Sphaerodactylus townsendi isolate TG3544 linkage group LG14, MPM_Stown_v2.3, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Lepidosauria; Squamata; Bifurcata; Gekkota; Sphaerodactylidae; Sphaerodactylus.
Chromosome-level genome assembly reveals dynamic sex chromosomes in Neotropical leaf-litter geckos (Sphaerodactylidae: Sphaerodactylus)
Publication Status: Available-Online prior to print
REFSEQ INFORMATION: The reference sequence is identical to\nCM037627.2.\nAssembly name: MPM_Stown_v2.3\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Marquette University on\n2022/04/08. The original whole-genome shotgun project has the\naccession JAHVXK000000000.2.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Marquette University\nAssembly Method :: SuperNova v. 2.1.1\nAssembly Name :: MPM_Stown_v2.3\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 160.0x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Sphaerodactylus townsendi 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.
RRAD, Ras related glycolysis inhibitor and calcium channel regulator, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
RRAD, Ras related glycolysis inhibitor and calcium channel regulator, transcript variant X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
CKLF like MARVEL transmembrane domain containing 3
CKLF-like MARVEL transmembrane domain-containing protein 3
CKLF like MARVEL transmembrane domain containing 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CKLF like MARVEL transmembrane domain containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CKLF-like MARVEL transmembrane domain-containing protein 4 isoform X2
CKLF-like MARVEL transmembrane domain-containing protein 4 isoform X1
dynein cytoplasmic 1 light intermediate chain 2
cytoplasmic dynein 1 light intermediate chain 2
telomere repeat binding bouquet formation protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
telomere repeats-binding bouquet formation protein 1
NEDD8-activating enzyme E1 regulatory subunit
carbonic anhydrase 7, 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 1 sample with support for all annotated introns
carbonic anhydrase 7, 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 1 sample with support for all annotated introns
pyruvate dehydrogenase phosphatase catalytic subunit 2
pyruvate dehydrogenase [acetyl-transferring]-phosphatase 2, mitochondrial
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
brain expressed associated with NEDD4 1, transcript variant X1
brain expressed associated with NEDD4 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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 7 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
A disintegrin and metalloproteinase with thrombospondin motifs 18
A disintegrin and metalloproteinase with thrombospondin motifs 18-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
nudix hydrolase 7, transcript variant X1
peroxisomal coenzyme A diphosphatase NUDT7 isoform X1
nudix hydrolase 7, transcript variant X2
peroxisomal coenzyme A diphosphatase NUDT7 isoform X2
synaptic vesicle membrane protein VAT-1 homolog-like
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
MAF bZIP transcription factor, transcript variant X1
MAF bZIP transcription factor, transcript variant X2
MAF bZIP transcription factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
chromodomain Y like 2, transcript variant X2
chromodomain Y like 2, transcript variant X1
chromodomain Y-like protein 2 isoform X2
chromodomain Y-like protein 2 isoform X1
C-X9-C motif containing 2, transcript variant X1
C-X9-C motif containing 2, transcript variant X2
C-X9-C motif containing 2, transcript variant X5
C-X9-C motif containing 2, transcript variant X4
C-X9-C motif containing 2, transcript variant X3
COX assembly mitochondrial protein 2 homolog
centromere protein N, 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
centromere protein N, transcript variant X3
centromere protein N, transcript variant X1
centromere protein N, transcript variant X5
centromere protein N, transcript variant X6
centromere protein N, transcript variant X7
centromere protein N, transcript variant X8
centromere protein N, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C16orf46 homolog
protein phosphatase 1 regulatory subunit 3E-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
glycine cleavage system H protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
polycystic kidney disease protein 1-like 2
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
c-Maf inducing protein, transcript variant X1
c-Maf inducing protein, transcript variant X3
c-Maf inducing protein, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2
solute carrier family 12 member 4, transcript variant X2
solute carrier family 12 member 4, transcript variant X1
solute carrier family 12 member 4, transcript variant X3
solute carrier family 12 member 4 isoform X2
solute carrier family 12 member 4 isoform X1
solute carrier family 12 member 4 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DDX28
dihydrouridine synthase 2, transcript variant X5
dihydrouridine synthase 2, transcript variant X6
dihydrouridine synthase 2, transcript variant X7
dihydrouridine synthase 2, transcript variant X4
dihydrouridine synthase 2, transcript variant X3
dihydrouridine synthase 2, transcript variant X1
dihydrouridine synthase 2, transcript variant X2
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X2
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X3
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X1
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X4
oxidative stress induced growth inhibitor 1
oxidative stress-induced growth inhibitor 1
N-terminal EF-hand calcium binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
N-terminal EF-hand calcium-binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
solute carrier family 38 member 8, transcript variant X1
solute carrier family 38 member 8, transcript variant X2
putative sodium-coupled neutral amino acid transporter 8 isoform X1
putative sodium-coupled neutral amino acid transporter 8 isoform X2
membrane bound transcription factor peptidase, site 1
membrane-bound transcription factor site-1 protease
hydroxysteroid dehydrogenase like 1, transcript variant X7
hydroxysteroid dehydrogenase like 1, transcript variant X8
hydroxysteroid dehydrogenase like 1, transcript variant X3
hydroxysteroid dehydrogenase like 1, transcript variant X6
hydroxysteroid dehydrogenase like 1, transcript variant X2
hydroxysteroid dehydrogenase like 1, transcript variant X4
hydroxysteroid dehydrogenase like 1, transcript variant X1
hydroxysteroid dehydrogenase like 1, transcript variant X5
inactive hydroxysteroid dehydrogenase-like protein 1
dynein axonemal assembly factor 1, transcript variant X1
dynein axonemal assembly factor 1, transcript variant X2
heat shock transcription factor 4, 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 2 samples with support for all annotated introns
heat shock transcription factor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heat shock transcription factor 4, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TNFRSF1A associated via death domain, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TNFRSF1A associated via death domain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tumor necrosis factor receptor type 1-associated DEATH domain protein isoform X1
TNFRSF1A associated via death domain, 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 4 samples with support for all annotated introns
TNFRSF1A associated via death domain, transcript variant X4
tumor necrosis factor receptor type 1-associated DEATH domain protein isoform X2
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9, transcript variant X2
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9, transcript variant X1
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9, transcript variant X3
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9
phagosome assembly factor 1, transcript variant X1
phagosome assembly factor 1, transcript variant X2
core-binding factor subunit beta, transcript variant X2
core-binding factor subunit beta, transcript variant X1
core-binding factor subunit beta isoform X1
core-binding factor subunit beta isoform X2
G protein subunit alpha o1, transcript variant 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 3 samples with support for all annotated introns
G protein subunit alpha o1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
G protein subunit alpha o1, transcript variant X2
guanine nucleotide-binding protein G(o) subunit alpha isoform X2
guanine nucleotide-binding protein G(o) subunit alpha isoform X1
guanine nucleotide-binding protein G(o) subunit alpha isoform X3
autocrine motility factor receptor, transcript variant X1
autocrine motility factor receptor, transcript variant X2
E3 ubiquitin-protein ligase AMFR isoform X2
E3 ubiquitin-protein ligase AMFR isoform X1
cleavage and polyadenylation specificity factor subunit 5
2-oxoglutarate and iron dependent oxygenase domain containing 1
DNA-directed RNA polymerase II subunit RPB3
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
nuclear pore complex protein Nup93 isoform X1
nuclear pore complex protein Nup93 isoform X2
nuclear pore complex protein Nup93 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
homocysteine inducible ER protein with ubiquitin like domain 1, transcript variant X1
homocysteine inducible ER protein with ubiquitin like domain 1, transcript variant X2
homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 1 protein isoform X1
homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 1 protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 25% 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
proteasome activator subunit 3 interacting protein 1, transcript variant X2
proteasome activator subunit 3 interacting protein 1, transcript variant X1
ring finger and SPRY domain containing 1
RING finger and SPRY domain-containing protein 1
ADP ribosylation factor like GTPase 2 binding protein
ADP-ribosylation factor-like protein 2-binding protein
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
C-X3-C motif chemokine ligand 1, transcript variant X2
C-X3-C motif chemokine ligand 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125443718, transcript variant X1
uncharacterized LOC125443718, transcript variant X2
uncharacterized protein LOC125443718 isoform X1
uncharacterized protein LOC125443718 isoform X2
dynein regulatory complex subunit 7, transcript variant X2
dynein regulatory complex subunit 7, transcript variant X1
dynein regulatory complex subunit 7 isoform X2
dynein regulatory complex subunit 7 isoform X1
pancreatic secretory granule membrane major glycoprotein GP2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor G5, 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 1 sample with support for all annotated introns
adhesion G protein-coupled receptor G5, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% 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: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: coiled-coil domain-containing protein 102A
docking protein 4, 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 2 samples with support for all annotated introns
docking protein 4, transcript variant X2
docking protein 4, transcript variant X1
docking protein 4, transcript variant X5
docking protein 4, transcript variant X3
ubiquinone biosynthesis protein COQ9, mitochondrial
cytokine induced apoptosis inhibitor 1, transcript variant X1
cytokine induced apoptosis inhibitor 1, transcript variant X2
probable D-lactate dehydrogenase, mitochondrial
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
BCAR1 scaffold protein, Cas family member
breast cancer anti-estrogen resistance protein 1
nuclear factor of activated T-cells, cytoplasmic 3
epithelial splicing regulatory protein 2, transcript variant X2
epithelial splicing regulatory protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
epithelial splicing regulatory protein 2 isoform X2
epithelial splicing regulatory protein 2 isoform X1
epithelial splicing regulatory protein 2, transcript variant X4
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
epithelial splicing regulatory protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
epithelial splicing regulatory protein 2 isoform X4
epithelial splicing regulatory protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sphingomyelin phosphodiesterase 3, transcript variant X1
sphingomyelin phosphodiesterase 3, transcript variant X2
protein arginine methyltransferase 7, transcript variant X2
protein arginine methyltransferase 7, transcript variant X1
protein arginine methyltransferase 7, transcript variant X3
protein arginine N-methyltransferase 7 isoform X1
protein arginine N-methyltransferase 7 isoform X2
solute carrier family 7 member 6 opposite strand
probable RNA polymerase II nuclear localization protein SLC7A6OS
solute carrier family 7 member 6, transcript variant X2
solute carrier family 7 member 6, transcript variant X1
solute carrier family 7 member 6, transcript variant X3
receptor-interacting serine/threonine-protein kinase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mixed lineage kinase domain like pseudokinase
mixed lineage kinase domain-like protein
pyruvate dehydrogenase phosphatase regulatory subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pyruvate dehydrogenase phosphatase regulatory subunit, transcript variant X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X1
pyruvate dehydrogenase phosphatase regulatory subunit, 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
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
CCAAT enhancer binding protein gamma, 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 10 samples with support for all annotated introns
CCAAT enhancer binding protein gamma, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 5 bases in 5 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% 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: deleted 5 bases in 5 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: malonyl-CoA decarboxylase, mitochondrial
malonyl-CoA decarboxylase, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: malonyl-CoA decarboxylase, mitochondrial-like
transfer RNA alanine (anticodon GGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X1
short-chain dehydrogenase/reductase family 42E member 1 isoform X1
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X2
short-chain dehydrogenase/reductase family 42E member 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
sodium-dependent noradrenaline transporter
lysophosphatidylcholine acyltransferase 2
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
iroquois homeobox 6, transcript variant X1
iroquois homeobox 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
iroquois homeobox 6, 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 2 samples with support for all annotated introns
iroquois homeobox 6, transcript variant X3
iroquois-class homeodomain protein IRX-6 isoform X1
iroquois-class homeodomain protein IRX-6 isoform X2
iroquois-class homeodomain protein IRX-6 isoform X3
iroquois-class homeodomain protein IRX-5
uncharacterized LOC125443827, transcript variant X3
uncharacterized LOC125443827, transcript variant X1
uncharacterized LOC125443827, transcript variant X6
uncharacterized LOC125443827, transcript variant X7
uncharacterized LOC125443827, transcript variant X4
uncharacterized LOC125443827, transcript variant X5
uncharacterized protein LOC125443827 isoform X1
uncharacterized LOC125443827, transcript variant X2
uncharacterized protein LOC125443827 isoform X2
iroquois-class homeodomain protein IRX-3
FTO alpha-ketoglutarate dependent dioxygenase, transcript variant X7
FTO alpha-ketoglutarate dependent dioxygenase, transcript variant X1
alpha-ketoglutarate-dependent dioxygenase FTO isoform X7
alpha-ketoglutarate-dependent dioxygenase FTO isoform X1
FTO alpha-ketoglutarate dependent dioxygenase, transcript variant X5
FTO alpha-ketoglutarate dependent dioxygenase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
alpha-ketoglutarate-dependent dioxygenase FTO isoform X5
alpha-ketoglutarate-dependent dioxygenase FTO isoform X4
FTO alpha-ketoglutarate dependent dioxygenase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
alpha-ketoglutarate-dependent dioxygenase FTO isoform X3
FTO alpha-ketoglutarate dependent dioxygenase, transcript variant X6
alpha-ketoglutarate-dependent dioxygenase FTO isoform X6
FTO alpha-ketoglutarate dependent dioxygenase, 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
alpha-ketoglutarate-dependent dioxygenase FTO isoform X2
AKT interacting protein, transcript variant X3
AKT interacting protein, transcript variant X2
AKT interacting protein, transcript variant X1
AKT interacting protein, transcript variant X5
AKT interacting protein, transcript variant X4
chromodomain helicase DNA binding protein 9, transcript variant X3
chromodomain helicase DNA binding protein 9, transcript variant X2
chromodomain helicase DNA binding protein 9, transcript variant X6
chromodomain helicase DNA binding protein 9, transcript variant X8
chromodomain helicase DNA binding protein 9, transcript variant X11
chromodomain helicase DNA binding protein 9, transcript variant X5
chromodomain helicase DNA binding protein 9, transcript variant X1
chromodomain helicase DNA binding protein 9, transcript variant X10
chromodomain helicase DNA binding protein 9, transcript variant X7
chromodomain helicase DNA binding protein 9, transcript variant X4
chromodomain helicase DNA binding protein 9, transcript variant X9
chromodomain helicase DNA binding protein 9, transcript variant X17
chromodomain helicase DNA binding protein 9, transcript variant X16
chromodomain helicase DNA binding protein 9, transcript variant X12
chromodomain helicase DNA binding protein 9, transcript variant X14
chromodomain helicase DNA binding protein 9, transcript variant X13
chromodomain helicase DNA binding protein 9, transcript variant X15
chromodomain-helicase-DNA-binding protein 9 isoform X10
chromodomain-helicase-DNA-binding protein 9 isoform X5
chromodomain-helicase-DNA-binding protein 9 isoform X9
chromodomain-helicase-DNA-binding protein 9 isoform X4
chromodomain-helicase-DNA-binding protein 9 isoform X3
chromodomain-helicase-DNA-binding protein 9 isoform X8
chromodomain-helicase-DNA-binding protein 9 isoform X2
chromodomain-helicase-DNA-binding protein 9 isoform X11
chromodomain-helicase-DNA-binding protein 9 isoform X7
chromodomain-helicase-DNA-binding protein 9 isoform X6
chromodomain-helicase-DNA-binding protein 9 isoform X1
chromodomain-helicase-DNA-binding protein 9 isoform X14
chromodomain-helicase-DNA-binding protein 9 isoform X13
chromodomain-helicase-DNA-binding protein 9 isoform X12
chromodomain-helicase-DNA-binding protein 9 isoform X15
TOX high mobility group box family member 3
uncharacterized LOC125443661, transcript variant X2
uncharacterized LOC125443661, transcript variant X1
spalt like transcription factor 1, transcript variant X1
spalt like transcription factor 1, transcript variant X2
CYLD lysine 63 deubiquitinase, transcript variant X5
CYLD lysine 63 deubiquitinase, transcript variant X1
CYLD lysine 63 deubiquitinase, transcript variant X4
CYLD lysine 63 deubiquitinase, transcript variant X3
CYLD lysine 63 deubiquitinase, transcript variant X2
ubiquitin carboxyl-terminal hydrolase CYLD isoform X2
ubiquitin carboxyl-terminal hydrolase CYLD isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NKD inhibitor of WNT signaling pathway 1, transcript variant X2
NKD inhibitor of WNT signaling pathway 1, transcript variant X1
protein naked cuticle homolog 1 isoform X2
protein naked cuticle homolog 1 isoform X1
bromodomain containing 7, transcript variant X1
bromodomain containing 7, transcript variant X2
bromodomain-containing protein 7 isoform X1
bromodomain-containing protein 7 isoform X2
terminal nucleotidyltransferase 4B, transcript variant X2
terminal nucleotidyltransferase 4B, transcript variant X1
terminal nucleotidyltransferase 4B isoform X2
terminal nucleotidyltransferase 4B isoform 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 7 samples with support for all annotated introns
CTD nuclear envelope phosphatase 1 regulatory subunit 1
nuclear envelope phosphatase-regulatory subunit 1
nuclear receptor coactivator 5-like, transcript variant X1
nuclear receptor coactivator 5-like, transcript variant X2
nuclear receptor coactivator 5-like, transcript variant X3
nuclear receptor coactivator 5-like isoform X1
nuclear receptor coactivator 5-like isoform X2
uncharacterized protein LOC125443464 isoform X3
zinc finger protein 423, transcript variant X1
zinc finger protein 423, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C16orf78 homolog
uncharacterized LOC125443608, transcript variant X1
uncharacterized LOC125443608, transcript variant X2
siah E3 ubiquitin protein ligase 1, transcript variant X2
siah E3 ubiquitin protein ligase 1, transcript variant X1
E3 ubiquitin-protein ligase SIAH1 isoform X1
E3 ubiquitin-protein ligase SIAH1 isoform X2
phosphorylase kinase regulatory subunit beta, transcript variant X5
phosphorylase kinase regulatory subunit beta, transcript variant X9
phosphorylase kinase regulatory subunit beta, transcript variant X6
phosphorylase kinase regulatory subunit beta, transcript variant X1
phosphorylase kinase regulatory subunit beta, transcript variant X2
phosphorylase kinase regulatory subunit beta, transcript variant X7
phosphorylase kinase regulatory subunit beta, transcript variant X4
phosphorylase kinase regulatory subunit beta, transcript variant X3
phosphorylase kinase regulatory subunit beta, transcript variant X8
phosphorylase b kinase regulatory subunit beta isoform X3
phosphorylase b kinase regulatory subunit beta isoform X6
phosphorylase b kinase regulatory subunit beta isoform X4
phosphorylase b kinase regulatory subunit beta isoform X1
phosphorylase b kinase regulatory subunit beta isoform X2
phosphorylase b kinase regulatory subunit beta isoform X5
integrin alpha FG-GAP repeat containing 1
neuropilin and tolloid like 2, transcript variant X1
neuropilin and tolloid like 2, transcript variant X2
neuropilin and tolloid-like protein 2 isoform X1
neuropilin and tolloid-like protein 2 isoform X2
DnaJ heat shock protein family (Hsp40) member A2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: myosin light chain kinase 3
origin recognition complex subunit 6, transcript variant X1
origin recognition complex subunit 6, transcript variant X2
origin recognition complex subunit 6 isoform X1
origin recognition complex subunit 6 isoform X2
vacuolar protein sorting-associated protein 35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome b-c1 complex subunit Rieske, mitochondrial
POP4 homolog, ribonuclease P/MRP subunit
pleckstrin homology and FYVE domain containing 1
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 7 samples with support for all annotated introns
pleckstrin homology domain-containing family F member 1
linkage group 14 C19orf12 homolog, transcript variant X2
linkage group 14 C19orf12 homolog, transcript variant X1
linkage group 14 C19orf12 homolog, transcript variant X3
uncharacterized protein F13E9.13, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: unconventional prefoldin RPB5 interactor 1
zinc finger protein 536, transcript variant X1
zinc finger protein 536, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
zinc finger protein 507, transcript variant X1
zinc finger protein 507, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain-containing protein 27
regulator of G protein signaling 9 binding protein
regulator of G-protein signaling 9-binding protein
tudor domain containing 12, transcript variant X1
tudor domain containing 12, transcript variant X3
tudor domain containing 12, transcript variant X2
tudor domain containing 12, transcript variant X4
putative ATP-dependent RNA helicase TDRD12 isoform X1
putative ATP-dependent RNA helicase TDRD12 isoform X3
putative ATP-dependent RNA helicase TDRD12 isoform X2
putative ATP-dependent RNA helicase TDRD12 isoform X4
centrosomal protein 89, transcript variant X6
centrosomal protein 89, transcript variant X1
centrosomal protein 89, transcript variant X3
centrosomal protein 89, transcript variant X2
centrosomal protein of 89 kDa isoform X1
centrosomal protein of 89 kDa isoform X3
centrosomal protein of 89 kDa isoform X2
centrosomal protein of 89 kDa isoform X5
centrosomal protein 89, transcript variant X4
centrosomal protein 89, transcript variant X5
centrosomal protein of 89 kDa isoform X4
FA core complex associated protein 24, transcript variant X1
FA core complex associated protein 24, transcript variant X2
Fanconi anemia core complex-associated protein 24 isoform X1
Fanconi anemia core complex-associated protein 24 isoform X2
rhophilin Rho GTPase binding protein 2, transcript variant X2
rhophilin Rho GTPase binding protein 2, transcript variant X1
G-patch domain containing 1, transcript variant X1
G-patch domain containing 1, transcript variant X2
G patch domain-containing protein 1 isoform X1
G patch domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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
low-density lipoprotein receptor-related protein 3
solute carrier family 7 member 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
asc-type amino acid transporter 1 isoform X1
solute carrier family 7 member 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
asc-type amino acid transporter 1 isoform X2
alanyl-tRNA synthetase 1, transcript variant X1
alanyl-tRNA synthetase 1, transcript variant X2
uncharacterized oxidoreductase C663.09c-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RHO family interacting cell polarization regulator 1, transcript variant X2
rho family-interacting cell polarization regulator 1 isoform X2
RHO family interacting cell polarization regulator 1, transcript variant X1
rho family-interacting cell polarization regulator 1 isoform X1
CCCTC-binding factor, transcript variant X2
CCCTC-binding factor, transcript variant X1
transcriptional repressor CTCF isoform X1
transcriptional repressor CTCF isoform X2
capping protein regulator and myosin 1 linker 2
capping protein, Arp2/3 and myosin-I linker protein 2
ACD shelterin complex subunit and telomerase recruitment factor, transcript variant X3
ACD shelterin complex subunit and telomerase recruitment factor, transcript variant X2
ACD shelterin complex subunit and telomerase recruitment factor, transcript variant X5
ACD shelterin complex subunit and telomerase recruitment factor, transcript variant X4
ACD shelterin complex subunit and telomerase recruitment factor, transcript variant X1
adrenocortical dysplasia protein homolog isoform X3
adrenocortical dysplasia protein homolog isoform X2
adrenocortical dysplasia protein homolog isoform X1
par-6 family cell polarity regulator alpha, transcript variant X1
par-6 family cell polarity regulator alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
par-6 family cell polarity regulator alpha, 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 10 samples with support for all annotated introns
partitioning defective 6 homolog alpha isoform X1
partitioning defective 6 homolog alpha isoform X2
partitioning defective 6 homolog alpha isoform X3
enkurin domain containing 1, transcript variant X2
enkurin domain containing 1, transcript variant X1
enkurin domain containing 1, transcript variant X3
glucose-fructose oxidoreductase domain containing 2, transcript variant X3
glucose-fructose oxidoreductase domain containing 2, transcript variant X2
glucose-fructose oxidoreductase domain containing 2, transcript variant X1
glucose-fructose oxidoreductase domain containing 2, transcript variant X5
glucose-fructose oxidoreductase domain containing 2, transcript variant X4
glucose-fructose oxidoreductase domain-containing protein 2
RAN binding protein 10, transcript variant X2
RAN binding protein 10, transcript variant X1
translin associated factor X interacting protein 1, transcript variant X1
translin associated factor X interacting protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
translin-associated factor X-interacting protein 1 isoform X1
translin-associated factor X-interacting protein 1 isoform X3
translin associated factor X interacting protein 1, transcript variant X2
translin-associated factor X-interacting protein 1 isoform X2
nuclear transport factor 2, transcript variant X2
nuclear transport factor 2, transcript variant X1
enhancer of mRNA decapping 4, transcript variant X1
enhancer of mRNA decapping 4, transcript variant X2
enhancer of mRNA-decapping protein 4 isoform X1
enhancer of mRNA-decapping protein 4 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 9 samples with support for all annotated introns
protein serine kinase H1, transcript variant X1
protein serine kinase H1, transcript variant X3
protein serine kinase H1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
exocyst complex component 3-like protein
E2F transcription factor 4, transcript variant X2
E2F transcription factor 4, transcript variant X1
engulfment and cell motility 3, transcript variant X1
engulfment and cell motility 3, transcript variant X2
F-box/LRR-repeat protein 2-like, transcript variant X3
F-box/LRR-repeat protein 2-like, transcript variant X2
F-box/LRR-repeat protein 2-like, transcript variant X1
F-box/LRR-repeat protein 2-like isoform X3
F-box/LRR-repeat protein 2-like isoform X2
F-box/LRR-repeat protein 2-like isoform X1
transmembrane protein 208, transcript variant X1
transmembrane protein 208, transcript variant X2
zinc finger DHHC-type containing 1, transcript variant X3
zinc finger DHHC-type containing 1, transcript variant X4
zinc finger DHHC-type containing 1, transcript variant X1
zinc finger DHHC-type containing 1, transcript variant X2
tubulin polymerization promoting protein family member 3, 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
tubulin polymerization promoting protein family member 3, transcript variant X6
tubulin polymerization promoting protein family member 3, transcript variant X5
tubulin polymerization-promoting protein family member 3 isoform X1
tubulin polymerization promoting protein family member 3, transcript variant X2
tubulin polymerization promoting protein family member 3, transcript variant X4
tubulin polymerization promoting protein family member 3, transcript variant X3
tubulin polymerization-promoting protein family member 3 isoform X2
heat shock factor binding protein 1, transcript variant X1
heat shock factor binding protein 1, transcript variant X2
potassium voltage-gated channel modifier subfamily G member 4
potassium voltage-gated channel subfamily G member 4
WAP four-disulfide core domain protein 1
ATPase secretory pathway Ca2+ transporting 2
calcium-transporting ATPase type 2C member 2
coactosin like F-actin binding protein 1
kelch like family member 36, transcript variant X2
kelch like family member 36, transcript variant X1
ubiquitin specific peptidase 10, transcript variant X1
ubiquitin specific peptidase 10, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 10 isoform X1
ubiquitin carboxyl-terminal hydrolase 10 isoform X2
cysteine rich secretory protein LCCL domain containing 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 91% 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cysteine-rich secretory protein LCCL domain-containing 2
hepatocyte nuclear factor 4-beta-like, transcript variant X1
hepatocyte nuclear factor 4-beta-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
hepatocyte nuclear factor 4-beta-like isoform X1
hepatocyte nuclear factor 4-beta-like isoform X2
zinc finger DHHC-type palmitoyltransferase 7
cytochrome c oxidase subunit 4 isoform 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
interferon regulatory factor 8, 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 1 sample with support for all annotated introns
interferon regulatory factor 8 isoform X1
interferon regulatory factor 8, transcript variant X2
interferon regulatory factor 8 isoform X2
methenyltetrahydrofolate synthetase domain containing, transcript variant X1
methenyltetrahydrofolate synthetase domain containing, transcript variant X2
methenyltetrahydrofolate synthase domain-containing protein isoform X1
methenyltetrahydrofolate synthase domain-containing protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125443705, transcript variant X2
uncharacterized LOC125443705, transcript variant X1
Gse1 coiled-coil protein, transcript variant X2
Gse1 coiled-coil protein, 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 3 samples with support for all annotated introns
Gse1 coiled-coil protein, transcript variant X3
Gse1 coiled-coil protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein KIAA0513 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
LOW QUALITY PROTEIN: F-box only protein 31
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
microtubule associated protein 1 light chain 3 beta
microtubule-associated proteins 1A/1B light chain 3B
zinc finger CCHC domain-containing protein 14
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
large neutral amino acids transporter small subunit 1
carbonic anhydrase 5A, transcript variant X1
carbonic anhydrase 5A, transcript variant X2
carbonic anhydrase 5A, mitochondrial isoform X1
carbonic anhydrase 5A, mitochondrial isoform X2
BTG3 associated nuclear protein, transcript variant X1
BTG3 associated nuclear protein, transcript variant X3
BTG3 associated nuclear protein, transcript variant X2
zinc finger protein 469, transcript variant X2
zinc finger protein 469, transcript variant X1
zinc finger protein 469, transcript variant X3
zinc finger protein, FOG family member 1
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 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein ZFPM1
thyrotropin-releasing hormone receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 18-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00324
SPG7 matrix AAA peptidase subunit, paraplegin, transcript variant X1
SPG7 matrix AAA peptidase subunit, paraplegin, transcript variant X2
ankyrin repeat domain containing 11, transcript variant X1
ankyrin repeat domain containing 11, transcript variant X4
ankyrin repeat domain containing 11, transcript variant X3
ankyrin repeat domain containing 11, transcript variant X2
ankyrin repeat domain-containing protein 11 isoform X1
ankyrin repeat domain-containing protein 11 isoform X2
putative solute carrier family 22 member 31
acyl-CoA synthetase family member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
acyl-CoA synthetase family member 3, 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 1 sample with support for all annotated introns
malonate--CoA ligase ACSF3, mitochondrial
CBFA2/RUNX1 partner transcriptional co-repressor 3, transcript variant X1
CBFA2/RUNX1 partner transcriptional co-repressor 3, transcript variant X3
CBFA2/RUNX1 partner transcriptional co-repressor 3, transcript variant X2
CBFA2/RUNX1 partner transcriptional co-repressor 3, transcript variant X4
CBFA2/RUNX1 partner transcriptional co-repressor 3, transcript variant X5
CBFA2/RUNX1 partner transcriptional co-repressor 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
embryonic polyadenylate-binding protein 2
trafficking protein particle complex subunit 2L
trafficking protein particle complex subunit 2-like protein
chromatin licensing and DNA replication factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear factor of activated T-cells 5-like
cytosolic thiouridylase subunit 2, transcript variant X2
cytosolic thiouridylase subunit 2, transcript variant X1
cytosolic thiouridylase subunit 2, transcript variant X3
cytoplasmic tRNA 2-thiolation protein 2 isoform X2
cytoplasmic tRNA 2-thiolation protein 2 isoform X1
cytoplasmic tRNA 2-thiolation protein 2 isoform X3
ring finger protein 166, transcript variant X1
E3 ubiquitin-protein ligase RNF166 isoform X1
ring finger protein 166, transcript variant X2
E3 ubiquitin-protein ligase RNF166 isoform X2
snail family transcriptional repressor 3, transcript variant X2
snail family transcriptional repressor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
charged multivesicular body protein 1A, transcript variant X2
charged multivesicular body protein 1A, transcript variant X1
charged multivesicular body protein 1A, transcript variant X3
charged multivesicular body protein 1a isoform X2
charged multivesicular body protein 1a isoform X1
charged multivesicular body protein 1a isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
spermatogenesis associated 2 like, transcript variant X1
spermatogenesis associated 2 like, transcript variant X2
spermatogenesis-associated protein 2-like protein
VPS9 domain containing 1, transcript variant X2
VPS9 domain containing 1, transcript variant X1
VPS9 domain-containing protein 1 isoform X2
VPS9 domain-containing protein 1 isoform X1
spire type actin nucleation factor 2, 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 1 sample with support for all annotated introns
spire type actin nucleation factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
differentially expressed in FDCP 8 homolog, transcript variant X2
differentially expressed in FDCP 8 homolog, transcript variant X1
differentially expressed in FDCP 8 homolog
dysbindin domain containing 1, transcript variant X1
dysbindin domain containing 1, transcript variant X2
dysbindin domain containing 1, transcript variant X3
dysbindin domain-containing protein 1 isoform X1
dysbindin domain-containing protein 1 isoform X2
dysbindin domain-containing protein 1 isoform X3
growth arrest specific 8, transcript variant X2
growth arrest specific 8, transcript variant X1
dynein regulatory complex subunit 4 isoform X1
dynein regulatory complex subunit 4 isoform X2
5-hydroxyisourate hydrolase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
5-hydroxyisourate hydrolase-like, transcript variant X1
5-hydroxyisourate hydrolase-like isoform X2
5-hydroxyisourate hydrolase-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transport and golgi organization 6 homolog, transcript variant X1
transport and golgi organization 6 homolog, transcript variant X2
transport and Golgi organization protein 6 homolog isoform X1
transport and Golgi organization protein 6 homolog isoform X2
basic salivary proline-rich protein 2-like
chromosome transmission fidelity protein 8 homolog
U3 small nucleolar RNA-associated protein 4 homolog
syntrophin beta 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 1 sample with support for all annotated introns
syntrophin beta 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
vacuolar protein sorting 4 homolog A, transcript variant X2
vacuolar protein sorting 4 homolog A, transcript variant X1
vacuolar protein sorting-associated protein 4A isoform X2
vacuolar protein sorting-associated protein 4A isoform X1
LOW QUALITY PROTEIN: peptide deformylase, mitochondrial
conserved oligomeric Golgi complex subunit 8
nucleolar pre-rRNA processing protein NIP7
60S ribosome subunit biogenesis protein NIP7 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
transmembrane emp24 domain-containing protein 6
nuclear factor of activated T cells 5, transcript variant X1
nuclear factor of activated T-cells 5 isoform X1
nuclear factor of activated T cells 5, transcript variant X2
nuclear factor of activated T cells 5, transcript variant X3
nuclear factor of activated T cells 5, transcript variant X4
nuclear factor of activated T-cells 5 isoform X2
NIN1 (RPN12) binding protein 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
NIN1 (RPN12) binding protein 1 homolog, 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 9 samples with support for all annotated introns
WW domain containing E3 ubiquitin protein ligase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
NEDD4-like E3 ubiquitin-protein ligase WWP2
LOW QUALITY PROTEIN: zinc finger homeobox protein 3
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: 51 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 10 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: pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16
dihydroorotate dehydrogenase (quinone), mitochondrial
polycystin 1 like 3, transient receptor potential channel interacting
polycystic kidney disease protein 1-like 3
zinc finger protein 821, transcript variant X1
zinc finger protein 821, transcript variant X2
adaptor related protein complex 1 subunit gamma 1, transcript variant X2
adaptor related protein complex 1 subunit gamma 1, transcript variant X1
adaptor related protein complex 1 subunit gamma 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TERF2 interacting protein, transcript variant X1
TERF2 interacting protein, transcript variant X2
telomeric repeat-binding factor 2-interacting protein 1 isoform X1
telomeric repeat-binding factor 2-interacting protein 1 isoform X2
lysyl-tRNA synthetase 1, transcript variant X2
lysyl-tRNA synthetase 1, transcript variant X3
lysyl-tRNA synthetase 1, transcript variant X1
adenosine deaminase tRNA specific 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
adenosine deaminase tRNA specific 1, transcript variant X1
adenosine deaminase tRNA specific 1, transcript variant X10
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 9 samples with support for all annotated introns
adenosine deaminase tRNA specific 1, transcript variant X2
adenosine deaminase tRNA specific 1, transcript variant X6
adenosine deaminase tRNA specific 1, transcript variant X7
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
adenosine deaminase tRNA specific 1, transcript variant X4
adenosine deaminase tRNA specific 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
adenosine deaminase tRNA specific 1, transcript variant X9
adenosine deaminase tRNA specific 1, transcript variant X8
tRNA-specific adenosine deaminase 1 isoform X1
tRNA-specific adenosine deaminase 1 isoform X2
tRNA-specific adenosine deaminase 1 isoform X3
tRNA-specific adenosine deaminase 1 isoform X7
tRNA-specific adenosine deaminase 1 isoform X4
tRNA-specific adenosine deaminase 1 isoform X5
tRNA-specific adenosine deaminase 1 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
potassium channel tetramerization domain containing 15, transcript variant X2
potassium channel tetramerization domain containing 15, transcript variant X1
BTB/POZ domain-containing protein KCTD15 isoform X1
BTB/POZ domain-containing protein KCTD15 isoform X2
LSM14A mRNA processing body assembly factor, transcript variant X2
LSM14A mRNA processing body assembly factor, transcript variant X1
granule associated Rac and RHOG effector 1, transcript variant X1
granule associated Rac and RHOG effector 1, transcript variant X2
granule associated Rac and RHOG effector protein 1
WT1 interacting protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
WT1 interacting protein, transcript variant X1
Wilms tumor protein 1-interacting protein isoform X2
Wilms tumor protein 1-interacting protein isoform X1
ubiquitin like modifier activating enzyme 2
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
fatty acyl-CoA hydrolase precursor, medium chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
cytosolic iron-sulfur assembly component 2B
uncharacterized protein KIAA0895-like homolog
phosphatidylcholine-sterol acyltransferase
SNF-related serine/threonine-protein kinase-like
uncharacterized LOC125443571, transcript variant X1
uncharacterized LOC125443571, transcript variant X2
hydroxysteroid 11-beta dehydrogenase 2, transcript variant X2
hydroxysteroid 11-beta dehydrogenase 2, transcript variant X1
11-beta-hydroxysteroid dehydrogenase type 2 isoform X2
11-beta-hydroxysteroid dehydrogenase type 2 isoform X1
formin homology 2 domain containing 1, transcript variant X2
formin homology 2 domain containing 1, transcript variant X1
FH1/FH2 domain-containing protein 1 isoform X2
FH1/FH2 domain-containing protein 1 isoform X1
pleckstrin homology and RhoGEF domain containing G4
potassium channel tetramerization domain containing 19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
BTB/POZ domain-containing protein KCTD19
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
leucine-rich repeat-containing protein 36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
ST3 beta-galactoside alpha-2,3-sialyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 2
conserved oligomeric Golgi complex subunit 4
COORDINATES: nucleotide motif:Rfam:12.0:RF00611
VAC14 component of PIKFYVE complex, transcript variant X2
VAC14 component of PIKFYVE complex, transcript variant X1
HYDIN axonemal central pair apparatus protein
aspartate aminotransferase, mitochondrial
solute carrier family 38 member 7, transcript variant X1
solute carrier family 38 member 7, transcript variant X2
putative sodium-coupled neutral amino acid transporter 7
CCR4-NOT transcription complex subunit 1, transcript variant X3
CCR4-NOT transcription complex subunit 1, transcript variant X1
CCR4-NOT transcription complex subunit 1, transcript variant X5
CCR4-NOT transcription complex subunit 1, transcript variant X4
CCR4-NOT transcription complex subunit 1, transcript variant X6
CCR4-NOT transcription complex subunit 1, transcript variant X7
CCR4-NOT transcription complex subunit 1, transcript variant X2
CCR4-NOT transcription complex subunit 1 isoform X1
CCR4-NOT transcription complex subunit 1 isoform X3
CCR4-NOT transcription complex subunit 1 isoform X2
CCR4-NOT transcription complex subunit 1 isoform X4
CCR4-NOT transcription complex subunit 1 isoform X5
COORDINATES: nucleotide motif:Rfam:12.0:RF00407
SET domain containing 6, protein lysine methyltransferase
NDRG family member 4, transcript variant X5
NDRG family member 4, transcript variant X2
NDRG family member 4, transcript variant X1
NDRG family member 4, transcript variant X4
NDRG family member 4, transcript variant X3
DNA replication complex GINS protein PSF3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 113, transcript variant X1
coiled-coil domain containing 113, transcript variant X2
coiled-coil domain-containing protein 113 isoform X1
coiled-coil domain-containing protein 113 isoform X2
casein kinase 2 alpha 2, transcript variant X2
casein kinase 2 alpha 2, transcript variant X1
uncharacterized LOC125443283, transcript variant X2
uncharacterized LOC125443283, transcript variant X1
uncharacterized protein LOC125443283 isoform X1
uncharacterized protein LOC125443283 isoform X2
cilia and flagella associated protein 20
cilia- and flagella-associated protein 20
U6 snRNA biogenesis phosphodiesterase 1, transcript variant X2
U6 snRNA biogenesis phosphodiesterase 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 1 sample with support for all annotated introns
testis, prostate and placenta-expressed protein
cyclic nucleotide-gated cation channel beta-1-like, transcript variant X1
cyclic nucleotide-gated cation channel beta-1-like, transcript variant X4
cyclic nucleotide-gated cation channel beta-1-like, transcript variant X2
cyclic nucleotide-gated cation channel beta-1-like, transcript variant X5
cyclic nucleotide-gated cation channel beta-1-like, transcript variant X3
cyclic nucleotide-gated cation channel beta-1-like isoform X4
cyclic nucleotide-gated cation channel beta-1-like isoform X5
cyclic nucleotide-gated cation channel beta-1-like isoform X1
cyclic nucleotide-gated cation channel beta-1-like isoform X2
cyclic nucleotide-gated cation channel beta-1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 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: 6 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: 39 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
TP53 induced glycolysis regulatory phosphatase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
fructose-2,6-bisphosphatase TIGAR isoform X2
TP53 induced glycolysis regulatory phosphatase, 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 7 samples with support for all annotated introns
fructose-2,6-bisphosphatase TIGAR isoform X1
TP53 induced glycolysis regulatory phosphatase, transcript variant X3
fructose-2,6-bisphosphatase TIGAR isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
dual specificity tyrosine phosphorylation regulated kinase 4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 4 codons; deleted 5 bases in 4 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 4 codons; deleted 5 bases in 4 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dual specificity tyrosine-phosphorylation-regulated kinase 4
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
NADH:ubiquinone oxidoreductase subunit A9
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9, mitochondrial
polypeptide N-acetylgalactosaminyltransferase 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
probable polypeptide N-acetylgalactosaminyltransferase 8
potassium voltage-gated channel subfamily A member 6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: potassium voltage-gated channel subfamily A member 6
potassium voltage-gated channel subfamily A member 1, transcript variant X2
potassium voltage-gated channel subfamily A member 1, transcript variant X1
potassium voltage-gated channel subfamily A member 1 isoform X2
potassium voltage-gated channel subfamily A member 1 isoform X1
potassium voltage-gated channel subfamily A member 5-like, transcript variant X2
potassium voltage-gated channel subfamily A member 5-like, transcript variant X1
potassium voltage-gated channel subfamily A member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 3 bases at 3 genomic stop codons; 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: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 5
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
dual specificity phosphatase 16, transcript variant X2
dual specificity phosphatase 16, transcript variant X1
cAMP responsive element binding protein like 2
cAMP-responsive element-binding protein-like 2
G protein-coupled receptor 19, transcript variant X3
G protein-coupled receptor 19, transcript variant X2
G protein-coupled receptor 19, transcript variant X1
probable G-protein coupled receptor 19 isoform X2
probable G-protein coupled receptor 19 isoform X1
cyclin-dependent kinase inhibitor 1-like, transcript variant X2
cyclin-dependent kinase inhibitor 1-like, transcript variant X4
cyclin-dependent kinase inhibitor 1-like, transcript variant X3
cyclin-dependent kinase inhibitor 1-like, transcript variant X1
cyclin-dependent kinase inhibitor 1-like isoform X2
cyclin-dependent kinase inhibitor 1-like isoform X1
cyclin-dependent kinase inhibitor 1-like isoform X3
potassium voltage-gated channel subfamily KQT member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
28S ribosomal protein S35, mitochondrial
parathyroid hormone like hormone, transcript variant X1
parathyroid hormone like hormone, transcript variant X2
coiled-coil domain containing 91, transcript variant X1
coiled-coil domain containing 91, transcript variant X3
coiled-coil domain containing 91, transcript variant X2
coiled-coil domain containing 91, transcript variant X4
coiled-coil domain containing 91, transcript variant X6
coiled-coil domain-containing protein 91 isoform X1
coiled-coil domain-containing protein 91 isoform X2
coiled-coil domain-containing protein 91 isoform X4
coiled-coil domain containing 91, transcript variant X5
coiled-coil domain-containing protein 91 isoform X3
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
LOW QUALITY PROTEIN: low-density lipoprotein receptor-related protein 6
apoptosis facilitator Bcl-2-like protein 14
COORDINATES: nucleotide motif:Rfam:12.0:RF00264
zinc finger CCCH-type antiviral protein 1-like, transcript variant X1
zinc finger CCCH-type antiviral protein 1-like, transcript variant X3
zinc finger CCCH-type antiviral protein 1-like isoform X1
zinc finger CCCH-type antiviral protein 1-like isoform X3
zinc finger CCCH-type antiviral protein 1-like, transcript variant X2
zinc finger CCCH-type antiviral protein 1-like isoform X2
polycystic kidney disease and receptor for egg jelly-related protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
cysteine rich DPF motif domain containing 1, transcript variant X1
cysteine rich DPF motif domain containing 1, transcript variant X2
cysteine-rich DPF motif domain-containing protein 1
peroxisome proliferator activated receptor alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
peroxisome proliferator-activated receptor alpha
Wnt family member 7B, transcript variant X2
Wnt family member 7B, transcript variant X3
Wnt family member 7B, transcript variant X1
Wnt family member 7B, transcript variant X4
structural maintenance of chromosomes 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes protein 1B
family with sequence similarity 118 member A, transcript variant X5
family with sequence similarity 118 member A, transcript variant X1
family with sequence similarity 118 member A, transcript variant X2
family with sequence similarity 118 member A, transcript variant X4
family with sequence similarity 118 member A, transcript variant X3
KIAA0930 ortholog, transcript variant X2
KIAA0930 ortholog, transcript variant X1
uncharacterized protein KIAA0930 homolog isoform X1
uncharacterized protein KIAA0930 homolog isoform X2
nuclear pore complex protein Nup50 isoform X3
nuclear pore complex protein Nup50 isoform X2
nuclear pore complex protein Nup50 isoform X1
PHD finger protein 21B, transcript variant X1
PHD finger protein 21B, transcript variant X2
PHD finger protein 21B, transcript variant X3
LOW QUALITY PROTEIN: metastasis-associated protein MTA1-like
phosphofurin acidic cluster sorting protein 2-like, transcript variant X2
phosphofurin acidic cluster sorting protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphofurin acidic cluster sorting protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
phosphofurin acidic cluster sorting protein 2-like, transcript variant X3
phosphofurin acidic cluster sorting protein 2-like isoform X2
phosphofurin acidic cluster sorting protein 2-like isoform X1
phosphofurin acidic cluster sorting protein 2-like isoform X4
phosphofurin acidic cluster sorting protein 2-like isoform X3
SEC22 homolog B, vesicle trafficking protein, transcript variant X1
SEC22 homolog B, vesicle trafficking protein, transcript variant X2
vesicle-trafficking protein SEC22b isoform X1
vesicle-trafficking protein SEC22b isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
polyunsaturated fatty acid 5-lipoxygenase
uncharacterized LOC125443560, transcript variant X2
uncharacterized LOC125443560, transcript variant X3
uncharacterized LOC125443560, transcript variant X5
uncharacterized LOC125443560, transcript variant X1
uncharacterized LOC125443560, transcript variant X4
uncharacterized protein LOC125443560 isoform X3
uncharacterized protein LOC125443560 isoform X1
uncharacterized protein LOC125443560 isoform X2
ribosome binding protein 1, transcript variant X2
ribosome binding protein 1, transcript variant X1
ribosome binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
barrier-to-autointegration factor-like protein
mitochondrial genome maintenance exonuclease 1, transcript variant X1
mitochondrial genome maintenance exonuclease 1, transcript variant X2
mitochondrial genome maintenance exonuclease 1, transcript variant X3
mitochondrial genome maintenance exonuclease 1, transcript variant X4
mitochondrial genome maintenance exonuclease 1 isoform X1
mitochondrial genome maintenance exonuclease 1 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 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: cysteine-rich protein 2-binding protein
double zinc ribbon and ankyrin repeat domains 1, transcript variant X2
double zinc ribbon and ankyrin repeat domains 1, transcript variant X1
double zinc ribbon and ankyrin repeat-containing protein 1
DNA-directed RNA polymerase III subunit RPC6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
START domain-containing protein 10-like, transcript variant X2
START domain-containing protein 10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
START domain-containing protein 10-like isoform X1
START domain-containing protein 10-like isoform X2
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3, 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
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3, transcript variant X4
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3, transcript variant X1
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3, transcript variant X2
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3, transcript variant X6
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
histone deacetylase 3, transcript variant X1
histone deacetylase 3, transcript variant X2
E3 ubiquitin-protein ligase MARCHF8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
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
protocadherin gamma-C5-like, transcript variant X9
protocadherin gamma-C5-like, transcript variant X18
protocadherin gamma-C5-like, transcript variant X10
protocadherin gamma-C5-like, transcript variant X14
protocadherin gamma-C5-like, transcript variant X19
protocadherin gamma-C5-like, transcript variant X15
protocadherin gamma-C5-like, transcript variant X16
protocadherin gamma-C5-like, transcript variant X17
protocadherin gamma-C5-like, transcript variant X13
protocadherin gamma-C5-like, transcript variant X12
protocadherin gamma-C5-like, transcript variant X5
protocadherin gamma-C5-like, transcript variant X11
protocadherin gamma-C5-like, transcript variant X2
protocadherin gamma-C5-like, transcript variant X3
protocadherin gamma-C5-like, transcript variant X22
protocadherin gamma-C5-like, transcript variant X23
protocadherin gamma-C5-like, transcript variant X20
protocadherin gamma-C5-like, transcript variant X21
protocadherin gamma-C5-like, transcript variant X6
protocadherin gamma-C5-like, transcript variant X8
protocadherin gamma-C5-like, transcript variant X1
protocadherin gamma-C5-like, transcript variant X4
protocadherin gamma-C5-like, transcript variant X7
protocadherin gamma-A12-like isoform X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
protocadherin gamma-A11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
protocadherin gamma-A11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 133 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
protocadherin gamma-A11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 133 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protocadherin gamma-B5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 136 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
protocadherin beta-16-like, transcript variant X2
protocadherin beta-16-like, transcript variant X6
protocadherin beta-16-like, transcript variant X3
protocadherin beta-16-like, transcript variant X10
protocadherin beta-16-like, transcript variant X5
protocadherin beta-16-like, transcript variant X1
protocadherin beta-16-like, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 164 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: 110 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
glucose-6-phosphatase catalytic subunit 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein L27, transcript variant X1
ribosomal protein L27, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
meiosis specific with coiled-coil domain, transcript variant X2
meiosis-specific coiled-coil domain-containing protein MEIOC isoform X2
meiosis specific with coiled-coil domain, transcript variant X1
meiosis specific with coiled-coil domain, transcript variant X3
meiosis-specific coiled-coil domain-containing protein MEIOC isoform X1
meiosis-specific coiled-coil domain-containing protein MEIOC isoform X3
coiled-coil domain-containing protein 43
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 134 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 169 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
protocadherin beta-16-like, transcript variant X7
protocadherin beta-16-like, transcript variant X9
protocadherin beta-16-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 6 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 6 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protocadherin alpha-C1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 172 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 207 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: 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 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: 178 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
protocadherin alpha-5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 199 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protocadherin alpha-5-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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 197 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: 178 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 169 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
protocadherin-10-like, transcript variant X1
protocadherin-10-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histidine--tRNA ligase, cytoplasmic-like
DND microRNA-mediated repression inhibitor 1
WD repeat domain 55, transcript variant X1
WD repeat domain 55, transcript variant X2
WD repeat-containing protein 55 isoform X1
WD repeat-containing protein 55 isoform X2
NADH:ubiquinone oxidoreductase subunit A2, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 isoform X2
NADH:ubiquinone oxidoreductase subunit A2, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 isoform X1
transmembrane and coiled-coil domains 6, transcript variant X1
transmembrane and coiled-coil domains 6, transcript variant X3
transmembrane and coiled-coil domains 6, transcript variant X2
transmembrane and coiled-coil domain-containing protein 6 isoform X1
transmembrane and coiled-coil domain-containing protein 6 isoform X2
probable UDP-sugar transporter protein SLC35A4
SLC35A4 upstream open reading frame protein-like
amyloid beta precursor protein binding family B member 3
amyloid-beta A4 precursor protein-binding family B member 3
uncharacterized LOC125443398, transcript variant X2
uncharacterized LOC125443398, transcript variant X1
ankyrin repeat and KH domain-containing protein 1-like
ankyrin repeat and KH domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ankyrin repeat and KH domain containing 1, transcript variant X4
ankyrin repeat and KH domain containing 1, transcript variant X6
ankyrin repeat and KH domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ankyrin repeat and KH domain containing 1, transcript variant X5
ankyrin repeat and KH domain containing 1, transcript variant X1
ankyrin repeat and KH domain-containing protein 1 isoform X3
ankyrin repeat and KH domain-containing protein 1 isoform X5
ankyrin repeat and KH domain-containing protein 1 isoform X2
ankyrin repeat and KH domain-containing protein 1 isoform X4
ankyrin repeat and KH domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
proheparin-binding EGF-like growth factor
cysteine rich transmembrane module containing 1
cysteine-rich and transmembrane domain-containing protein 1
pro-neuregulin-2, membrane-bound isoform
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
CXXC finger protein 5, transcript variant X3
CXXC finger protein 5, transcript variant X1
CXXC finger protein 5, transcript variant X2
CXXC-type zinc finger protein 5 isoform X2
CXXC-type zinc finger protein 5 isoform X1
ubiquitin conjugating enzyme E2 D2, transcript variant X1
ubiquitin conjugating enzyme E2 D2, transcript variant X2
ubiquitin-conjugating enzyme E2 D2 isoform X1
ubiquitin-conjugating enzyme E2 D2 isoform X2
stimulator of interferon response cGAMP interactor 1
family with sequence similarity 193 member A, transcript variant X5
family with sequence similarity 193 member A, transcript variant X3
family with sequence similarity 193 member A, transcript variant X6
family with sequence similarity 193 member A, transcript variant X4
family with sequence similarity 193 member A, transcript variant X1
family with sequence similarity 193 member A, transcript variant X2
uncharacterized protein KIAA0232 homolog
coiled-coil domain-containing protein 96
sortilin related VPS10 domain containing receptor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
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: VPS10 domain-containing receptor SorCS2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
synapse differentiation-inducing gene protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
SEC23 homolog B, COPII coat complex component
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: 1 Protein, and 53% coverage of the annotated genomic feature by RNAseq alignments
SCP2 sterol-binding domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sodium/potassium/calcium exchanger 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
Ras and Rab interactor 2, transcript variant X1
Ras and Rab interactor 2, transcript variant X2
Ras and Rab interactor 2, transcript variant X3
Ras and Rab interactor 2, transcript variant X4
N-alpha-acetyltransferase 20, NatB catalytic subunit, transcript variant X1
N-alpha-acetyltransferase 20, NatB catalytic subunit, transcript variant X2
cilia and flagella associated protein 61
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 61
Ral GTPase activating protein catalytic subunit alpha 2
ral GTPase-activating protein subunit alpha-2
centrosomal protein kizuna-like, transcript variant X1
centrosomal protein kizuna-like, transcript variant X2
centrosomal protein kizuna-like isoform X1
centrosomal protein kizuna-like isoform X2
5'-3' exoribonuclease 2, transcript variant X2
5'-3' exoribonuclease 2, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
chaperonin containing TCP1 subunit 5, transcript variant X2
chaperonin containing TCP1 subunit 5, transcript variant X1
ATP synthase c subunit lysine N-methyltransferase, transcript variant X1
ATP synthase c subunit lysine N-methyltransferase, transcript variant X2
ATP synthase c subunit lysine N-methyltransferase, transcript variant X4
ATP synthase c subunit lysine N-methyltransferase, transcript variant X3
ATP synthase subunit C lysine N-methyltransferase
5-methyltetrahydrofolate-homocysteine methyltransferase reductase
FAST kinase domains 3, transcript variant X2
FAST kinase domains 3, transcript variant X3
FAST kinase domains 3, transcript variant X1
FAST kinase domain-containing protein 3, mitochondrial
LOW QUALITY PROTEIN: adenylate cyclase type 2
terminal nucleotidyltransferase 4A, 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 6 samples with support for all annotated introns
terminal nucleotidyltransferase 4A, transcript variant X2
terminal nucleotidyltransferase 4A isoform X1
terminal nucleotidyltransferase 4A isoform X2
ankyrin repeat domain 33B, transcript variant X2
ankyrin repeat domain 33B, transcript variant X1
ankyrin repeat domain-containing protein 33B
E3 ubiquitin-protein ligase MARCHF6-like
small nuclear ribonucleoprotein U11/U12 subunit 48
U11/U12 small nuclear ribonucleoprotein 48 kDa protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
carboxymethylenebutenolidase homolog, transcript variant X1
carboxymethylenebutenolidase homolog, transcript variant X2
carboxymethylenebutenolidase homolog, transcript variant X3
carboxymethylenebutenolidase homolog isoform X1
carboxymethylenebutenolidase homolog isoform X2
nuclear transcription factor, X-box binding 1, transcript variant X3
nuclear transcription factor, X-box binding 1, transcript variant X2
nuclear transcription factor, X-box binding 1, transcript variant X1
transcriptional repressor NF-X1 isoform X3
transcriptional repressor NF-X1 isoform X1
transcriptional repressor NF-X1 isoform X2
ankyrin repeat and sterile alpha motif domain containing 6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ankyrin repeat and SAM domain-containing protein 6
polypeptide N-acetylgalactosaminyltransferase 12
LOW QUALITY PROTEIN: polypeptide N-acetylgalactosaminyltransferase 12
gamma-aminobutyric acid type B receptor subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
elongator acetyltransferase complex subunit 2, transcript variant X2
elongator acetyltransferase complex subunit 2, transcript variant X1
elongator acetyltransferase complex subunit 2, transcript variant X3
elongator acetyltransferase complex subunit 2, transcript variant X4
catenin alpha like 1, transcript variant X2
catenin alpha like 1, transcript variant X1
catenin alpha like 1, transcript variant X5
catenin alpha like 1, transcript variant X3
catenin alpha like 1, transcript variant X4
solute carrier family 39 member 6, transcript variant X4
solute carrier family 39 member 6, transcript variant X2
solute carrier family 39 member 6, transcript variant X1
solute carrier family 39 member 6, transcript variant X3
solute carrier family 12 member 7, transcript variant X4
solute carrier family 12 member 7, transcript variant X2
solute carrier family 12 member 7, transcript variant X1
solute carrier family 12 member 7, transcript variant X5
solute carrier family 12 member 7, transcript variant X6
solute carrier family 12 member 7 isoform X5
solute carrier family 12 member 7 isoform X4
solute carrier family 12 member 7 isoform X2
solute carrier family 12 member 7 isoform X1
solute carrier family 12 member 7 isoform X6
solute carrier family 12 member 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 12 member 7 isoform X3
membrane anchored junction protein, transcript variant X1
membrane anchored junction protein, transcript variant X2
membrane-anchored junction protein isoform X1
membrane-anchored junction protein isoform X2
sodium-dependent neutral amino acid transporter B(0)AT1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
sodium-dependent neutral amino acid transporter B(0)AT3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
cleft lip and palate transmembrane protein 1-like protein
lysophosphatidylcholine acyltransferase 1
39S ribosomal protein L36, mitochondrial
NADH:ubiquinone oxidoreductase subunit S6, transcript variant X1
NADH:ubiquinone oxidoreductase subunit S6, transcript variant X2
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial isoform X1
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial isoform X2
iroquois-class homeodomain protein IRX-4-like
LOW QUALITY PROTEIN: iroquois-class homeodomain protein IRX-4-like
iroquois homeobox 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
iroquois-class homeodomain protein IRX-4 isoform X1
iroquois homeobox 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
iroquois-class homeodomain protein IRX-4 isoform X2
iroquois homeobox 2, transcript variant X1
iroquois homeobox 2, transcript variant X2
iroquois-class homeodomain protein IRX-2
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
iroquois homeobox 1, transcript variant X2
iroquois homeobox 1, transcript variant X1
iroquois-class homeodomain protein IRX-1 isoform X1
iroquois-class homeodomain protein IRX-1 isoform X2
ADAM metallopeptidase with thrombospondin type 1 motif 16
A disintegrin and metalloproteinase with thrombospondin motifs 16
little elongation complex subunit 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 10
ubiquitin conjugating enzyme E2 Q family like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-conjugating enzyme E2Q-like protein 1
RNA cytosine C(5)-methyltransferase NSUN2