-containing protein 60-like, transcript variant X4
coiled-coil domain-containing protein 60-like, transcript variant X3
coiled-coil domain-containing protein 60-like, transcript variant X2
coiled-coil domain-containing protein 60-like isoform X1
coiled-coil domain-containing protein 60-like isoform X3
coiled-coil domain-containing protein 60-like isoform X2
X-box binding 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 21 samples with support for all annotated introns
X-box binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
zinc and ring finger 3, 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 9 samples with support for all annotated introns
zinc and ring finger 3, 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 15 samples with support for all annotated introns
E3 ubiquitin-protein ligase znrf3 isoform X1
E3 ubiquitin-protein ligase znrf3 isoform X2
kringle containing transmembrane protein 1
sushi domain containing 2, transcript variant X7
sushi domain containing 2, transcript variant X2
sushi domain containing 2, transcript variant X1
sushi domain containing 2, transcript variant X3
sushi domain-containing protein 2 isoform X5
sushi domain-containing protein 2 isoform X1
sushi domain containing 2, transcript variant X4
sushi domain-containing protein 2 isoform X2
sushi domain containing 2, transcript variant X6
sushi domain containing 2, transcript variant X5
sushi domain-containing protein 2 isoform X4
sushi domain-containing protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
synergin gamma-like, transcript variant X3
synergin gamma-like, transcript variant X1
synergin gamma-like, transcript variant X2
solute carrier family 35 member E4, transcript variant X1
solute carrier family 35 member E4, transcript variant X2
chromosome 25 C12orf43 homolog, transcript variant X2
chromosome 25 C12orf43 homolog, 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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 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: 12 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
hepatocyte nuclear factor 1-alpha isoform X2
hepatocyte nuclear factor 1-alpha isoform X1
hepatocyte nuclear factor 1-alpha isoform X3
signal peptide peptidase 3, transcript variant X2
signal peptide peptidase-like 3 isoform X2
signal peptide peptidase 3, transcript variant X1
signal peptide peptidase-like 3 isoform X1
signal peptide peptidase 3, transcript variant X3
signal peptide peptidase-like 3 isoform 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 22 samples with support for all annotated introns
short-chain specific acyl-CoA dehydrogenase, mitochondrial
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
calcium binding protein 1a, transcript variant X1
calcium binding protein 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
calcium binding protein 1a, 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 4 samples with support for all annotated introns
uncharacterized LOC125463976, transcript variant X2
uncharacterized LOC125463976, transcript variant X4
uncharacterized LOC125463976, transcript variant X3
uncharacterized LOC125463976, transcript variant X1
uncharacterized protein LOC125463976 isoform X3
uncharacterized protein LOC125463976 isoform X2
uncharacterized protein LOC125463976 isoform X1
POP5 homolog, ribonuclease P/MRP subunit
ring finger protein 10, transcript variant X2
ring finger protein 10, transcript variant X3
ring finger protein 10, transcript variant X1
coenzyme Q5, methyltransferase, transcript variant X1
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial isoform X1
coenzyme Q5, methyltransferase, transcript variant X2
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial isoform X2
uncharacterized LOC125463973, transcript variant X1
uncharacterized LOC125463973, transcript variant X2
serine/arginine-rich splicing factor 1-like, 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 19 samples with support for all annotated introns
serine/arginine-rich splicing factor 1-like, 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 24 samples with support for all annotated introns
serine/arginine-rich splicing factor 1-like isoform X1
serine/arginine-rich splicing factor 1-like isoform X2
glutamyl-tRNA amidotransferase subunit C
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial
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
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cytochrome c oxidase subunit 6A1, mitochondrial-like
uncharacterized LOC125463907, transcript variant X2
uncharacterized LOC125463907, transcript variant X1
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
solute carrier family 2, facilitated glucose transporter member 11-like
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X2
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 16 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X1
solute carrier family 2, facilitated glucose transporter member 11-like isoform X1
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X4
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 1 sample with support for all annotated introns
solute carrier family 2, facilitated glucose transporter member 11-like isoform X2
solute carrier family 2, facilitated glucose transporter member 11-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 2 member 11b, transcript variant X5
solute carrier family 2 member 11b, transcript variant X3
solute carrier family 2 member 11b, transcript variant X2
solute carrier family 2 member 11b, transcript variant X4
solute carrier family 2 member 11b, transcript variant X1
solute carrier family 2 member 11b, transcript variant X6
solute carrier family 2, facilitated glucose transporter member 11b isoform X3
solute carrier family 2, facilitated glucose transporter member 11b isoform X2
solute carrier family 2, facilitated glucose transporter member 11b isoform X4
solute carrier family 2, facilitated glucose transporter member 11b isoform X1
solute carrier family 2, facilitated glucose transporter member 11b isoform X5
citron rho-interacting serine/threonine kinase a, 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
citron rho-interacting serine/threonine kinase a, transcript variant X2
citron Rho-interacting kinase isoform X2
citron Rho-interacting kinase isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
BICD family like cargo adaptor 1, transcript variant X1
BICD family like cargo adaptor 1, transcript variant X2
BICD family like cargo adaptor 1, transcript variant X3
BICD family like cargo adaptor 1, transcript variant X5
BICD family like cargo adaptor 1, transcript variant X4
BICD family like cargo adaptor 1, transcript variant X6
BICD family-like cargo adapter 1 isoform X1
BICD family-like cargo adapter 1 isoform X2
BICD family-like cargo adapter 1 isoform X3
transmembrane protein 233, 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 9 samples with support for all annotated introns
transmembrane protein 233, transcript variant X1
5'-AMP-activated protein kinase subunit beta-1, transcript variant X4
5'-AMP-activated protein kinase subunit beta-1, transcript variant X1
5'-AMP-activated protein kinase subunit beta-1, transcript variant X3
5'-AMP-activated protein kinase subunit beta-1, transcript variant X2
5'-AMP-activated protein kinase subunit beta-1 isoform X2
5'-AMP-activated protein kinase subunit beta-1 isoform X1
ADP-ribose pyrophosphatase, mitochondrial-like, transcript variant X1
ADP-ribose pyrophosphatase, mitochondrial-like, transcript variant X3
ADP-ribose pyrophosphatase, mitochondrial-like, transcript variant X2
ADP-ribose pyrophosphatase, mitochondrial-like isoform X1
ADP-ribose pyrophosphatase, mitochondrial-like isoform X2
transcobalamin-2-like, transcript variant X2
transcobalamin-2-like, transcript variant X1
coiled-coil domain-containing protein 117-like, transcript variant X2
coiled-coil domain-containing protein 117-like, transcript variant X4
coiled-coil domain-containing protein 117-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 23 samples with support for all annotated introns
coiled-coil domain-containing protein 117-like, transcript variant X5
coiled-coil domain-containing protein 117-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 20 samples with support for all annotated introns
coiled-coil domain-containing protein 117-like, transcript variant X7
coiled-coil domain-containing protein 117-like, transcript variant X6
coiled-coil domain-containing protein 117-like
oxysterol-binding protein 2-like, transcript variant X4
oxysterol-binding protein 2-like, transcript variant X3
oxysterol-binding protein 2-like, transcript variant X2
oxysterol-binding protein 2-like, transcript variant X1
oxysterol-binding protein 2-like, transcript variant X5
oxysterol-binding protein 2-like, transcript variant X6
oxysterol-binding protein 2-like isoform X4
oxysterol-binding protein 2-like isoform X3
oxysterol-binding protein 2-like isoform X2
oxysterol-binding protein 2-like isoform X1
oxysterol-binding protein 2-like isoform X5
oxysterol-binding protein 2-like isoform X6
mitotic spindle organizing protein 2B, transcript variant X3
mitotic spindle organizing protein 2B, transcript variant X2
mitotic spindle organizing protein 2B, transcript variant X1
mitotic spindle organizing protein 2B, transcript variant X4
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 24 samples with support for all annotated introns
mitotic-spindle organizing protein 2 isoform X1
mitotic-spindle organizing protein 2 isoform X3
mitotic-spindle organizing protein 2 isoform X2
mitotic-spindle organizing protein 2 isoform X4
apoptosis-inducing factor 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
apoptosis-inducing factor 3, transcript variant X4
apoptosis-inducing factor 3, transcript variant X9
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 6 samples with support for all annotated introns
apoptosis-inducing factor 3, transcript variant X6
apoptosis-inducing factor 3, 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 6 samples with support for all annotated introns
apoptosis-inducing factor 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 5 samples with support for all annotated introns
apoptosis-inducing factor 3, transcript variant X2
apoptosis-inducing factor 3, transcript variant X3
apoptosis-inducing factor 3, transcript variant X8
apoptosis-inducing factor 3, transcript variant X10
leucine-zipper-like transcription regulator 1
leucine-zipper-like transcriptional regulator 1
uncharacterized LOC125464359, transcript variant X2
uncharacterized LOC125464359, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
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 9 samples with support for all annotated introns
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 8 samples with support for all annotated introns
NAD-dependent protein lipoamidase sirtuin-4, mitochondrial isoform X1
NAD-dependent protein lipoamidase sirtuin-4, mitochondrial isoform X2
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X1
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X2
uncharacterized protein DDB_G0284459-like, transcript variant X6
uncharacterized protein DDB_G0284459-like, transcript variant X1
uncharacterized protein DDB_G0284459-like, transcript variant X2
uncharacterized protein DDB_G0284459-like, transcript variant X3
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
uncharacterized protein DDB_G0284459-like isoform X5
uncharacterized protein DDB_G0284459-like isoform X1
uncharacterized protein DDB_G0284459-like isoform X2
uncharacterized protein DDB_G0284459-like isoform X3
uncharacterized protein DDB_G0284459-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein DDB_G0284459-like, transcript variant X4
uncharacterized protein DDB_G0284459-like isoform X4
immunoglobulin lambda-1 light chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC393431 homolog, transcript variant X3
uncharacterized protein LOC393431 homolog, transcript variant X1
uncharacterized protein LOC393431 homolog, transcript variant X4
uncharacterized protein LOC393431 homolog, transcript variant X2
uncharacterized LOC125464256, transcript variant X2
uncharacterized LOC125464256, transcript variant X1
transfer RNA phenylalanine (anticodon AAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
CDC45 cell division cycle 45 homolog (S. cerevisiae), transcript variant X2
CDC45 cell division cycle 45 homolog (S. cerevisiae), transcript variant X1
cell division control protein 45 homolog isoform X2
cell division control protein 45 homolog isoform X1
ubiquitin recognition factor in ER associated degradation 1
ubiquitin recognition factor in ER-associated degradation protein 1
peptidyl-prolyl cis-trans isomerase FKBP8-like
peptidyl-prolyl cis-trans isomerase FKBP8-like, transcript variant X4
peptidyl-prolyl cis-trans isomerase FKBP8-like, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP8-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase FKBP8-like, transcript variant X3
peptidyl-prolyl cis-trans isomerase FKBP8-like isoform X3
peptidyl-prolyl cis-trans isomerase FKBP8-like isoform X1
peptidyl-prolyl cis-trans isomerase FKBP8-like isoform X2
chromosome 25 C22orf39 homolog, transcript variant X2
UPF0545 protein C22orf39 homolog isoform X2
chromosome 25 C22orf39 homolog, transcript variant X1
UPF0545 protein C22orf39 homolog isoform X1
mitochondrial ribosomal protein L40, transcript variant X2
mitochondrial ribosomal protein L40, transcript variant X1
mitochondrial ribosomal protein L40, transcript variant X3
39S ribosomal protein L40, mitochondrial isoform X2
39S ribosomal protein L40, mitochondrial isoform X1
39S ribosomal protein L40, mitochondrial isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin lambda constant 7-like, transcript variant X2
immunoglobulin lambda constant 7-like isoform 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 10 samples with support for all annotated introns
peptidylprolyl isomerase (cyclophilin)-like 2
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 24 samples with support for all annotated introns
RING-type E3 ubiquitin-protein ligase PPIL2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
protein phosphatase, Mg2+/Mn2+ dependent, 1F, 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 5 samples with support for all annotated introns
protein phosphatase, Mg2+/Mn2+ dependent, 1F, 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
DNA topoisomerase III beta, transcript variant X1
DNA topoisomerase III beta, transcript variant X2
ras-related protein Rab-35, transcript variant X2
ras-related protein Rab-35, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RAB36, member RAS oncogene family, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RAB36, member RAS oncogene family, transcript variant X2
RAB36, member RAS oncogene family, transcript variant X4
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 5 samples with support for all annotated introns
RAB36, member RAS oncogene family, transcript variant X5
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
RAB36, member RAS oncogene family, transcript variant X8
RAB36, member RAS oncogene family, transcript variant X7
RAB36, member RAS oncogene family, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RAB36, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide binding protein (G protein), alpha z polypeptide, transcript variant X1
guanine nucleotide binding protein (G protein), alpha z polypeptide, transcript variant X2
guanine nucleotide-binding protein G(z) subunit alpha
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X1
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X2
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X3
DEP domain containing 5, GATOR1 subcomplex subunit, transcript variant X4
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, eta polypeptide, transcript variant X1
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, eta polypeptide, transcript variant X2
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 7 samples with support for all annotated introns
uncharacterized wu:fi75a02, transcript variant X2
uncharacterized wu:fi75a02, transcript variant X1
uncharacterized wu:fi75a02, transcript variant X3
uncharacterized wu:fi75a02, transcript variant X4
uncharacterized wu:fi75a02, transcript variant X5
uncharacterized protein wu:fi75a02 isoform X1
uncharacterized protein wu:fi75a02 isoform X2
uncharacterized protein wu:fi75a02 isoform X3
uncharacterized protein wu:fi75a02 isoform X4
phosphatidylserine decarboxylase, 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 6 samples with support for all annotated introns
phosphatidylserine decarboxylase, 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 19 samples with support for all annotated introns
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X2
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X3
phosphatidylserine decarboxylase, 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 15 samples with support for all annotated introns
phosphatidylserine decarboxylase, 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 16 samples with support for all annotated introns
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X4
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X1
phosphatidylserine decarboxylase, transcript variant X5
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X3
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
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X1
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant 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 20 samples with support for all annotated introns
eukaryotic translation initiation factor 4E transporter isoform X1
eukaryotic translation initiation factor 4E transporter isoform X2
eukaryotic translation initiation factor 4E transporter isoform X3
developmentally regulated GTP binding protein 1, transcript variant X2
developmentally regulated GTP binding protein 1, transcript variant X1
developmentally-regulated GTP-binding protein 1 isoform X2
developmentally-regulated GTP-binding protein 1 isoform X1
POZ/BTB and AT hook containing zinc finger 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
POZ/BTB and AT hook containing zinc finger 1, 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 9 samples with support for all annotated introns
POZ (BTB) and AT hook-containing zinc finger 1 isoform X1
POZ (BTB) and AT hook-containing zinc finger 1 isoform 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 2 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 51
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 4 catalytic subunit, transcript variant X2
serine/threonine-protein phosphatase 4 catalytic subunit isoform X2
serine/threonine-protein phosphatase 4 catalytic subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
serine/threonine-protein phosphatase 4 catalytic subunit isoform X1
v-crk avian sarcoma virus CT10 oncogene homolog-like
kelch-like family member 22, 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
kelch-like family member 22, 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 10 samples with support for all annotated introns
kelch-like family member 22, transcript variant X1
glutathione S-transferase theta-1-like, transcript variant X3
glutathione S-transferase theta-1-like isoform X3
D-dopachrome tautomerase, transcript variant X4
D-dopachrome tautomerase, transcript variant X1
D-dopachrome tautomerase, transcript variant X3
D-dopachrome tautomerase, transcript variant X2
glutathione S-transferase theta-1-like, transcript variant X2
glutathione S-transferase theta-1-like isoform X2
glutathione S-transferase theta-1-like, transcript variant X1
glutathione S-transferase theta-1-like isoform X1
glutathione hydrolase 1 proenzyme-like, 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 3 samples with support for all annotated introns
glutathione hydrolase 1 proenzyme-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
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
uncharacterized protein LOC101885505 homolog, transcript variant X2
uncharacterized protein LOC101885505 homolog, transcript variant X1
uncharacterized protein LOC101885505 homolog, transcript variant X4
uncharacterized protein LOC101885505 homolog, transcript variant X3
coiled-coil domain-containing protein 74B
mediator complex subunit 15, transcript variant X2
mediator complex subunit 15, transcript variant X4
mediator complex subunit 15, transcript variant X3
mediator complex subunit 15, transcript variant X1
mediator of RNA polymerase II transcription subunit 15 isoform X2
mediator of RNA polymerase II transcription subunit 15 isoform X4
mediator of RNA polymerase II transcription subunit 15 isoform X3
mediator of RNA polymerase II transcription subunit 15 isoform X1
guanylyl cyclase domain containing 1, transcript variant X2
guanylyl cyclase domain containing 1, transcript variant X1
ureidopropionase, beta, transcript variant X3
ureidopropionase, beta, transcript variant X4
ureidopropionase, beta, transcript variant X6
ureidopropionase, beta, transcript variant X1
ureidopropionase, beta, transcript variant X2
ureidopropionase, beta, transcript variant X5
transfer RNA arginine (anticodon CCU); 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: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1-like a, transcript variant 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 13 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1-like a, transcript variant X3
sperm antigen with calponin homology and coiled-coil domains 1-like a, 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 8 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1-like a, transcript variant X1
sperm antigen with calponin homology and coiled-coil domains 1-like a, transcript variant X5
PH_BCR_vertebrate and RhoGAP_Bcr domain-containing protein, transcript variant X2
PH_BCR_vertebrate and RhoGAP_Bcr domain-containing protein, transcript variant X1
PH_BCR_vertebrate and RhoGAP_Bcr domain-containing protein isoform X2
PH_BCR_vertebrate and RhoGAP_Bcr domain-containing protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, 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 17 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, transcript variant X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, transcript variant X3
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 24 samples with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 isoform X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform 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
coiled-coil-helix-coiled-coil-helix domain containing 10
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
uncharacterized protein C22orf15, transcript variant X6
uncharacterized protein C22orf15, transcript variant X2
uncharacterized protein C22orf15, transcript variant X5
uncharacterized protein C22orf15, transcript variant X1
uncharacterized protein C22orf15, transcript variant X7
uncharacterized protein C22orf15, transcript variant X3
uncharacterized protein C22orf15, transcript variant X4
uncharacterized protein LOC125464124 isoform X6
uncharacterized protein C22orf15 isoform X2
uncharacterized protein LOC125464124 isoform X5
uncharacterized protein C22orf15 isoform X1
uncharacterized protein LOC125464124 isoform X7
uncharacterized protein C22orf15 isoform X3
uncharacterized protein C22orf15 isoform X4
thyroid adenoma-associated protein homolog
testis-specific serine/threonine-protein kinase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
DiGeorge syndrome critical region gene 2, transcript variant X4
DiGeorge syndrome critical region gene 2, transcript variant X3
DiGeorge syndrome critical region gene 2, transcript variant X1
DiGeorge syndrome critical region gene 2, transcript variant X2
integral membrane protein DGCR2/IDD isoform X3
integral membrane protein DGCR2/IDD isoform X4
integral membrane protein DGCR2/IDD isoform X1
integral membrane protein DGCR2/IDD isoform X2
phosphoinositide-3-kinase interacting protein 1
phosphoinositide-3-kinase-interacting protein 1
uncharacterized LOC125464224, transcript variant X2
uncharacterized LOC125464224, transcript variant X1