Sphaerodactylus townsendi isolate TG3544 linkage group LG17, 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\nCM037630.2.\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.
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
COORDINATES: polyA evidence [ECO:0006239]
family with sequence similarity 214 member A
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 6 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 6 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
pyruvate kinase M1/2, transcript variant X2
pyruvate kinase M1/2, transcript variant X1
GRAM domain containing 2A, 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 8 samples with support for all annotated introns
GRAM domain containing 2A, 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
GRAM domain-containing protein 2A isoform X1
GRAM domain containing 2A, 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 7 samples with support for all annotated introns
GRAM domain-containing protein 2A isoform X3
GRAM domain containing 2A, 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
GRAM domain-containing protein 2A isoform X2
SUMO peptidase family member, NEDD8 specific, transcript variant X6
SUMO peptidase family member, NEDD8 specific, transcript variant X1
SUMO peptidase family member, NEDD8 specific, transcript variant X3
SUMO peptidase family member, NEDD8 specific, transcript variant X2
SUMO peptidase family member, NEDD8 specific, transcript variant X5
SUMO peptidase family member, NEDD8 specific, transcript variant X4
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: 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor subfamily 2 group E member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 2 group E member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
photoreceptor-specific nuclear receptor isoform X2
photoreceptor-specific nuclear receptor isoform X1
cytoplasmic polyadenylation element binding protein 1, transcript variant X1
cytoplasmic polyadenylation element binding protein 1, transcript variant X2
cytoplasmic polyadenylation element-binding protein 1 isoform X1
cytoplasmic polyadenylation element-binding protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00056
RNA binding protein, mRNA processing factor 2, transcript variant X2
RNA binding protein, mRNA processing factor 2, transcript variant X1
RNA-binding protein with multiple splicing 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
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: ornithine decarboxylase antizyme 2
zinc finger protein 609, transcript variant X4
zinc finger protein 609, transcript variant X1
zinc finger protein 609, transcript variant X2
zinc finger protein 609, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 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: 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: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
SEC11 homolog A, signal peptidase complex subunit
signal peptidase complex catalytic subunit SEC11A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
sodium/nucleoside cotransporter 1-like, transcript variant X3
sodium/nucleoside cotransporter 1-like, transcript variant X2
sodium/nucleoside cotransporter 1-like, transcript variant X1
sodium/nucleoside cotransporter 2-like isoform X1
sodium/nucleoside cotransporter 1-like isoform X3
sodium/nucleoside cotransporter 1-like isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
SH2 domain-containing adapter protein F-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SH2 domain-containing adapter protein F-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
SH2 domain-containing adapter protein F-like
poly(ADP-ribose) polymerase family member 6
protein mono-ADP-ribosyltransferase PARP6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ariadne RBR E3 ubiquitin protein ligase 1, transcript variant X1
ariadne RBR E3 ubiquitin protein ligase 1, transcript variant X2
E3 ubiquitin-protein ligase ARIH1 isoform X1
E3 ubiquitin-protein ligase ARIH1 isoform X2
ADP dependent glucokinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ADP dependent glucokinase, 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
ADP dependent glucokinase, transcript variant 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: 5 Proteins, and 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: 9 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
hyperpolarization activated cyclic nucleotide gated potassium channel 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4
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
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
caseinolytic mitochondrial matrix peptidase chaperone subunit X
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: 10 Proteins, and 53% 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: ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial
kelch repeat and BTB domain containing 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
kelch repeat and BTB domain-containing protein 13
mitochondrial methionyl-tRNA formyltransferase, 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
mitochondrial methionyl-tRNA formyltransferase, 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
methionyl-tRNA formyltransferase, mitochondrial isoform X1
methionyl-tRNA formyltransferase, mitochondrial isoform X2
protein mono-ADP-ribosyltransferase PARP16-like
immunoglobulin superfamily DCC subclass member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
immunoglobulin superfamily DCC subclass member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 3
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: integrator complex subunit 14
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: 7 Proteins, and 93% 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; substituted 7 bases at 7 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: C-myc promoter-binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 59% coverage of the annotated genomic feature by RNAseq alignments
multiple epidermal growth factor-like domains protein 11
COORDINATES: nucleotide motif:Rfam:12.0:RF00582
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mothers against decapentaplegic homolog 6
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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
mothers against decapentaplegic homolog 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: mothers against decapentaplegic homolog 3-like
mitogen-activated protein kinase kinase 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
dual specificity mitogen-activated protein kinase kinase 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
IQ domain-containing protein H-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
IQ domain-containing protein H-like, transcript variant X2
IQ domain-containing protein H-like, transcript variant X4
IQ domain-containing protein H-like, transcript variant X3
IQ domain-containing protein H-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
SKI family transcriptional corepressor 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 4 samples with support for all annotated introns
SKI family transcriptional corepressor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SKI family transcriptional corepressor 1 isoform X1
SKI family transcriptional corepressor 1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: kinesin-like protein KIF23
TLE family member 3, transcriptional corepressor, transcript variant X5
TLE family member 3, transcriptional corepressor, transcript variant X3
TLE family member 3, transcriptional corepressor, transcript variant X6
TLE family member 3, transcriptional corepressor, transcript variant X4
TLE family member 3, transcriptional corepressor, transcript variant X2
TLE family member 3, transcriptional corepressor, transcript variant X1
transducin-like enhancer protein 3 isoform X5
transducin-like enhancer protein 3 isoform X3
transducin-like enhancer protein 3 isoform X6
transducin-like enhancer protein 3 isoform X4
transducin-like enhancer protein 3 isoform X2
transducin-like enhancer protein 3 isoform X1
uveal autoantigen with coiled-coil domains and ankyrin repeats
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 7-like
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
cytosolic iron-sulfur assembly component 2A
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 10 samples with support for all annotated introns
SPG11 vesicle trafficking associated, spatacsin, transcript variant X1
SPG11 vesicle trafficking associated, spatacsin, transcript variant X2
SPG11 vesicle trafficking associated, spatacsin, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit J
golgi membrane protein 2, transcript variant X4
golgi membrane protein 2, transcript variant X3
golgi membrane protein 2, transcript variant X5
golgi membrane protein 2, transcript variant X1
golgi membrane protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 69% 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 6 samples with support for all annotated introns
mannosidase alpha class 2A member 2, transcript variant X4
mannosidase alpha class 2A member 2, transcript variant X1
mannosidase alpha class 2A member 2, transcript variant X3
mannosidase alpha class 2A member 2, transcript variant X2
unc-45 myosin chaperone A, transcript variant X1
unc-45 myosin chaperone A, transcript variant X2
RCC1 domain containing 1, transcript variant X2
RCC1 domain containing 1, transcript variant X1
RCC1 domain-containing protein 1 isoform X2
RCC1 domain-containing protein 1 isoform X1
protein regulator of cytokinesis 1, transcript variant X1
protein regulator of cytokinesis 1, transcript variant X2
protein regulator of cytokinesis 1, transcript variant X3
protein regulator of cytokinesis 1 isoform X2
protein regulator of cytokinesis 1 isoform X1
protein regulator of cytokinesis 1 isoform X3
isocitrate dehydrogenase [NADP], mitochondrial
basic salivary proline-rich protein 3-like
zinc finger protein 710, transcript variant X2
zinc finger protein 710, transcript variant X1
alanyl aminopeptidase, membrane, transcript variant X3
alanyl aminopeptidase, membrane, transcript variant X2
alanyl aminopeptidase, membrane, transcript variant X1
alanyl aminopeptidase, membrane, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gonadotropin-releasing hormone II receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Ras protein specific guanine nucleotide releasing factor 1
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
ras-specific guanine nucleotide-releasing factor 1
furin, paired basic amino acid cleaving enzyme
serine incorporator 4, 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 5 samples with support for all annotated introns
serine incorporator 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine incorporator 4, transcript variant X2
serine incorporator 4, transcript variant X1
serine incorporator 4, transcript variant X4
peptidyl-prolyl cis-trans isomerase FKBP8-like, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP8-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase FKBP8-like
protein disulfide isomerase family A member 3
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
diphosphoinositol pentakisphosphate kinase 1, transcript variant X1
diphosphoinositol pentakisphosphate kinase 1, transcript variant X2
diphosphoinositol pentakisphosphate kinase 1, transcript variant X3
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1 isoform X1
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1 isoform X2
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1 isoform X3
microtubule associated protein 1A, transcript variant X1
microtubule associated protein 1A, transcript variant X2
microtubule-associated protein 1A isoform X1
microtubule-associated protein 1A isoform X2
tumor protein p53 binding protein 1, transcript variant X1
tumor protein p53 binding protein 1, transcript variant X3
tumor protein p53 binding protein 1, transcript variant X2
tubulin gamma complex associated protein 4, transcript variant X1
tubulin gamma complex associated protein 4, transcript variant X2
tubulin gamma complex associated protein 4, transcript variant X5
tubulin gamma complex associated protein 4, transcript variant X4
tubulin gamma complex associated protein 4, transcript variant X3
tubulin gamma complex associated protein 4, transcript variant X7
tubulin gamma complex associated protein 4, transcript variant X6
gamma-tubulin complex component 4 isoform X1
gamma-tubulin complex component 4 isoform X2
gamma-tubulin complex component 4 isoform X5
gamma-tubulin complex component 4 isoform X3
gamma-tubulin complex component 4 isoform X4
IQ motif containing GTPase activating protein 1
ras GTPase-activating-like protein IQGAP1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 81% 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, and 98% coverage of the annotated genomic feature by RNAseq alignments
probable ribosome biogenesis protein RLP24
RAB27A, member RAS oncogene family, transcript variant X2
RAB27A, member RAS oncogene family, transcript variant X1
RAB27A, member RAS oncogene family, transcript variant X4
RAB27A, member RAS oncogene family, transcript variant X6
RAB27A, member RAS oncogene family, transcript variant X3
RAB27A, member RAS oncogene family, transcript variant X5
phosphatidylinositol glycan anchor biosynthesis class B, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis class B, transcript variant X2
cell cycle progression 1, transcript variant X3
cell cycle progression 1, transcript variant X1
cell cycle progression 1, transcript variant X2
cell cycle progression protein 1 isoform X2
cell cycle progression protein 1 isoform X1
dynein axonemal assembly factor 4, transcript variant X2
dynein axonemal assembly factor 4, transcript variant X1
dynein axonemal assembly factor 4 isoform X2
dynein axonemal assembly factor 4 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: 6 Proteins, and 98% 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: 21 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
class I histocompatibility antigen, F10 alpha chain-like, transcript variant X1
class I histocompatibility antigen, F10 alpha chain-like, transcript variant X2
class I histocompatibility antigen, F10 alpha chain-like isoform X1
class I histocompatibility antigen, F10 alpha chain-like isoform X2
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
meiosis-specific nuclear structural 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; 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 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: zinc finger protein 280D
transcription factor 12, transcript variant X1
transcription factor 12, transcript variant X2
transcription factor 12, transcript variant X3
transcription factor 12, transcript variant X4
transcription factor 12, transcript variant X5
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; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cingulin-like protein 1
aldehyde dehydrogenase 1 family member A2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 96% 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: retinal dehydrogenase 2
tetratricopeptide repeat protein 24-like
lipase C, hepatic type, transcript variant X1
hepatic triacylglycerol lipase isoform X1
lipase C, hepatic type, transcript variant X2
lipase C, hepatic type, transcript variant X3
hepatic triacylglycerol lipase isoform X2
hepatic triacylglycerol lipase isoform X3
disintegrin and metalloproteinase domain-containing protein 10
LOW QUALITY PROTEIN: ubiquitin carboxyl-terminal hydrolase MINDY-2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 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: E3 ubiquitin-protein ligase Arkadia
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
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
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; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: unconventional myosin-Ie
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 81 member A, 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 1 sample with support for all annotated introns
family with sequence similarity 81 member A, 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
death associated protein kinase 2, 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
death associated protein kinase 2, transcript variant X2
death-associated protein kinase 2 isoform X2
death-associated protein kinase 2 isoform X1
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1
probable E3 ubiquitin-protein ligase HERC1
F-box and leucine rich repeat protein 22
ubiquitin specific peptidase 3, transcript variant X1
ubiquitin specific peptidase 3, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 3 isoform X1
ubiquitin carboxyl-terminal hydrolase 3 isoform X2
carbonic anhydrase 12, 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
carbonic anhydrase 12, 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
carbonic anhydrase 12, transcript variant X3
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 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: 42 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: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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; substituted 9 bases at 9 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
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 4 bases in 3 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 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: intermembrane lipid transfer protein VPS13C
complement decay-accelerating factor-like
interactor of little elongation complex ELL subunit 2, transcript variant X1
interactor of little elongation complex ELL subunit 2, transcript variant X2
little elongation complex subunit 2 isoform X1
little elongation complex subunit 2 isoform X2
uncharacterized LOC125424763, transcript variant X1
uncharacterized LOC125424763, transcript variant X2
BCL2 interacting protein 2, transcript variant X1
BCL2 interacting protein 2, transcript variant X3
BCL2 interacting protein 2, transcript variant X5
BCL2 interacting protein 2, transcript variant X4
BCL2 interacting protein 2, transcript variant X2
BCL2/adenovirus E1B 19 kDa protein-interacting protein 2 isoform X4
BCL2/adenovirus E1B 19 kDa protein-interacting protein 2 isoform X1
BCL2/adenovirus E1B 19 kDa protein-interacting protein 2 isoform X2
BCL2/adenovirus E1B 19 kDa protein-interacting protein 2 isoform X3
general transcription factor IIA subunit 2, transcript variant X1
general transcription factor IIA subunit 2, transcript variant X2
transcription initiation factor IIA subunit 2
glucosaminyl (N-acetyl) transferase 3, mucin type
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
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3
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 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 88% 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 4 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: OTU domain-containing protein 7A
Kruppel like factor 13, 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
Kruppel like factor 13, 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
transient receptor potential cation channel subfamily M member 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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: 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: transient receptor potential cation channel subfamily M member 1
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: myotubularin-related protein 10-like
FANCD2 and FANCI associated nuclease 1, transcript variant X5
FANCD2 and FANCI associated nuclease 1, transcript variant X2
FANCD2 and FANCI associated nuclease 1, transcript variant X4
FANCD2 and FANCI associated nuclease 1, transcript variant X3
FANCD2 and FANCI associated nuclease 1, transcript variant X6
FANCD2 and FANCI associated nuclease 1, transcript variant X1
fanconi-associated nuclease 1 isoform X2
fanconi-associated nuclease 1 isoform X1
U3 small nucleolar ribonucleoprotein protein MPP10
methylmalonyl-CoA epimerase, mitochondrial
amyloid beta precursor protein binding family A member 2, transcript variant X1
amyloid beta precursor protein binding family A member 2, transcript variant X3
amyloid beta precursor protein binding family A member 2, transcript variant X2
amyloid-beta A4 precursor protein-binding family A member 2 isoform X1
amyloid-beta A4 precursor protein-binding family A member 2 isoform X2
endosomal transmembrane epsin interactor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 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: 3 Proteins, and 15% 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% 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: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: adenosine deaminase-like protein
threonine--tRNA ligase 1, cytoplasmic-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
La ribonucleoprotein 6, translational regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeat-containing protein 49
thrombospondin type-1 domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 97% 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha, transcript variant X1
isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha, transcript variant X2
isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha, transcript variant X3
isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isoform X1
isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial isoform X2
acyl-CoA synthetase bubblegum family member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA synthetase bubblegum family member 1, 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
acyl-CoA synthetase bubblegum family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase ACSBG1 isoform X2
long-chain-fatty-acid--CoA ligase ACSBG1 isoform X3
long-chain-fatty-acid--CoA ligase ACSBG1 isoform X1
DnaJ heat shock protein family (Hsp40) member A4
cellular retinoic acid binding protein 1, transcript variant X2
cellular retinoic acid-binding protein 1 isoform X2
cellular retinoic acid binding protein 1, transcript variant X1
cellular retinoic acid-binding protein 1 isoform X1
SIN3 transcription regulator family member A
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 4 bases at 4 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: paired amphipathic helix protein Sin3a
protein tyrosine phosphatase non-receptor type 9
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 94% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: tyrosine-protein phosphatase non-receptor type 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 3 like 1
outer dense fiber protein 3-like 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 4 samples with support for all annotated introns
leucine rich repeat and Ig domain containing 1
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
LOW QUALITY PROTEIN: leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1
high mobility group 20A, transcript variant X3
high mobility group 20A, transcript variant X1
high mobility group 20A, transcript variant X2
high mobility group protein 20A isoform X2
high mobility group protein 20A isoform X1
pseudopodium enriched atypical kinase 1, transcript variant X3
pseudopodium enriched atypical kinase 1, transcript variant X1
pseudopodium enriched atypical kinase 1, transcript variant X2
inactive tyrosine-protein kinase PEAK1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: inactive tyrosine-protein kinase PEAK1-like
proline-serine-threonine phosphatase interacting protein 1
proline-serine-threonine phosphatase-interacting protein 1
S-phase cyclin A associated protein in the ER
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
S phase cyclin A-associated protein in the endoplasmic reticulum
S phase cyclin A-associated protein in the endoplasmic reticulum-like
electron transfer flavoprotein subunit alpha, transcript variant X2
electron transfer flavoprotein subunit alpha, transcript variant X1
electron transfer flavoprotein subunit alpha, mitochondrial isoform X1
electron transfer flavoprotein subunit alpha, mitochondrial isoform X2
pro-neuregulin-4, membrane-bound isoform isoform X1
pro-neuregulin-4, membrane-bound isoform isoform X2
ubiquitin conjugating enzyme E2 Q2, transcript variant X1
ubiquitin conjugating enzyme E2 Q2, transcript variant X2
ubiquitin-conjugating enzyme E2 Q2 isoform X2
ubiquitin-conjugating enzyme E2 Q2 isoform X1
cholinergic receptor nicotinic beta 4 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
neuronal acetylcholine receptor subunit beta-4
cholinergic receptor nicotinic alpha 3 subunit
neuronal acetylcholine receptor subunit alpha-3
cholinergic receptor nicotinic alpha 5 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-5
proteasome 20S subunit alpha 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
proteasome 20S subunit alpha 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
hydroxylysine kinase, transcript variant X2
hydroxylysine kinase, transcript variant X3
hydroxylysine kinase, transcript variant X1
iron responsive element binding protein 2
iron-responsive element-binding protein 2
mannosidase alpha class 2C member 1, transcript variant X1
mannosidase alpha class 2C member 1, transcript variant X2
nei like DNA glycosylase 1, transcript variant X2
nei like DNA glycosylase 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
COMM domain containing 4, transcript variant X2
COMM domain containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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: 24 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: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
immunoglobulin superfamily containing leucine rich repeat 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
immunoglobulin superfamily containing leucine-rich repeat protein 2
immunoglobulin superfamily containing leucine-rich repeat protein-like
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
signaling receptor and transporter of retinol STRA6, transcript variant X5
signaling receptor and transporter of retinol STRA6, transcript variant X4
signaling receptor and transporter of retinol STRA6, transcript variant X3
signaling receptor and transporter of retinol STRA6, transcript variant X1
signaling receptor and transporter of retinol STRA6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 33
COORDINATES: nucleotide motif:Rfam:12.0:RF00264
semaphorin 7A (John Milton Hagen blood group)
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, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ubiquitin-like protein 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 628 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
AT-rich interaction domain 3B, transcript variant X1
AT-rich interaction domain 3B, transcript variant X3
AT-rich interaction domain 3B, transcript variant X4
AT-rich interaction domain 3B, transcript variant X5
AT-rich interaction domain 3B, transcript variant X2
AT-rich interactive domain-containing protein 3B isoform X1
AT-rich interactive domain-containing protein 3B isoform X2
AT-rich interactive domain-containing protein 3B isoform X3
AT-rich interactive domain-containing protein 3B isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
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 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: enhancer of mRNA-decapping protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
C-terminal Src kinase, transcript variant X2
C-terminal Src kinase, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine/threonine-protein kinase ULK3
secretory carrier-associated membrane protein 2
family with sequence similarity 219 member B
cytochrome c oxidase subunit 5A, mitochondrial
secretory carrier-associated membrane protein 5
phosphopantothenoylcysteine decarboxylase, transcript variant X2
phosphopantothenoylcysteine decarboxylase, transcript variant X3
phosphopantothenoylcysteine decarboxylase, transcript variant X4
phosphopantothenoylcysteine decarboxylase, transcript variant X1
phosphopantothenoylcysteine decarboxylase, transcript variant X5
phosphopantothenoylcysteine decarboxylase isoform X1
phosphopantothenoylcysteine decarboxylase isoform X2
linkage group 17 C15orf39 homolog, transcript variant X2
linkage group 17 C15orf39 homolog, transcript variant X1
uncharacterized protein C15orf39 homolog isoform X1
uncharacterized protein C15orf39 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 47% 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 10 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: 15 Proteins, and 99% 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: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
guanine nucleotide-binding protein subunit beta-5
LEO1 homolog, Paf1/RNA polymerase II complex component
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tropomodulin-3-like, transcript variant X2
tropomodulin-3-like, transcript variant X4
tropomodulin-3-like, transcript variant X3
tropomodulin-3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lysM and putative peptidoglycan-binding domain-containing protein 2
adaptor related protein complex 4 subunit epsilon 1
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: AP-4 complex subunit epsilon-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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: tumor necrosis factor alpha-induced protein 8-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 87% 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: 7 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: 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: 81% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 24 member 5, transcript variant X1
solute carrier family 24 member 5, transcript variant X2
sodium/potassium/calcium exchanger 5 isoform X1
sodium/potassium/calcium exchanger 5 isoform X2
solute carrier family 24 member 5, transcript variant X3
sodium/potassium/calcium exchanger 5 isoform X3
myelin expression factor 2, transcript variant X2
myelin expression factor 2, transcript variant X3
myelin expression factor 2, transcript variant X1
myelin expression factor 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial
centrosomal protein 152, transcript variant X4
centrosomal protein 152, transcript variant X6
centrosomal protein 152, transcript variant X2
centrosomal protein 152, transcript variant X3
centrosomal protein 152, transcript variant X1
centrosomal protein 152, transcript variant X5
centrosomal protein of 152 kDa isoform X4
centrosomal protein of 152 kDa isoform X6
centrosomal protein of 152 kDa isoform X2
centrosomal protein of 152 kDa isoform X3
centrosomal protein of 152 kDa isoform X1
centrosomal protein of 152 kDa isoform X5
SHC adaptor protein 4, transcript variant X2
SHC adaptor protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SECIS binding protein 2 like, transcript variant X1
SECIS binding protein 2 like, transcript variant X2
selenocysteine insertion sequence-binding protein 2-like isoform X2
selenocysteine insertion sequence-binding protein 2-like isoform X1
COP9 signalosome subunit 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
COP9 signalosome subunit 2, transcript variant X2
COP9 signalosome subunit 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
COP9 signalosome subunit 2, transcript variant X1
COP9 signalosome complex subunit 2 isoform X4
COP9 signalosome complex subunit 2 isoform X2
COP9 signalosome complex subunit 2 isoform X3
COP9 signalosome complex subunit 2 isoform X1
LOW QUALITY PROTEIN: N-acetylgalactosamine kinase
family with sequence similarity 227 member B
fibroblast growth factor 7, transcript variant X1
fibroblast growth factor 7, transcript variant X2
fibroblast growth factor 7, transcript variant X3
NAD(P) transhydrogenase, mitochondrial-like
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: NAD(P) transhydrogenase, mitochondrial-like
ATPase phospholipid transporting 8B4 (putative)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
probable phospholipid-transporting ATPase IM
spermatogenesis-associated protein 5-like protein 1
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
normal mucosa of esophagus-specific gene 1 protein
biogenesis of lysosomal organelles complex 1 subunit 6
biogenesis of lysosome-related organelles complex 1 subunit 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
sulfide:quinone oxidoreductase, mitochondrial
signal peptide peptidase like 2A, transcript variant X2
signal peptide peptidase like 2A, transcript variant X1
signal peptide peptidase-like 2A isoform X1
signal peptide peptidase-like 2A isoform X2
transient receptor potential cation channel subfamily M member 7
LOW QUALITY PROTEIN: transient receptor potential cation channel subfamily M member 7
inactive ubiquitin carboxyl-terminal hydrolase 50
ubiquitin specific peptidase 8, transcript variant X6
ubiquitin specific peptidase 8, transcript variant X5
ubiquitin specific peptidase 8, transcript variant X7
ubiquitin specific peptidase 8, transcript variant X4
ubiquitin specific peptidase 8, transcript variant X3
ubiquitin specific peptidase 8, transcript variant X1
ubiquitin specific peptidase 8, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 8 isoform X5
ubiquitin carboxyl-terminal hydrolase 8 isoform X4
ubiquitin carboxyl-terminal hydrolase 8 isoform X6
ubiquitin carboxyl-terminal hydrolase 8 isoform X3
ubiquitin carboxyl-terminal hydrolase 8 isoform X2
ubiquitin carboxyl-terminal hydrolase 8 isoform X1
GA binding protein transcription factor subunit beta 1, transcript variant X2
GA binding protein transcription factor subunit beta 1, transcript variant X1
GA binding protein transcription factor subunit beta 1, transcript variant X3
GA-binding protein subunit beta-1 isoform X1
GA-binding protein subunit beta-1 isoform X2
histidine decarboxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
histidine decarboxylase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 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: 16 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: very long-chain acyl-CoA synthetase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
glycine amidinotransferase, mitochondrial
phosphodiesterase 8A, transcript variant X1
phosphodiesterase 8A, transcript variant X2
phosphodiesterase 8A, transcript variant X3
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A isoform X1
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A isoform X2
fibronectin type III and SPRY domain containing 2
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
fibronectin type III and SPRY domain-containing protein 2
WASP homolog associated with actin, golgi membranes and microtubules, transcript variant X2
WASP homolog associated with actin, golgi membranes and microtubules, transcript variant X1
WASP homolog-associated protein with actin, membranes and microtubules isoform X1
WASP homolog-associated protein with actin, membranes and microtubules isoform X2
homer scaffold protein 2, transcript variant X2
homer scaffold protein 2, transcript variant X1
RNA guanine-7 methyltransferase activating subunit, transcript variant X1
RNA guanine-7 methyltransferase activating subunit, transcript variant X2
RNA guanine-N7 methyltransferase activating subunit
transmembrane 6 superfamily member 1, transcript variant X2
transmembrane 6 superfamily member 1 isoform X2
transmembrane 6 superfamily member 1, transcript variant X3
transmembrane 6 superfamily member 1, transcript variant X1
transmembrane 6 superfamily member 1, transcript variant X4
transmembrane 6 superfamily member 1 isoform X1
transmembrane 6 superfamily member 1 isoform X3
transmembrane 6 superfamily member 1 isoform X4
transmembrane 6 superfamily member 1, transcript variant X6
transmembrane 6 superfamily member 1, transcript variant X5
transmembrane 6 superfamily member 1 isoform X5
hepatoma-derived growth factor-related protein 3
SH3 domain containing GRB2 like 3, endophilin A3, transcript variant X1
SH3 domain containing GRB2 like 3, endophilin A3, transcript variant X2
lamin-L(III)-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lamin-L(III)-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
elongation factor like GTPase 1, transcript variant X4
elongation factor like GTPase 1, transcript variant X5
elongation factor like GTPase 1, transcript variant X2
elongation factor like GTPase 1, transcript variant X3
elongation factor like GTPase 1, transcript variant X1
elongation factor-like GTPase 1 isoform X1
elongation factor-like GTPase 1 isoform X2
elongation factor-like GTPase 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
cilia and flagella associated protein 161, transcript variant X1
cilia and flagella associated protein 161, transcript variant X3
cilia and flagella associated protein 161, transcript variant X2
cilia- and flagella-associated protein 161 isoform X1
cilia- and flagella-associated protein 161 isoform X3
cilia- and flagella-associated protein 161 isoform X2
StAR related lipid transfer domain containing 5
talin rod 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 7 samples with support for all annotated introns
talin rod domain containing 1, transcript variant X1
cell migration inducing hyaluronidase 1, transcript variant X3
cell migration inducing hyaluronidase 1, transcript variant X1
cell migration inducing hyaluronidase 1, transcript variant X2
cell migration inducing hyaluronidase 1, transcript variant X4
cell migration-inducing and hyaluronan-binding protein isoform X2
cell migration-inducing and hyaluronan-binding protein isoform X1
cell migration inducing hyaluronidase 1, transcript variant X5
cell migration-inducing and hyaluronan-binding protein isoform X3
abhydrolase domain containing 17C, depalmitoylase
alpha/beta hydrolase domain-containing protein 17C
aryl hydrocarbon receptor nuclear translocator 2, 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
aryl hydrocarbon receptor nuclear translocator 2 isoform X1
aryl hydrocarbon receptor nuclear translocator 2, transcript variant X2
aryl hydrocarbon receptor nuclear translocator 2 isoform X2
cortexin domain containing 1, transcript variant X1
cortexin domain containing 1, transcript variant X2
fumarylacetoacetate hydrolase, transcript variant X1
fumarylacetoacetate hydrolase, transcript variant X2
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 61% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: AN1-type zinc finger protein 6
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: bcl-2-related protein A1
uncharacterized LOC125424732, transcript variant X1
uncharacterized LOC125424732, transcript variant X2
membrane integral NOTCH2 associated receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
major intrinsically disordered Notch2-binding receptor 1
LOW QUALITY PROTEIN: WD repeat-containing protein 93
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
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
ras-related and estrogen-regulated growth inhibitor-like protein, 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 2 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like protein, transcript variant X3
ras-related and estrogen-regulated growth inhibitor-like protein, transcript variant X1
ras-related and estrogen-regulated growth inhibitor-like protein isoform X2
ras-related and estrogen-regulated growth inhibitor-like protein isoform X1
kinesin family member 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kinesin family member 7, transcript variant X2
TOPBP1 interacting checkpoint and replication regulator
Rh family C glycoprotein, 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 1 sample with support for all annotated introns
Rh family C glycoprotein, 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 2 samples with support for all annotated introns
Rh family C glycoprotein, transcript variant X2
Rh family C glycoprotein, transcript variant X6
Rh family C glycoprotein, transcript variant X5
Rh family C glycoprotein, transcript variant X4
ADAM metallopeptidase with thrombospondin type 1 motif 17
A disintegrin and metalloproteinase with thrombospondin motifs 17
ceramide synthase 3, 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
ceramide synthase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat and SOCS box containing 7
aldehyde dehydrogenase 1 family member A3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aldehyde dehydrogenase family 1 member A3
leucine rich repeat kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine rich repeat kinase 1, transcript variant X2
leucine-rich repeat serine/threonine-protein kinase 1 isoform X1
leucine-rich repeat serine/threonine-protein kinase 1 isoform X2
small nuclear ribonucleoprotein polypeptide A'
proprotein convertase subtilisin/kexin type 6, transcript variant X2
proprotein convertase subtilisin/kexin type 6, transcript variant X1
proprotein convertase subtilisin/kexin type 6 isoform X2
proprotein convertase subtilisin/kexin type 6 isoform X1
proprotein convertase subtilisin/kexin type 6, transcript variant X3
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 1 sample with support for all annotated introns
proprotein convertase subtilisin/kexin type 6 isoform X3
pleckstrin homology domain containing O2, transcript variant X2
pleckstrin homology domain-containing family O member 2 isoform X2
pleckstrin homology domain containing O2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
pleckstrin homology domain-containing family O member 2 isoform X1
A-kinase anchor protein 13-like, transcript variant X1
A-kinase anchor protein 13-like, transcript variant X2
A-kinase anchoring protein 13, transcript variant X1
A-kinase anchoring protein 13, transcript variant X2
A-kinase anchoring protein 13, transcript variant X3
A-kinase anchoring protein 13, transcript variant X4
A-kinase anchoring protein 13, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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: 17 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
LOW QUALITY PROTEIN: NT-3 growth factor receptor-like
39S ribosomal protein L46, mitochondrial
mitochondrial ribosomal protein S11, transcript variant X1
mitochondrial ribosomal protein S11, transcript variant X2
28S ribosomal protein S11, mitochondrial isoform X1
28S ribosomal protein S11, mitochondrial isoform X2
DET1 partner of COP1 E3 ubiquitin ligase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
hyaluronan and proteoglycan link protein 3, transcript variant X2
hyaluronan and proteoglycan link protein 3, transcript variant X1
hyaluronan and proteoglycan link protein 3
milk fat globule EGF and factor V/VIII domain containing, transcript variant X2
milk fat globule EGF and factor V/VIII domain containing, transcript variant X1
abhydrolase domain containing 2, acylglycerol lipase
retinaldehyde binding protein 1, transcript variant X2
retinaldehyde binding protein 1, transcript variant X1
retinaldehyde-binding protein 1 isoform X2
retinaldehyde-binding protein 1 isoform X1
FA complementation group I, transcript variant X2
FA complementation group I, transcript variant X1
FA complementation group I, transcript variant X3
LysM domain containing 4, transcript variant X1
lysM and putative peptidoglycan-binding domain-containing protein 4 isoform X1
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LysM domain containing 4, transcript variant X2
lysM and putative peptidoglycan-binding domain-containing protein 4 isoform X2
myocyte enhancer factor 2A, transcript variant X2
myocyte enhancer factor 2A, transcript variant X6
myocyte enhancer factor 2A, transcript variant X4
myocyte enhancer factor 2A, transcript variant X1
myocyte enhancer factor 2A, transcript variant X7
myocyte enhancer factor 2A, transcript variant X5
myocyte enhancer factor 2A, transcript variant X3
myocyte enhancer factor 2A, transcript variant X8
myocyte-specific enhancer factor 2A isoform X5
myocyte-specific enhancer factor 2A isoform X3
myocyte-specific enhancer factor 2A isoform X1
myocyte-specific enhancer factor 2A isoform X6
myocyte-specific enhancer factor 2A isoform X4
myocyte-specific enhancer factor 2A isoform X2
myocyte-specific enhancer factor 2A isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
leucine rich repeat containing 28, transcript variant X2
leucine rich repeat containing 28, transcript variant X3
leucine rich repeat containing 28, transcript variant X1
leucine rich repeat containing 28, transcript variant X4
leucine-rich repeat-containing protein 28 isoform X2
leucine-rich repeat-containing protein 28 isoform X1
leucine-rich repeat-containing protein 28 isoform X3
pyroglutamyl-peptidase I like, transcript variant X1
pyroglutamyl-peptidase I like, transcript variant X2
pyroglutamyl-peptidase 1-like protein isoform X1
pyroglutamyl-peptidase 1-like protein isoform X2
protein FAM169B-like, transcript variant X2
protein FAM169B-like, transcript variant X1
protein FAM169B-like, transcript variant X3
nuclear receptor subfamily 2 group F member 2, transcript variant X4
nuclear receptor subfamily 2 group F member 2, transcript variant X3
nuclear receptor subfamily 2 group F member 2, transcript variant X1
nuclear receptor subfamily 2 group F member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
multiple C2 and transmembrane domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
multiple C2 and transmembrane domain-containing protein 2
repulsive guidance molecule BMP co-receptor a
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: 25 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 3 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; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: repulsive guidance molecule A
chromodomain-helicase-DNA-binding protein 2-like
chromodomain helicase DNA binding protein 2, transcript variant X1
chromodomain-helicase-DNA-binding protein 2 isoform X1
chromodomain helicase DNA binding protein 2, transcript variant X2
chromodomain-helicase-DNA-binding protein 2 isoform X2
chromodomain helicase DNA binding protein 2, 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 4 samples with support for all annotated introns
chromodomain-helicase-DNA-binding protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
F-actin-capping protein subunit alpha-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 32% coverage of the annotated genomic feature by RNAseq alignments
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2, transcript variant X2
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2, transcript variant X1
alpha-2,8-sialyltransferase 8B isoform X2
alpha-2,8-sialyltransferase 8B isoform X1
solute carrier organic anion transporter family member 3A1
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: solute carrier organic anion transporter family member 3A1
synaptic vesicle glycoprotein 2B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
synaptic vesicle glycoprotein 2B, 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 2 samples with support for all annotated introns
synaptic vesicle glycoprotein 2B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
synaptic vesicle glycoprotein 2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
synaptic vesicle glycoprotein 2B, transcript variant X3
ankyrin repeat and death domain containing 1A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ankyrin repeat and death domain-containing protein 1A
SPG21 abhydrolase domain containing, maspardin