Chiloscyllium plagiosum isolate BGI_BamShark_2017 chromosome 25, ASM401019v2, whole genome shotgun sequence.
Chiloscyllium plagiosum (whitespotted bambooshark)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Hemiscylliidae; Chiloscyllium.
REFSEQ INFORMATION: The reference sequence is identical to\nCM012980.1.\nAssembly name: ASM401019v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the BGI on 2019/01/10. The\noriginal whole-genome shotgun project has the accession\nQPFF00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: BGI\nAssembly Method :: platanus v. 1.2.4; 3ddna v. 170123\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 280.0x\nSequencing Technology :: BGIseq-500\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Chiloscyllium plagiosum 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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 92, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
coiled-coil domain containing 92, transcript variant X2
coiled-coil domain-containing protein 92
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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
scavenger receptor class B member 1-like isoform X2
scavenger receptor class B member 1-like isoform X1
adhesion G protein-coupled receptor D1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
adhesion G-protein coupled receptor D1 isoform X3
adhesion G protein-coupled receptor D1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
adhesion G-protein coupled receptor D1 isoform X1
adhesion G protein-coupled receptor D1, 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 10 samples with support for all annotated introns
adhesion G-protein coupled receptor D1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
splicing factor SWAP, transcript variant X4
splicing factor SWAP, transcript variant X2
splicing factor SWAP, transcript variant X1
splicing factor SWAP, transcript variant X3
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 X4
splicing factor, suppressor of white-apricot homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase ULK1-like, transcript variant X1
serine/threonine-protein kinase ULK1-like, transcript variant X2
serine/threonine-protein kinase ULK1-like, transcript variant X3
serine/threonine-protein kinase ULK1-like, transcript variant X4
serine/threonine-protein kinase ULK1-like isoform X1
serine/threonine-protein kinase ULK1-like isoform X2
serine/threonine-protein kinase ULK1-like isoform X3
serine/threonine-protein kinase ULK1-like isoform X4
E1A binding protein p400, transcript variant X1
E1A binding protein p400, transcript variant X3
E1A binding protein p400, transcript variant X6
E1A binding protein p400, transcript variant X2
E1A binding protein p400, transcript variant X4
E1A binding protein p400, transcript variant X8
E1A binding protein p400, transcript variant X5
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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC122562508, 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 2 samples with support for all annotated introns
uncharacterized LOC122562508, transcript variant X3
uncharacterized LOC122562508, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 9
uncharacterized LOC122562510, 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 6 samples with support for all annotated introns
uncharacterized LOC122562510, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
hypermethylated in cancer 2, transcript variant X15
hypermethylated in cancer 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 2 samples with support for all annotated introns
hypermethylated in cancer 2, transcript variant X8
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 4 samples with support for all annotated introns
hypermethylated in cancer 2, transcript variant X11
hypermethylated in cancer 2, transcript variant X6
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 26 samples with support for all annotated introns
hypermethylated in cancer 2, transcript variant X4
hypermethylated in cancer 2, transcript variant X10
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 6 samples with support for all annotated introns
hypermethylated in cancer 2, transcript variant X7
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
hypermethylated in cancer 2, transcript variant X2
hypermethylated in cancer 2, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
hypermethylated in cancer 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
hypermethylated in cancer 2, transcript variant X9
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 3 samples with support for all annotated introns
hypermethylated in cancer 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 8 samples with support for all annotated introns
hypermethylated in cancer 2 protein isoform X4
hypermethylated in cancer 2 protein isoform X3
hypermethylated in cancer 2 protein isoform X2
hypermethylated in cancer 2 protein isoform X5
hypermethylated in cancer 2 protein isoform X1
hypermethylated in cancer 2 protein isoform X6
hypermethylated in cancer 2, transcript variant X14
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
hypermethylated in cancer 2, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
YdjC chitooligosaccharide deacetylase homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
phosphatidylinositol 4-kinase alpha-like, transcript variant X2
phosphatidylinositol 4-kinase alpha-like, transcript variant X1
phosphatidylinositol 4-kinase alpha-like isoform X2
phosphatidylinositol 4-kinase alpha-like isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: heparin cofactor 2-like
tricarboxylate transport protein, mitochondrial
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 26 samples with support for all annotated introns
uncharacterized LOC122562518, transcript variant X2
uncharacterized LOC122562518, transcript variant X1
clathrin heavy chain 1-like, transcript variant X6
clathrin heavy chain 1-like, transcript variant X4
clathrin heavy chain 1-like, transcript variant X2
clathrin heavy chain 1-like, transcript variant X5
clathrin heavy chain 1-like, transcript variant X3
clathrin heavy chain 1-like, transcript variant X1
uncharacterized LOC122562446, transcript variant X2
uncharacterized LOC122562446, transcript variant X1
T-box transcription factor 1, transcript variant X1
T-box transcription factor 1, transcript variant X2
T-box transcription factor TBX1 isoform X1
T-box transcription factor TBX1 isoform X2
guanine nucleotide binding protein (G protein), beta polypeptide 1-like, transcript variant X4
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 (G protein), beta polypeptide 1-like, transcript variant X1
guanine nucleotide binding protein (G protein), beta polypeptide 1-like, transcript variant X5
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X3
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X1
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X2
catechol O-methyltransferase-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 1 sample with support for all annotated introns
catechol O-methyltransferase-like isoform X2
thioredoxin reductase 2, tandem duplicate 2
catechol O-methyltransferase-like, 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
catechol O-methyltransferase-like isoform X1
catechol O-methyltransferase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
catechol O-methyltransferase-like, 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 6 samples with support for all annotated introns
catechol O-methyltransferase-like isoform X3
ARVCF delta catenin family member b, transcript variant X2
ARVCF delta catenin family member b, transcript variant X4
ARVCF delta catenin family member b, transcript variant X15
ARVCF delta catenin family member b, transcript variant X3
ARVCF delta catenin family member b, transcript variant X12
ARVCF delta catenin family member b, transcript variant X6
ARVCF delta catenin family member b, transcript variant X7
ARVCF delta catenin family member b, transcript variant X1
ARVCF delta catenin family member b, transcript variant X11
ARVCF delta catenin family member b, transcript variant X9
ARVCF delta catenin family member b, transcript variant X5
ARVCF delta catenin family member b, transcript variant X13
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 X8
ARVCF delta catenin family member b isoform X3
ARVCF delta catenin family member b isoform X5
ARVCF delta catenin family member b isoform X2
ARVCF delta catenin family member b isoform X1
ARVCF delta catenin family member b isoform X6
ARVCF delta catenin family member b isoform X4
ARVCF delta catenin family member b isoform X7
transport and golgi organization 2 homolog (Drosophila)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transport and Golgi organization protein 2 homolog
DGCR8 microprocessor complex subunit, transcript variant X1
DGCR8 microprocessor complex subunit, transcript variant X2
microprocessor complex subunit DGCR8 isoform X1
microprocessor complex subunit DGCR8 isoform X2
tRNA methyltransferase 2 homolog A, transcript variant X2
tRNA (uracil-5-)-methyltransferase homolog A isoform X2
tRNA methyltransferase 2 homolog A, 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 10 samples with support for all annotated introns
tRNA methyltransferase 2 homolog A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tRNA methyltransferase 2 homolog A, 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 14 samples with support for all annotated introns
tRNA (uracil-5-)-methyltransferase homolog A isoform X4
tRNA (uracil-5-)-methyltransferase homolog A isoform X3
tRNA (uracil-5-)-methyltransferase homolog A isoform X1
RAN binding protein 1, transcript variant X2
ran-specific GTPase-activating protein isoform X2
RAN binding protein 1, transcript variant X1
ran-specific GTPase-activating protein isoform X1
zinc finger DHHC-type palmitoyltransferase 8b
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
PGAM family member 5, serine/threonine protein phosphatase, mitochondrial, transcript variant X1
PGAM family member 5, serine/threonine protein phosphatase, mitochondrial, transcript variant X2
serine/threonine-protein phosphatase PGAM5, mitochondrial isoform X1
serine/threonine-protein phosphatase PGAM5, mitochondrial isoform X2
ankyrin repeat and LEM domain containing 2, 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 6 samples with support for all annotated introns
ankyrin repeat and LEM domain containing 2, transcript variant X2
ankyrin repeat and LEM domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
ankyrin repeat and LEM domain containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ankyrin repeat and LEM domain-containing protein 2 isoform X1
ankyrin repeat and LEM domain-containing protein 2 isoform X2
uncharacterized si:dkey-112e17.1, transcript variant X2
uncharacterized si:dkey-112e17.1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein si:dkey-112e17.1 isoform X2
uncharacterized protein si:dkey-112e17.1 isoform X1
checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase
autism susceptibility gene 2 protein isoform X8
autism susceptibility gene 2 protein isoform X3
autism susceptibility gene 2 protein isoform X6
autism susceptibility gene 2 protein isoform X5
autism susceptibility gene 2 protein isoform X2
autism susceptibility gene 2 protein isoform X4
autism susceptibility gene 2 protein isoform X1
autism susceptibility gene 2 protein isoform X10
autism susceptibility gene 2 protein isoform X9
autism susceptibility gene 2 protein isoform X7
autism susceptibility gene 2 protein isoform X11
uncharacterized LOC122562541, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC122562541, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
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 31 samples with support for all annotated introns
stromal cell-derived factor 2-like protein 1
ferritin, heavy subunit-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 1 sample with support for all annotated introns
ferritin, heavy subunit-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
WSC domain containing 2, transcript variant X3
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 5 samples with support for all annotated introns
WSC domain containing 2, transcript variant X4
WSC domain containing 2, transcript variant X2
uncharacterized LOC122562450, transcript variant X2
uncharacterized LOC122562450, transcript variant X1
uncharacterized LOC122562450, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 23 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 13 samples with support for all annotated introns
leucine-rich repeat-containing protein 74B-like
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
solute carrier family 7 member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples 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: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DiGeorge syndrome critical region gene 6, transcript variant X3
DiGeorge syndrome critical region gene 6, transcript variant X2
DiGeorge syndrome critical region gene 6, transcript variant X1
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Hermansky-Pudlak syndrome 4 protein isoform X1
Hermansky-Pudlak syndrome 4 protein isoform X2
uncharacterized protein LOC571755 homolog
uncharacterized protein si:ch211-170d8.2
aspartate beta-hydroxylase domain containing 2, transcript variant X1
aspartate beta-hydroxylase domain containing 2, transcript variant X3
aspartate beta-hydroxylase domain containing 2, transcript variant X4
aspartate beta-hydroxylase domain containing 2, transcript variant X2
aspartate beta-hydroxylase domain-containing protein 2
seizure 6-like protein, transcript variant X1
seizure 6-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
potassium channel tetramerization domain containing 10, transcript variant X1
potassium channel tetramerization domain containing 10, transcript variant X2
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
potassium channel tetramerization domain containing 10, transcript variant X3
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X3
potassium channel tetramerization domain containing 10, transcript variant X4
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X4
small G protein signaling modulator 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
small G protein signaling modulator 1-like, transcript variant X2
small G protein signaling modulator 1-like isoform X1
small G protein signaling modulator 1-like isoform X2
small G protein signaling modulator 1-like, 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 2 samples with support for all annotated introns
small G protein signaling modulator 1-like isoform X3
ubiquitin carboxyl-terminal hydrolase 30-like
alkB homolog 2, alpha-ketoglutarate dependent dioxygenase
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
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
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: acetyl-CoA carboxylase 1-like
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 29 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 72% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 222 member A
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
transient receptor potential cation channel subfamily V member 4-like
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
trichoplein, keratin filament binding, 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 11 samples with support for all annotated introns
trichoplein, keratin filament binding, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
trichoplein, keratin filament binding, 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 18 samples with support for all annotated introns
trichoplein keratin filament-binding protein isoform X1
trichoplein keratin filament-binding protein isoform X2
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X3
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X2
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 X1
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X15
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X6
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X14
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X5
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X8
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X7
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X9
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X11
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X12
ARF GTPase-activating protein GIT2a isoform X15
ARF GTPase-activating protein GIT2a isoform X3
ARF GTPase-activating protein GIT2a isoform X12
ARF GTPase-activating protein GIT2a isoform X6
ARF GTPase-activating protein GIT2a isoform X9
ARF GTPase-activating protein GIT2a isoform X2
ARF GTPase-activating protein GIT2a isoform X14
ARF GTPase-activating protein GIT2a isoform X13
ARF GTPase-activating protein GIT2a isoform X11
ARF GTPase-activating protein GIT2a isoform X5
ARF GTPase-activating protein GIT2a isoform X8
ARF GTPase-activating protein GIT2a isoform X4
ARF GTPase-activating protein GIT2a isoform X7
ARF GTPase-activating protein GIT2a isoform X1
G protein-coupled receptor kinase interacting ArfGAP 2a, transcript variant X10
ARF GTPase-activating protein GIT2a isoform X10
ankyrin repeat domain 13A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ankyrin repeat domain 13A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ankyrin repeat domain 13A, transcript variant X1
ankyrin repeat domain-containing protein 13A isoform X2
ankyrin repeat domain-containing protein 13A isoform X1
solute carrier family 6 member 4b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 6 member 4b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 6 member 4b isoform X2
solute carrier family 6 member 4b isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
D-amino-acid oxidase, tandem duplicate 2
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 21 samples with support for all annotated introns
protein phosphatase Slingshot homolog 1-like, transcript variant X1
protein phosphatase Slingshot homolog 1-like, transcript variant X3
protein phosphatase Slingshot homolog 1-like, transcript variant X2
protein phosphatase Slingshot homolog 1-like, transcript variant X4
protein phosphatase Slingshot homolog 1-like isoform X1
protein phosphatase Slingshot homolog 1-like isoform X3
protein phosphatase Slingshot homolog 1-like isoform X2
protein phosphatase Slingshot homolog 1-like isoform X4
protein phosphatase Slingshot homolog 1-like, transcript variant X5
protein phosphatase Slingshot homolog 1-like isoform X5
coronin, actin binding protein, 1Cb, transcript variant X1
uncharacterized protein coro1cb isoform X1
coronin, actin binding protein, 1Cb, transcript variant X2
protein tyrosine phosphatase non-receptor type 11a, transcript variant X1
protein tyrosine phosphatase non-receptor type 11a, transcript variant X2
tyrosine-protein phosphatase non-receptor type 11
rabphilin-3A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
rabphilin-3A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rabphilin-3A-like, transcript variant X1
rabphilin-3A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
rabphilin-3A-like, transcript variant X3
sodium- and chloride-dependent GABA transporter 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1-like isoform X2
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: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1-like, transcript variant X3
sodium- and chloride-dependent GABA transporter 1-like, transcript variant X4
sodium- and chloride-dependent GABA transporter 1-like isoform X3
acyl-CoA dehydrogenase family member 10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
acyl-CoA dehydrogenase family member 10-like, 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 16 samples with support for all annotated introns
acyl-CoA dehydrogenase family member 10-like
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
endoplasmic reticulum resident protein 29-like
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X3
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X1
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X2
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X3
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X1
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X2
TRAF-type zinc finger domain containing 1, transcript variant X1
TRAF-type zinc finger domain containing 1, transcript variant X2
TRAF-type zinc finger domain containing 1, transcript variant X3
TRAF-type zinc finger domain containing 1, transcript variant X4
TRAF-type zinc finger domain-containing protein 1 isoform X2
TRAF-type zinc finger domain-containing protein 1 isoform X3
TRAF-type zinc finger domain-containing protein 1 isoform X4
TRAF-type zinc finger domain-containing protein 1 isoform X1
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 7 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 7 samples with support for all annotated introns
uncharacterized protein LOC122562594 isoform X1
uncharacterized protein LOC122562594 isoform 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
general transcriptional corepressor trfA-like isoform X4
inositol polyphosphate-5-phosphatase Jb, transcript variant X2
inositol polyphosphate-5-phosphatase Jb, 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 14 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
inositol polyphosphate-5-phosphatase Jb, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X1
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 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: 14 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
polyubiquitin-like, transcript variant X2
polyubiquitin-like, transcript variant X1
P2X purinoceptor 2-like, transcript variant X3
P2X purinoceptor 2-like, transcript variant X4
P2X purinoceptor 2-like, transcript variant X6
P2X purinoceptor 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
P2X purinoceptor 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
P2X purinoceptor 2-like, transcript variant X1
polymerase (DNA directed), epsilon, 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 2 samples with support for all annotated introns
polymerase (DNA directed), epsilon, transcript variant X1
DNA polymerase epsilon catalytic subunit A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
acylphosphatase 1, erythrocyte (common) type
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC122562605, transcript variant X4
uncharacterized LOC122562605, transcript variant X3
uncharacterized LOC122562605, transcript variant X1
uncharacterized LOC122562605, transcript variant X2
uncharacterized protein LOC122562605 isoform X1
uncharacterized protein LOC122562605 isoform X2
uncharacterized protein LOC122562605 isoform X3
uncharacterized LOC122562609, transcript variant X2
uncharacterized LOC122562609, transcript variant X1
beta-crystallin B3-like, transcript variant X1
beta-crystallin B3-like, transcript variant X2
beta-crystallin B2-like, transcript variant X2
beta-crystallin B2-like, transcript variant X1
uncharacterized LOC122562614, transcript variant X5
uncharacterized LOC122562614, transcript variant X3
uncharacterized LOC122562614, transcript variant X1
uncharacterized LOC122562614, transcript variant X4
uncharacterized LOC122562614, transcript variant X2
G protein-coupled receptor kinase 3, transcript variant X2
G protein-coupled receptor kinase 3, 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 10 samples with support for all annotated introns
beta-adrenergic receptor kinase 2 isoform X2
beta-adrenergic receptor kinase 2 isoform X1
uncharacterized LOC122562613, 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 18 samples with support for all annotated introns
uncharacterized LOC122562613, 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
uncharacterized LOC122562613, transcript variant X2
uncharacterized protein LOC122562613 isoform X1
uncharacterized protein LOC122562613 isoform X3
uncharacterized protein LOC122562613 isoform X2
protein-tyrosine sulfotransferase 2-like, 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 9 samples with support for all annotated introns
protein-tyrosine sulfotransferase 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 7 samples with support for all annotated introns
protein-tyrosine sulfotransferase 2-like, transcript variant X1
protein-tyrosine sulfotransferase 2-like isoform X1
protein-tyrosine sulfotransferase 2-like isoform X3
protein-tyrosine sulfotransferase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
clustered mitochondria protein homolog, transcript variant X1
clustered mitochondria protein homolog, transcript variant X2
clustered mitochondria protein homolog isoform X1
clustered mitochondria protein homolog isoform X2
SRR1 domain containing, transcript variant X5
SRR1 domain containing, transcript variant X2
SRR1 domain containing, transcript variant X4
SRR1 domain containing, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SRR1 domain containing, 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
SRR1 domain containing, transcript variant X1
tetratricopeptide repeat domain 28, transcript variant X1
tetratricopeptide repeat domain 28, 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 4 samples with support for all annotated introns
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 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
transcriptional activator MN1 isoform X3
transcriptional activator MN1 isoform X1
transcriptional activator MN1 isoform X4
transcriptional activator MN1 isoform X2
uncharacterized LOC122562461, transcript variant X2
uncharacterized LOC122562461, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 51% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC122562405
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
proline dehydrogenase 1, mitochondrial-like
THO complex subunit 5 homolog isoform X1
THO complex subunit 5 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized protein LOC564476 homolog, transcript variant X1
uncharacterized protein LOC564476 homolog, transcript variant X3
uncharacterized protein zgc:193801 isoform X1
uncharacterized protein zgc:193801 isoform X3
uncharacterized protein LOC564476 homolog, transcript variant X2
uncharacterized protein zgc:193801 isoform X2
AP-1 complex subunit beta-1, 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 15 samples with support for all annotated introns
AP-1 complex subunit beta-1, transcript variant X2
AP-1 complex subunit beta-1, transcript variant X4
AP-1 complex subunit beta-1, transcript variant X1
AP-1 complex subunit beta-1, transcript variant X3
rhomboid domain-containing protein 3-like
EMI domain-containing protein 1-like, transcript variant X1
EMI domain-containing protein 1-like, transcript variant X2
EMI domain-containing protein 1-like isoform X1
EMI domain-containing protein 1-like isoform X2
EMI domain-containing protein 1-like, transcript variant X3
EMI domain-containing protein 1-like isoform X3
ABC transporter B family member 1-like, 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 1 sample with support for all annotated introns
ABC transporter B family member 1-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 3 samples with support for all annotated introns
ABC transporter B family member 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 4 samples with support for all annotated introns
ABC transporter B family member 1-like isoform X3
ABC transporter B family member 1-like isoform X2
ABC transporter B family member 1-like isoform X1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
rasGAP-activating-like protein 1, 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 3 samples with support for all annotated introns
rasGAP-activating-like protein 1, transcript variant X1
rasGAP-activating-like protein 1 isoform X2
rasGAP-activating-like protein 1 isoform X1
cytosolic arginine sensor for mTORC1 subunit 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
cytosolic arginine sensor for mTORC1 subunit 2-like isoform X2
cytosolic arginine sensor for mTORC1 subunit 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytosolic arginine sensor for mTORC1 subunit 2-like isoform X1
galactose-3-O-sulfotransferase 1a, transcript variant X1
galactose-3-O-sulfotransferase 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
galactose-3-O-sulfotransferase 1a, 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
zona pellucida sperm-binding protein 3-like
mitochondrial fission process 1, transcript variant X1
mitochondrial fission process 1, transcript variant X2
mitochondrial fission process protein 1 isoform X2
mitochondrial fission process protein 1 isoform X1
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 16 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 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 157
coiled-coil domain-containing protein 157-like
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
PH domain containing endocytic trafficking adaptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 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 77% coverage of the annotated genomic feature by RNAseq alignments
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 61% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1, catalytic subunit, gamma isozyme
serine/threonine-protein phosphatase PP1-gamma catalytic subunit A
hydrogen voltage-gated channel 1, 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 8 samples with support for all annotated introns
hydrogen voltage-gated channel 1, 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 1 sample with support for all annotated introns
hydrogen voltage-gated channel 1, 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 4 samples with support for all annotated introns
hydrogen voltage-gated channel 1, 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 25 samples with support for all annotated introns
VPS29 retromer complex component, transcript variant X1
VPS29 retromer complex component, transcript variant X2
vacuolar protein sorting-associated protein 29 isoform X1
vacuolar protein sorting-associated protein 29 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC122562661, transcript variant X3
uncharacterized LOC122562661, transcript variant X2
uncharacterized LOC122562661, transcript variant 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), transcript variant X2
ubiquitin-conjugating enzyme E2G 1b (UBC7 homolog, yeast), transcript variant X3
ubiquitin-conjugating enzyme E2G 1b (UBC7 homolog, yeast), transcript variant X1
anaphase promoting complex subunit 7, transcript variant X1
anaphase promoting complex subunit 7, transcript variant X2
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 14 samples with support for all annotated introns
anaphase promoting complex subunit 7, 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 18 samples with support for all annotated introns
anaphase promoting complex subunit 7, transcript variant X5
anaphase-promoting complex subunit 7 isoform X1
anaphase-promoting complex subunit 7 isoform X2
anaphase-promoting complex subunit 7 isoform X3
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 X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
intraflagellar transport protein 81 homolog isoform X1
intraflagellar transport 81 homolog, transcript variant X2
intraflagellar transport protein 81 homolog isoform 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 9 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X1
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X5
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X3
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X2
calcium/calmodulin-dependent protein kinase kinase 2-like isoform X3
calcium/calmodulin-dependent protein kinase kinase 2-like isoform X1
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X4
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 5 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase kinase 2-like isoform X2
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase kinase 2-like isoform X4
calcium/calmodulin-dependent protein kinase kinase 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase kinase 2-like isoform X5
ring finger protein 34a, transcript variant X3
E3 ubiquitin-protein ligase RNF34a isoform X3
ring finger protein 34a, transcript variant X1
ring finger protein 34a, transcript variant X2
E3 ubiquitin-protein ligase RNF34a isoform X1
E3 ubiquitin-protein ligase RNF34a isoform X2
lysine-specific demethylase 2B, transcript variant X4
lysine-specific demethylase 2B, transcript variant X3
lysine-specific demethylase 2B, transcript variant X11
lysine-specific demethylase 2B, transcript variant X2
lysine-specific demethylase 2B, transcript variant X1
lysine-specific demethylase 2B, transcript variant X13
lysine-specific demethylase 2B, transcript variant X6
lysine-specific demethylase 2B, transcript variant X9
lysine-specific demethylase 2B, transcript variant X8
lysine-specific demethylase 2B, transcript variant X7
lysine-specific demethylase 2B, transcript variant X5
lysine-specific demethylase 2B, transcript variant X12
lysine-specific demethylase 2B, transcript variant X10
lysine-specific demethylase 2B, transcript variant X14
lysine-specific demethylase 2B isoform X4
lysine-specific demethylase 2B isoform X3
lysine-specific demethylase 2B isoform X11
lysine-specific demethylase 2B isoform X2
lysine-specific demethylase 2B isoform X1
lysine-specific demethylase 2B isoform X6
lysine-specific demethylase 2B isoform X8
lysine-specific demethylase 2B isoform X7
lysine-specific demethylase 2B isoform X5
lysine-specific demethylase 2B isoform X9
lysine-specific demethylase 2B isoform X10
lysine-specific demethylase 2B isoform X12
lysine-specific demethylase 2B isoform X13
calcium release-activated calcium channel protein 1-like
MORN repeat containing 3, 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 18 samples with support for all annotated introns
MORN repeat containing 3, transcript variant X2
MORN repeat containing 3, transcript variant X1
transmembrane protein 120B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protein 120B, transcript variant X2
transmembrane protein 120B, transcript variant X1
transmembrane protein 120B, transcript variant X3
transmembrane protein 120B, transcript variant X4
transmembrane protein 120B, 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 3 samples with support for all annotated introns
ras homolog family member F, 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 17 samples with support for all annotated introns
ras homolog family member F, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
rho-related GTP-binding protein RhoF isoform X2
rho-related GTP-binding protein RhoF isoform X1
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X3
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X1
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X4
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X5
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X6
SET domain containing 1B, histone lysine methyltransferase a, transcript variant X2
histone-lysine N-methyltransferase SETD1B-A isoform X1
histone-lysine N-methyltransferase SETD1B-A isoform X2
histone-lysine N-methyltransferase SETD1B-A isoform X3
histone-lysine N-methyltransferase SETD1B-A isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 9
cilia and flagella associated protein 251
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
cilia- and flagella-associated protein 251
BAF chromatin remodeling complex subunit BCL7A, transcript variant X2
BAF chromatin remodeling complex subunit BCL7A, transcript variant X3
BAF chromatin remodeling complex subunit BCL7A, transcript variant X1
B-cell CLL/lymphoma 7 protein family member A isoform X1
B-cell CLL/lymphoma 7 protein family member A isoform X2
leucine-rich repeat-containing protein 43-like
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4-like
diablo homolog, mitochondrial-like, transcript variant X3
diablo homolog, mitochondrial-like, transcript variant X2
diablo homolog, mitochondrial-like, transcript variant X1
diablo homolog, mitochondrial-like isoform X2
diablo homolog, mitochondrial-like isoform X3
diablo homolog, mitochondrial-like isoform X1
VPS33A core subunit of CORVET and HOPS complexes, transcript variant X1
VPS33A core subunit of CORVET and HOPS complexes, transcript variant X2
vacuolar protein sorting-associated protein 33A isoform X1
vacuolar protein sorting-associated protein 33A isoform X2
CAP-GLY domain containing linker protein 1a
CAP-Gly domain-containing linker protein 1
zinc finger CCHC domain-containing protein 8
uncharacterized protein LOC562347 homolog
uncharacterized protein si:ch211-110p13.9
arginine/serine-rich coiled-coil 2, transcript variant X1
arginine/serine-rich coiled-coil 2, transcript variant X2
arginine/serine-rich coiled-coil protein 2 isoform X1
arginine/serine-rich coiled-coil protein 2 isoform X2
kinetochore associated 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kinetochore associated 1, 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
kinetochore-associated protein 1 isoform X2
kinetochore-associated protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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: 2 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
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
density-regulated protein, transcript variant X2
density-regulated protein, transcript variant X1
density-regulated protein, transcript variant X3
coiled-coil domain containing 62, 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 17 samples with support for all annotated introns
coiled-coil domain containing 62, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
coiled-coil domain-containing protein 62 isoform X1
coiled-coil domain-containing protein 62 isoform X2
coiled-coil domain containing 62, 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 26 samples with support for all annotated introns
coiled-coil domain-containing protein 62 isoform X3
coiled-coil domain containing 62, 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 10 samples with support for all annotated introns
coiled-coil domain-containing protein 62 isoform X4
huntingtin-interacting protein 1-related protein-like, transcript variant X1
huntingtin-interacting protein 1-related protein-like, transcript variant X2
huntingtin-interacting protein 1-related protein-like isoform X1
huntingtin-interacting protein 1-related protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glycosyltransferase 1 domain containing 1, 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 20 samples with support for all annotated introns
glycosyltransferase 1 domain-containing protein 1 isoform X1
glycosyltransferase 1 domain containing 1, transcript variant X4
glycosyltransferase 1 domain-containing protein 1 isoform X4
glycosyltransferase 1 domain containing 1, transcript variant X2
glycosyltransferase 1 domain-containing protein 1 isoform X2
glycosyltransferase 1 domain containing 1, transcript variant X3
glycosyltransferase 1 domain-containing protein 1 isoform X3
solute carrier family 15 member 4, 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 3 samples with support for all annotated introns
solute carrier family 15 member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 15 member 4, 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 2 samples with support for all annotated introns
solute carrier family 15 member 4, transcript variant X5
solute carrier family 15 member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
solute carrier family 15 member 4 isoform X1
solute carrier family 15 member 4 isoform X2
solute carrier family 15 member 4 isoform X4
solute carrier family 15 member 4 isoform X5
solute carrier family 15 member 4 isoform X3
transmembrane protein 132C-like, transcript variant X1
transmembrane protein 132C-like, transcript variant X2
transmembrane protein 132C-like, transcript variant X4
transmembrane protein 132C-like, transcript variant X7
transmembrane protein 132C-like, transcript variant X8
transmembrane protein 132C-like, transcript variant X3
transmembrane protein 132C-like, transcript variant X6
transmembrane protein 132C-like, transcript variant X5
transmembrane protein 132C-like, transcript variant X9
transmembrane protein 132C-like isoform X1
transmembrane protein 132C-like isoform X2
transmembrane protein 132C-like isoform X4
transmembrane protein 132C-like isoform X3
transmembrane protein 132C-like isoform X5
acetoacetyl-CoA synthetase, transcript variant X2
acetoacetyl-CoA synthetase, transcript variant X1
acetoacetyl-CoA synthetase, 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 11 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 27 samples with support for all annotated introns
DEAH (Asp-Glu-Ala-His) box polypeptide 37
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
squamous cell carcinoma antigen recognized by T-cells 3
myotubularin related protein 3, transcript variant X2
myotubularin related protein 3, transcript variant X1
myotubularin related protein 3, transcript variant X3
myotubularin related protein 3, transcript variant X4
myotubularin related protein 3, transcript variant X8
myotubularin related protein 3, transcript variant X5
myotubularin-related protein 3 isoform X8
myotubularin-related protein 3 isoform X3
myotubularin-related protein 3 isoform X4
myotubularin-related protein 3 isoform X1
myotubularin-related protein 3 isoform X2
myotubularin-related protein 3 isoform X5
myotubularin related protein 3, transcript variant X6
myotubularin-related protein 3 isoform X6
myotubularin related protein 3, transcript variant X7
myotubularin-related protein 3 isoform X7
activating signal cointegrator 1 complex subunit 2, transcript variant X2
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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 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
zinc finger, matrin-type 5, transcript variant X1
zinc finger, matrin-type 5, transcript variant X2
zinc finger matrin-type protein 5 isoform X1
zinc finger matrin-type protein 5 isoform X2
calcium-binding protein 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
calcium-binding protein 7, transcript variant X4
calcium-binding protein 7, transcript variant X3
calcium-binding protein 7, 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine dehydratase-like, transcript variant X4
serine dehydratase-like, transcript variant X3
serine dehydratase-like, transcript variant X5
serine dehydratase-like, transcript variant X1
serine dehydratase-like, transcript variant X6
serine dehydratase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 13 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
RBPJ-interacting and tubulin-associated protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 5 samples with support for all annotated introns
RBPJ-interacting and tubulin-associated protein 1-like
DEAD (Asp-Glu-Ala-Asp) box polypeptide 54
cilia and flagella associated protein 73, transcript variant X1
cilia and flagella associated protein 73, transcript variant X2
coiled-coil domain-containing protein 42 homolog isoform X2
coiled-coil domain-containing protein 42 homolog 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 25 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
RNA binding motif protein 19, transcript variant X3
RNA binding motif protein 19, transcript variant X2
probable RNA-binding protein 19 isoform X1
probable RNA-binding protein 19 isoform X2
RNA binding motif protein 19, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable RNA-binding protein 19 isoform X3
uncharacterized LOC122562476, transcript variant X2
uncharacterized LOC122562476, transcript variant X1
uncharacterized LOC122562476, transcript variant X3
uncharacterized LOC122562477, transcript variant X1
uncharacterized LOC122562477, transcript variant X2
T-box transcription factor 5b, transcript variant X2
T-box transcription factor 5b, transcript variant X3
T-box transcription factor 5b, transcript variant X1
T-box transcription factor 5b, transcript variant X4
T-box transcription factor TBX5b isoform X2
T-box transcription factor TBX5b isoform X1
uncharacterized LOC122562730, transcript variant X2
uncharacterized LOC122562730, transcript variant X1
uncharacterized LOC122562731, transcript variant X4
uncharacterized LOC122562731, transcript variant X2
uncharacterized LOC122562731, transcript variant X1
uncharacterized LOC122562731, transcript variant X3
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 13-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 13-like isoform X2
mediator of RNA polymerase II transcription subunit 13-like isoform X1
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ring finger protein, transmembrane 2, transcript variant X1
ring finger protein, transmembrane 2, transcript variant X2
RING finger and transmembrane domain-containing protein 2 isoform X1
RING finger and transmembrane domain-containing protein 2 isoform X2
V-set and immunoglobulin domain containing 10
V-set and immunoglobulin domain-containing protein 10
WD repeat and SOCS box containing 2, transcript variant X5
WD repeat and SOCS box containing 2, transcript variant X6
WD repeat and SOCS box containing 2, transcript variant X4
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 25 samples with support for all annotated introns
WD repeat and SOCS box containing 2, transcript variant X1
WD repeat and SOCS box containing 2, transcript variant X2
WD repeat and SOCS box containing 2, transcript variant X3
WD repeat and SOCS box-containing protein 2 isoform X3
WD repeat and SOCS box-containing protein 2 isoform X4
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 subunit 5 isoform 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 X1
replication factor C subunit 5 isoform X3
kinase suppressor of ras 2, transcript variant X1
kinase suppressor of ras 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122562744, transcript variant X2
uncharacterized LOC122562744, transcript variant X1
SDS3 homolog, SIN3A corepressor complex component
sin3 histone deacetylase corepressor complex component SDS3
serine/threonine-protein kinase TAO3 isoform X1
serine/threonine-protein kinase TAO3 isoform X2
phosphatidylethanolamine binding protein 1
phosphatidylethanolamine-binding protein 1
nitric oxide synthase 1 (neuronal), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nitric oxide synthase 1 (neuronal), transcript variant X2
nitric oxide synthase 1 (neuronal), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/arginine repetitive matrix 4, transcript variant X1
serine/arginine repetitive matrix 4, transcript variant X2
serine/arginine repetitive matrix protein 4 isoform X1
serine/arginine repetitive matrix protein 4 isoform X2
uncharacterized LOC122562481, transcript variant X2
uncharacterized LOC122562481, transcript variant X3
uncharacterized LOC122562481, 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 7 samples with support for all annotated introns
coiled-coil domain-containing protein 60-like, transcript variant X4
coiled-coil domain-containing protein 60-like, transcript variant X6
coiled-coil domain-containing protein 60-like, 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 5 samples with support for all annotated introns
coiled-coil domain-containing protein 60-like, transcript variant X2
coiled-coil domain-containing protein 60-like, transcript variant X3
coiled-coil domain-containing protein 60-like, transcript variant X1
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
coiled-coil domain-containing protein 60-like, transcript variant X7
coiled-coil domain-containing protein 60-like isoform X4
collagen alpha-1(III) chain-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized LOC122562757, transcript variant X1
uncharacterized LOC122562757, transcript variant X2
zinc and ring finger 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc and ring finger 3, transcript variant X2
E3 ubiquitin-protein ligase znrf3 isoform X1
E3 ubiquitin-protein ligase znrf3 isoform X2
zinc and ring finger 3, transcript variant X3
E3 ubiquitin-protein ligase znrf3 isoform X3
zinc and ring finger 3, transcript variant X4
zinc and ring finger 3, transcript variant X5
E3 ubiquitin-protein ligase znrf3 isoform X4
E3 ubiquitin-protein ligase znrf3 isoform X5
kringle containing transmembrane protein 1, transcript variant X2
kringle containing transmembrane protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
kringle containing transmembrane protein 1, transcript variant X3
sushi domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sushi domain-containing protein 2 isoform X1
sushi domain containing 2, 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 9 samples with support for all annotated introns
sushi domain containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sushi domain-containing protein 2 isoform X4
sushi domain-containing protein 2 isoform X5
sushi domain containing 2, 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 5 samples with support for all annotated introns
sushi domain-containing protein 2 isoform X3
sushi domain containing 2, transcript variant X6
sushi domain containing 2, transcript variant X2
sushi domain-containing protein 2 isoform X6
sushi domain-containing protein 2 isoform X2
dual specificity protein phosphatase 18-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC122562763, transcript variant X3
uncharacterized LOC122562763, transcript variant X1
uncharacterized LOC122562763, transcript variant X2
synergin gamma-like, transcript variant X6
synergin gamma-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
synergin gamma-like, transcript variant X3
synergin gamma-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 16 samples with support for all annotated introns
synergin gamma-like, transcript variant X4
synergin gamma-like, transcript variant X5
synergin gamma-like, transcript variant X8
synergin gamma-like, transcript variant X7
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
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
acyl-CoA dehydrogenase short chain, 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 26 samples with support for all annotated introns
acyl-CoA dehydrogenase short chain, transcript variant X2
acyl-CoA dehydrogenase short chain, 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 10 samples with support for all annotated introns
short-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1
short-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2
unc-119 homolog 1, transcript variant X1
unc-119 homolog 1, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
calcium binding protein 1a, 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 2 samples with support for all annotated introns
calcium binding protein 1a, 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 10 samples with support for all annotated introns
calcium binding protein 1a, 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 2 samples with support for all annotated introns
calcium binding protein 1a, transcript variant X3
uncharacterized LOC122562775, transcript variant X2
uncharacterized LOC122562775, transcript variant X1
uncharacterized LOC122562775, transcript variant X3
uncharacterized protein LOC122562775 isoform X1
uncharacterized protein LOC122562775 isoform X3
uncharacterized protein LOC122562775 isoform X2
POP5 homolog, ribonuclease P/MRP subunit
ring finger protein 10, transcript variant X5
ring finger protein 10, transcript variant X2
ring finger protein 10, transcript variant X4
ring finger protein 10, transcript variant X3
ring finger protein 10, transcript variant X1
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial
serine/arginine-rich splicing factor 1B-like
glutamyl-tRNA amidotransferase subunit C, transcript variant X2
glutamyl-tRNA amidotransferase subunit C, transcript variant X1
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial isoform X1
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial isoform X2
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cytochrome c oxidase subunit 6A, mitochondrial-like, transcript variant X1
cytochrome c oxidase subunit 6A, mitochondrial-like, transcript variant X2
cytochrome c oxidase subunit 6A, mitochondrial-like isoform X2
cytochrome c oxidase subunit 6A, mitochondrial-like isoform X1
RNA-binding protein Musashi homolog 1-like
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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X3
solute carrier family 2, facilitated glucose transporter member 11-like isoform X3
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X4
solute carrier family 2, facilitated glucose transporter member 11-like, transcript variant X2
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 isoform X2
solute carrier family 2, facilitated glucose transporter member 11-like
solute carrier family 2, facilitated glucose transporter member 11b
citron rho-interacting serine/threonine kinase a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
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 X4
BICD family-like cargo adapter 1 isoform X1
BICD family-like cargo adapter 1 isoform X2
BICD family-like cargo adapter 1 isoform X3
5'-AMP-activated protein kinase subunit beta-1-like, 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 21 samples with support for all annotated introns
5'-AMP-activated protein kinase subunit beta-1-like isoform X3
5'-AMP-activated protein kinase subunit beta-1-like, transcript variant X2
5'-AMP-activated protein kinase subunit beta-1-like, transcript variant X1
5'-AMP-activated protein kinase subunit beta-1-like isoform X2
5'-AMP-activated protein kinase subunit beta-1-like isoform X1
ADP-ribose pyrophosphatase, mitochondrial-like
transcobalamin-2-like, transcript variant X2
transcobalamin-2-like, transcript variant X1
transcobalamin-2-like, transcript variant X3
coiled-coil domain containing 117, transcript variant X4
coiled-coil domain containing 117, transcript variant X1
coiled-coil domain containing 117, transcript variant X3
coiled-coil domain containing 117, transcript variant X2
coiled-coil domain-containing protein 117 isoform X1
coiled-coil domain-containing protein 117 isoform X2
uncharacterized protein si:ch211-102c2.8
oxysterol-binding protein 2-like, transcript variant X1
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 X9
oxysterol-binding protein 2-like, transcript variant X7
oxysterol-binding protein 2-like, transcript variant X8
oxysterol-binding protein 2-like, transcript variant X14
oxysterol-binding protein 2-like, transcript variant X6
oxysterol-binding protein 2-like, transcript variant X11
oxysterol-binding protein 2-like, transcript variant X13
oxysterol-binding protein 2-like, transcript variant X5
oxysterol-binding protein 2-like, transcript variant X10
oxysterol-binding protein 2-like, transcript variant X12
oxysterol-binding protein 2-like isoform X2
oxysterol-binding protein 2-like isoform X1
oxysterol-binding protein 2-like isoform X3
oxysterol-binding protein 2-like isoform X4
oxysterol-binding protein 2-like isoform X6
oxysterol-binding protein 2-like isoform X8
oxysterol-binding protein 2-like isoform X5
oxysterol-binding protein 2-like isoform X7
oxysterol-binding protein 2-like isoform X9
mitotic spindle organizing protein 2B, transcript variant X1
mitotic spindle organizing protein 2B, transcript variant X4
mitotic spindle organizing protein 2B, transcript variant X2
mitotic spindle organizing protein 2B, transcript variant X3
mitotic spindle organizing protein 2B, transcript variant X5
mitotic-spindle organizing protein 2 isoform X1
mitotic-spindle organizing protein 2 isoform X2
mitotic-spindle organizing protein 2 isoform X3
mitotic-spindle organizing protein 2 isoform X4
mitotic-spindle organizing protein 2 isoform X5
apoptosis-inducing factor 3, transcript variant X3
apoptosis-inducing factor 3, transcript variant X2
apoptosis-inducing factor 3, transcript variant X6
apoptosis-inducing factor 3, transcript variant X5
apoptosis-inducing factor 3, transcript variant X4
apoptosis-inducing factor 3, transcript variant X1
leucine-zipper-like transcription regulator 1
leucine-zipper-like transcriptional regulator 1
protein piccolo-like, transcript variant X2
protein piccolo-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 4 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 3 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
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X3
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X2
cytoplasmic tRNA 2-thiolation protein 1 isoform X2
cytosolic thiouridylase subunit 1 homolog (S. pombe), transcript variant X1
cytoplasmic tRNA 2-thiolation protein 1 isoform X1
cytoplasmic tRNA 2-thiolation protein 1 isoform X3
uncharacterized protein DDB_G0284459-like isoform X1
uncharacterized protein DDB_G0284459-like isoform X3
uncharacterized protein DDB_G0284459-like isoform X5
uncharacterized protein DDB_G0284459-like isoform X4
uncharacterized protein DDB_G0284459-like isoform X2
uncharacterized protein DDB_G0284459-like isoform X6
uncharacterized protein LOC122562805 isoform X7
ribosomal protein, large, P0, transcript variant X1
60S acidic ribosomal protein P0 isoform X1
ribosomal protein, large, P0, transcript variant X2
60S acidic ribosomal protein P0 isoform X2
immunoglobulin lambda-1 light chain-like
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 15 samples with support for all annotated introns
uncharacterized protein LOC393431 homolog
uncharacterized LOC122562811, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC122562811, transcript variant X1
CDC45 cell division cycle 45 homolog (S. cerevisiae), 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
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
CDC45 cell division cycle 45 homolog (S. cerevisiae), transcript variant X4
cell division control protein 45 homolog isoform X3
ubiquitin recognition factor in ER associated degradation 1
ubiquitin recognition factor in ER-associated degradation protein 1
peptidyl-prolyl cis-trans isomerase FKBP8-like
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
39S ribosomal protein L40, mitochondrial isoform X2
39S ribosomal protein L40, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122562486, transcript variant X1
uncharacterized LOC122562486, transcript variant X2
uncharacterized LOC122562827, transcript variant X3
uncharacterized LOC122562827, transcript variant X2
uncharacterized LOC122562827, transcript variant X1
peptidylprolyl isomerase (cyclophilin)-like 2, transcript variant X2
peptidylprolyl isomerase (cyclophilin)-like 2, transcript variant X1
RING-type E3 ubiquitin-protein ligase PPIL2 isoform X1
RING-type E3 ubiquitin-protein ligase PPIL2 isoform X2
protein phosphatase, Mg2+/Mn2+ dependent, 1F
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
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 26 samples with support for all annotated introns
RAB35, member RAS oncogene family b, transcript variant X2
RAB35, member RAS oncogene family b, transcript variant X1
phospholipase A2-like, transcript variant X3
phospholipase A2-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 5 samples with support for all annotated introns
phospholipase A2, minor isoenzyme-like isoform X2
phospholipase A2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phospholipase A2, minor isoenzyme-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RAB36, member RAS oncogene family, transcript variant X1
RAB36, member RAS oncogene family, transcript variant X4
RAB36, member RAS oncogene family, transcript variant X2
RAB36, member RAS oncogene family, transcript variant X3
RAB36, member RAS oncogene family, transcript variant X5
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
guanine nucleotide binding protein (G protein), alpha z polypeptide
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 126 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
guanine nucleotide-binding protein G(z) subunit alpha
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
pleckstrin homology domain-containing family A member 7-like, transcript variant X2
pleckstrin homology domain-containing family A member 7-like, transcript variant X1
pleckstrin homology domain-containing family A member 7-like isoform X2
pleckstrin homology domain-containing family A member 7-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized wu:fi75a02, transcript variant X1
uncharacterized wu:fi75a02, transcript variant X3
uncharacterized wu:fi75a02, transcript variant X4
uncharacterized wu:fi75a02, transcript variant X2
uncharacterized wu:fi75a02, transcript variant X5
uncharacterized protein wu:fi75a02 isoform X1
uncharacterized protein wu:fi75a02 isoform X2
uncharacterized protein wu:fi75a02 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylserine decarboxylase, transcript variant X1
phosphatidylserine decarboxylase, transcript variant X2
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X1
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X2
phosphatidylserine decarboxylase, transcript variant X4
phosphatidylserine decarboxylase, transcript variant X5
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X4
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X5
phosphatidylserine decarboxylase, transcript variant X8
phosphatidylserine decarboxylase, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phosphatidylserine decarboxylase, transcript variant X3
phosphatidylserine decarboxylase, transcript variant X6
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X6
phosphatidylserine decarboxylase proenzyme, mitochondrial isoform X3
SFI1 centrin binding protein, transcript variant X2
SFI1 centrin binding protein, transcript variant X3
SFI1 centrin binding protein, transcript variant X1
SFI1 centrin binding protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 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 26 samples with support for all annotated introns
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X2
eukaryotic translation initiation factor 4E nuclear import factor 1, transcript variant X5
eukaryotic translation initiation factor 4E transporter isoform X1
eukaryotic translation initiation factor 4E transporter isoform X2
eukaryotic translation initiation factor 4E transporter isoform X5
eukaryotic translation initiation factor 4E transporter isoform X3
eukaryotic translation initiation factor 4E transporter isoform X4
developmentally regulated GTP binding protein 1
developmentally-regulated GTP-binding protein 1
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 10 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
POZ-, AT hook-, and zinc finger-containing protein 1 isoform X1
POZ-, AT hook-, and zinc finger-containing protein 1 isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 51
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 27 samples with support for all annotated introns
uncharacterized LOC122562853, 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 19 samples with support for all annotated introns
uncharacterized LOC122562853, 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 13 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 17 samples with support for all annotated introns
calcineurin binding protein 1, transcript variant X1
calcineurin binding protein 1, transcript variant X4
calcineurin binding protein 1, transcript variant X2
calcineurin binding protein 1, transcript variant X3
calcineurin-binding protein cabin-1 isoform X1
calcineurin-binding protein cabin-1 isoform X4
calcineurin-binding protein cabin-1 isoform X3
calcineurin-binding protein cabin-1 isoform X2
DEP domain containing 5, GATOR1 subcomplex subunit
uncharacterized LOC122562859, transcript variant X4
uncharacterized LOC122562859, transcript variant X2
uncharacterized LOC122562859, transcript variant X1
uncharacterized LOC122562859, transcript variant X5
uncharacterized LOC122562859, transcript variant X3
uncharacterized protein LOC122562859 isoform X2
uncharacterized protein LOC122562859 isoform X1
uncharacterized protein LOC122562859 isoform X3
serine/threonine-protein phosphatase 4 catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
v-crk avian sarcoma virus CT10 oncogene homolog-like
uncharacterized LOC122562490, transcript variant X2
uncharacterized LOC122562490, transcript variant X3
uncharacterized LOC122562490, transcript variant X5
uncharacterized LOC122562490, transcript variant X4
uncharacterized LOC122562490, transcript variant X1
kelch-like family member 22, transcript variant X3
kelch-like family member 22, transcript variant X1
kelch-like family member 22, transcript variant X2
glutathione S-transferase theta-3-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 31 samples with support for all annotated introns
glutathione S-transferase theta-3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
glutathione S-transferase theta-3-like isoform X2
glutathione S-transferase theta-3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 185, transcript variant X6
ring finger protein 185, transcript variant X2
ring finger protein 185, 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 13 samples with support for all annotated introns
ring finger protein 185, transcript variant X5
ring finger protein 185, transcript variant X1
ring finger protein 185, transcript variant X3
E3 ubiquitin-protein ligase RNF185 isoform X6
E3 ubiquitin-protein ligase RNF185 isoform X2
E3 ubiquitin-protein ligase RNF185 isoform X5
E3 ubiquitin-protein ligase RNF185 isoform X4
E3 ubiquitin-protein ligase RNF185 isoform X3
E3 ubiquitin-protein ligase RNF185 isoform X1
phosphoinositide-3-kinase interacting protein 1, transcript variant X2
phosphoinositide-3-kinase interacting protein 1, transcript variant X1
phosphoinositide-3-kinase-interacting protein 1 isoform X1
phosphoinositide-3-kinase-interacting protein 1 isoform X2
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 X2
integral membrane protein DGCR2/IDD isoform X3
integral membrane protein DGCR2/IDD isoform X1
testis-specific serine/threonine-protein kinase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
ess-2 splicing factor homolog, 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 29 samples with support for all annotated introns
splicing factor ESS-2 homolog isoform X1
ess-2 splicing factor homolog, 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 25 samples with support for all annotated introns
splicing factor ESS-2 homolog isoform X2
thyroid adenoma-associated protein homolog, transcript variant X1
thyroid adenoma-associated protein homolog, transcript variant X3
thyroid adenoma-associated protein homolog, transcript variant X2
thyroid adenoma-associated protein homolog, transcript variant X5
thyroid adenoma-associated protein homolog isoform X1
thyroid adenoma-associated protein homolog isoform X3
thyroid adenoma-associated protein homolog isoform X2
thyroid adenoma-associated protein homolog isoform X5
thyroid adenoma-associated protein homolog, transcript variant X4
thyroid adenoma-associated protein homolog isoform X4
coiled-coil-helix-coiled-coil-helix domain containing 10
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
stromelysin-3-like, transcript variant X1
stromelysin-3-like, transcript variant X2
stromelysin-3-like, transcript variant X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, transcript variant X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, transcript variant X5
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A, transcript variant X6
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 X5
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1 isoform X6
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 X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily B member 1-A isoform X2
breakpoint cluster region protein-like, transcript variant X3
breakpoint cluster region protein-like, transcript variant X1
breakpoint cluster region protein-like, transcript variant X2
breakpoint cluster region protein-like isoform X1
breakpoint cluster region protein-like isoform X2
breakpoint cluster region protein-like isoform X3
sperm antigen with calponin homology and coiled-coil domains 1-like a, transcript variant X2
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 X4
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 X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
ureidopropionase, beta, transcript variant X2
ureidopropionase, beta, transcript variant X1
mediator complex subunit 15, transcript variant X1
mediator complex subunit 15, transcript variant X5
mediator complex subunit 15, transcript variant X2
mediator of RNA polymerase II transcription subunit 15 isoform X1
mediator of RNA polymerase II transcription subunit 15 isoform X5
mediator of RNA polymerase II transcription subunit 15 isoform X2
mediator complex subunit 15, transcript variant X3
mediator of RNA polymerase II transcription subunit 15 isoform X3
mediator complex subunit 15, transcript variant X4
mediator of RNA polymerase II transcription subunit 15 isoform X4
mediator complex subunit 15, transcript variant X6
mediator of RNA polymerase II transcription subunit 15 isoform X6
uncharacterized LOC122562887, transcript variant X1
uncharacterized LOC122562887, transcript variant X2
coiled-coil domain-containing protein 74B-like
transfer RNA serine (anticodon GGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
sphingomyelin phosphodiesterase 4, transcript variant X3
sphingomyelin phosphodiesterase 4, transcript variant X2
sphingomyelin phosphodiesterase 4, transcript variant X1
sphingomyelin phosphodiesterase 4, transcript variant X5
sphingomyelin phosphodiesterase 4, transcript variant X4
sphingomyelin phosphodiesterase 4 isoform X3
sphingomyelin phosphodiesterase 4 isoform X5
sphingomyelin phosphodiesterase 4 isoform X2
sphingomyelin phosphodiesterase 4 isoform X4
sphingomyelin phosphodiesterase 4 isoform X1
leucine-rich repeat-containing protein 75B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
gastrula zinc finger protein XlCGF17.1-like, transcript variant X3
gastrula zinc finger protein XlCGF17.1-like, transcript variant X2
gastrula zinc finger protein XlCGF17.1-like, transcript variant X1
gastrula zinc finger protein XlCGF17.1-like
transfer RNA valine (anticodon UAC); 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: 8 Proteins