Silurus meridionalis isolate SWU-2019-XX chromosome 29, ASM1480568v1, whole genome shotgun sequence.
Silurus meridionalis (Silurus soldatovi meridionalis)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Ostariophysi; Siluriformes; Siluridae; Silurus.
Chromosome-level assembly of southern catfish (silurus meridionalis) provides insights into visual adaptation to nocturnal and benthic lifestyles
REFSEQ INFORMATION: The reference sequence is identical to\nCM025913.1.\nAssembly name: ASM1480568v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Southwest University on\n2020/10/02. The original whole-genome shotgun project has the\naccession JABFDY000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Southwest University\nAssembly Method :: WTDBG v. 1.2.8\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 97.83x\nSequencing Technology :: Oxford Nanopore PromethION\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Silurus meridionalis Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X8
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
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X6
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
Rho guanine nucleotide exchange factor (GEF) 1a, 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 6 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X4
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X1
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X7
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X9
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X10
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 12 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 1a, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
rho guanine nucleotide exchange factor 1a isoform X8
rho guanine nucleotide exchange factor 1a isoform X6
rho guanine nucleotide exchange factor 1a isoform X5
rho guanine nucleotide exchange factor 1a isoform X3
rho guanine nucleotide exchange factor 1a isoform X2
rho guanine nucleotide exchange factor 1a isoform X4
rho guanine nucleotide exchange factor 1a isoform X1
rho guanine nucleotide exchange factor 1a isoform X7
rho guanine nucleotide exchange factor 1a isoform X9
rho guanine nucleotide exchange factor 1a isoform X10
rho guanine nucleotide exchange factor 1a isoform X12
rho guanine nucleotide exchange factor 1a isoform X11
death-associated protein kinase 2, transcript variant X1
death-associated protein kinase 2, transcript variant X4
death-associated protein kinase 2, transcript variant X2
death-associated protein kinase 2, transcript variant X3
uncharacterized protein si:ch73-109i22.2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: translocon-associated protein subunit beta
growth factor receptor-bound protein 10-like, transcript variant X3
growth factor receptor-bound protein 10-like, transcript variant X1
growth factor receptor-bound protein 10-like, transcript variant X2
growth factor receptor-bound protein 10-like, transcript variant X4
growth factor receptor-bound protein 10-like isoform X1
growth factor receptor-bound protein 10-like isoform X2
growth factor receptor-bound protein 10-like, transcript variant X5
growth factor receptor-bound protein 10-like isoform X3
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger DHHC-type palmitoyltransferase 18b, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 18b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
palmitoyltransferase ZDHHC18-B isoform X1
palmitoyltransferase ZDHHC18-B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC124382157, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124382157, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: opioid receptor, delta 1a
phosphatase and actin regulator 4a, transcript variant X4
phosphatase and actin regulator 4a, transcript variant X3
phosphatase and actin regulator 4a, transcript variant X5
phosphatase and actin regulator 4a, transcript variant X6
phosphatase and actin regulator 4a, transcript variant X2
phosphatase and actin regulator 4a, transcript variant X1
phosphatase and actin regulator 4a, transcript variant X7
phosphatase and actin regulator 4a, transcript variant X8
phosphatase and actin regulator 4A isoform X3
phosphatase and actin regulator 4A isoform X2
phosphatase and actin regulator 4A isoform X5
phosphatase and actin regulator 4A isoform X4
phosphatase and actin regulator 4A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor HIVEP3
protein tyrosine phosphatase receptor type Ua, transcript variant X2
protein tyrosine phosphatase receptor type Ua, transcript variant X5
protein tyrosine phosphatase receptor type Ua, transcript variant X4
protein tyrosine phosphatase receptor type Ua, transcript variant X3
protein tyrosine phosphatase receptor type Ua, transcript variant X1
receptor-type tyrosine-protein phosphatase U isoform X2
receptor-type tyrosine-protein phosphatase U isoform X5
receptor-type tyrosine-protein phosphatase U isoform X4
receptor-type tyrosine-protein phosphatase U isoform X3
receptor-type tyrosine-protein phosphatase U isoform X1
glucocorticoid modulatory element binding protein 1, transcript variant X3
glucocorticoid modulatory element binding protein 1, transcript variant X1
glucocorticoid modulatory element binding protein 1, transcript variant X2
glucocorticoid modulatory element-binding protein 1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
small nucleolar RNA SNORA16B/SNORA16A family
COORDINATES: nucleotide motif:Rfam:12.0:RF00190
COORDINATES: nucleotide motif:Rfam:12.0:RF00188
COORDINATES: nucleotide motif:Rfam:12.0:RF00608
Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 4a
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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein phosphatase 1, regulatory subunit 8a, transcript variant X2
protein phosphatase 1, regulatory subunit 8a, transcript variant X1
protein phosphatase 1, regulatory subunit 8a, transcript variant X3
protein phosphatase 1, regulatory subunit 8a, transcript variant X4
protein phosphatase 1, regulatory subunit 8a, transcript variant X5
protein phosphatase 1, regulatory subunit 8a, transcript variant X7
protein phosphatase 1, regulatory subunit 8a, transcript variant X8
protein phosphatase 1, regulatory subunit 8a, transcript variant X6
protein phosphatase 1, regulatory subunit 8a isoform X1
protein phosphatase 1, regulatory subunit 8a isoform X2
protein phosphatase 1, regulatory subunit 8a isoform X3
protein phosphatase 1, regulatory subunit 8a isoform X4
protein phosphatase 1, regulatory subunit 8a isoform X5
PDLIM1 interacting kinase 1 like, transcript variant X1
PDLIM1 interacting kinase 1 like, transcript variant X2
PDLIM1 interacting kinase 1 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycoprotein endo-alpha-1,2-mannosidase-like protein
ubiquitin-conjugating enzyme E2 E1, transcript variant X1
ubiquitin-conjugating enzyme E2 E2 isoform X1
ubiquitin-conjugating enzyme E2 E1, transcript variant X2
ubiquitin-conjugating enzyme E2 E1 isoform X2
NFKB inhibitor interacting Ras-like 1, transcript variant X1
NFKB inhibitor interacting Ras-like 1, transcript variant X6
NFKB inhibitor interacting Ras-like 1, transcript variant X3
NFKB inhibitor interacting Ras-like 1, transcript variant X4
NFKB inhibitor interacting Ras-like 1, transcript variant X5
NFKB inhibitor interacting Ras-like 1, transcript variant X2
NF-kappa-B inhibitor-interacting Ras-like protein 1
nuclear receptor subfamily 1, group D, member 2b
nuclear receptor subfamily 1 group D member 2b
thyroid hormone receptor beta, transcript variant X4
thyroid hormone receptor beta, transcript variant X5
thyroid hormone receptor beta, transcript variant X1
thyroid hormone receptor beta, transcript variant X2
thyroid hormone receptor beta, transcript variant X3
thyroid hormone receptor beta isoform X4
thyroid hormone receptor beta isoform X3
thyroid hormone receptor beta isoform X2
thyroid hormone receptor beta isoform X1
retinoic acid receptor beta-like, transcript variant X1
retinoic acid receptor beta-like isoform X1
retinoic acid receptor beta-like, transcript variant X2
retinoic acid receptor beta-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
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: peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase
activity-dependent neuroprotector homeobox protein 2b
ATPase H+ transporting V1 subunit C1b, transcript variant X1
ATPase H+ transporting V1 subunit C1b, transcript variant X2
brain and acute leukemia cytoplasmic protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
spire-type actin nucleation factor 1a, transcript variant X1
spire-type actin nucleation factor 1a, transcript variant X2
spire-type actin nucleation factor 1a, transcript variant X3
spire-type actin nucleation factor 1a, transcript variant X4
spire-type actin nucleation factor 1a, transcript variant X5
kelch-like family member 38a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
kelch-like family member 38a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
family with sequence similarity 91 member A1, transcript variant X1
family with sequence similarity 91 member A1, transcript variant X2
family with sequence similarity 91 member A1, transcript variant X3
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
CBY1 interacting BAR domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
CBY1 interacting BAR domain containing 1, transcript variant X1
triple QxxK/R motif containing, transcript variant X1
triple QxxK/R motif containing, transcript variant X2
triple QxxK/R motif containing, transcript variant X3
RUNX1 partner transcriptional co-repressor 1
leucine-rich repeat-containing protein 69
LOW QUALITY PROTEIN: deubiquitinase OTUD6B
zinc finger MYM-type containing 4, tandem duplicate 1, transcript variant X1
zinc finger MYM-type containing 4, tandem duplicate 1, transcript variant X2
zinc finger MYM-type containing 4, tandem duplicate 1, transcript variant X3
splicing factor proline/glutamine-rich, transcript variant X2
splicing factor proline/glutamine-rich, transcript variant X1
splicing factor, proline- and glutamine-rich
uncharacterized LOC124381948, transcript variant X1
adhesion G protein-coupled receptor B2, transcript variant X1
adhesion G protein-coupled receptor B2, transcript variant X5
adhesion G protein-coupled receptor B2, transcript variant X6
adhesion G protein-coupled receptor B2, transcript variant X2
adhesion G protein-coupled receptor B2, transcript variant X4
adhesion G protein-coupled receptor B2, transcript variant X7
adhesion G protein-coupled receptor B2, transcript variant X3
adhesion G protein-coupled receptor B2, transcript variant X8
uncharacterized LOC124381948, transcript variant X2
adhesion G protein-coupled receptor B2 isoform X1
adhesion G protein-coupled receptor B2 isoform X5
adhesion G protein-coupled receptor B2 isoform X6
adhesion G protein-coupled receptor B2 isoform X2
adhesion G protein-coupled receptor B2 isoform X4
adhesion G protein-coupled receptor B2 isoform X7
adhesion G protein-coupled receptor B2 isoform X3
adhesion G protein-coupled receptor B2 isoform X8
LOW QUALITY PROTEIN: collagen alpha-1(XVI) chain
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
PHD finger protein 14, transcript variant X3
PHD finger protein 14, transcript variant X4
PHD finger protein 14, transcript variant X1
PHD finger protein 14, transcript variant X2
thrombospondin, type I, domain containing 7Aa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
thrombospondin type-1 domain-containing protein 7A
intracellular protein transport protein USO1-like
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
CAP-Gly domain-containing linker protein 1-like
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
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
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 80% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: myosin-2 heavy chain-like
calponin homology domain-containing protein DDB_G0272472-like
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
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
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
trichohyalin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
trichohyalin-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphatidylinositol-4,5-bisphosphate 4-phosphatase 2
type 2 phosphatidylinositol 4,5-bisphosphate 4-phosphatase
N-terminal EF-hand calcium binding protein 1
N-terminal EF-hand calcium-binding protein 1
BCL2 associated athanogene 6, like, transcript variant X1
BCL2 associated athanogene 6, like, transcript variant X2
BCL2 associated athanogene 6, like, transcript variant X3
BCL2 associated athanogene 6, like, transcript variant X4
large proline-rich protein BAG6 isoform X1
large proline-rich protein BAG6 isoform X2
large proline-rich protein BAG6 isoform X3
large proline-rich protein BAG6 isoform X4
LOW QUALITY PROTEIN: uncharacterized protein C6orf136 homolog
ATP-binding cassette, sub-family F (GCN20), member 1, transcript variant X2
ATP-binding cassette, sub-family F (GCN20), member 1, transcript variant X1
ATP-binding cassette sub-family F member 1 isoform X1
ATP-binding cassette sub-family F member 1 isoform X2
28S ribosomal protein S18b, mitochondrial
protein phosphatase 1, regulatory subunit 10
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 98% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine/threonine-protein phosphatase 1 regulatory subunit 10
KH domain containing, RNA binding, signal transduction associated 1b, transcript variant X2
KH domain containing, RNA binding, signal transduction associated 1b, transcript variant X1
KH domain-containing, RNA-binding, signal transduction-associated protein 1b
karyopherin alpha 6 (importin alpha 7), transcript variant X2
karyopherin alpha 6 (importin alpha 7), transcript variant X1
karyopherin alpha 6 (importin alpha 7), transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
eukaryotic translation initiation factor 3, subunit I
LOW QUALITY PROTEIN: eukaryotic translation initiation factor 3 subunit I
chromodomain-helicase-DNA-binding protein 4-like
LOW QUALITY PROTEIN: chromodomain-helicase-DNA-binding protein 4-like
cell division control protein 42 homolog
pre-B-cell leukemia homeobox interacting protein 1a, transcript variant X1
pre-B-cell leukemia homeobox interacting protein 1a, transcript variant X2
pre-B-cell leukemia transcription factor-interacting protein 1 isoform X1
pre-B-cell leukemia transcription factor-interacting protein 1 isoform X2
S100 calcium binding protein S, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
S100 calcium binding protein S, transcript variant X1
S100 calcium binding protein S, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
S100 calcium binding protein S, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
S100 calcium binding protein S isoform X1
S100 calcium binding protein S isoform X2
pygopus homolog 2 (Drosophila), transcript variant X3
pygopus homolog 2 (Drosophila), transcript variant X1
pygopus homolog 2 (Drosophila), transcript variant X2
ubiquitin associated protein 2-like, transcript variant X2
ubiquitin associated protein 2-like, transcript variant X1
ubiquitin associated protein 2-like, transcript variant X6
ubiquitin associated protein 2-like, transcript variant X3
ubiquitin associated protein 2-like, transcript variant X4
ubiquitin associated protein 2-like, transcript variant X5
ubiquitin-associated protein 2-like isoform X1
ubiquitin-associated protein 2-like isoform X5
ubiquitin-associated protein 2-like isoform X2
ubiquitin-associated protein 2-like isoform X3
ubiquitin-associated protein 2-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger protein 687b, transcript variant X3
zinc finger protein 687b, transcript variant X2
zinc finger protein 687b, transcript variant X1
zinc finger protein 687b, transcript variant X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00396
CDC28 protein kinase regulatory subunit 1B
cyclin-dependent kinases regulatory subunit 1
cholinergic receptor, nicotinic, alpha 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 46b, transcript variant X2
tripartite motif-containing 46b isoform X2
tripartite motif containing 46b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tripartite motif containing 46b, transcript variant X6
tripartite motif containing 46b, transcript variant X3
tripartite motif containing 46b, transcript variant X5
tripartite motif containing 46b, transcript variant X7
tripartite motif containing 46b, transcript variant X1
tripartite motif-containing 46b isoform X1
tripartite motif-containing 46b isoform X3
tripartite motif-containing 46b isoform X4
tripartite motif-containing 46b isoform X5
dolichyl-phosphate mannosyltransferase subunit 3, regulatory, transcript variant X1
dolichyl-phosphate mannosyltransferase subunit 3, regulatory, transcript variant X2
dolichol-phosphate mannosyltransferase subunit 3
uncharacterized LOC124381983, transcript variant X2
uncharacterized LOC124381983, transcript variant X1
uncharacterized LOC124381984, transcript variant X1
uncharacterized LOC124381984, transcript variant X2
uncharacterized LOC124381984, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
oxidoreductase NAD-binding domain containing 1
LOW QUALITY PROTEIN: oxidoreductase NAD-binding domain-containing protein 1
insulin-like growth factor 2 mRNA binding protein 3
LOW QUALITY PROTEIN: insulin-like growth factor 2 mRNA-binding protein 3
coiled-coil domain containing 126, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
coiled-coil domain containing 126, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
coiled-coil domain-containing protein 126
LOW QUALITY PROTEIN: oxysterol-binding protein-related protein 3a
protein associated with LIN7 2, MAGUK p55 family member b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: MAGUK p55 subfamily member 6b
LOW QUALITY PROTEIN: deleted in azoospermia-like
LOW QUALITY PROTEIN: TBC1 domain family member 5
potassium voltage-gated channel, subfamily H (eag-related), member 8
potassium voltage-gated channel subfamily H member 8
K(lysine) acetyltransferase 2B, transcript variant X1
histone acetyltransferase KAT2B isoform X1
K(lysine) acetyltransferase 2B, transcript variant X2
histone acetyltransferase KAT2B isoform X2
K(lysine) acetyltransferase 2B, transcript variant X3
histone acetyltransferase KAT2B isoform X3
AT rich interactive domain 1Ab (SWI-like)
AT-rich interactive domain-containing protein 1A
nuclear receptor subfamily 0, group B, member 2b
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 11% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: nuclear receptor subfamily 0, group B, member 2b
trophoblast glycoprotein a, transcript variant X2
trophoblast glycoprotein a, transcript variant X3
trophoblast glycoprotein a, transcript variant X1
SH3 domain binding glutamate-rich protein like 3
SH3 domain-binding glutamic acid-rich-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
erythrocyte membrane protein band 4.1a, transcript variant X6
erythrocyte membrane protein band 4.1a, transcript variant X2
erythrocyte membrane protein band 4.1a, transcript variant X5
erythrocyte membrane protein band 4.1a, transcript variant X11
erythrocyte membrane protein band 4.1a, transcript variant X10
erythrocyte membrane protein band 4.1a, transcript variant X9
erythrocyte membrane protein band 4.1a, transcript variant X7
erythrocyte membrane protein band 4.1a, transcript variant X8
erythrocyte membrane protein band 4.1a, transcript variant X1
erythrocyte membrane protein band 4.1a, transcript variant X3
erythrocyte membrane protein band 4.1a, transcript variant X4
erythrocyte membrane protein band 4.1a, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
RNA polymerase II subunit A C-terminal domain phosphatase
zinc finger and BTB domain containing 22b
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 17 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 22b
retinoid x receptor, beta a, transcript variant X2
retinoid x receptor, beta a, transcript variant X1
retinoic acid receptor RXR-beta-A isoform X2
retinoic acid receptor RXR-beta-A isoform X1
death-domain associated protein, transcript variant X4
death-domain associated protein, transcript variant X1
death-domain associated protein, transcript variant X3
death-domain associated protein, transcript variant X2
death domain-associated protein 6 isoform X1
death domain-associated protein 6 isoform X2
transfer RNA tyrosine (anticodon GUA); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC124382212, transcript variant X5
uncharacterized LOC124382212, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC124382212, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC124382212, 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 6 samples with support for all annotated introns
uncharacterized LOC124382212, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC124382212, 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 10 samples with support for all annotated introns
uncharacterized protein LOC124382212 isoform X3
uncharacterized protein LOC124382212 isoform X2
uncharacterized protein LOC124382212 isoform X1
LOW QUALITY PROTEIN: protein capicua homolog
carcinoembryonic antigen-related cell adhesion molecule 20
guanine nucleotide binding protein (G protein), beta polypeptide 3b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-3b
succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial
uncharacterized LOC124382096, transcript variant X1
uncharacterized LOC124382096, 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 7 samples with support for all annotated introns
uncharacterized protein LOC124382096 isoform X1
uncharacterized protein LOC124382096 isoform X2
uncharacterized LOC124382097, 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 4 samples with support for all annotated introns
uncharacterized LOC124382097, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ETS domain-containing transcription factor ERF
POU domain, class 2, transcription factor 2
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
ATPase Na+/K+ transporting subunit alpha 3a
sodium/potassium-transporting ATPase subunit alpha-3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
transfer RNA glutamic acid (anticodon UUC); 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: 87% 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: 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol-4-phosphate 5-kinase, type I, alpha, a, transcript variant X2
phosphatidylinositol-4-phosphate 5-kinase, type I, alpha, a, transcript variant X4
phosphatidylinositol-4-phosphate 5-kinase, type I, alpha, a, transcript variant X1
phosphatidylinositol-4-phosphate 5-kinase, type I, alpha, a, transcript variant X3
phosphatidylinositol-4-phosphate 5-kinase, type I, alpha, a isoform X1
phosphatidylinositol-4-phosphate 5-kinase, type I, alpha, a isoform X2
proteasome 26S subunit ubiquitin receptor, non-ATPase 4a
26S proteasome non-ATPase regulatory subunit 4a
zinc finger protein 271, transcript variant X2
zinc finger protein 271, transcript variant X4
zinc finger protein 271, transcript variant X1
zinc finger protein 271, transcript variant X3
uncharacterized protein si:ch73-347e22.4 isoform X2
uncharacterized protein si:ch73-347e22.4 isoform X3
apolipoprotein Ea, transcript variant X2
apolipoprotein Ea, transcript variant X1
apolipoprotein A-IV a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
apolipoprotein A-IV a, 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 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 29% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
translocase of outer mitochondrial membrane 40 homolog, like
mitochondrial import receptor subunit TOM40B
probable ATP-dependent RNA helicase ddx6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
sodium/hydrogen exchanger 3-like, transcript variant X1
sodium/hydrogen exchanger 3-like isoform X1
sodium/hydrogen exchanger 3-like, transcript variant X2
sodium/hydrogen exchanger 3-like isoform X2
argonaute RISC catalytic component 3b, transcript variant X2
argonaute RISC catalytic component 3b, transcript variant X1
oleoyl-ACP hydrolase, transcript variant X3
oleoyl-ACP hydrolase, transcript variant X1
oleoyl-ACP hydrolase, transcript variant X2
S-acyl fatty acid synthase thioesterase, medium chain isoform X1
S-acyl fatty acid synthase thioesterase, medium chain isoform X3
S-acyl fatty acid synthase thioesterase, medium chain isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon CGA); 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: 4 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: 52 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
upstream transcription factor 2, c-fos interacting
fMet-Leu-Phe receptor-like, transcript variant X2
fMet-Leu-Phe receptor-like, transcript variant X1
fMet-Leu-Phe receptor-like, transcript variant X3
uncharacterized LOC124382200, transcript variant X3
uncharacterized LOC124382200, transcript variant X2
uncharacterized protein LOC124382200 isoform X2
uncharacterized LOC124382200, transcript variant X1
uncharacterized LOC124382200, transcript variant X4
uncharacterized protein LOC124382200 isoform X1
uncharacterized protein LOC124382200 isoform X4
uncharacterized protein LOC124382200 isoform X3
solute carrier family 2, facilitated glucose transporter member 3a
neuronal pentraxin-2, transcript variant X3
neuronal pentraxin-2, transcript variant X1
neuronal pentraxin-2, transcript variant X2
calcium channel, voltage-dependent, gamma subunit 6a, transcript variant X2
calcium channel, voltage-dependent, gamma subunit 6a, transcript variant X1
calcium channel, voltage-dependent, gamma subunit 6a, transcript variant X3
calcium channel, voltage-dependent, gamma subunit 6a, transcript variant X4
calcium channel, voltage-dependent, gamma subunit 6a isoform X1
calcium channel, voltage-dependent, gamma subunit 6a isoform X2
calcium channel, voltage-dependent, gamma subunit 8a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ceramide synthase 2a
cugbp, Elav-like family member 3a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cugbp, Elav-like family member 3a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cugbp, Elav-like family member 3a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cugbp, Elav-like family member 3a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cugbp, Elav-like family member 3a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
CUGBP Elav-like family member 3 isoform X2
CUGBP Elav-like family member 3 isoform X1
regulation of nuclear pre-mRNA domain containing 2a
regulation of nuclear pre-mRNA domain-containing protein 2a
28S ribosomal protein S21, mitochondrial
cellular retinoic acid binding protein 2, b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cellular retinoic acid-binding protein 2b
secretory carrier membrane protein 3, transcript variant X1
secretory carrier membrane protein 3, transcript variant X2
secretory carrier-associated membrane protein 3 isoform X1
secretory carrier-associated membrane protein 3 isoform X2
ash1 (absent, small, or homeotic)-like (Drosophila)
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 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: histone-lysine N-methyltransferase ASH1L
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: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: leucine-rich repeat-containing protein 71
SET domain bifurcated histone lysine methyltransferase 1a, transcript variant X1
SET domain bifurcated histone lysine methyltransferase 1a, transcript variant X4
SET domain bifurcated histone lysine methyltransferase 1a, transcript variant X5
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 16 samples with support for all annotated introns
SET domain bifurcated histone lysine methyltransferase 1a, transcript variant X2
SET domain bifurcated histone lysine methyltransferase 1a, transcript variant X3
histone-lysine N-methyltransferase SETDB1-A isoform X1
histone-lysine N-methyltransferase SETDB1-A isoform X2
histone-lysine N-methyltransferase SETDB1-A isoform X3
CDC-like kinase 2a, transcript variant X1
dual specificity protein kinase CLK2 isoform X1
CDC-like kinase 2a, transcript variant X2
dual specificity protein kinase CLK2 isoform X2
uncharacterized protein LOC560648 homolog, transcript variant X2
uncharacterized protein LOC560648 homolog, transcript variant X1
hyperpolarization activated cyclic nucleotide-gated potassium channel 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2
NADH:ubiquinone oxidoreductase core subunit V1
LOW QUALITY PROTEIN: NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial
lysine (K)-specific methyltransferase 2Ba
origin recognition complex subunit 4, transcript variant X2
origin recognition complex subunit 4, transcript variant X1
origin recognition complex subunit 4, transcript variant X4
origin recognition complex subunit 4, transcript variant X5
origin recognition complex subunit 4, transcript variant X6
origin recognition complex subunit 4, transcript variant X3
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 5 samples with support for all annotated introns
family with sequence similarity 131 member Ba, transcript variant X1
family with sequence similarity 131 member Ba, transcript variant X3
family with sequence similarity 131 member Ba, transcript variant X4
family with sequence similarity 131 member Ba, transcript variant X2
family with sequence similarity 131 member Ba, transcript variant X6
uncharacterized protein fam131ba isoform X1
uncharacterized protein fam131ba isoform X2
uncharacterized protein fam131ba isoform X3
uncharacterized protein fam131ba isoform X4
family with sequence similarity 131 member Ba, transcript variant X5
uncharacterized protein fam131ba isoform X5
uncharacterized protein fam131ba isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine/tyrosine kinase 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
serine/threonine/tyrosine kinase 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tyrosine-protein kinase STYK1 isoform X1
tyrosine-protein kinase STYK1 isoform X2
uncharacterized protein LOC572203 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC572203 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC572203 homolog, transcript variant X3
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 1 sample with support for all annotated introns
germ cell-specific gene 1-like protein isoform X1
germ cell-specific gene 1-like protein isoform X3
germ cell-specific gene 1-like protein isoform X2
coiled-coil domain containing 106b, transcript variant X3
coiled-coil domain containing 106b, transcript variant X2
coiled-coil domain containing 106b, transcript variant X5
coiled-coil domain containing 106b, transcript variant X4
coiled-coil domain containing 106b, transcript variant X1
coiled-coil domain-containing protein 106b
U2 small nuclear RNA auxiliary factor 2b, transcript variant X3
U2 small nuclear RNA auxiliary factor 2b, transcript variant X1
U2 small nuclear RNA auxiliary factor 2b, transcript variant X2
U2 small nuclear RNA auxiliary factor 2b, transcript variant X10
U2 small nuclear RNA auxiliary factor 2b, transcript variant X9
U2 small nuclear RNA auxiliary factor 2b, transcript variant X4
U2 small nuclear RNA auxiliary factor 2b, transcript variant X5
U2 small nuclear RNA auxiliary factor 2b isoform X1
U2 small nuclear RNA auxiliary factor 2b isoform X2
U2 small nuclear RNA auxiliary factor 2b isoform X4
U2 small nuclear RNA auxiliary factor 2b isoform X5
U2 small nuclear RNA auxiliary factor 2b isoform X3
U2 small nuclear RNA auxiliary factor 2b isoform X10
U2 small nuclear RNA auxiliary factor 2b isoform X9
U2 small nuclear RNA auxiliary factor 2b, transcript variant X7
U2 small nuclear RNA auxiliary factor 2b isoform X7
U2 small nuclear RNA auxiliary factor 2b, transcript variant X6
U2 small nuclear RNA auxiliary factor 2b, transcript variant X8
U2 small nuclear RNA auxiliary factor 2b isoform X6
U2 small nuclear RNA auxiliary factor 2b isoform X8
CCR4-NOT transcription complex, subunit 3b
LOW QUALITY PROTEIN: CCR4-NOT transcription complex subunit 3b
shisa family member 7, transcript variant X1
shisa family member 7, transcript variant X3
shisa family member 7, transcript variant X2
LOW QUALITY PROTEIN: zinc finger protein 865
D site albumin promoter binding protein a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
D site albumin promoter binding protein a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
D site albumin promoter binding protein a isoform X1
D site albumin promoter binding protein a isoform X2
glutamate receptor, ionotropic, N-methyl D-aspartate 2D, a
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: glutamate receptor ionotropic, NMDA 2D
fibronectin type III domain containing 5b
LOW QUALITY PROTEIN: fibronectin type III domain-containing protein 5
low density lipoprotein receptor adaptor protein 1a
low density lipoprotein receptor adapter protein 1a
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 8 samples with support for all annotated introns
lysophosphatidylcholine acyltransferase 1, transcript variant X2
lysophosphatidylcholine acyltransferase 1, transcript variant X3
lysophosphatidylcholine acyltransferase 1, transcript variant X1
lysophosphatidylcholine acyltransferase 1, transcript variant X4
lysophosphatidylcholine acyltransferase 1 isoform X1
lysophosphatidylcholine acyltransferase 1 isoform X2
39S ribosomal protein L36, mitochondrial
NADH:ubiquinone oxidoreductase subunit S6
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; 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
LOW QUALITY PROTEIN: iroquois-class homeodomain protein IRX-4b
iroquois homeobox 1b, transcript variant X1
iroquois homeobox 1b, transcript variant X2
iroquois-class homeodomain protein IRX-1b isoform X1
iroquois-class homeodomain protein IRX-1b isoform X2
mediator of RNA polymerase II transcription subunit 10
ubiquitin-conjugating enzyme E2Q family-like 1
ubiquitin-conjugating enzyme E2Q-like protein 1
RNA cytosine C(5)-methyltransferase NSUN2
steroid-5-alpha-reductase, alpha polypeptide 1 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 1)
LOW QUALITY PROTEIN: terminal nucleotidyltransferase 4A
adenylate cyclase 2b (brain), transcript variant X1
adenylate cyclase 2b (brain), transcript variant X2
alpha tubulin acetyltransferase 1, transcript variant X1
alpha-tubulin N-acetyltransferase 1 isoform X1
alpha tubulin acetyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
alpha tubulin acetyltransferase 1, transcript variant X3
alpha tubulin acetyltransferase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
alpha tubulin acetyltransferase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
alpha tubulin acetyltransferase 1, transcript variant X4
alpha-tubulin N-acetyltransferase 1 isoform X2
alpha-tubulin N-acetyltransferase 1 isoform X4
alpha-tubulin N-acetyltransferase 1 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00276
chromosome 29 C6orf47 homolog, transcript variant X1
chromosome 29 C6orf47 homolog, transcript variant X2
protein phosphatase 1, regulatory (inhibitor) subunit 11
valyl-tRNA synthetase 2, mitochondrial, transcript variant X2
valyl-tRNA synthetase 2, mitochondrial, transcript variant X1
valyl-tRNA synthetase 2, mitochondrial, transcript variant X3
valine--tRNA ligase, mitochondrial isoform X1
valine--tRNA ligase, mitochondrial isoform X2
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase b, transcript variant X1
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase b isoform X1
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase b, transcript variant X2
alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase b isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B, transcript variant X4
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B, transcript variant X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B isoform X1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B isoform X3
DNA-directed RNA polymerase I subunit RPA12
general transcription factor IIH, polypeptide 4
general transcription factor IIH subunit 4
SH3-binding domain protein 5-like, b, transcript variant X1
SH3-binding domain protein 5-like, b, transcript variant X2
SH3 domain-binding protein 5-like isoform X1
SH3 domain-binding protein 5-like isoform X2
gamma-aminobutyric acid (GABA) B receptor, 1b
LOW QUALITY PROTEIN: gamma-aminobutyric acid type B receptor subunit 1
tumor necrosis factor a (TNF superfamily, member 2)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
SAC1 like phosphatidylinositide phosphatase a
phosphatidylinositol-3-phosphatase SAC1-A
zinc finger and BTB domain-containing protein 12-like
negative elongation factor complex member E
SKI2 homolog, superkiller viralicidic activity 2-like
transmembrane protein 268, transcript variant X2
transmembrane protein 268, transcript variant X1
casein kinase 2, beta polypeptide, transcript variant X1
casein kinase 2, beta polypeptide, transcript variant X3
casein kinase 2, beta polypeptide, transcript variant X2
casein kinase II subunit beta isoform X1
casein kinase II subunit beta isoform X2
protein disulfide isomerase family A, member 8
integrator complex subunit 3, transcript variant X1
integrator complex subunit 3, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: atrial natriuretic peptide receptor 1
myosin regulatory light chain interacting protein a
LOW QUALITY PROTEIN: dystrobrevin binding protein 1b
jumonji, AT rich interactive domain 2b, transcript variant X2
jumonji, AT rich interactive domain 2b, transcript variant X1
jumonji, AT rich interactive domain 2b, transcript variant X3
par-6 family cell polarity regulator gamma b
biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino
biogenesis of lysosome-related organelles complex 1 subunit 4
asparagine synthetase, transcript variant X2
asparagine synthetase, transcript variant X1
asparagine synthetase [glutamine-hydrolyzing]
succinate dehydrogenase complex assembly factor 3
succinate dehydrogenase assembly factor 3, mitochondrial
collagen, type XXVIII, alpha 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
collagen, type XXVIII, alpha 1a, transcript variant X2
UBAP1-MVB12-associated (UMA) domain containing 1
UBAP1-MVB12-associated (UMA)-domain containing protein 1
LOW QUALITY PROTEIN: glucocorticoid induced 1a
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
regulating synaptic membrane exocytosis 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulating synaptic membrane exocytosis 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
regulating synaptic membrane exocytosis 3, transcript variant X2
regulating synaptic membrane exocytosis protein 3 isoform X1
regulating synaptic membrane exocytosis protein 3 isoform X2
protein tyrosine phosphatase 4A3a, transcript variant X1
protein tyrosine phosphatase 4A3a, transcript variant X4
protein tyrosine phosphatase 4A3a, transcript variant X2
protein tyrosine phosphatase 4A3a, transcript variant X3
low affinity immunoglobulin epsilon Fc receptor-like, transcript variant X2
low affinity immunoglobulin epsilon Fc receptor-like, transcript variant X1
low affinity immunoglobulin epsilon Fc receptor-like
C-type lectin domain family 3 member A-like
C-type lectin domain family 4 member E-like
C-type lectin domain family 6 member A-like, transcript variant X1
C-type lectin domain family 6 member A-like, transcript variant X2
C-type lectin domain family 4 member E-like isoform X1
C-type lectin domain family 6 member A-like isoform X2
C-type lectin domain family 4 member E-like, transcript variant X1
C-type lectin domain family 4 member E-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC571482 homolog
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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: cyclin-dependent kinase 5 activator 1
uncharacterized si:dkey-154b15.1, transcript variant X2
uncharacterized si:dkey-154b15.1, transcript variant X3
uncharacterized si:dkey-154b15.1, transcript variant X1
uncharacterized protein si:dkey-154b15.1
COORDINATES: nucleotide motif:Rfam:12.0:RF00411
class I histocompatibility antigen, F10 alpha chain-like, transcript variant X1
class I histocompatibility antigen, F10 alpha chain-like, transcript variant X2
class I histocompatibility antigen, F10 alpha chain-like isoform X1
T-cell surface glycoprotein CD1b4-like isoform X2
EYA transcriptional coactivator and phosphatase 3, transcript variant X2
EYA transcriptional coactivator and phosphatase 3, transcript variant X1
EYA transcriptional coactivator and phosphatase 3, transcript variant X6
EYA transcriptional coactivator and phosphatase 3, transcript variant X5
EYA transcriptional coactivator and phosphatase 3, transcript variant X7
EYA transcriptional coactivator and phosphatase 3, transcript variant X4
EYA transcriptional coactivator and phosphatase 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
forkhead box protein K2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
forkhead box protein K2-like, transcript variant X1
HLF transcription factor, PAR bZIP family member a
monocyte to macrophage differentiation-associated
monocyte to macrophage differentiation factor
chromobox homolog 2 (Drosophila Pc class)
ectonucleotide pyrophosphatase/phosphodiesterase family member 7-like
RNA binding protein fox-1 homolog 3-like, transcript variant X3
RNA binding protein fox-1 homolog 3-like, transcript variant X1
RNA binding protein fox-1 homolog 3-like, transcript variant X5
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
RNA binding protein fox-1 homolog 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RNA binding protein fox-1 homolog 3-like isoform X2
RNA binding protein fox-1 homolog 3-like isoform X1
RNA binding protein fox-1 homolog 3-like isoform X3
RNA binding protein fox-1 homolog 3-like, transcript variant X4
RNA binding protein fox-1 homolog 3-like isoform X4
RNA binding protein fox-1 homolog 3-like isoform X5
uncharacterized LOC124382011, transcript variant X1
uncharacterized protein LOC124382011 isoform X1
uncharacterized LOC124382011, transcript variant X2
uncharacterized protein LOC124382011 isoform X2
uncharacterized LOC124382012, transcript variant X1
uncharacterized LOC124382012, transcript variant X3
uncharacterized LOC124382012, transcript variant X2
uncharacterized LOC124381928, transcript variant X5
uncharacterized LOC124381928, transcript variant X3
uncharacterized LOC124381928, transcript variant X2
uncharacterized LOC124381928, transcript variant X1
uncharacterized LOC124381928, transcript variant X4
uncharacterized protein LOC124381928 isoform X2
uncharacterized protein LOC124381928 isoform X4
uncharacterized protein LOC124381928 isoform X5
uncharacterized protein LOC124381928 isoform X3
uncharacterized protein LOC124381928 isoform X1
NACHT, LRR and PYD domains-containing protein 12-like
LOW QUALITY PROTEIN: NACHT, LRR and PYD domains-containing protein 12-like
uncharacterized LOC124381765, transcript variant X1
uncharacterized protein LOC124381765 isoform X1
uncharacterized LOC124381765, transcript variant X4
uncharacterized LOC124381765, transcript variant X2
uncharacterized LOC124381765, transcript variant X3
uncharacterized protein LOC124381765 isoform X2
uncharacterized protein LOC124381765 isoform X4
uncharacterized protein LOC124381765 isoform X3
uncharacterized LOC124381764, transcript variant X5
uncharacterized LOC124381764, transcript variant X3
uncharacterized LOC124381764, transcript variant X7
uncharacterized LOC124381764, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC124381764, transcript variant X6
uncharacterized protein LOC124381764 isoform X1
uncharacterized LOC124381764, transcript variant X2
uncharacterized LOC124381764, transcript variant X4
uncharacterized protein LOC124381764 isoform X2
uncharacterized LOC124381763, transcript variant X2
uncharacterized LOC124381763, transcript variant X1
Jupiter microtubule associated homolog 1b
NACHT, LRR and PYD domains-containing protein 5-like, transcript variant X4
NACHT, LRR and PYD domains-containing protein 5-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 5-like, transcript variant X3
NACHT, LRR and PYD domains-containing protein 5-like, transcript variant X1
uncharacterized protein LOC124381758 isoform X4
NACHT, LRR and PYD domains-containing protein 5-like isoform X2
NACHT, LRR and PYD domains-containing protein 5-like isoform X3
uncharacterized protein LOC124381758 isoform X1
NLR family CARD domain-containing protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
NLR family CARD domain-containing protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
NLR family CARD domain-containing protein 3-like isoform X2
NLR family CARD domain-containing protein 3-like isoform X1
golgi associated, gamma adaptin ear containing, ARF binding protein 3b, transcript variant X1
golgi associated, gamma adaptin ear containing, ARF binding protein 3b, transcript variant X2
ADP-ribosylation factor-binding protein GGA3 isoform X2
ADP-ribosylation factor-binding protein GGA3 isoform X1
LOW QUALITY PROTEIN: fas-binding factor 1 homolog
COORDINATES: nucleotide motif:Rfam:12.0:RF00213
COORDINATES: nucleotide motif:Rfam:12.0:RF00277
sphingosine kinase 2-like, transcript variant X1
sphingosine kinase 2-like, transcript variant X2
cysteine protease ATG4D-like, transcript variant X2
cysteine protease ATG4D-like, transcript variant X1
microtubule associated serine/threonine kinase 1b, transcript variant X3
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 10 samples with support for all annotated introns
microtubule associated serine/threonine kinase 1b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
microtubule associated serine/threonine kinase 1b, 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 9 samples with support for all annotated introns
microtubule associated serine/threonine kinase 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
microtubule associated serine/threonine kinase 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
microtubule-associated serine/threonine-protein kinase 1 isoform X2
microtubule-associated serine/threonine-protein kinase 1 isoform X3
microtubule-associated serine/threonine-protein kinase 1 isoform X4
microtubule-associated serine/threonine-protein kinase 1 isoform X1
JunB proto-oncogene, AP-1 transcription factor subunit b
hook microtubule-tethering protein 2, transcript variant X1
hook microtubule-tethering protein 2, transcript variant X2
telomerase RNA component interacting RNase
trafficking protein particle complex subunit 5-like
protein kinase N1b, transcript variant X2
protein kinase N1b, transcript variant X3
serine/threonine-protein kinase N1b isoform X2
protein kinase N1b, transcript variant X1
serine/threonine-protein kinase N1b isoform X1
LOW QUALITY PROTEIN: transforming growth factor beta receptor type 3
volume-regulated anion channel subunit LRRC8D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
volume-regulated anion channel subunit LRRC8D, transcript variant X2
volume-regulated anion channel subunit LRRC8D isoform X1
volume-regulated anion channel subunit LRRC8D isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39Ab, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39Ab isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39Ab, transcript variant X1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39Ab, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39Ab isoform X1
LOW QUALITY PROTEIN: ran GTPase-activating protein 1a
zinc finger CCCH-type containing 7Ba, transcript variant X1
zinc finger CCCH-type containing 7Ba, transcript variant X2
zinc finger CCCH-type containing 7Ba isoform X1
zinc finger CCCH-type containing 7Ba isoform X2
TEF transcription factor, PAR bZIP family member b, transcript variant X2
TEF transcription factor, PAR bZIP family member b, transcript variant X3
TEF transcription factor, PAR bZIP family member b, transcript variant X4
TEF transcription factor, PAR bZIP family member b isoform X2
TEF transcription factor, PAR bZIP family member b isoform X3
TEF transcription factor, PAR bZIP family member b, transcript variant X1
TEF transcription factor, PAR bZIP family member b isoform X1
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X3
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X1
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X2
DNA-directed RNA polymerase III subunit RPC8
cold shock domain containing C2, RNA binding b
phosphomannomutase 1, transcript variant X2
phosphomannomutase 1, transcript variant X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
nuclear body protein SP140-like protein, transcript variant X4
nuclear body protein SP140-like protein, transcript variant X2
nuclear body protein SP140-like protein, transcript variant X3
nuclear body protein SP140-like protein, transcript variant X5
nuclear body protein SP140-like protein, transcript variant X1
nuclear body protein SP140-like isoform X4
nuclear body protein SP140-like isoform X2
nuclear body protein SP140-like isoform X3
nuclear body protein SP140-like isoform X1
nuclear body protein SP140-like protein isoform X5
nuclear body protein SP140-like protein isoform X2
nuclear body protein SP140-like protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes protein 4-like
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 15 samples with support for all annotated introns
cell division cycle 27, transcript variant X1
cell division cycle 27, transcript variant X2
cell division cycle protein 27 homolog isoform X1
cell division cycle protein 27 homolog isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
LOW QUALITY PROTEIN: KAT8 regulatory NSL complex subunit 1
microtubule-associated protein tau b, transcript variant X2
microtubule-associated protein tau b, transcript variant X1
microtubule-associated protein tau b, transcript variant X6
microtubule-associated protein tau b, transcript variant X5
microtubule-associated protein tau b, transcript variant X7
microtubule-associated protein tau b, transcript variant X3
microtubule-associated protein tau isoform X4
microtubule-associated protein tau isoform X5
microtubule-associated protein tau isoform X3
microtubule-associated protein tau isoform X1
microtubule-associated protein tau b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
microtubule-associated protein tau isoform X2
zinc finger protein, FOG family member 2b
CD209 antigen-like protein C, transcript variant X3
CD209 antigen-like protein C, transcript variant X2
CD209 antigen-like protein C, transcript variant X1
sodium channel, voltage-gated, type IV, alpha, b
sodium channel protein type 4 subunit alpha B
myosin, light chain 4, alkali; atrial, embryonic, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
myosin, light chain 4, alkali; atrial, embryonic, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
low density lipoprotein receptor-related protein 12
low-density lipoprotein receptor-related protein 12
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: 55 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: thrombospondin-3b-like
uncharacterized LOC124382074, transcript variant X1
uncharacterized LOC124382074, transcript variant X2
DNA-directed RNA polymerase III subunit RPC7-like, transcript variant X2
DNA-directed RNA polymerase III subunit RPC7-like, transcript variant X3
DNA-directed RNA polymerase III subunit RPC7-like, transcript variant X1
DNA-directed RNA polymerase III subunit RPC7-like isoform X1
DNA-directed RNA polymerase III subunit RPC7-like isoform X2
XK-related protein 8-like, 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 3 samples with support for all annotated introns
XK-related protein 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
XK-related protein 8-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
XK-related protein 8-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
XK-related protein 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
endonuclease/exonuclease/phosphatase family domain containing 1
endonuclease/exonuclease/phosphatase family domain-containing protein 1
LOW QUALITY PROTEIN: uncharacterized protein KIAA0895
SNAP associated protein, transcript variant X2
SNAP associated protein, transcript variant X1
SMAD family member 10a, transcript variant X2
SMAD family member 10a, transcript variant X1
mothers against decapentaplegic homolog 4 isoform X1
mothers against decapentaplegic homolog 4 isoform X2
synaptotagmin XIa, transcript variant X1
synaptotagmin XIa, transcript variant X2
uncharacterized LOC124381793, transcript variant X3
uncharacterized LOC124381793, transcript variant X2
uncharacterized LOC124381793, transcript variant X1
Ras-related and estrogen-regulated growth inhibitor-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
THAP domain containing 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
THAP domain containing 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
THAP domain-containing protein 7 isoform X2
THAP domain-containing protein 7 isoform X1
uncharacterized LOC124381781, transcript variant X1
uncharacterized LOC124381781, transcript variant X2
uncharacterized protein LOC124381781 isoform X1
uncharacterized protein LOC124381781 isoform X2
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ab, transcript variant X3
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ab, transcript variant X2
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ab, transcript variant X5
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ab, transcript variant X4
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ab, transcript variant X7
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ab, transcript variant X6
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ab, transcript variant X1
uncharacterized protein LOC100034657 homolog, transcript variant X1
uncharacterized protein LOC100034657 homolog, transcript variant X2
uncharacterized protein si:dkey-81h8.1 isoform X1
high affinity immunoglobulin epsilon receptor subunit beta isoform X2
nuclear transcription factor Y subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
dual specificity mitogen-activated protein kinase kinase 4, transcript variant X1
dual specificity mitogen-activated protein kinase kinase 4, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 4, transcript variant X3
dual specificity mitogen-activated protein kinase kinase 4, transcript variant X5
dual specificity mitogen-activated protein kinase kinase 4, transcript variant X4
dual specificity mitogen-activated protein kinase kinase 4 isoform X3
dual specificity mitogen-activated protein kinase kinase 4 isoform X2
dual specificity mitogen-activated protein kinase kinase 4 isoform X1
dual specificity mitogen-activated protein kinase kinase 4 isoform X4
dual specificity mitogen-activated protein kinase kinase 4 isoform X5
transmembrane protein 220, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
transmembrane protein 220, transcript variant X1
solute carrier family 25 member 19, transcript variant X1
solute carrier family 25 member 19, transcript variant X2
mitochondrial thiamine pyrophosphate carrier isoform X1
mitochondrial thiamine pyrophosphate carrier isoform X2
N-acetylglucosamine-6-phosphate deacetylase
NLR family CARD domain-containing protein 3-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, and 66% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: NLR family CARD domain-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like
uncharacterized LOC124381868, transcript variant X1
uncharacterized LOC124381868, transcript variant X5
uncharacterized LOC124381868, transcript variant X2
uncharacterized protein LOC124381868 isoform X1
uncharacterized protein LOC124381868 isoform X2
uncharacterized protein LOC124381868 isoform X5
uncharacterized LOC124381868, transcript variant X4
uncharacterized LOC124381868, transcript variant X3
uncharacterized protein LOC124381868 isoform X3
uncharacterized protein LOC124381868 isoform X4
Tu translation elongation factor, mitochondrial
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X3
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X2
HSPA (heat shock 70kDa) binding protein, cytoplasmic cochaperone 1, transcript variant X1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase a, transcript variant X1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase a isoform X1
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase a, transcript variant X2
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase a isoform X2
complement C1q tumor necrosis factor-related protein 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 6-like
interleukin 2 receptor, beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
interleukin 2 receptor, beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
interleukin-2 receptor subunit beta isoform X2
interleukin-2 receptor subunit beta isoform X1
uncharacterized LOC124382256, transcript variant X1
uncharacterized LOC124382256, transcript variant X2
MIEF1 upstream open reading frame protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
LOW QUALITY PROTEIN: histone acetyltransferase p300
X-prolyl aminopeptidase 3, mitochondrial, transcript variant X2
X-prolyl aminopeptidase 3, mitochondrial, transcript variant X1
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 239-like, transcript variant X4
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X24
zinc finger protein 239-like, transcript variant X23
zinc finger protein 420-like isoform X15
zinc finger protein 239-like, transcript variant X9
zinc finger protein 239-like, transcript variant X6
zinc finger protein 239-like, transcript variant X19
zinc finger protein 239-like, transcript variant X10
zinc finger protein 239-like, transcript variant X17
zinc finger protein 239-like, transcript variant X12
zinc finger protein 239-like, transcript variant X21
zinc finger protein 239-like, transcript variant X11
zinc finger protein 658B-like isoform X10
zinc finger protein 658B-like isoform X12
zinc finger protein 239-like, transcript variant X25
zinc finger protein 239-like, transcript variant X18
zinc finger protein 239-like, transcript variant X20
zinc finger protein 729-like isoform X16
zinc finger protein 239-like, transcript variant X13
zinc finger protein 239-like, transcript variant X7
zinc finger protein 239-like, transcript variant X8
zinc finger protein 239-like, transcript variant X16
zinc finger protein 239-like, transcript variant X15
zinc finger protein 239-like, transcript variant X14
zinc finger protein 239-like isoform X11
zinc finger protein 239-like, transcript variant X5
zinc finger protein 239-like, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 262 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger protein 239-like isoform X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC124381917, transcript variant X1
uncharacterized LOC124381917, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 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: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 218 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
DEAD (Asp-Glu-Ala-Asp) box polypeptide 47, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 47, transcript variant X1
probable ATP-dependent RNA helicase DDX47 isoform X2
probable ATP-dependent RNA helicase DDX47 isoform X1
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC393524 homolog, transcript variant X1
uncharacterized protein LOC393524 homolog, transcript variant X3
uncharacterized protein LOC393524 homolog, transcript variant X2
peripheral myelin protein 22-like, transcript variant X1
peripheral myelin protein 22-like, transcript variant X2
germ cell-specific gene 1-like protein, transcript variant X1
germ cell-specific gene 1-like protein, transcript variant X2
LOW QUALITY PROTEIN: transcription factor 20
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: 33 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: glutamate receptor ionotropic, NMDA 2B
interferon-induced very large GTPase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: interferon-induced very large GTPase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: postacrosomal sheath WW domain-binding protein
ribosomal RNA-processing protein 7 homolog A
polymerase (DNA-directed), delta interacting protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
polymerase (DNA-directed), delta interacting protein 3, transcript variant X3
polymerase (DNA-directed), delta interacting protein 3, transcript variant X1
polymerase delta-interacting protein 3 isoform X2
polymerase delta-interacting protein 3 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
family with sequence similarity 234 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
essential MCU regulator, mitochondrial-like
NADH:ubiquinone oxidoreductase subunit A6
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6
serine/arginine repetitive matrix protein 1-like, transcript variant X1
serine/arginine repetitive matrix protein 2-like isoform X1
serine/arginine repetitive matrix protein 1-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like isoform X2
nucleolar protein 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
nucleolar protein 12, transcript variant X1
sterol regulatory element binding transcription factor 2
sterol regulatory element-binding protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
LOW QUALITY PROTEIN: GTPase IMAP family member 7-like
GTPase IMAP family member 4-like, transcript variant X2
GTPase IMAP family member 4-like, transcript variant X1
GTPase IMAP family member 4-like isoform X2
GTPase IMAP family member 4-like isoform X1
coiled-coil domain-containing protein 134
meiosis inhibitor protein 1-like, transcript variant X3
meiosis inhibitor protein 1-like isoform X3
meiosis inhibitor protein 1-like, transcript variant X2
meiosis inhibitor protein 1-like, transcript variant X1
meiosis inhibitor protein 1-like, transcript variant X5
meiosis inhibitor protein 1-like, transcript variant X7
meiosis inhibitor protein 1-like isoform X2
meiosis inhibitor protein 1-like isoform X1
meiosis inhibitor protein 1-like isoform X5
meiosis inhibitor protein 1-like isoform X6
meiosis inhibitor protein 1-like, transcript variant X4
meiosis inhibitor protein 1-like isoform X4
meiosis inhibitor protein 1-like, transcript variant X6
KDEL endoplasmic reticulum protein retention receptor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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
KDEL endoplasmic reticulum protein retention receptor 3, transcript variant X3
KDEL endoplasmic reticulum protein retention receptor 3, transcript variant X1
potassium inwardly rectifying channel subfamily J member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 12
DNA-directed RNA polymerases I, II, and III subunit RPABC2
trinucleotide repeat-containing gene 6B protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
trinucleotide repeat-containing gene 6B protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
trinucleotide repeat-containing gene 6B protein-like, 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 14 samples with support for all annotated introns
trinucleotide repeat-containing gene 6B protein-like isoform X2
trinucleotide repeat-containing gene 6B protein-like isoform X1
caspase recruitment domain-containing protein 11
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: caspase recruitment domain-containing protein 11
interferon-induced very large GTPase 1-like, transcript variant X2
interferon-induced very large GTPase 1-like, transcript variant X1
interferon-induced very large GTPase 1-like, transcript variant X3
interferon-induced very large GTPase 1-like, transcript variant X5
interferon-induced very large GTPase 1-like, transcript variant X4
protein interacting with prkca 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 18 samples with support for all annotated introns
protein interacting with prkca 1, transcript variant X1
protein interacting with prkca 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phospholipase B domain containing 1a, transcript variant X1
phospholipase B domain containing 1a, transcript variant X2
protein shisa-8-like, transcript variant X1
protein shisa-8-like, transcript variant X2
protein shisa-8-like, transcript variant X3
protein shisa-8-like, transcript variant X5
protein shisa-8-like, transcript variant X6
uncharacterized protein LOC124382280 isoform X3
protein shisa-8-like, transcript variant X4