Sceloporus undulatus isolate JIND9_A2432 ecotype Alabama chromosome 11, SceUnd_v1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Lepidosauria; Squamata; Bifurcata; Unidentata; Episquamata; Toxicofera; Iguania; Phrynosomatidae; Phrynosomatinae; Sceloporus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM032829.1.\nAssembly name: SceUnd_v1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Auburn University on\n2021/07/08. The original whole-genome shotgun project has the\naccession JAGXEY000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Auburn University\nAssembly Date :: 01-AUG-2017\nAssembly Method :: SuperNova v. 2016; HiRise v. August 2017;\n PBJelly v. September 2017\nAssembly Name :: SceUnd_v1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 4859.0x\nSequencing Technology :: Illumina HiSeq; PacBio\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Sceloporus undulatus 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##
the sample came from two individuals: brain sample from one juvenile (IND9) and blood, liver, muscle, tail, brain samples from one adult (Adult2432)
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 98% coverage of the annotated genomic feature by RNAseq alignments
polypeptide N-acetylgalactosaminyltransferase 17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
autism susceptibility gene 2 protein-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: autism susceptibility gene 2 protein-like
autism susceptibility gene 2 protein homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
autism susceptibility gene 2 protein homolog isoform X2
autism susceptibility gene 2 protein homolog, transcript variant X1
autism susceptibility gene 2 protein homolog isoform X1
autism susceptibility gene 2 protein homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
autism susceptibility gene 2 protein homolog isoform X5
autism susceptibility gene 2 protein homolog, transcript variant X3
autism susceptibility gene 2 protein homolog isoform X3
autism susceptibility gene 2 protein homolog, transcript variant X4
autism susceptibility gene 2 protein homolog isoform X4
CAP-Gly domain-containing linker protein 2-like
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 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: 2 Proteins, and 55% 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: neutrophil cytosol factor 1-like
cytosolic arginine sensor for mTORC1 subunit 2
COORDINATES: polyA evidence [ECO:0006239]
RCC1-like G exchanging factor-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: neutrophil cytosol factor 1
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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: general transcription factor II-I
general transcription factor II-I repeat domain-containing protein 1
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: 12 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: CAP-Gly domain-containing linker protein 2-like
linker for activation of T-cells family member 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
linker for activation of T-cells family member 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
linker for activation of T-cells family member 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
linker for activation of T-cells family member 2-like isoform X1
linker for activation of T-cells family member 2-like isoform X2
eukaryotic translation initiation factor 4H, transcript variant X2
eukaryotic translation initiation factor 4H, transcript variant X1
eukaryotic translation initiation factor 4H isoform X2
eukaryotic translation initiation factor 4H isoform X1
MYB binding protein 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
MYB binding protein 1a, transcript variant X1
sphingolipid transporter 2, transcript variant X1
sphingolipid transporter 2, transcript variant X2
sphingolipid transporter 3 (putative), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sphingolipid transporter 3 (putative), transcript variant X3
sphingolipid transporter 3 (putative), transcript variant X4
sphingolipid transporter 3 (putative), transcript variant X5
sphingolipid transporter 3 (putative), 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
ubiquitin conjugating enzyme E2 G1, transcript variant X3
ubiquitin conjugating enzyme E2 G1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
ubiquitin conjugating enzyme E2 G1, transcript variant X1
ubiquitin-conjugating enzyme E2 G1 isoform X1
ubiquitin-conjugating enzyme E2 G1 isoform X2
ankyrin repeat and FYVE domain containing 1
uroplakin-3b-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uroplakin-3b-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 8 samples with support for all annotated introns
zinc finger ZZ-type and EF-hand domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
zinc finger ZZ-type and EF-hand domain-containing protein 1-like, transcript variant X1
zinc finger ZZ-type and EF-hand domain-containing protein 1-like, transcript variant X2
zinc finger ZZ-type and EF-hand domain-containing protein 1-like isoform X1
zinc finger ZZ-type and EF-hand domain-containing protein 1-like isoform X2
zinc finger ZZ-type and EF-hand domain-containing protein 1-like, transcript variant X3
zinc finger ZZ-type and EF-hand domain-containing protein 1-like isoform X3
sarcoplasmic/endoplasmic reticulum calcium ATPase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
purinergic receptor P2X 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
purinergic receptor P2X 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
purinergic receptor P2X 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
purinergic receptor P2X 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
calcium/calmodulin dependent protein kinase kinase 1
calcium/calmodulin-dependent protein kinase kinase 1
complement component 1 Q subcomponent-binding protein, mitochondrial
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 2 bases in 2 codons
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 2 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
MIS12 kinetochore complex component, transcript variant X1
MIS12 kinetochore complex component, transcript variant X2
coiled-coil domain-containing protein 74A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% 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 99% coverage of the annotated genomic feature by RNAseq alignments
RNA polymerase II subunit J, transcript variant X2
DNA-directed RNA polymerase II subunit RPB11-a isoform X2
RNA polymerase II subunit J, transcript variant X1
DNA-directed RNA polymerase II subunit RPB11-a isoform X1
leucine rich repeats and WD repeat domain containing 1
leucine-rich repeat and WD repeat-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
alpha-ketoglutarate-dependent dioxygenase alkB homolog 4
ORAI calcium release-activated calcium modulator 2
PRKR interacting protein 1, transcript variant X2
PRKR interacting protein 1, transcript variant X1
SH2B adaptor protein 2, 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
SH2B adaptor protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
SH2B adaptor protein 2, transcript variant X4
SH2B adaptor protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
cut like homeobox 1, transcript variant X4
cut like homeobox 1, transcript variant X5
cut like homeobox 1, transcript variant X3
cut like homeobox 1, transcript variant X2
cut like homeobox 1, transcript variant X1
collagen type XXVI alpha 1 chain, transcript variant X6
collagen type XXVI alpha 1 chain, transcript variant X5
collagen type XXVI alpha 1 chain, transcript variant X2
collagen type XXVI alpha 1 chain, transcript variant X4
collagen type XXVI alpha 1 chain, transcript variant X1
collagen type XXVI alpha 1 chain, 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
intraflagellar transport 22, transcript variant X1
intraflagellar transport 22, transcript variant X2
intraflagellar transport protein 22 homolog
rabaptin, RAB GTPase binding effector protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
deltex E3 ubiquitin ligase 2, transcript variant X2
deltex E3 ubiquitin ligase 2, transcript variant X1
probable E3 ubiquitin-protein ligase DTX2 isoform X2
probable E3 ubiquitin-protein ligase DTX2 isoform X1
scavenger receptor cysteine rich family member with 4 domains, transcript variant X2
scavenger receptor cysteine rich family member with 4 domains, transcript variant X1
scavenger receptor cysteine rich family member with 4 domains, transcript variant X3
scavenger receptor cysteine rich family member with 4 domains, transcript variant X4
scavenger receptor cysteine-rich domain-containing group B protein isoform X1
scavenger receptor cysteine-rich domain-containing group B protein isoform X2
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma
heat shock protein family B (small) member 1
serine/arginine repetitive matrix 3, transcript variant X2
serine/arginine repetitive matrix 3, transcript variant X3
serine/arginine repetitive matrix 3, transcript variant X4
serine/arginine repetitive matrix 3, transcript variant X1
serine/arginine repetitive matrix protein 3 isoform X2
serine/arginine repetitive matrix protein 3 isoform X1
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, including 1 sample with support for all annotated introns
serine/threonine/tyrosine interacting like 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 25% 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 2 codons; deleted 2 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine/threonine/tyrosine-interacting-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: NADPH--cytochrome P450 reductase
transmembrane protease serine 11E-like, transcript variant X4
transmembrane protease serine 11E-like, transcript variant X6
transmembrane protease serine 11E-like, transcript variant X3
transmembrane protease serine 11E-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protease serine 11E-like isoform X2
transmembrane protease serine 11E-like, transcript variant X2
transmembrane protease serine 11E-like, transcript variant X1
transmembrane protease serine 11E-like isoform X1
transmembrane protease serine 11E-like isoform X3
BAF chromatin remodeling complex subunit BCL7B, transcript variant X2
BAF chromatin remodeling complex subunit BCL7B, transcript variant X1
B-cell CLL/lymphoma 7 protein family member B
BUD23 rRNA methyltransferase and ribosome maturation factor
probable 18S rRNA (guanine-N(7))-methyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
MLX interacting protein like, transcript variant X1
MLX interacting protein like, transcript variant X6
MLX interacting protein like, transcript variant X3
MLX interacting protein like, transcript variant X2
MLX interacting protein like, transcript variant X4
MLX interacting protein like, transcript variant X5
MLX interacting protein like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
carbohydrate-responsive element-binding protein isoform X1
carbohydrate-responsive element-binding protein isoform X6
carbohydrate-responsive element-binding protein isoform X3
carbohydrate-responsive element-binding protein isoform X2
carbohydrate-responsive element-binding protein isoform X4
carbohydrate-responsive element-binding protein isoform X5
DnaJ heat shock protein family (Hsp40) member C30
dnaJ homolog subfamily C member 30, mitochondrial
vacuolar protein sorting-associated protein 37D
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PICALM interacting mitotic regulator, transcript variant X2
PICALM interacting mitotic regulator, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TSPO associated protein 1, transcript variant X6
TSPO associated protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TSPO associated protein 1, transcript variant X3
TSPO associated protein 1, transcript variant X4
TSPO associated protein 1, transcript variant X1
TSPO associated protein 1, transcript variant X2
peripheral-type benzodiazepine receptor-associated protein 1 isoform X3
peripheral-type benzodiazepine receptor-associated protein 1 isoform X2
peripheral-type benzodiazepine receptor-associated protein 1 isoform X1
SPT4 homolog, DSIF elongation factor subunit
ring finger protein 43, transcript variant X1
ring finger protein 43, transcript variant X2
E3 ubiquitin-protein ligase RNF43 isoform X1
E3 ubiquitin-protein ligase RNF43 isoform X2
myotubularin related protein 4, transcript variant X1
myotubularin related protein 4, transcript variant X2
abhydrolase domain containing 11, transcript variant X1
abhydrolase domain containing 11, transcript variant X2
transmembrane protein 270, transcript variant X2
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 8 samples with support for all annotated introns
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 270, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
tRNA-yW synthesizing protein 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
tRNA-yW synthesizing protein 1 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase TYW1 isoform X1
S-adenosyl-L-methionine-dependent tRNA 4-demethylwyosine synthase TYW1 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00414
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
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: inactive C-alpha-formylglycine-generating enzyme 2
phosphorylase kinase catalytic subunit gamma 1
phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform
coiled-coil-helix-coiled-coil-helix domain containing 2
coiled-coil-helix-coiled-coil-helix domain-containing protein 2
nuclear protein 2, transcriptional regulator, transcript variant X1
nuclear protein 2, transcriptional regulator, transcript variant X2
vitamin K epoxide reductase complex subunit 1 like 1
vitamin K epoxide reductase complex subunit 1-like protein 1
argininosuccinate lyase, transcript variant X3
argininosuccinate lyase, transcript variant X4
argininosuccinate lyase, transcript variant X1
argininosuccinate lyase, transcript variant X2
CGRP receptor component, transcript variant X2
CGRP receptor component, transcript variant X1
DNA-directed RNA polymerase III subunit RPC9 isoform X1
DNA-directed RNA polymerase III subunit RPC9 isoform X2
tyrosylprotein sulfotransferase 1, transcript variant X5
tyrosylprotein sulfotransferase 1, transcript variant X6
tyrosylprotein sulfotransferase 1, transcript variant X3
tyrosylprotein sulfotransferase 1, transcript variant X1
tyrosylprotein sulfotransferase 1, transcript variant X2
tyrosylprotein sulfotransferase 1, transcript variant X8
tyrosylprotein sulfotransferase 1, transcript variant X4
tyrosylprotein sulfotransferase 1, transcript variant X7
protein-tyrosine sulfotransferase 1 isoform X2
protein-tyrosine sulfotransferase 1 isoform X1
potassium channel tetramerization domain containing 7, transcript variant X2
potassium channel tetramerization domain containing 7, transcript variant X4
potassium channel tetramerization domain containing 7, transcript variant X3
potassium channel tetramerization domain containing 7, transcript variant X1
BTB/POZ domain-containing protein KCTD7 isoform X1
BTB/POZ domain-containing protein KCTD7 isoform X2
RAB guanine nucleotide exchange factor 1, transcript variant X1
RAB guanine nucleotide exchange factor 1, transcript variant X2
uncharacterized LOC121917053, transcript variant X3
uncharacterized LOC121917053, transcript variant X2
uncharacterized LOC121917053, transcript variant X1
uncharacterized LOC121917054, transcript variant X1
uncharacterized LOC121917054, transcript variant X2
ring finger and FYVE like domain containing E3 ubiquitin protein ligase, transcript variant X2
ring finger and FYVE like domain containing E3 ubiquitin protein ligase, transcript variant X3
ring finger and FYVE like domain containing E3 ubiquitin protein ligase, transcript variant X5
ring finger and FYVE like domain containing E3 ubiquitin protein ligase, transcript variant X6
ring finger and FYVE like domain containing E3 ubiquitin protein ligase, transcript variant X4
ring finger and FYVE like domain containing E3 ubiquitin protein ligase, transcript variant X1
E3 ubiquitin-protein ligase rififylin isoform X1
E3 ubiquitin-protein ligase rififylin isoform X2
unc-45 myosin chaperone B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DNA repair protein RAD51 homolog 4 isoform X1
DNA repair protein RAD51 homolog 4 isoform X2
unc-45 myosin chaperone B, transcript variant X4
unc-45 myosin chaperone B, transcript variant X3
unc-45 myosin chaperone B, transcript variant X5
unc-45 myosin chaperone B, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00288
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 23 samples with support for all annotated introns
adaptor related protein complex 2 subunit beta 1, transcript variant X1
adaptor related protein complex 2 subunit beta 1, transcript variant X2
RAS like family 10 member B, 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 3 samples with support for all annotated introns
RAS like family 10 member B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RAS like family 10 member B, 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 5 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 71% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C17orf50 homolog
TATA-box binding protein associated factor 15
TATA-binding protein-associated factor 2N
MKS transition zone complex subunit 1, transcript variant X1
MKS transition zone complex subunit 1, transcript variant X2
Meckel syndrome type 1 protein isoform X1
MKS transition zone complex subunit 1, transcript variant X3
Meckel syndrome type 1 protein isoform X2
maestro heat-like repeat-containing protein family member 2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized protein C2orf72 homolog, transcript variant X1
uncharacterized protein C2orf72 homolog, transcript variant X2
uncharacterized protein C2orf72 homolog isoform X1
uncharacterized protein C2orf72 homolog isoform X2
bromodomain adjacent to zinc finger domain 1B
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
leucine-rich repeat-containing protein 75A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: transmembrane protein 248
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
solute carrier family 13 member 5, transcript variant X1
solute carrier family 13 member 5, transcript variant X2
solute carrier family 13 member 5 isoform X1
solute carrier family 13 member 5 isoform X2
mediator of RNA polymerase II transcription subunit 31
thioredoxin domain-containing protein 17
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: membrane-associated phosphatidylinositol transfer protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
huntingtin interacting protein 1, transcript variant X2
huntingtin-interacting protein 1 isoform X2
huntingtin interacting protein 1, transcript variant X1
huntingtin-interacting protein 1 isoform X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nuclear envelope pore membrane protein POM 121C
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase TRIM50-like
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 20 samples with support for all annotated introns
DEAH-box helicase 40, transcript variant X3
probable ATP-dependent RNA helicase DHX40 isoform X3
DEAH-box helicase 40, transcript variant X2
DEAH-box helicase 40, transcript variant X1
probable ATP-dependent RNA helicase DHX40 isoform X1
probable ATP-dependent RNA helicase DHX40 isoform X2
clathrin heavy chain, 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 4 samples with support for all annotated introns
clathrin heavy chain, transcript variant X1
peptidyl-tRNA hydrolase 2, transcript variant X1
peptidyl-tRNA hydrolase 2, transcript variant X2
peptidyl-tRNA hydrolase 2, transcript variant X3
peptidyl-tRNA hydrolase 2, mitochondrial
vacuole membrane protein 1, transcript variant X1
vacuole membrane protein 1, 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 16 samples with support for all annotated introns
vacuole membrane protein 1, transcript variant X3
vacuole membrane protein 1, transcript variant X2
uncharacterized LOC121917130, transcript variant X2
uncharacterized LOC121917130, 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 16 samples with support for all annotated introns
ribosomal protein S6 kinase B1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
ribosomal protein S6 kinase B1, transcript variant X2
ribosomal protein S6 kinase beta-1 isoform X1
ribosomal protein S6 kinase beta-1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 13-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 13-like
SET and MYND domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutathione S-transferase theta-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutathione S-transferase theta-1-like, transcript variant X1
glutathione S-transferase theta-1-like isoform X2
glutathione S-transferase theta-3-like isoform X1
large neutral amino acids transporter small subunit 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon, transcript variant X2
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon, transcript variant X1
inositol polyphosphate-5-phosphatase K, transcript variant X1
inositol polyphosphate-5-phosphatase K, transcript variant X3
inositol polyphosphate-5-phosphatase K, transcript variant X5
inositol polyphosphate-5-phosphatase K, transcript variant X2
inositol polyphosphate-5-phosphatase K, transcript variant X4
inositol polyphosphate 5-phosphatase K isoform X5
inositol polyphosphate 5-phosphatase K isoform X4
inositol polyphosphate 5-phosphatase K isoform X2
inositol polyphosphate 5-phosphatase K isoform X3
inositol polyphosphate 5-phosphatase K isoform X1
phosphatidylinositol transfer protein alpha
phosphatidylinositol transfer protein alpha isoform
uncharacterized LOC121917105, transcript variant X1
uncharacterized LOC121917105, transcript variant X3
uncharacterized LOC121917105, transcript variant X4
uncharacterized LOC121917105, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 89% 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: large neutral amino acids transporter small subunit 4
scavenger receptor class F member 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
scavenger receptor class F member 1, transcript variant X2
scavenger receptor class F member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
scavenger receptor class F member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
scavenger receptor class F member 1 isoform X4
scavenger receptor class F member 1 isoform X2
scavenger receptor class F member 1 isoform X3
scavenger receptor class F member 1 isoform X1
tyrosine-protein kinase JAK3-like, transcript variant X2
tyrosine-protein kinase JAK3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tyrosine-protein kinase JAK3-like, transcript variant X4
tyrosine-protein kinase JAK3-like, transcript variant X5
tyrosine-protein kinase JAK3-like, transcript variant X6
tyrosine-protein kinase JAK3-like, transcript variant X1
uncharacterized protein LOC121917103 isoform X2
uncharacterized protein LOC121917103 isoform X3
uncharacterized protein LOC121917103 isoform X1
uncharacterized protein LOC121917103 isoform X4
uncharacterized protein LOC121917103 isoform X5
tyrosine-protein kinase JAK3-like isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
SMG6 nonsense mediated mRNA decay factor
DNA polymerase delta interacting protein 2
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
LOW QUALITY PROTEIN: polymerase delta-interacting protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 37% 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 1 base in 1 codon; deleted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transmembrane protein 199
sterile alpha and TIR motif containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
apoptosis-inducing factor 3-like, transcript variant X2
apoptosis-inducing factor 3-like, transcript variant X1
SET and MYND domain-containing protein 4
WD repeat domain 81, 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 23 samples with support for all annotated introns
WD repeat domain 81, transcript variant X2
serpin family F member 2, transcript variant X1
serpin family F member 2, transcript variant X3
serpin family F member 2, transcript variant X4
serpin family F member 2, transcript variant X2
serpin family F member 2, transcript variant X5
serpin family F member 2, transcript variant X6
serpin family F member 1, transcript variant X2
serpin family F member 1, transcript variant X1
pigment epithelium-derived factor isoform X1
pigment epithelium-derived factor isoform X2
replication protein A 70 kDa DNA-binding subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: 2-(3-amino-3-carboxypropyl)histidine synthase subunit 1
OVCA2 serine hydrolase domain containing
TNF receptor associated factor 4, transcript variant X2
TNF receptor associated factor 4, transcript variant X1
TNF receptor associated factor 4, transcript variant X3
TNF receptor associated factor 4, transcript variant X6
TNF receptor associated factor 4, transcript variant X5
TNF receptor associated factor 4, transcript variant X7
TNF receptor associated factor 4, transcript variant X4
TNF receptor-associated factor 4 isoform X2
TNF receptor-associated factor 4 isoform X1
TNF receptor-associated factor 4 isoform X5
TNF receptor-associated factor 4 isoform X3
TNF receptor-associated factor 4 isoform X4
TNF receptor-associated factor 4 isoform X6
NIMA related kinase 8, 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 7 samples with support for all annotated introns
NIMA related kinase 8, transcript variant X2
NIMA related kinase 8, 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
serine/threonine-protein kinase Nek8 isoform X1
serine/threonine-protein kinase Nek8 isoform X2
serine/threonine-protein kinase Nek8 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00150
RAB34, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
RAB34, member RAS oncogene family, transcript variant X2
RAB34, member RAS oncogene family, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
adenine phosphoribosyltransferase-like, transcript variant X2
adenine phosphoribosyltransferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
SPT6 homolog, histone chaperone and transcription elongation factor, transcript variant X1
SPT6 homolog, histone chaperone and transcription elongation factor, 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 6 samples with support for all annotated introns
ribosomal protein S6 kinase-related protein
aldolase, fructose-bisphosphate C, transcript variant X1
aldolase, fructose-bisphosphate C, transcript variant X2
aldolase, fructose-bisphosphate C, transcript variant X3
aldolase, fructose-bisphosphate C, transcript variant X4
phosphatidylinositol glycan anchor biosynthesis class S
unc-119 lipid binding chaperone, 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 13 samples with support for all annotated introns
unc-119 lipid binding chaperone, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
family with sequence similarity 222 member B, transcript variant X1
family with sequence similarity 222 member B, transcript variant X2
Era like 12S mitochondrial rRNA chaperone 1, transcript variant X2
Era like 12S mitochondrial rRNA chaperone 1, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 13
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 13 samples with support for all annotated introns
LOW QUALITY PROTEIN: PHD finger protein 12
seizure related 6 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
seizure related 6 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
seizure related 6 homolog, transcript variant X3
seizure related 6 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
unconventional myosin-XVIIIa isoform X10
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
crystallin beta A1, transcript variant X1
crystallin beta A1, transcript variant X2
nuclear fragile X mental retardation-interacting protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ARF GTPase-activating protein GIT1 isoform X4
ARF GTPase-activating protein GIT1 isoform X3
ARF GTPase-activating protein GIT1 isoform X5
ARF GTPase-activating protein GIT1 isoform X2
ARF GTPase-activating protein GIT1 isoform X1
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: 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ankyrin repeat domain-containing protein 13B
slingshot protein phosphatase 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 9 samples with support for all annotated introns
slingshot protein phosphatase 2, 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 10 samples with support for all annotated introns
protein phosphatase Slingshot homolog 2 isoform X1
protein phosphatase Slingshot homolog 2 isoform X2
EF-hand calcium binding domain 5, 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
EF-hand calcium binding domain 5, transcript variant X2
EF-hand calcium-binding domain-containing protein 5
nuclear speckle splicing regulatory protein 1, transcript variant X1
nuclear speckle splicing regulatory protein 1, transcript variant X2
nuclear speckle splicing regulatory protein 1 isoform X1
nuclear speckle splicing regulatory protein 1, transcript variant X3
nuclear speckle splicing regulatory protein 1 isoform X2
nuclear speckle splicing regulatory protein 1 isoform X3
solute carrier family 6 member 4, transcript variant X4
solute carrier family 6 member 4, transcript variant X1
solute carrier family 6 member 4, transcript variant X3
solute carrier family 6 member 4, transcript variant X2
transmembrane and immunoglobulin domain containing 1, 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 6 samples with support for all annotated introns
transmembrane and immunoglobulin domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane and immunoglobulin domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane and immunoglobulin domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
golgi SNAP receptor complex member 1, transcript variant X1
golgi SNAP receptor complex member 1, transcript variant X2
Golgi SNAP receptor complex member 1 isoform X1
Golgi SNAP receptor complex member 1 isoform X2
trafficking regulator of GLUT4 (SLC2A4) 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ABR activator of RhoGEF and GTPase, transcript variant X1
active breakpoint cluster region-related protein isoform X1
ABR activator of RhoGEF and GTPase, transcript variant X2
active breakpoint cluster region-related protein isoform X2
ABR activator of RhoGEF and GTPase, transcript variant X3
active breakpoint cluster region-related protein isoform X3
ABR activator of RhoGEF and GTPase, transcript variant X4
active breakpoint cluster region-related protein isoform X4
ABR activator of RhoGEF and GTPase, transcript variant X5
active breakpoint cluster region-related protein isoform X5
translocase of inner mitochondrial membrane 22
mitochondrial import inner membrane translocase subunit Tim22
sperm antigen with calponin homology and coiled-coil domains 1
zinc finger SWIM-type containing 7, transcript variant X4
zinc finger SWIM-type containing 7, transcript variant X5
zinc finger SWIM-type containing 7, transcript variant X3
adenosine A2b receptor, transcript variant X1
adenosine A2b receptor, transcript variant X2
zinc finger SWIM-type containing 7, transcript variant X2
zinc finger SWIM-type containing 7, transcript variant X6
zinc finger SWIM-type containing 7, transcript variant X7
zinc finger SWIM-type containing 7, transcript variant X1
zinc finger SWIM domain-containing protein 7 isoform X2
zinc finger SWIM domain-containing protein 7 isoform X1
tetratricopeptide repeat protein 19, mitochondrial
nuclear receptor corepressor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
nuclear receptor corepressor 1-like isoform X1
nuclear receptor corepressor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
nuclear receptor corepressor 1-like isoform X2
phosphatidylinositol glycan anchor biosynthesis class L
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase
transient receptor potential cation channel subfamily V member 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transient receptor potential cation channel subfamily V member 1-like, transcript variant X3
transient receptor potential cation channel subfamily V member 1-like isoform X2
transient receptor potential cation channel subfamily V member 1-like, transcript variant X1
transient receptor potential cation channel subfamily V member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transient receptor potential cation channel subfamily V member 1-like isoform X1
sedoheptulokinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sedoheptulokinase, 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 8 samples with support for all annotated introns
sedoheptulokinase, transcript variant X3
sedoheptulokinase, 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 4 samples with support for all annotated introns
sedoheptulokinase, transcript variant X1
cystinosin, lysosomal cystine transporter
Tax1 binding protein 3, transcript variant X2
Tax1 binding protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transient receptor potential cation channel subfamily V member 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transient receptor potential cation channel subfamily V member 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily V member 2-like
transient receptor potential cation channel subfamily V member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 18 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium-transporting ATPase subunit alpha-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 237 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
A-kinase anchor protein 10, mitochondrial
unc-51 like autophagy activating kinase 2, transcript variant X2
unc-51 like autophagy activating kinase 2, transcript variant X6
serine/threonine-protein kinase ULK2 isoform X2
serine/threonine-protein kinase ULK2 isoform X6
unc-51 like autophagy activating kinase 2, transcript variant X8
unc-51 like autophagy activating kinase 2, transcript variant X7
unc-51 like autophagy activating kinase 2, transcript variant X5
serine/threonine-protein kinase ULK2 isoform X5
unc-51 like autophagy activating kinase 2, transcript variant X1
unc-51 like autophagy activating kinase 2, transcript variant X3
unc-51 like autophagy activating kinase 2, transcript variant X4
serine/threonine-protein kinase ULK2 isoform X1
serine/threonine-protein kinase ULK2 isoform X4
serine/threonine-protein kinase ULK2 isoform X3
serine/threonine-protein kinase ULK2 isoform X7
aldehyde dehydrogenase 3 family member A2, transcript variant X1
aldehyde dehydrogenase 3 family member A2, transcript variant X2
aldehyde dehydrogenase family 3 member A2 isoform X2
aldehyde dehydrogenase family 3 member A2 isoform X1
multidrug and toxin extrusion protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
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
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 23 samples with support for all annotated introns
gem nuclear organelle associated protein 4, transcript variant X2
gem nuclear organelle associated protein 4, transcript variant X1
probable ATP-dependent RNA helicase DDX52
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 15 samples with support for all annotated introns
transcriptional adaptor 2A, transcript variant X2
transcriptional adaptor 2A, transcript variant X1
transcriptional adapter 2-alpha isoform X2
transcriptional adapter 2-alpha isoform X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: acetyl-CoA carboxylase 1
apoptosis antagonizing transcription factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
apoptosis antagonizing transcription factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 13-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 7 bases in 6 codons; 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: inserted 7 bases in 6 codons; deleted 2 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mediator of RNA polymerase II transcription subunit 13-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: integrator complex subunit 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: rRNA methyltransferase 1, mitochondrial
gametogenetin binding protein 2, transcript variant X2
gametogenetin binding protein 2, transcript variant X1
gametogenetin binding protein 2, transcript variant X3
gametogenetin-binding protein 2 isoform X2
gametogenetin-binding protein 2 isoform X1
gametogenetin-binding protein 2 isoform X3
phosphatidylinositol glycan anchor biosynthesis class W, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis class W, 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 22 samples with support for all annotated introns
phosphatidylinositol-glycan biosynthesis class W protein isoform X2
phosphatidylinositol-glycan biosynthesis class W protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger HIT domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
protein phosphatase, Mg2+/Mn2+ dependent 1D
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 42% 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 1 base in 1 codon; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein phosphatase 1D
ubiquitin specific peptidase 32, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ubiquitin specific peptidase 32, 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 13 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 32 isoform X2
ubiquitin carboxyl-terminal hydrolase 32 isoform X1
uncharacterized protein C17orf64 homolog
amyloid beta precursor protein binding protein 2
BCAS3 microtubule associated cell migration factor
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
LOW QUALITY PROTEIN: BCAS3 microtubule associated cell migration factor
T-box transcription factor 2, transcript variant X1
T-box transcription factor 2, transcript variant X2
SMG8 nonsense mediated mRNA decay factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
glycerophosphodiester phosphodiesterase domain containing 1
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
spindle and kinetochore associated complex subunit 2, transcript variant X1
spindle and kinetochore-associated protein 2 isoform X1
spindle and kinetochore associated complex subunit 2, transcript variant X2
spindle and kinetochore-associated protein 2 isoform X2
tripartite motif containing 37, transcript variant X2
tripartite motif containing 37, transcript variant X1
protein phosphatase, Mg2+/Mn2+ dependent 1E, transcript variant X2
protein phosphatase, Mg2+/Mn2+ dependent 1E, transcript variant X3
protein phosphatase, Mg2+/Mn2+ dependent 1E, transcript variant X1
testis expressed 14, intercellular bridge forming factor
inactive serine/threonine-protein kinase TEX14
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 382 Proteins
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
double C2-like domain-containing protein beta
rabphilin 3A like (without C2 domains), transcript variant X1
rabphilin 3A like (without C2 domains), transcript variant X2
rabphilin 3A like (without C2 domains), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
VPS53 subunit of GARP complex, transcript variant X1
VPS53 subunit of GARP complex, transcript variant X2
vacuolar protein sorting-associated protein 53 homolog isoform X1
vacuolar protein sorting-associated protein 53 homolog isoform X2
RNA-binding protein Musashi homolog 2-like, transcript variant X3
RNA-binding protein Musashi homolog 2-like, transcript variant X1
RNA-binding protein Musashi homolog 2-like, transcript variant X12
RNA-binding protein Musashi homolog 2-like, transcript variant X9
RNA-binding protein Musashi homolog 2-like, transcript variant X2
RNA-binding protein Musashi homolog 2-like, transcript variant X4
RNA-binding protein Musashi homolog 2-like, transcript variant X5
RNA-binding protein Musashi homolog 2-like, transcript variant X10
RNA-binding protein Musashi homolog 2-like, transcript variant X6
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
RNA-binding protein Musashi homolog 2-like, transcript variant X11
RNA-binding protein Musashi homolog 2-like, transcript variant X8
RNA-binding protein Musashi homolog 2-like isoform X1
RNA-binding protein Musashi homolog 2-like isoform X3
RNA-binding protein Musashi homolog 2-like isoform X9
RNA-binding protein Musashi homolog 2-like isoform X4
RNA-binding protein Musashi homolog 2-like isoform X10
RNA-binding protein Musashi homolog 2-like isoform X12
RNA-binding protein Musashi homolog 2-like isoform X2
RNA-binding protein Musashi homolog 2-like isoform X6
RNA-binding protein Musashi homolog 2-like isoform X11
RNA-binding protein Musashi homolog 2-like isoform X5
RNA-binding protein Musashi homolog 2-like isoform X8
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 24 samples with support for all annotated introns
kinase suppressor of ras 1, transcript variant X5
kinase suppressor of ras 1, transcript variant X7
kinase suppressor of ras 1, transcript variant X8
kinase suppressor of ras 1, transcript variant X6
kinase suppressor of ras 1, transcript variant X4
kinase suppressor of ras 1, transcript variant X1
kinase suppressor of ras 1, transcript variant X2
kinase suppressor of ras 1, transcript variant X3
WD repeat and SOCS box-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
oligodendrocyte myelin glycoprotein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
oligodendrocyte myelin glycoprotein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ecotropic viral integration site 2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
ecotropic viral integration site 2B, 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 9 samples with support for all annotated introns
A-kinase anchoring protein 1, transcript variant X2
A-kinase anchoring protein 1, transcript variant X1
A-kinase anchor protein 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
RNA-binding protein Musashi homolog 2-like, transcript variant X7
RNA-binding protein Musashi homolog 2-like isoform 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
coiled-coil domain-containing protein 182
mitochondrial ribosomal protein S23, transcript variant X2
mitochondrial ribosomal protein S23, transcript variant X1
28S ribosomal protein S23, mitochondrial isoform X2
28S ribosomal protein S23, mitochondrial isoform X1
CUE domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
CUE domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
CUE domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
vascular endothelial zinc finger 1, transcript variant X4
vascular endothelial zinc finger 1, transcript variant X3
vascular endothelial zinc finger 1, transcript variant X1
vascular endothelial zinc finger 1, transcript variant X5
vascular endothelial zinc finger 1, transcript variant X2
vascular endothelial zinc finger 1 isoform X5
vascular endothelial zinc finger 1 isoform X2
vascular endothelial zinc finger 1 isoform X4
vascular endothelial zinc finger 1 isoform X3
vascular endothelial zinc finger 1 isoform X1
serine and arginine rich splicing factor 1, transcript variant X2
serine and arginine rich splicing factor 1, transcript variant X1
serine/arginine-rich splicing factor 1 isoform X2
serine/arginine-rich splicing factor 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 74% 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 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: hepatocyte nuclear factor 1-beta-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 82% 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 4 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nitric oxide synthase, inducible-like
LYR motif containing 9, transcript variant X2
LYR motif containing 9, transcript variant X1
LYR motif containing 9, transcript variant X3
serine/threonine-protein kinase NLK isoform X1
serine/threonine-protein kinase NLK isoform X2
LOW QUALITY PROTEIN: intraflagellar transport protein 20 homolog
TNF alpha induced protein 1, transcript variant X6
TNF alpha induced protein 1, transcript variant X4
TNF alpha induced protein 1, transcript variant X1
TNF alpha induced protein 1, transcript variant X2
TNF alpha induced protein 1, transcript variant X3
TNF alpha induced protein 1, transcript variant X5
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2
small G protein signaling modulator 2, transcript variant X1
small G protein signaling modulator 2, transcript variant X2
small G protein signaling modulator 2, transcript variant X3
small G protein signaling modulator 2 isoform X1
small G protein signaling modulator 2 isoform X2
small G protein signaling modulator 2 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
MAX network transcriptional repressor, transcript variant X1
MAX network transcriptional repressor, transcript variant X2
platelet activating factor acetylhydrolase 1b regulatory subunit 1
platelet-activating factor acetylhydrolase IB subunit beta
clustered mitochondria homolog, transcript variant X2
clustered mitochondria homolog, transcript variant X3
clustered mitochondria homolog, transcript variant X1
clustered mitochondria protein homolog isoform X2
clustered mitochondria protein homolog isoform X1
clustered mitochondria protein homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns