Aythya fuligula isolate bAytFul2 chromosome 10, bAytFul2.pri, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Galloanserae; Anseriformes; Anatidae; Aythyinae; Aythya.
REFSEQ INFORMATION: The reference sequence is identical to\nCM020309.1.\nAssembly name: bAytFul2.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2019/12/31. The original whole-genome shotgun project has the\naccession WNMM00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 20-SEP-2019\nAssembly Method :: FALCON v. 2018.31.08-03.06; FALCON-Unzip\n v. 6.0.0.47841; purge_haplotigs v.\n v1.0.3+ 1.Nov.2018; scaff10x v. 4.1.0;\n Bionano Solve DLS v. 3.2.1; Salsa HiC v.\n 2.2; Arrow smrtanalysis Pacbio polishing\n & gap filling v. 6.0.0.47841; longranger\n align v. 2.2.2; freebayes Illumina\n polishing v. 1.3; gEVAL manual curation\n v. 2019-09-20; VGP assembly pipeline\n individual v. 1.5\nAssembly Name :: bAytFul2.pri\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 64.03x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Aythya fuligula Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.3\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Patrik Ellstrom, Mahmoud Naguib, Josef Jarhult
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: 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: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
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: homeobox expressed in ES cells 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
Rho guanine nucleotide exchange factor 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 3 isoform X4
Rho guanine nucleotide exchange factor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
rho guanine nucleotide exchange factor 3 isoform X2
Rho guanine nucleotide exchange factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
rho guanine nucleotide exchange factor 3 isoform X1
Rho guanine nucleotide exchange factor 3, transcript variant X3
rho guanine nucleotide exchange factor 3 isoform X3
transcription activation suppressor, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription activation suppressor, 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 3 samples with support for all annotated introns
transcription activation suppressor, 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
transcription activation suppressor, transcript variant X3
transcription activation suppressor, transcript variant X4
transcription activation suppressor, transcript variant X7
transcription activation suppressor, transcript variant X5
coiled-coil domain containing 66, transcript variant X3
coiled-coil domain containing 66, transcript variant X2
coiled-coil domain containing 66, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain containing 66, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain containing 66, transcript variant X1
coiled-coil domain-containing protein 66 isoform X2
coiled-coil domain-containing protein 66 isoform X1
ELKS/RAB6-interacting/CAST family member 2, transcript variant X1
ELKS/RAB6-interacting/CAST family member 2, transcript variant X3
ELKS/RAB6-interacting/CAST family member 2, transcript variant X4
ELKS/RAB6-interacting/CAST family member 2, transcript variant X6
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
ELKS/RAB6-interacting/CAST family member 2, transcript variant X7
ELKS/RAB6-interacting/CAST family member 2, transcript variant X5
ELKS/RAB6-interacting/CAST family member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium voltage-gated channel auxiliary subunit alpha2delta 3, transcript variant X8
calcium voltage-gated channel auxiliary subunit alpha2delta 3, 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
calcium voltage-gated channel auxiliary subunit alpha2delta 3, transcript variant X1
calcium voltage-gated channel auxiliary subunit alpha2delta 3, transcript variant X4
calcium voltage-gated channel auxiliary subunit alpha2delta 3, transcript variant X5
calcium voltage-gated channel auxiliary subunit alpha2delta 3, transcript variant X3
calcium voltage-gated channel auxiliary subunit alpha2delta 3, transcript variant X6
calcium voltage-gated channel auxiliary subunit alpha2delta 3, transcript variant X7
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X3
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X4
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X1
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X5
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X6
leucine rich repeats and transmembrane domains 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
leucine-rich repeat and transmembrane domain-containing protein 1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium voltage-gated channel subunit alpha1 D
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 9 bases in 7 codons; deleted 6 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 9 bases in 7 codons; deleted 6 bases in 6 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: voltage-dependent L-type calcium channel subunit alpha-1D
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphoenolpyruvate carboxykinase [GTP], mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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: phosphoenolpyruvate carboxykinase [GTP], mitochondrial-like
zinc finger CCCH domain-containing protein 11A-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: 4 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: zinc finger CCCH domain-containing protein 11A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 40, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protein 40, transcript variant X1
BICD cargo adaptor 2, 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 3 samples with support for all annotated introns
BICD cargo adaptor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BICD cargo adaptor 2, transcript variant X3
BICD cargo adaptor 2, transcript variant X4
BICD cargo adaptor 2, transcript variant X5
BICD cargo adaptor 2, transcript variant X6
FYVE, RhoGEF and PH domain containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
FYVE, RhoGEF and PH domain-containing protein 3 isoform X1
FYVE, RhoGEF and PH domain containing 3, transcript variant X2
FYVE, RhoGEF and PH domain containing 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FYVE, RhoGEF and PH domain-containing protein 3 isoform X2
FYVE, RhoGEF and PH domain-containing protein 3 isoform X4
FYVE, RhoGEF and PH domain containing 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
FYVE, RhoGEF and PH domain-containing protein 3 isoform X3
FYVE, RhoGEF and PH domain containing 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FYVE, RhoGEF and PH domain-containing protein 3 isoform X5
sushi domain containing 3, transcript variant X1
sushi domain-containing protein 3 isoform X1
sushi domain containing 3, transcript variant X2
sushi domain-containing protein 3 isoform X2
caspase recruitment domain family member 19, transcript variant X3
caspase recruitment domain family member 19, transcript variant X2
caspase recruitment domain-containing protein 19 isoform X2
caspase recruitment domain family member 19, transcript variant X1
caspase recruitment domain family member 19, transcript variant X4
caspase recruitment domain-containing protein 19 isoform X3
caspase recruitment domain-containing protein 19 isoform 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 3 samples with support for all annotated introns
WNK lysine deficient protein kinase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
WNK lysine deficient protein kinase 2, transcript variant X1
WNK lysine deficient protein kinase 2, transcript variant X3
WNK lysine deficient protein kinase 2, transcript variant X2
WNK lysine deficient protein kinase 2, transcript variant X5
WNK lysine deficient protein kinase 2, transcript variant X6
serine/threonine-protein kinase WNK2 isoform X4
serine/threonine-protein kinase WNK2 isoform X1
serine/threonine-protein kinase WNK2 isoform X3
serine/threonine-protein kinase WNK2 isoform X2
serine/threonine-protein kinase WNK2 isoform X5
serine/threonine-protein kinase WNK2 isoform X6
family with sequence similarity 120A, transcript variant X1
family with sequence similarity 120A, transcript variant X2
constitutive coactivator of PPAR-gamma-like protein 1 isoform X1
constitutive coactivator of PPAR-gamma-like protein 1 isoform X2
PHD finger protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
PHD finger protein 2, transcript variant X2
lysine-specific demethylase PHF2 isoform X1
lysine-specific demethylase PHF2 isoform X2
protein tyrosine phosphatase domain containing 1, transcript variant X5
protein tyrosine phosphatase domain-containing protein 1 isoform X4
protein tyrosine phosphatase domain containing 1, transcript variant X2
protein tyrosine phosphatase domain containing 1, transcript variant X4
protein tyrosine phosphatase domain containing 1, transcript variant X3
protein tyrosine phosphatase domain containing 1, transcript variant X1
protein tyrosine phosphatase domain-containing protein 1 isoform X1
protein tyrosine phosphatase domain-containing protein 1 isoform X2
protein tyrosine phosphatase domain-containing protein 1 isoform X3
protein tyrosine phosphatase domain containing 1, transcript variant X6
protein tyrosine phosphatase domain-containing protein 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
uncharacterized LOC116493043, transcript variant X3
uncharacterized LOC116493043, transcript variant X2
uncharacterized LOC116493043, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
histone deacetylase 11, transcript variant X1
histone deacetylase 11, transcript variant X4
histone deacetylase 11, transcript variant X7
histone deacetylase 11, transcript variant X3
histone deacetylase 11, transcript variant X5
histone deacetylase 11, transcript variant X6
histone deacetylase 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
IQ motif and Sec7 domain ArfGEF 1, transcript variant X10
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
IQ motif and Sec7 domain ArfGEF 1, transcript variant X1
IQ motif and Sec7 domain ArfGEF 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
IQ motif and Sec7 domain ArfGEF 1, transcript variant X3
IQ motif and Sec7 domain ArfGEF 1, transcript variant X4
IQ motif and Sec7 domain ArfGEF 1, transcript variant X5
IQ motif and SEC7 domain-containing protein 1 isoform X1
IQ motif and SEC7 domain-containing protein 1 isoform X2
IQ motif and SEC7 domain-containing protein 1 isoform X3
IQ motif and SEC7 domain-containing protein 1 isoform X4
IQ motif and SEC7 domain-containing protein 1 isoform X5
IQ motif and SEC7 domain-containing protein 1 isoform X10
IQ motif and Sec7 domain ArfGEF 1, transcript variant X9
IQ motif and SEC7 domain-containing protein 1 isoform X9
IQ motif and Sec7 domain ArfGEF 1, transcript variant X6
IQ motif and SEC7 domain-containing protein 1 isoform X6
IQ motif and Sec7 domain ArfGEF 1, transcript variant X7
IQ motif and Sec7 domain ArfGEF 1, transcript variant X8
IQ motif and SEC7 domain-containing protein 1 isoform X7
IQ motif and SEC7 domain-containing protein 1 isoform X8
complex I assembly factor ACAD9, mitochondrial
cilia and flagella associated protein 92
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein KIAA1257 homolog
EF-hand and coiled-coil domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
EF-hand and coiled-coil domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
haloacid dehalogenase-like hydrolase domain-containing 5
CCHC-type zinc finger nucleic acid binding protein, transcript variant X1
CCHC-type zinc finger nucleic acid binding protein, transcript variant X3
CCHC-type zinc finger nucleic acid binding protein, transcript variant X2
CCHC-type zinc finger nucleic acid binding protein, transcript variant X4
cellular nucleic acid-binding protein isoform X4
cellular nucleic acid-binding protein isoform X3
cellular nucleic acid-binding protein isoform X2
cellular nucleic acid-binding protein isoform X1
Raf-1 proto-oncogene, serine/threonine kinase, transcript variant X1
Raf-1 proto-oncogene, serine/threonine kinase, transcript variant X2
RAF proto-oncogene serine/threonine-protein kinase isoform X1
RAF proto-oncogene serine/threonine-protein kinase isoform X2
Raf-1 proto-oncogene, serine/threonine kinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Raf-1 proto-oncogene, serine/threonine kinase, transcript variant X4
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
RAF proto-oncogene serine/threonine-protein kinase isoform X3
RAF proto-oncogene serine/threonine-protein kinase isoform X4
makorin ring finger protein 2, transcript variant X2
makorin ring finger protein 2, transcript variant X1
probable E3 ubiquitin-protein ligase makorin-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxisome proliferator activated receptor gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
peroxisome proliferator-activated receptor gamma
TAM41 mitochondrial translocator assembly and maintenance homolog
phosphatidate cytidylyltransferase, mitochondrial
vestigial like family member 4, transcript variant X2
transcription cofactor vestigial-like protein 4 isoform X2
vestigial like family member 4, transcript variant X1
transcription cofactor vestigial-like protein 4 isoform X1
vestigial like family member 4, transcript variant X4
vestigial like family member 4, transcript variant X3
transcription cofactor vestigial-like protein 4 isoform X3
autophagy related 7, transcript variant X3
autophagy related 7, transcript variant X1
autophagy related 7, transcript variant X2
ubiquitin-like modifier-activating enzyme ATG7 isoform X2
ubiquitin-like modifier-activating enzyme ATG7 isoform X1
histamine receptor H1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histamine receptor H1, transcript variant X1
solute carrier family 6 member 1, 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
solute carrier family 6 member 1, transcript variant X2
sodium- and chloride-dependent GABA transporter 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 3
ATPase plasma membrane Ca2+ transporting 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
plasma membrane calcium-transporting ATPase 2
uncharacterized LOC116492957, transcript variant X1
uncharacterized LOC116492957, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01229
nucleolar protein 8, transcript variant X1
nucleolar protein 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 88% 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: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
shisa family member 5, transcript variant X1
shisa family member 5, transcript variant X2
ring finger protein 123, transcript variant X1
E3 ubiquitin-protein ligase RNF123 isoform X1
ring finger protein 123, transcript variant X2
E3 ubiquitin-protein ligase RNF123 isoform X2
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, including 3 samples with support for all annotated introns
mannose-1-phosphate guanyltransferase beta
inositol hexakisphosphate kinase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inositol hexakisphosphate kinase 1, transcript variant X1
inositol hexakisphosphate kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin like modifier activating enzyme 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-like modifier-activating enzyme 7
T-cell leukemia translocation-altered gene protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% 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: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% 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: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 58% 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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: acylamino-acid-releasing enzyme
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
TRAF interacting protein, transcript variant X2
TRAF interacting protein, transcript variant X1
TRAF interacting protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin-protein ligase TRAIP isoform X2
E3 ubiquitin-protein ligase TRAIP isoform X1
E3 ubiquitin-protein ligase TRAIP isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
caM kinase-like vesicle-associated protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
MON1 homolog A, secretory trafficking associated, transcript variant X2
MON1 homolog A, secretory trafficking associated, transcript variant X1
vacuolar fusion protein MON1 homolog A isoform X2
vacuolar fusion protein MON1 homolog A isoform X1
RNA binding motif protein 6, transcript variant X1
RNA binding motif protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
BRICK1 subunit of SCAR/WAVE actin nucleating complex
glutathione peroxidase 1, transcript variant X2
glutathione peroxidase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
testis expressed 264, ER-phagy receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
testis expressed 264, ER-phagy receptor, transcript variant X3
testis expressed 264, ER-phagy receptor, transcript variant X2
testis expressed 264, ER-phagy receptor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ribosomal RNA processing 9, U3 small nucleolar RNA binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
U3 small nucleolar RNA-interacting protein 2
troponin C1, slow skeletal and cardiac type
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
troponin C, slow skeletal and cardiac muscles
5'-nucleotidase domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein-like 3
COORDINATES: nucleotide motif:Rfam:12.0:RF00569
COORDINATES: nucleotide motif:Rfam:12.0:RF00574
glycosyltransferase 8 domain containing 1
glycosyltransferase 8 domain-containing protein 1
NIMA related kinase 4, transcript variant X2
NIMA related kinase 4, transcript variant X1
NIMA related kinase 4, transcript variant X3
NIMA related kinase 4, transcript variant X4
serine/threonine-protein kinase Nek4 isoform X2
serine/threonine-protein kinase Nek4 isoform X1
serine/threonine-protein kinase Nek4 isoform X3
inter-alpha-trypsin inhibitor heavy chain H3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
inter-alpha-trypsin inhibitor heavy chain 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
inter-alpha-trypsin inhibitor heavy chain H4
musculoskeletal embryonic nuclear protein 1, transcript variant X1
musculoskeletal embryonic nuclear protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
store-operated calcium entry regulator STIMATE isoform X2
musculoskeletal embryonic nuclear protein 1 isoform X1
scm-like with four MBT domains protein 1
protein kinase C delta, transcript variant X1
protein kinase C delta, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 4, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 4, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 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 1 sample with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4 isoform X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4 isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4 isoform X3
6-phosphofructo-2-kinase/fructose-2, 6-biphosphatase 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 62% 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 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tumor suppressor 2, mitochondrial calcium regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras association domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYND domain-containing protein 10
cytochrome b561 domain-containing protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome b561 domain-containing protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytochrome b561 domain-containing protein 2 isoform X1
cytochrome b561 domain-containing protein 2 isoform X2
calcium voltage-gated channel auxiliary subunit alpha2delta 2, transcript variant X4
calcium voltage-gated channel auxiliary subunit alpha2delta 2, transcript variant X2
calcium voltage-gated channel auxiliary subunit alpha2delta 2, transcript variant X3
calcium voltage-gated channel auxiliary subunit alpha2delta 2, transcript variant X1
calcium voltage-gated channel auxiliary subunit alpha2delta 2, transcript variant X5
voltage-dependent calcium channel subunit alpha-2/delta-2 isoform X4
voltage-dependent calcium channel subunit alpha-2/delta-2 isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-2 isoform X3
voltage-dependent calcium channel subunit alpha-2/delta-2 isoform X1
voltage-dependent calcium channel subunit alpha-2/delta-2 isoform X5
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
chromosome 10 C3orf18 homolog, transcript variant X1
chromosome 10 C3orf18 homolog, transcript variant X3
chromosome 10 C3orf18 homolog, transcript variant X2
HemK methyltransferase family member 1, transcript variant X2
HemK methyltransferase family member 1, transcript variant X1
MTRF1L release factor glutamine methyltransferase
cytokine inducible SH2 containing protein
cytokine-inducible SH2-containing protein
MAPK activated protein kinase 3, transcript variant X2
MAPK activated protein kinase 3, transcript variant X1
dedicator of cytokinesis 3, transcript variant X1
dedicator of cytokinesis 3, transcript variant X2
dedicator of cytokinesis 3, transcript variant X3
dedicator of cytokinesis 3, transcript variant X4
dedicator of cytokinesis 3, transcript variant X5
dedicator of cytokinesis 3, transcript variant X8
dedicator of cytokinesis 3, transcript variant X6
dedicator of cytokinesis 3, transcript variant X7
dedicator of cytokinesis 3, transcript variant X10
dedicator of cytokinesis 3, transcript variant X9
dedicator of cytokinesis protein 3 isoform X1
dedicator of cytokinesis protein 3 isoform X2
dedicator of cytokinesis protein 3 isoform X8
dedicator of cytokinesis protein 3 isoform X3
dedicator of cytokinesis protein 3 isoform X6
dedicator of cytokinesis protein 3 isoform X9
dedicator of cytokinesis protein 3 isoform X7
dedicator of cytokinesis protein 3 isoform X4
dedicator of cytokinesis protein 3 isoform X10
dedicator of cytokinesis protein 3 isoform X5
mesencephalic astrocyte derived neurotrophic factor
mesencephalic astrocyte-derived neurotrophic factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 80, NatH catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 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: 19 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine rich single-pass membrane protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 25% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich single-pass membrane protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
2'-5'-oligoadenylate synthase-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium-coupled neutral amino acid transporter 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
guanine nucleotide-binding protein G(i) subunit alpha-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(t) subunit alpha-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 3 samples with support for all annotated introns
RNA binding motif protein 5, transcript variant X2
RNA binding motif protein 5, transcript variant X1
poly(ADP-ribose) polymerase family member 3
protein mono-ADP-ribosyltransferase PARP3
aminoacylase-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
aminoacylase-1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aminoacylase-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
aminoacylase-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BRCA1 associated protein 1, transcript variant X1
BRCA1 associated protein 1, transcript variant X2
ubiquitin carboxyl-terminal hydrolase BAP1 isoform X1
ubiquitin carboxyl-terminal hydrolase BAP1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dynein heavy chain 1, axonemal
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein phosphatase, Mg2+/Mn2+ dependent 1M
twinfilin actin binding protein 2, transcript variant X1
twinfilin actin binding protein 2, transcript variant X2
twinfilin actin binding protein 2, transcript variant X3
5-aminolevulinate synthase, nonspecific, mitochondrial
ankyrin repeat and SOCS box containing 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 37% 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 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: 10 Proteins, and 92% 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: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sarcolemma associated protein, transcript variant X3
sarcolemma associated protein, transcript variant X11
sarcolemma associated protein, transcript variant X15
sarcolemma associated protein, transcript variant X6
sarcolemma associated protein, transcript variant X4
sarcolemma associated protein, transcript variant X13
sarcolemma associated protein, transcript variant X17
sarcolemma associated protein, transcript variant X1
sarcolemma associated protein, transcript variant X10
sarcolemma associated protein, transcript variant X9
sarcolemma associated protein, transcript variant X2
sarcolemma associated protein, transcript variant X12
sarcolemma associated protein, transcript variant X16
sarcolemma associated protein, transcript variant X5
sarcolemma associated protein, transcript variant X14
sarcolemma associated protein, transcript variant X18
sarcolemma associated protein, transcript variant X7
sarcolemma associated protein, transcript variant X8
sarcolemmal membrane-associated protein isoform X3
sarcolemmal membrane-associated protein isoform X1
sarcolemmal membrane-associated protein isoform X11
sarcolemmal membrane-associated protein isoform X6
sarcolemmal membrane-associated protein isoform X7
sarcolemmal membrane-associated protein isoform X10
sarcolemmal membrane-associated protein isoform X4
sarcolemmal membrane-associated protein isoform X9
sarcolemmal membrane-associated protein isoform X13
sarcolemmal membrane-associated protein isoform X17
sarcolemmal membrane-associated protein isoform X2
sarcolemmal membrane-associated protein isoform X12
sarcolemmal membrane-associated protein isoform X8
sarcolemmal membrane-associated protein isoform X16
sarcolemmal membrane-associated protein isoform X5
sarcolemmal membrane-associated protein isoform X15
sarcolemmal membrane-associated protein isoform X14
sarcolemmal membrane-associated protein isoform X18
sarcolemma associated protein, transcript variant X19
sarcolemmal membrane-associated protein isoform X19
sarcolemma associated protein, transcript variant X20
sarcolemmal membrane-associated protein isoform X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
abhydrolase domain containing 6, acylglycerol lipase, transcript variant X2
abhydrolase domain containing 6, acylglycerol lipase, transcript variant X1
cadherin EGF LAG seven-pass G-type receptor 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
cytochrome b-c1 complex subunit 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxymethylcytosine binding, ES cell specific
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
RAB7A, member RAS oncogene family, transcript variant X2
RAB7A, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DnaJ heat shock protein family (Hsp40) member B8
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
LOW QUALITY PROTEIN: dnaJ homolog subfamily B member 8
eukaryotic elongation factor, selenocysteine-tRNA specific, transcript variant X1
eukaryotic elongation factor, selenocysteine-tRNA specific, transcript variant X2
eukaryotic elongation factor, selenocysteine-tRNA specific, transcript variant X4
eukaryotic elongation factor, selenocysteine-tRNA specific, transcript variant X3
selenocysteine-specific elongation factor isoform X1
selenocysteine-specific elongation factor isoform X2
protein transport protein Sec61 subunit alpha
kelch repeat and BTB domain containing 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
kelch repeat and BTB domain-containing protein 12
ankyrin repeat and BTB domain containing 1
ankyrin repeat and BTB/POZ domain-containing protein 1
minichromosome maintenance complex component 2
transmembrane protein adipocyte associated 1, transcript variant X1
transmembrane protein adipocyte associated 1, transcript variant X4
transmembrane protein adipocyte associated 1, transcript variant X3
transmembrane protein adipocyte associated 1, transcript variant X2
transmembrane protein adipocyte-associated 1
coiled-coil-helix-coiled-coil-helix domain containing 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% 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: tRNAscan-SE.
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 41 member 3, transcript variant X4
solute carrier family 41 member 3, transcript variant X3
solute carrier family 41 member 3, transcript variant X1
solute carrier family 41 member 3, transcript variant X2
solute carrier family 41 member 3 isoform X1
solute carrier family 41 member 3 isoform X2
Kruppel like factor 15, transcript variant X1
Kruppel like factor 15, transcript variant X2
cilia and flagella associated protein 100
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 100
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 55% 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 2 samples with support for all annotated introns
coiled-coil-helix-coiled-coil-helix domain containing 4
mitochondrial intermembrane space import and assembly protein 40
XPC complex subunit, DNA damage recognition and repair factor, transcript variant X1
DNA repair protein complementing XP-C cells isoform X1
XPC complex subunit, DNA damage recognition and repair factor, transcript variant X2
DNA repair protein complementing XP-C cells isoform X2
LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated
U6 snRNA-associated Sm-like protein LSm3
uncharacterized LOC116493178, transcript variant X1
uncharacterized LOC116493178, transcript variant X2
solute carrier family 6 member 6, transcript variant X3
solute carrier family 6 member 6, transcript variant X4
solute carrier family 6 member 6, transcript variant X7
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
solute carrier family 6 member 6, transcript variant X1
solute carrier family 6 member 6, transcript variant X2
sodium- and chloride-dependent taurine transporter isoform X1
sodium- and chloride-dependent taurine transporter isoform X2
solute carrier family 6 member 6, transcript variant X5
sodium- and chloride-dependent taurine transporter isoform X3
solute carrier family 6 member 6, transcript variant X6
sodium- and chloride-dependent taurine transporter isoform X4
glutamate receptor interacting protein 2
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
glutamate receptor-interacting protein 2
coiled-coil domain containing 174, transcript variant X1
coiled-coil domain containing 174, transcript variant X2
coiled-coil domain-containing protein 174 isoform X1
coiled-coil domain-containing protein 174 isoform X2
coiled-coil domain containing 51, transcript variant X1
coiled-coil domain containing 51, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 24% coverage of the annotated genomic feature by RNAseq alignments
SET domain containing 5, transcript variant X1
SET domain containing 5, transcript variant X2
SET domain containing 5, transcript variant X5
SET domain containing 5, transcript variant X4
histone-lysine N-methyltransferase SETD5 isoform X1
histone-lysine N-methyltransferase SETD5 isoform X2
histone-lysine N-methyltransferase SETD5 isoform X4
SET domain containing 5, transcript variant X3
histone-lysine N-methyltransferase SETD5 isoform X3
LHFPL tetraspan subfamily member 4 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
bromodomain and PHD finger containing 1, transcript variant X1
bromodomain and PHD finger containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
calcium/calmodulin dependent protein kinase I
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type 1
actin related protein 2/3 complex subunit 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
actin-related protein 2/3 complex subunit 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 5% 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 70% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial mRNA pseudouridine synthase RPUSD3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 44% 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 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: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
coiled-coil domain-containing protein 71
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 19, transcript variant X4
ubiquitin specific peptidase 19, transcript variant X5
ubiquitin specific peptidase 19, transcript variant X1
ubiquitin specific peptidase 19, transcript variant X3
ubiquitin specific peptidase 19, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 19 isoform X3
ubiquitin carboxyl-terminal hydrolase 19 isoform X4
ubiquitin carboxyl-terminal hydrolase 19 isoform X1
ubiquitin carboxyl-terminal hydrolase 19 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium- and chloride-dependent creatine transporter 1
epidermal differentiation-specific protein-like
inosine monophosphate dehydrogenase 2, transcript variant X1
inosine monophosphate dehydrogenase 2, transcript variant X2
inosine-5'-monophosphate dehydrogenase 2 isoform X1
inosine-5'-monophosphate dehydrogenase 2 isoform X2
NADH:ubiquinone oxidoreductase complex assembly factor 3
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3
DALR anticodon binding domain containing 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
DALR anticodon-binding domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 52% 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: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ariadne RBR E3 ubiquitin protein ligase 2, transcript variant X3
ariadne RBR E3 ubiquitin protein ligase 2, transcript variant X1
ariadne RBR E3 ubiquitin protein ligase 2, transcript variant X2
mitochondrial carnitine/acylcarnitine carrier protein
protein kinase cAMP-dependent type II regulatory subunit alpha
cAMP-dependent protein kinase type II-alpha regulatory subunit
hydroxyacyl-thioester dehydratase type 2
hydroxyacyl-thioester dehydratase type 2, mitochondrial
PX domain containing serine/threonine kinase like, transcript variant X1
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 3 samples with support for all annotated introns
PX domain containing serine/threonine kinase like, transcript variant X2
PX domain containing serine/threonine kinase like, transcript variant X4
PX domain containing serine/threonine kinase like, transcript variant X5
PX domain containing serine/threonine kinase like, transcript variant X6
PX domain containing serine/threonine kinase like, transcript variant X3
PX domain-containing protein kinase-like protein isoform X1
PX domain-containing protein kinase-like protein isoform X2
PX domain-containing protein kinase-like protein isoform X4
PX domain-containing protein kinase-like protein isoform X5
PX domain-containing protein kinase-like protein isoform X3
pyruvate dehydrogenase E1 component subunit beta, mitochondrial
potassium channel tetramerization domain containing 6, transcript variant X1
potassium channel tetramerization domain containing 6, transcript variant X2
potassium channel tetramerization domain containing 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
family with sequence similarity 107 member A
FAM3 metabolism regulating signaling molecule D
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
chromosome 10 C3orf67 homolog, transcript variant X2
chromosome 10 C3orf67 homolog, transcript variant X3
chromosome 10 C3orf67 homolog, transcript variant X4
chromosome 10 C3orf67 homolog, transcript variant X1
uncharacterized protein C3orf67 homolog isoform X2
uncharacterized protein C3orf67 homolog isoform X1
fragile histidine triad diadenosine triphosphatase
protein tyrosine phosphatase receptor type G
receptor-type tyrosine-protein phosphatase gamma
chromosome 10 C3orf14 homolog, transcript variant X1
chromosome 10 C3orf14 homolog, transcript variant X2
uncharacterized protein C3orf14 homolog isoform X1
uncharacterized protein C3orf14 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
calcium dependent secretion activator, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium dependent secretion activator, transcript variant X4
calcium dependent secretion activator, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium dependent secretion activator, transcript variant X2
calcium dependent secretion activator, transcript variant X1
calcium-dependent secretion activator 1 isoform X5
calcium-dependent secretion activator 1 isoform X4
calcium-dependent secretion activator 1 isoform X3
calcium-dependent secretion activator 1 isoform X2
calcium-dependent secretion activator 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 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: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 9, transcript variant X1
ADAM metallopeptidase with thrombospondin type 1 motif 9, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 9 isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 9 isoform X2
ADAM metallopeptidase with thrombospondin type 1 motif 9, transcript variant X3
A disintegrin and metalloproteinase with thrombospondin motifs 9 isoform X3
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X6
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X9
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X8
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X7
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X5
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X1
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
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X10
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X6
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X3
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X9
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X8
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X7
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X5
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X2
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X4
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X1
membrane associated guanylate kinase, WW and PDZ domain containing 1, transcript variant X11
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
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 isoform X11
S-adenosylmethionine mitochondrial carrier protein
leucine rich repeats and immunoglobulin like domains 1
leucine-rich repeats and immunoglobulin-like domains protein 1
kelch repeat and BTB domain containing 8
kelch repeat and BTB domain-containing protein 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
succinate-CoA ligase GDP-forming subunit beta
succinate--CoA ligase [GDP-forming] subunit beta, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
EGF domain specific O-linked N-acetylglucosamine transferase, transcript variant X2
EGF domain specific O-linked N-acetylglucosamine transferase, transcript variant X1
EGF domain-specific O-linked N-acetylglucosamine transferase
ubiquitin like modifier activating enzyme 3, transcript variant X1
ubiquitin like modifier activating enzyme 3, transcript variant X2
ubiquitin like modifier activating enzyme 3, transcript variant X3
ubiquitin like modifier activating enzyme 3, transcript variant X4
NEDD8-activating enzyme E1 catalytic subunit isoform X2
NEDD8-activating enzyme E1 catalytic subunit isoform X1
NEDD8-activating enzyme E1 catalytic subunit isoform X3
ADP ribosylation factor like GTPase 6 interacting protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
melanocyte inducing transcription factor, transcript variant X1
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 3 samples with support for all annotated introns
melanocyte inducing transcription factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
melanocyte inducing transcription factor, transcript variant X3
melanocyte inducing transcription factor, transcript variant X4
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 3 samples with support for all annotated introns
microphthalmia-associated transcription factor isoform X1
microphthalmia-associated transcription factor isoform X2
microphthalmia-associated transcription factor isoform X3
microphthalmia-associated transcription factor isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 19% coverage of the annotated genomic feature by RNAseq alignments
MyoD family inhibitor domain containing 2, transcript variant X2
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
MyoD family inhibitor domain containing 2, transcript variant X1
myoD family inhibitor domain-containing protein 2 isoform X2
myoD family inhibitor domain-containing protein 2 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
eukaryotic translation initiation factor 4E family member 3, transcript variant X1
eukaryotic translation initiation factor 4E family member 3, transcript variant X2
eukaryotic translation initiation factor 4E type 3 isoform X1
eukaryotic translation initiation factor 4E type 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 6 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
SHQ1, H/ACA ribonucleoprotein assembly factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 4 regulatory subunit 2
serine/threonine-protein phosphatase 4 regulatory subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cell adhesion molecule L1 like, transcript variant X7
cell adhesion molecule L1 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cell adhesion molecule L1 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cell adhesion molecule L1 like, transcript variant X4
cell adhesion molecule L1 like, transcript variant X8
cell adhesion molecule L1 like, transcript variant X6
cell adhesion molecule L1 like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cell adhesion molecule L1 like, transcript variant X3
neural cell adhesion molecule L1-like protein isoform X4
neural cell adhesion molecule L1-like protein isoform X1
neural cell adhesion molecule L1-like protein isoform X2
neural cell adhesion molecule L1-like protein isoform X5
neural cell adhesion molecule L1-like protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
tRNA nucleotidyl transferase 1, transcript variant X2
tRNA nucleotidyl transferase 1, transcript variant X1
CCA tRNA nucleotidyltransferase 1, mitochondrial isoform X1
CCA tRNA nucleotidyltransferase 1, mitochondrial isoform X2
leucine rich repeat neuronal 1, transcript variant X2
leucine rich repeat neuronal 1, transcript variant X1
histone-lysine N-methyltransferase SETMAR
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inositol 1,4,5-trisphosphate receptor type 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: inositol 1,4,5-trisphosphate receptor type 1
basic helix-loop-helix family member e40
class E basic helix-loop-helix protein 40
ER degradation enhancing alpha-mannosidase like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ER degradation-enhancing alpha-mannosidase-like protein 1
uncharacterized LOC116493249, transcript variant X1
uncharacterized LOC116493249, transcript variant X3
uncharacterized LOC116493249, transcript variant X2
glutamate metabotropic receptor 7, transcript variant X4
glutamate metabotropic receptor 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glutamate metabotropic receptor 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutamate metabotropic receptor 7, transcript variant X3
metabotropic glutamate receptor 7 isoform X2
metabotropic glutamate receptor 7 isoform X1
metabotropic glutamate receptor 7 isoform X3
LIM and cysteine rich domains 1, transcript variant X2
LIM and cysteine rich domains 1, transcript variant X1
LIM and cysteine rich domains 1, transcript variant X3
LIM and cysteine rich domains 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 67% 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: 11 Proteins, and 98% 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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SLIT-ROBO Rho GTPase activating protein 3, transcript variant X2
SLIT-ROBO Rho GTPase activating protein 3, transcript variant X1
SLIT-ROBO Rho GTPase-activating protein 3 isoform X2
SLIT-ROBO Rho GTPase-activating protein 3 isoform X1
SLIT-ROBO Rho GTPase activating protein 3, transcript variant X3
SLIT-ROBO Rho GTPase-activating protein 3 isoform X3
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, including 3 samples with support for all annotated introns
von Hippel-Lindau disease tumor suppressor
interleukin-1 receptor-associated kinase-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SEC13 homolog, nuclear pore and COPII coat complex component
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
cullin-associated NEDD8-dissociated protein 1-like
methyl-CpG binding domain 4, DNA glycosylase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
intraflagellar transport protein 122 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 Proteins, and 9% 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane and coiled-coil domain family 1, transcript variant X3
transmembrane and coiled-coil domain family 1, transcript variant X2
transmembrane and coiled-coil domain family 1, transcript variant X5
transmembrane and coiled-coil domain family 1, transcript variant X4
transmembrane and coiled-coil domain family 1, transcript variant X1
transmembrane and coiled-coil domain family 1, transcript variant X7
transmembrane and coiled-coil domain family 1, transcript variant X8
transmembrane and coiled-coil domain family 1, transcript variant X6
transmembrane and coiled-coil domains protein 1 isoform X1
transmembrane and coiled-coil domains protein 1 isoform X2
transmembrane and coiled-coil domains protein 1 isoform X4
transmembrane and coiled-coil domains protein 1 isoform X5
transmembrane and coiled-coil domains protein 1 isoform X3
rabenosyn, RAB effector, transcript variant X1
rabenosyn, RAB effector, transcript variant X2
28S ribosomal protein S25, mitochondrial
nuclear receptor subfamily 2 group C member 2, transcript variant X6
nuclear receptor subfamily 2 group C member 2, transcript variant X2
nuclear receptor subfamily 2 group C member 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor subfamily 2 group C member 2, transcript variant X3
nuclear receptor subfamily 2 group C member 2, transcript variant X1
nuclear receptor subfamily 2 group C member 2, transcript variant X5
nuclear receptor subfamily 2 group C member 2 isoform X1
nuclear receptor subfamily 2 group C member 2 isoform X2
FYVE, RhoGEF and PH domain-containing protein 5