Coregonus clupeaformis isolate EN_2021a chromosome 4, ASM2061545v1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Protacanthopterygii; Salmoniformes; Salmonidae; Coregoninae; Coregonus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM036435.1.\nAssembly name: ASM2061545v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Laval University on\n2021/11/04. The original whole-genome shotgun project has the\naccession JAJAFO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Laval University\nAssembly Date :: 14-SEP-2021\nAssembly Method :: Flye v. 2.5\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 20.0x\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 :: Coregonus clupeaformis Annotation\n Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
transcription factor ETV6, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
transcription factor ETV6, transcript variant X1
transcription factor ETV6, transcript variant X4
transcription factor ETV6, transcript variant X3
transcription factor ETV6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
ubl carboxyl-terminal hydrolase 18, transcript variant X1
ubl carboxyl-terminal hydrolase 18, transcript variant X2
ubl carboxyl-terminal hydrolase 18 isoform X1
ubl carboxyl-terminal hydrolase 18 isoform X2
G1/S-specific cyclin-D2, 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 6 samples with support for all annotated introns
G1/S-specific cyclin-D2, transcript variant X1
fructose-2,6-bisphosphatase TIGAR B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
fructose-2,6-bisphosphatase TIGAR B-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 18 samples with support for all annotated introns
fructose-2,6-bisphosphatase TIGAR B-like isoform X2
fructose-2,6-bisphosphatase TIGAR B-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
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 19 samples with support for all annotated introns
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like, 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 1 sample with support for all annotated introns
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like, 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 3 samples with support for all annotated introns
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like, transcript variant X4
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like isoform X1
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like isoform X2
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like isoform X4
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like isoform X5
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like, transcript variant X3
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2-like isoform X3
fatty acyl-CoA reductase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
fatty acyl-CoA reductase 1, 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 5 samples with support for all annotated introns
endoplasmic reticulum-Golgi intermediate compartment protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
cystine/glutamate transporter-like, transcript variant X2
cystine/glutamate transporter-like, transcript variant X1
forkhead box protein M1, transcript variant X5
forkhead box protein M1, transcript variant X4
forkhead box protein M1, transcript variant X1
forkhead box protein M1, transcript variant X3
forkhead box protein M1, transcript variant X2
TUB like protein 3, transcript variant X3
TUB like protein 3, transcript variant X2
TUB like protein 3, transcript variant X1
protein mono-ADP-ribosyltransferase TIPARP-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
pleiotrophin-A-like, transcript variant X2
pleiotrophin-A-like, transcript variant X1
muscarinic acetylcholine receptor M2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
muscarinic acetylcholine receptor M2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
muscarinic acetylcholine receptor M2-like, 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 4 samples with support for all annotated introns
muscarinic acetylcholine receptor M2-like
guanine nucleotide-binding protein G(i) subunit alpha-1
semaphorin-3C-like, transcript variant X1
semaphorin-3C-like, transcript variant X2
semaphorin-3C-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
GAS2-like protein 3, transcript variant X2
GAS2-like protein 3, transcript variant X1
transmembrane 7 superfamily member 3-like
mediator of RNA polymerase II transcription subunit 21
aryl hydrocarbon receptor nuclear translocator-like protein 1, transcript variant X4
aryl hydrocarbon receptor nuclear translocator-like protein 1 isoform X4
aryl hydrocarbon receptor nuclear translocator-like protein 1, transcript variant X1
aryl hydrocarbon receptor nuclear translocator-like protein 1, transcript variant X2
aryl hydrocarbon receptor nuclear translocator-like protein 1, transcript variant X3
aryl hydrocarbon receptor nuclear translocator-like protein 2 isoform X1
aryl hydrocarbon receptor nuclear translocator-like protein 2 isoform X2
aryl hydrocarbon receptor nuclear translocator-like protein 1, transcript variant X5
aryl hydrocarbon receptor nuclear translocator-like protein 2 isoform X3
aryl hydrocarbon receptor nuclear translocator-like protein 1 isoform X5
neurofilament heavy polypeptide, 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 5 samples with support for all annotated introns
neurofilament heavy polypeptide, 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 21 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GFGX01042058.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 246 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 118 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
solute carrier family 39 member 10, transcript variant X1
solute carrier family 39 member 10, 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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
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.
nucleic acid binding protein 1a, transcript variant X2
nucleic acid binding protein 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
striated muscle preferentially expressed protein kinase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
striated muscle preferentially expressed protein kinase
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1, transcript variant X2
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 isoform X2
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1, transcript variant X1
uncharacterized protein LOC121550903 isoform X1
obscurin like cytoskeletal adaptor 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
obscurin like cytoskeletal adaptor 1b, transcript variant X10
obscurin like cytoskeletal adaptor 1b, transcript variant X8
obscurin like cytoskeletal adaptor 1b, transcript variant X6
obscurin like cytoskeletal adaptor 1b, transcript variant X3
obscurin like cytoskeletal adaptor 1b, transcript variant X4
obscurin like cytoskeletal adaptor 1b, transcript variant X9
obscurin like cytoskeletal adaptor 1b, transcript variant X7
obscurin like cytoskeletal adaptor 1b, transcript variant X5
obscurin like cytoskeletal adaptor 1b, transcript variant X1
collagen alpha-1(XVIII) chain, transcript variant X4
collagen alpha-1(XVIII) chain, transcript variant X5
collagen alpha-1(XVIII) chain isoform X4
collagen alpha-1(XVIII) chain isoform X5
collagen alpha-1(XVIII) chain, transcript variant X1
collagen alpha-1(XVIII) chain, transcript variant X2
collagen alpha-1(XVIII) chain, transcript variant X3
collagen alpha-1(XVIII) chain isoform X1
collagen alpha-1(XVIII) chain isoform X2
collagen alpha-1(XVIII) chain isoform X3
poly(rC)-binding protein 3, transcript variant X2
poly(rC)-binding protein 3, transcript variant X3
poly(rC)-binding protein 3, transcript variant X1
poly(rC)-binding protein 3, transcript variant X5
poly(rC)-binding protein 3, transcript variant X6
poly(rC)-binding protein 3, transcript variant X7
poly(rC)-binding protein 3, transcript variant X8
poly(rC)-binding protein 3, transcript variant X9
poly(rC)-binding protein 3, transcript variant X4
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
poly(rC)-binding protein 3, transcript variant X10
leucine-rich repeat-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121555670, 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 LOC121555670, transcript variant X2
collagen alpha-3(VI) chain, transcript variant X5
collagen alpha-3(VI) chain, transcript variant X3
collagen alpha-3(VI) chain, transcript variant X2
collagen alpha-3(VI) chain, transcript variant X1
collagen alpha-3(VI) chain, transcript variant X4
melanophilin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
melanophilin-like, 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
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
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X15
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
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X1
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X4
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X9
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X2
leucine rich repeat (in FLII) interacting protein 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 3 samples with support for all annotated introns
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X7
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X5
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X11
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
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X8
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X12
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
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X13
leucine rich repeat (in FLII) interacting protein 1a, transcript variant X14
leucine-rich repeat flightless-interacting protein 2 isoform X15
uncharacterized protein lrrfip1a isoform X1
uncharacterized protein lrrfip1a isoform X4
uncharacterized protein lrrfip1a isoform X6
uncharacterized protein lrrfip1a isoform X9
uncharacterized protein lrrfip1a isoform X2
uncharacterized protein lrrfip1a isoform X3
uncharacterized protein lrrfip1a isoform X7
leucine-rich repeat flightless-interacting protein 1 isoform X10
uncharacterized protein lrrfip1a isoform X5
leucine-rich repeat flightless-interacting protein 1 isoform X11
uncharacterized protein lrrfip1a isoform X8
leucine-rich repeat flightless-interacting protein 1 isoform X12
leucine-rich repeat flightless-interacting protein 1 isoform X13
leucine-rich repeat flightless-interacting protein 1 isoform X14
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
m-AAA protease-interacting protein 1, mitochondrial-like
E3 ubiquitin-protein ligase HECW2, transcript variant X2
E3 ubiquitin-protein ligase HECW2, transcript variant X1
E3 ubiquitin-protein ligase HECW2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin-protein ligase HECW2 isoform X1
E3 ubiquitin-protein ligase HECW2 isoform X2
zinc finger BED domain-containing 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 39 samples with support for all annotated introns
serine/threonine kinase 17b (apoptosis-inducing)
chromosome 4 C2orf69 homolog, transcript variant X1
chromosome 4 C2orf69 homolog, transcript variant X2
UPF0565 protein C2orf69 homolog isoform X1
UPF0565 protein C2orf69 homolog isoform X2
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X5
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X1
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X3
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X4
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X6
formiminotransferase cyclodeaminase N-terminal like 1, transcript variant X2
formiminotransferase N-terminal subdomain-containing protein isoform X1
formiminotransferase N-terminal subdomain-containing protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments
ly6/PLAUR domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
solute carrier family 35 member F5, transcript variant X3
solute carrier family 35 member F5, transcript variant X5
solute carrier family 35 member F5, transcript variant X1
solute carrier family 35 member F5, transcript variant X4
solute carrier family 35 member F5, transcript variant X2
solute carrier family 35 member F5, transcript variant X6
solute carrier family 35 member F5 isoform X2
solute carrier family 35 member F5 isoform X1
solute carrier family 35 member F5 isoform X3
inactive dipeptidyl peptidase 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
inactive dipeptidyl peptidase 10 isoform X1
inactive dipeptidyl peptidase 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
inactive dipeptidyl peptidase 10 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
gap junction gamma-1 protein, transcript variant X1
gap junction gamma-1 protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
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
histone deacetylase 4, transcript variant X1
histone deacetylase 4, transcript variant X2
histone deacetylase 4, transcript variant X3
ankyrin repeat and SOCS box containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
TNF receptor-associated factor 3 interacting protein 1, transcript variant X2
TNF receptor-associated factor 3 interacting protein 1, transcript variant X1
adenosine deaminase RNA specific B1b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
adenosine deaminase RNA specific B1b, 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 11 samples with support for all annotated introns
adenosine deaminase RNA specific B1b, 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 11 samples with support for all annotated introns
double-stranded RNA-specific editase 1 isoform X2
double-stranded RNA-specific editase 1 isoform X1
double-stranded RNA-specific editase 1 isoform 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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
integrin beta-2-like, transcript variant X6
integrin beta-2-like, transcript variant X4
integrin beta-2-like, transcript variant X2
integrin beta-2-like, transcript variant X3
integrin beta-2-like, transcript variant X1
integrin beta-2-like, transcript variant X5
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
uncharacterized protein LOC327557 homolog, transcript variant X1
uncharacterized protein LOC327557 homolog, transcript variant X2
uncharacterized protein LOC327557 homolog, transcript variant X3
peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform X1
peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform X2
peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform X3
uncharacterized protein LOC327557 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform X4
sterol 26-hydroxylase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 142, transcript variant X1
zinc finger protein 142, transcript variant X2
phospholipase C, delta 4b, transcript variant X1
phospholipase C, delta 4b, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-4 isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-4 isoform X2
CCR4-NOT transcription complex subunit 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 37-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 37-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 37-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 37-like
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 39 samples with support for all annotated introns
minichromosome maintenance complex component 3 associated protein, transcript variant X2
minichromosome maintenance complex component 3 associated protein, transcript variant X1
germinal-center associated nuclear protein
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase), transcript variant X1
lanosterol synthase (2,3-oxidosqualene-lanosterol cyclase), transcript variant X2
small membrane A-kinase anchor protein-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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 126 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
PMS1 homolog 1, mismatch repair system component, 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 7 samples with support for all annotated introns
PMS1 homolog 1, mismatch repair system component, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
PMS1 homolog 1, mismatch repair system component, transcript variant X3
ORMDL sphingolipid biosynthesis regulator 1
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
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable inactive tRNA-specific adenosine deaminase-like protein 3
O-sialoglycoprotein endopeptidase-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
probable tRNA N6-adenosine threonylcarbamoyltransferase, mitochondrial
ankyrin and armadillo repeat-containing protein
uncharacterized protein LOC678627 homolog
asparagine synthetase domain containing 1
asparagine synthetase domain-containing protein 1
ASNSD1 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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
glutaminase kidney isoform, mitochondrial-like
signal transducer and activator of transcription 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
signal transducer and activator of transcription 1b, transcript variant X1
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 5 samples with support for all annotated introns
signal transducer and activator of transcription 1b isoform X2
signal transducer and activator of transcription 1b isoform X1
signal transducer and activator of transcription 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
signal transducer and activator of transcription 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
signal transducer and activator of transcription 4 isoform X5
signal transducer and activator of transcription 4 isoform X4
signal transducer and activator of transcription 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
signal transducer and activator of transcription 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
signal transducer and activator of transcription 4, transcript variant X1
signal transducer and activator of transcription 4 isoform X3
signal transducer and activator of transcription 4 isoform X2
signal transducer and activator of transcription 4 isoform X1
mannose-1-phosphate guanyltransferase alpha-A, transcript variant X1
mannose-1-phosphate guanyltransferase alpha-A, transcript variant X2
mannose-1-phosphate guanyltransferase alpha-A isoform X1
mannose-1-phosphate guanyltransferase alpha-A isoform X2
mannose-1-phosphate guanyltransferase alpha-A, transcript variant X3
mannose-1-phosphate guanyltransferase alpha-A isoform X3
acid-sensing ion channel 4-A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
acid-sensing ion channel 4-A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 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
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 15 samples with support for all annotated introns
cyclin-dependent kinase 5 activator 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
myosin light chain kinase, smooth muscle, 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
myosin light chain kinase, smooth muscle, 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 2 samples with support for all annotated introns
myosin light chain kinase, smooth muscle isoform X1
myosin light chain kinase, smooth muscle isoform X2
formin-like protein 2, transcript variant X1
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
formin-like protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
formin-like protein 2, transcript variant X2
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
pre-mRNA-processing factor 40 homolog A, transcript variant X2
pre-mRNA-processing factor 40 homolog A, transcript variant X1
pre-mRNA-processing factor 40 homolog A, transcript variant X3
pre-mRNA-processing factor 40 homolog A isoform X3
pre-mRNA-processing factor 40 homolog A isoform X2
pre-mRNA-processing factor 40 homolog A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
polypeptide N-acetylgalactosaminyltransferase 13, 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 1 sample with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 13, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 13 isoform X2
polypeptide N-acetylgalactosaminyltransferase 13 isoform X1
G protein-activated inward rectifier potassium channel 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
nuclear receptor subfamily 4 group A member 2
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 23 samples with support for all annotated introns
glycerol-3-phosphate dehydrogenase, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycerol-3-phosphate dehydrogenase, mitochondrial, transcript variant X2
glycerol-3-phosphate dehydrogenase, mitochondrial isoform X1
glycerol-3-phosphate dehydrogenase, mitochondrial isoform X2
polypeptide N-acetylgalactosaminyltransferase 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
activin receptor type-1C-like, transcript variant X2
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 1 sample with support for all annotated introns
activin receptor type-1C-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
activin receptor type-1C-like isoform X2
activin receptor type-1C-like isoform X1
activin receptor type-1, transcript variant X4
activin receptor type-1, transcript variant X3
activin receptor type-1, transcript variant X5
activin receptor type-1, transcript variant X1
activin receptor type-1, transcript variant X2
uncharacterized protein C7orf57 homolog, transcript variant X1
uncharacterized protein C7orf57 homolog, transcript variant X2
uncharacterized protein C7orf57 homolog isoform X1
uncharacterized protein C7orf57 homolog isoform X2
coiled-coil domain-containing protein 148, transcript variant X3
coiled-coil domain-containing protein 148, transcript variant X1
coiled-coil domain-containing protein 148, transcript variant X2
coiled-coil domain-containing protein 148 isoform X2
coiled-coil domain-containing protein 148 isoform X1
insulin-like growth factor-binding protein 2-B, 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 22 samples with support for all annotated introns
insulin-like growth factor-binding protein 2-B, 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 15 samples with support for all annotated introns
insulin-like growth factor-binding protein 2-B, transcript variant X1
insulin-like growth factor-binding protein 2-B isoform X2
insulin-like growth factor-binding protein 2-B isoform X1
insulin-like growth factor-binding protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase FKBP7
major facilitator superfamily domain-containing protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
nuclear envelope integral membrane protein 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 8 samples with support for all annotated introns
neuronal membrane glycoprotein M6-b, transcript variant X3
neuronal membrane glycoprotein M6-b isoform X3
neuronal membrane glycoprotein M6-b, transcript variant X1
neuronal membrane glycoprotein M6-b, transcript variant X2
neuronal membrane glycoprotein M6-b isoform X1
neuronal membrane glycoprotein M6-b isoform X2
OFD1 centriole and centriolar satellite protein
oral-facial-digital syndrome 1 protein homolog
trafficking protein particle complex subunit 2
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 45 samples with support for all annotated introns
ras-related protein Rab-9A, transcript variant X1
ras-related protein Rab-9A, transcript variant X3
ras-related protein Rab-9A, transcript variant X4
ras-related protein Rab-9A, transcript variant X2
EGF-like-domain, multiple 6, transcript variant X1
EGF-like-domain, multiple 6, transcript variant X6
EGF-like-domain, multiple 6, transcript variant X4
EGF-like-domain, multiple 6, transcript variant X3
EGF-like-domain, multiple 6, transcript variant X2
EGF-like-domain, multiple 6, transcript variant X5
epidermal growth factor-like protein 6 isoform X6
epidermal growth factor-like protein 6 isoform X5
epidermal growth factor-like protein 6 isoform X4
epidermal growth factor-like protein 6 isoform X3
epidermal growth factor-like protein 6 isoform X2
epidermal growth factor-like protein 6 isoform X1
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
FERM and PDZ domain-containing protein 4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
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: FERM and PDZ domain-containing protein 4-like
LOW QUALITY PROTEIN: rho GTPase-activating protein 6-like
E3 ubiquitin-protein ligase Midline-1, transcript variant X3
E3 ubiquitin-protein ligase Midline-1, transcript variant X4
E3 ubiquitin-protein ligase Midline-1, transcript variant X2
E3 ubiquitin-protein ligase Midline-1, transcript variant X1
E3 ubiquitin-protein ligase Midline-1, transcript variant X5
E3 ubiquitin-protein ligase Midline-1 isoform X1
E3 ubiquitin-protein ligase Midline-1 isoform X2
component of oligomeric golgi complex 3, transcript variant X1
component of oligomeric golgi complex 3, transcript variant X2
conserved oligomeric Golgi complex subunit 3 isoform X1
conserved oligomeric Golgi complex subunit 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 24 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 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
SLIT and NTRK-like protein 5, 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 6 samples with support for all annotated introns
SLIT and NTRK-like protein 5, 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 8 samples with support for all annotated introns
homeobox protein PKNOX1-like, 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 19 samples with support for all annotated introns
homeobox protein PKNOX1-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 13 samples with support for all annotated introns
homeobox protein PKNOX1-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 28 samples with support for all annotated introns
homeobox protein PKNOX1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, transcript variant X3
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, transcript variant X6
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, transcript variant X2
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, transcript variant X5
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, transcript variant X1
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A, transcript variant X4
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X3
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X2
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X1
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X5
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A isoform X4
glucose-6-phosphate exchanger SLC37A1, 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 22 samples with support for all annotated introns
glucose-6-phosphate exchanger SLC37A1 isoform X1
glucose-6-phosphate exchanger SLC37A1, transcript variant X2
glucose-6-phosphate exchanger SLC37A1 isoform X2
transmembrane protein 50B, transcript variant X2
transmembrane protein 50B, 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 47 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
interferon alpha/beta receptor 1a, 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
interferon alpha/beta receptor 1a, 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 17 samples with support for all annotated introns
interferon alpha/beta receptor 1a isoform X2
interferon alpha/beta receptor 1a isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
interleukin-10 receptor subunit beta, transcript variant X2
interleukin-10 receptor subunit beta, transcript variant X1
interleukin-10 receptor subunit beta isoform X2
interleukin-10 receptor subunit beta isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
uncharacterized LOC121552784, transcript variant X3
uncharacterized LOC121552784, transcript variant X4
uncharacterized LOC121552784, transcript variant X5
uncharacterized LOC121552784, transcript variant X1
uncharacterized LOC121552784, transcript variant X2
uncharacterized protein LOC121552784 isoform X3
uncharacterized protein LOC121552784 isoform X1
uncharacterized protein LOC121552784 isoform X2
uncharacterized protein C21orf62 homolog
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 13 samples with support for all annotated introns
T-lymphocyte activation antigen CD80, transcript variant X2
T-lymphocyte activation antigen CD80, transcript variant X1
arginine and glutamate rich 1a, transcript variant X1
arginine and glutamate rich 1a, transcript variant X2
arginine and glutamate-rich protein 1-A isoform X1
arginine and glutamate-rich protein 1-A isoform 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
nucleolus and neural progenitor protein, 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
nucleolus and neural progenitor protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
nucleolus and neural progenitor protein isoform X1
nucleolus and neural progenitor protein isoform X2
testis-expressed protein 30, transcript variant X1
testis-expressed protein 30, transcript variant X2
syntaxin binding protein 5L, transcript variant X11
syntaxin binding protein 5L, transcript variant X9
syntaxin binding protein 5L, transcript variant X7
syntaxin binding protein 5L, transcript variant X4
syntaxin binding protein 5L, transcript variant X10
syntaxin binding protein 5L, transcript variant X8
syntaxin binding protein 5L, transcript variant X6
syntaxin binding protein 5L, transcript variant X3
syntaxin binding protein 5L, transcript variant X5
syntaxin binding protein 5L, transcript variant X2
syntaxin binding protein 5L, transcript variant X1
syntaxin-binding protein 5-like isoform X11
syntaxin-binding protein 5-like isoform X9
syntaxin-binding protein 5-like isoform X7
syntaxin-binding protein 5-like isoform X4
syntaxin-binding protein 5-like isoform X10
syntaxin-binding protein 5-like isoform X8
syntaxin-binding protein 5-like isoform X6
syntaxin-binding protein 5-like isoform X3
syntaxin-binding protein 5-like isoform X5
syntaxin-binding protein 5-like isoform X2
syntaxin-binding protein 5-like isoform X1
general transcription factor IIE, polypeptide 1, alpha
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 34 samples with support for all annotated introns
general transcription factor IIE subunit 1
RAB, member of RAS oncogene family-like 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 36 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like
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 25 samples with support for all annotated introns
transcription factor Sp3, transcript variant X3
transcription factor Sp3, transcript variant X1
transcription factor Sp3, transcript variant X2
transcription factor Sp3, transcript variant X4
cell division cycle associated 7a, transcript variant X2
cell division cycle associated 7a, transcript variant X1
cell division cycle-associated protein 7a isoform X2
cell division cycle-associated protein 7a isoform X1
mitogen-activated protein kinase kinase kinase 20, transcript variant X1
mitogen-activated protein kinase kinase kinase 20, transcript variant X2
mitogen-activated protein kinase kinase kinase 20 isoform X1
mitogen-activated protein kinase kinase kinase 20, transcript variant X3
mitogen-activated protein kinase kinase kinase 20 isoform X2
rap guanine nucleotide exchange factor 4-like, transcript variant X3
rap guanine nucleotide exchange factor 4-like, transcript variant X2
rap guanine nucleotide exchange factor 4-like, transcript variant X1
rap guanine nucleotide exchange factor 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121556137, transcript variant X3
uncharacterized LOC121556137, transcript variant X1
uncharacterized LOC121556137, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
histone acetyltransferase type B catalytic subunit, transcript variant X3
histone acetyltransferase type B catalytic subunit, transcript variant X2
histone acetyltransferase type B catalytic subunit, transcript variant X1
histone acetyltransferase type B catalytic subunit, transcript variant X5
histone acetyltransferase type B catalytic subunit, transcript variant X4
histone acetyltransferase type B catalytic subunit isoform X5
histone acetyltransferase type B catalytic subunit isoform X3
histone acetyltransferase type B catalytic subunit isoform X2
histone acetyltransferase type B catalytic subunit isoform X1
histone acetyltransferase type B catalytic subunit isoform X4
calcium-binding mitochondrial carrier protein Aralar1-like, transcript variant X2
calcium-binding mitochondrial carrier protein Aralar1-like, transcript variant X1
calcium-binding mitochondrial carrier protein Aralar1-like isoform X1
calcium-binding mitochondrial carrier protein Aralar1-like isoform X2
dynein, cytoplasmic 1, intermediate chain 2a, transcript variant X2
dynein, cytoplasmic 1, intermediate chain 2a, transcript variant X1
dynein, cytoplasmic 1, intermediate chain 2a isoform X2
dynein, cytoplasmic 1, intermediate chain 2a isoform X1
plasma membrane ascorbate-dependent reductase CYBRD1, transcript variant X2
plasma membrane ascorbate-dependent reductase CYBRD1 isoform X2
plasma membrane ascorbate-dependent reductase CYBRD1, transcript variant X1
plasma membrane ascorbate-dependent reductase CYBRD1 isoform X1
methyltransferase 8, methylcytidine, transcript variant X1
methyltransferase 8, methylcytidine, transcript variant X2
mRNA N(3)-methylcytidine methyltransferase METTL8 isoform X1
mRNA N(3)-methylcytidine methyltransferase METTL8 isoform X2
serine/threonine-protein kinase tousled-like 1-B
Golgi reassembly-stacking protein 2, transcript variant X1
Golgi reassembly-stacking protein 2, transcript variant X2
Golgi reassembly-stacking protein 2 isoform X2
Golgi reassembly-stacking protein 2 isoform X1
glutamate decarboxylase 1-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 23 samples with support for all annotated introns
glutamate decarboxylase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
glutamate decarboxylase 1-like isoform X2
glutamate decarboxylase 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase ubr3-like, transcript variant X4
E3 ubiquitin-protein ligase ubr3-like, transcript variant X3
E3 ubiquitin-protein ligase ubr3-like, transcript variant X2
E3 ubiquitin-protein ligase ubr3-like, transcript variant X1
E3 ubiquitin-protein ligase ubr3-like isoform X4
E3 ubiquitin-protein ligase ubr3-like isoform X3
E3 ubiquitin-protein ligase ubr3-like isoform X2
E3 ubiquitin-protein ligase ubr3-like isoform X1
methyltransferase 5, N6-adenosine, transcript variant X2
methyltransferase 5, N6-adenosine, transcript variant X1
rRNA N6-adenosine-methyltransferase METTL5 isoform X2
rRNA N6-adenosine-methyltransferase METTL5 isoform X1
lupus La protein homolog B, transcript variant X2
lupus La protein homolog B, transcript variant X1
kelch-like family member 23, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
kelch-like family member 23, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
FAST kinase domains 1, 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 31 samples with support for all annotated introns
FAST kinase domains 1, transcript variant X2
FAST kinase domains 1, transcript variant X3
FAST kinase domain-containing protein 1, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: kelch-like protein 41a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 89
low density lipoprotein receptor-related protein 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
low-density lipoprotein receptor-related protein 2a
retinol dehydrogenase 1, transcript variant X1
retinol dehydrogenase 1, transcript variant X2
retinol dehydrogenase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ATP-binding cassette, sub-family B (MDR/TAP), member 11a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
SPC25 component of NDC80 kinetochore complex
nitric oxide synthase trafficking, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nitric oxide synthase trafficking, transcript variant X1
serine threonine kinase 39, transcript variant X1
serine threonine kinase 39, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
STE20/SPS1-related proline-alanine-rich protein kinase isoform X1
STE20/SPS1-related proline-alanine-rich protein kinase isoform X2
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 1b, transcript variant X3
E3 SUMO-protein ligase ZBED1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
E3 SUMO-protein ligase ZBED1-like isoform X1
E3 SUMO-protein ligase ZBED1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
E3 SUMO-protein ligase ZBED1-like isoform X2
xin actin binding repeat containing 2b, transcript variant X4
LIM domain and actin-binding protein 1 isoform X4
xin actin binding repeat containing 2b, 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 2 samples with support for all annotated introns
xin actin binding repeat containing 2b, transcript variant X3
xin actin binding repeat containing 2b, transcript variant X1
xin actin-binding repeat-containing protein 2 isoform X2
xin actin-binding repeat-containing protein 2 isoform X3
xin actin-binding repeat-containing protein 2 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 3 (GalNAc-T3), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 3 (GalNAc-T3), 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 8 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
sodium channel protein type 2 subunit alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
sodium channel protein type 2 subunit alpha, transcript variant X1
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 1 sample with support for all annotated introns
sodium channel protein type 2 subunit alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein type 2 subunit alpha isoform X3
sodium channel protein type 2 subunit alpha isoform X2
sodium channel protein type 2 subunit alpha isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
cordon-bleu WH2 repeat protein-like 1b, transcript variant X2
cordon-bleu WH2 repeat protein-like 1b, transcript variant X1
cordon-bleu WH2 repeat protein-like 1b, transcript variant X4
cordon-bleu WH2 repeat protein-like 1b, transcript variant X3
growth factor receptor-bound protein 14, transcript variant X2
growth factor receptor-bound protein 14, 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 15 samples with support for all annotated introns
growth factor receptor-bound protein 14, transcript variant X3
growth factor receptor-bound protein 14, transcript variant X1
growth factor receptor-bound protein 14 isoform X1
growth factor receptor-bound protein 14 isoform X2
growth factor receptor-bound protein 14 isoform X3
growth factor receptor-bound protein 14, transcript variant X5
growth factor receptor-bound protein 14 isoform X4
potassium voltage-gated channel subfamily H member 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily H member 7, 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 4 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 7 isoform X1
potassium voltage-gated channel subfamily H member 7 isoform X2
interferon induced with helicase C domain 1
interferon-induced helicase C domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
sodium-driven chloride bicarbonate exchanger-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium-driven chloride bicarbonate exchanger-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium-driven chloride bicarbonate exchanger-like isoform X2
sodium-driven chloride bicarbonate exchanger-like isoform X1
uncharacterized LOC121552041, 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 46 samples with support for all annotated introns
uncharacterized LOC121552041, 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 54 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 17 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 1, transcript variant X6
RNA-binding motif, single-stranded-interacting protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 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 39 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 1 isoform X1
RNA-binding motif, single-stranded-interacting protein 1 isoform X6
RNA-binding motif, single-stranded-interacting protein 1 isoform X2
RNA-binding motif, single-stranded-interacting protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 1 isoform X3
RNA-binding motif, single-stranded-interacting protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 1, transcript variant X4
RNA-binding motif, single-stranded-interacting protein 1, transcript variant X5
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 38 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 1 isoform X4
RNA-binding motif, single-stranded-interacting protein 1 isoform X5
RNA-binding motif, single-stranded-interacting protein 1 isoform X7
RNA-binding motif, single-stranded-interacting protein 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RNA-binding motif, single-stranded-interacting protein 1 isoform X8
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X1
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X13
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X11
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X2
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X3
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X5
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X14
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X6
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X7
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X8
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X9
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X10
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X16
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X12
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X4
bromodomain adjacent to zinc finger domain protein 2B-like, transcript variant X15
bromodomain adjacent to zinc finger domain protein 2B-like isoform X1
bromodomain adjacent to zinc finger domain protein 2B-like isoform X13
bromodomain adjacent to zinc finger domain protein 2B-like isoform X11
bromodomain adjacent to zinc finger domain protein 2B-like isoform X2
bromodomain adjacent to zinc finger domain protein 2B-like isoform X3
bromodomain adjacent to zinc finger domain protein 2B-like isoform X5
bromodomain adjacent to zinc finger domain protein 2B-like isoform X14
bromodomain adjacent to zinc finger domain protein 2B-like isoform X6
bromodomain adjacent to zinc finger domain protein 2B-like isoform X7
bromodomain adjacent to zinc finger domain protein 2B-like isoform X8
bromodomain adjacent to zinc finger domain protein 2B-like isoform X9
bromodomain adjacent to zinc finger domain protein 2B-like isoform X10
bromodomain adjacent to zinc finger domain protein 2B-like isoform X16
bromodomain adjacent to zinc finger domain protein 2B-like isoform X12
bromodomain adjacent to zinc finger domain protein 2B-like isoform X4
bromodomain adjacent to zinc finger domain protein 2B-like isoform X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 11% coverage of the annotated genomic feature by RNAseq alignments
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1b, transcript variant X1
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1b, transcript variant X2
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1b, transcript variant X3
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1b, transcript variant X4
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1b, transcript variant X5
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1b, transcript variant X6
death-associated protein-like 1-A, transcript variant X1
death-associated protein-like 1-A, transcript variant X2
death-associated protein-like 1-A isoform X2
death-associated protein-like 1-A isoform X1
similar to RNA sequence (same species):INSD:GFGX01006554.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 166 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 58 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: nucleotide motif:Rfam:12.0:RF00397
calcium channel, voltage-dependent, L type, alpha 1C subunit, 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 1 sample with support for all annotated introns
voltage-dependent L-type calcium channel subunit alpha-1C isoform X1
calcium channel, voltage-dependent, L type, alpha 1C subunit, transcript variant X2
voltage-dependent L-type calcium channel subunit alpha-1C isoform X2
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X2
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X2
N-acyl phosphatidylethanolamine phospholipase D, transcript variant X1
N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D isoform X1
fibroblast growth factor receptor substrate 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
fibroblast growth factor receptor substrate 2a, transcript variant X2
fibroblast growth factor receptor substrate 2a
YEATS domain containing 4, transcript variant X1
YEATS domain containing 4, transcript variant X2
YEATS domain-containing protein 4 isoform X1
YEATS domain-containing protein 4 isoform X2
cleavage and polyadenylation specific factor 6, transcript variant X5
cleavage and polyadenylation specific factor 6, transcript variant X4
cleavage and polyadenylation specific factor 6, transcript variant X3
cleavage and polyadenylation specific factor 6, transcript variant X2
cleavage and polyadenylation specific factor 6, transcript variant X1
cleavage and polyadenylation specific factor 6, transcript variant X6
cleavage and polyadenylation specificity factor subunit 6 isoform X5
cleavage and polyadenylation specificity factor subunit 6 isoform X4
cleavage and polyadenylation specificity factor subunit 6 isoform X3
cleavage and polyadenylation specificity factor subunit 6 isoform X2
cleavage and polyadenylation specificity factor subunit 6 isoform X1
cleavage and polyadenylation specificity factor subunit 6 isoform X6
cleavage and polyadenylation specific factor 6, transcript variant X8
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 28 samples with support for all annotated introns
cleavage and polyadenylation specificity factor subunit 6 isoform X8
cleavage and polyadenylation specific factor 6, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
cleavage and polyadenylation specificity factor subunit 6 isoform X7
chaperonin containing TCP1, subunit 2 (beta)
COORDINATES: nucleotide motif:Rfam:12.0:RF01234
COORDINATES: nucleotide motif:Rfam:12.0:RF00191
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
RAB3A interacting protein (rabin3), transcript variant X2
RAB3A interacting protein (rabin3), transcript variant X1
RAB3A interacting protein (rabin3), transcript variant X5
RAB3A interacting protein (rabin3), transcript variant X6
RAB3A interacting protein (rabin3), transcript variant X7
RAB3A interacting protein (rabin3), transcript variant X4
RAB3A interacting protein (rabin3), transcript variant X3
CCR4-NOT transcription complex subunit 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
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: CCR4-NOT transcription complex subunit 2
calcium-activated potassium channel subunit beta-4
receptor-type tyrosine-protein phosphatase beta-like
interleukin-1 receptor-associated kinase 3, transcript variant X1
interleukin-1 receptor-associated kinase 3, transcript variant X2
interleukin-1 receptor-associated kinase 3 isoform X1
interleukin-1 receptor-associated kinase 3 isoform 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 16 samples with support for all annotated introns
glutamate receptor interacting protein 1, transcript variant X8
glutamate receptor interacting protein 1, transcript variant X6
glutamate receptor interacting protein 1, transcript variant X5
glutamate receptor interacting protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glutamate receptor interacting protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glutamate receptor interacting protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glutamate receptor interacting protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glutamate receptor interacting protein 1, transcript variant X2
glutamate receptor-interacting protein 1 isoform X8
glutamate receptor-interacting protein 1 isoform X6
glutamate receptor-interacting protein 1 isoform X5
glutamate receptor-interacting protein 1 isoform X7
glutamate receptor-interacting protein 1 isoform X3
glutamate receptor-interacting protein 1 isoform X4
glutamate receptor-interacting protein 1 isoform X1
glutamate receptor-interacting protein 1 isoform X2
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cullin-associated and neddylation-dissociated 1, transcript variant X1
cullin-associated and neddylation-dissociated 1, transcript variant X2
cullin-associated NEDD8-dissociated protein 1 isoform X1
cullin-associated NEDD8-dissociated protein 1 isoform X2
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform X1
dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform X2
CWF19-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
CWF19-like protein 1, transcript variant X4
CWF19-like protein 1, transcript variant X3
CWF19-like protein 1, transcript variant X2
cyclin D binding myb-like transcription factor 1, transcript variant X2
cyclin D binding myb-like transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
cyclin-D-binding Myb-like transcription factor 1 isoform X1
cyclin-D-binding Myb-like transcription factor 1 isoform X2
transmembrane protein 243, mitochondrial b, transcript variant X4
transmembrane protein 243, mitochondrial b, transcript variant X3
transmembrane protein 243, mitochondrial b, transcript variant X2
transmembrane protein 243, mitochondrial b, transcript variant X1
meiosis expressed gene 1 protein homolog
DNA cross-link repair 1C, PSO2 homolog (S. cerevisiae)
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 1 sample with support for all annotated introns
beta-galactoside alpha-2,6-sialyltransferase 2-like, transcript variant X2
beta-galactoside alpha-2,6-sialyltransferase 2-like, transcript variant X1
beta-galactoside alpha-2,6-sialyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
S-adenosylmethionine-dependent methyltransferase domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
transcription factor Dp-1, transcript variant X3
transcription factor Dp-1, transcript variant X1
transcription factor Dp-1, transcript variant X4
transcription factor Dp-1, transcript variant X2
transcription factor Dp-1, transcript variant X6
transcription factor Dp-1, transcript variant X5
DCN1-like protein 2, transcript variant X5
DCN1-like protein 2, transcript variant X4
DCN1-like protein 2, transcript variant X6
DCN1-like protein 2, transcript variant X3
DCN1-like protein 2, transcript variant X2
DCN1-like protein 2, transcript variant X1
DCN1-like protein 2, transcript variant X7
growth hormone-regulated TBC protein 1-A
lysosome-associated membrane glycoprotein 1
T-cell surface glycoprotein CD3 zeta chain-like
POU domain, class 2, transcription factor 1-like, transcript variant X8
POU domain, class 2, transcription factor 1-like, transcript variant X2
POU domain, class 2, transcription factor 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
POU domain, class 2, transcription factor 1-like, transcript variant X3
POU domain, class 2, transcription factor 1-like, transcript variant X1
POU domain, class 2, transcription factor 1-like, transcript variant X7
POU domain, class 2, transcription factor 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
POU domain, class 2, transcription factor 1-like, transcript variant X4
POU domain, class 2, transcription factor 1-like isoform X7
POU domain, class 2, transcription factor 1-like isoform X6
POU domain, class 2, transcription factor 1-like isoform X5
POU domain, class 2, transcription factor 1-like isoform X4
POU domain, class 2, transcription factor 1-like isoform X8
POU domain, class 2, transcription factor 1-like isoform X3
POU domain, class 2, transcription factor 1-like isoform X2
POU domain, class 2, transcription factor 1-like isoform X1
immunoglobulin-like domain-containing receptor 2, transcript variant X1
immunoglobulin-like domain-containing receptor 2, transcript variant X2
immunoglobulin-like domain-containing receptor 2, transcript variant X4
immunoglobulin-like domain-containing receptor 2, transcript variant X3
immunoglobulin-like domain-containing receptor 2 isoform X1
immunoglobulin-like domain-containing receptor 2 isoform X2
immunoglobulin-like domain-containing receptor 2 isoform X4
immunoglobulin-like domain-containing receptor 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
malic enzyme 3, NADP(+)-dependent, mitochondrial, transcript variant X2
malic enzyme 3, NADP(+)-dependent, mitochondrial, transcript variant X1
NADP-dependent malic enzyme, mitochondrial
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
ddb1 and cul4 associated factor 6, transcript variant X1
ddb1 and cul4 associated factor 6, transcript variant X3
ddb1 and cul4 associated factor 6, transcript variant X2
ddb1 and cul4 associated factor 6, transcript variant X5
ddb1 and cul4 associated factor 6, transcript variant X4
ddb1 and cul4 associated factor 6, transcript variant X6
ddb1 and cul4 associated factor 6, transcript variant X7
DDB1- and CUL4-associated factor 6 isoform X1
DDB1- and CUL4-associated factor 6 isoform X3
DDB1- and CUL4-associated factor 6 isoform X4
DDB1- and CUL4-associated factor 6 isoform X2
DDB1- and CUL4-associated factor 6 isoform X5
DDB1- and CUL4-associated factor 6 isoform X6
DDB1- and CUL4-associated factor 6 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein arginine methyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein arginine methyltransferase 2, transcript variant X1
uncharacterized si:ch211-218d20.15, transcript variant X2
uncharacterized si:ch211-218d20.15, 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 25 samples with support for all annotated introns
uncharacterized si:ch211-218d20.15, transcript variant X1
uncharacterized protein si:ch211-218d20.15 isoform X2
uncharacterized protein si:ch211-218d20.15 isoform X1
mediator complex subunit 14, 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 30 samples with support for all annotated introns
mediator complex subunit 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 14 isoform X2
mediator of RNA polymerase II transcription subunit 14 isoform X1
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X3
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X1
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X2
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X5
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X6
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X4
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X7
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X9
probable ubiquitin carboxyl-terminal hydrolase FAF-X, transcript variant X8
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X1
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X3
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X2
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X5
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X6
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X4
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X7
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X8
probable ubiquitin carboxyl-terminal hydrolase FAF-X isoform X9
DEAD-box helicase 3 X-linked a, transcript variant X1
DEAD-box helicase 3 X-linked a, transcript variant X2
DEAD-box helicase 3 X-linked a, transcript variant X4
DEAD-box helicase 3 X-linked a, transcript variant X3
DEAD-box helicase 3 X-linked a, transcript variant X5
DEAD-box helicase 3 X-linked a, transcript variant X6
DEAD-box helicase 3 X-linked a, transcript variant X7
DEAD-box helicase 3 X-linked a isoform X1
DEAD-box helicase 3 X-linked a isoform X2
DEAD-box helicase 3 X-linked a isoform X4
DEAD-box helicase 3 X-linked a isoform X3
DEAD-box helicase 3 X-linked a isoform X5
DEAD-box helicase 3 X-linked a isoform X6
DEAD-box helicase 3 X-linked a isoform X7
calcium/calmodulin-dependent serine protein kinase a, transcript variant X17
calcium/calmodulin-dependent serine protein kinase a, transcript variant X15
calcium/calmodulin-dependent serine protein kinase a, 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 4 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, transcript variant X3
calcium/calmodulin-dependent serine protein kinase a, 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 9 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, transcript variant X10
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 6 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, transcript variant X7
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
calcium/calmodulin-dependent serine protein kinase a, transcript variant X2
calcium/calmodulin-dependent serine protein kinase a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, transcript variant X6
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
calcium/calmodulin-dependent serine protein kinase a, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, transcript variant X9
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 5 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, transcript variant X5
calcium/calmodulin-dependent serine protein kinase a, transcript variant X1
calcium/calmodulin-dependent serine protein kinase a, transcript variant X16
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 13 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, transcript variant X13
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 12 samples with support for all annotated introns
calcium/calmodulin-dependent serine protein kinase a, 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 12 samples with support for all annotated introns
peripheral plasma membrane protein CASK isoform X16
peripheral plasma membrane protein CASK isoform X13
peripheral plasma membrane protein CASK isoform X17
peripheral plasma membrane protein CASK isoform X8
peripheral plasma membrane protein CASK isoform X15
peripheral plasma membrane protein CASK isoform X12
peripheral plasma membrane protein CASK isoform X10
peripheral plasma membrane protein CASK isoform X7
peripheral plasma membrane protein CASK isoform X2
peripheral plasma membrane protein CASK isoform X11
peripheral plasma membrane protein CASK isoform X4
peripheral plasma membrane protein CASK isoform X6
peripheral plasma membrane protein CASK isoform X14
peripheral plasma membrane protein CASK isoform X9
peripheral plasma membrane protein CASK isoform X5
peripheral plasma membrane protein CASK isoform X3
peripheral plasma membrane protein CASK isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
EF-hand domain (C-terminal) containing 2
EF-hand domain-containing family member C2
transfer RNA glycine (anticodon UCC); 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
lysine (K)-specific demethylase 6A, transcript variant X1
lysine (K)-specific demethylase 6A, transcript variant X4
lysine (K)-specific demethylase 6A, transcript variant X2
lysine (K)-specific demethylase 6A, transcript variant X3
lysine-specific demethylase 6A isoform X1
lysine-specific demethylase 6A isoform X4
lysine-specific demethylase 6A isoform X2
lysine-specific demethylase 6A isoform X3
lysine (K)-specific demethylase 6A, transcript variant X5
lysine-specific demethylase 6A isoform X5
lysine (K)-specific demethylase 6A, transcript variant X6
lysine-specific demethylase 6A isoform X6
divergent protein kinase domain 2B, transcript variant X1
divergent protein kinase domain 2B, transcript variant X2
divergent protein kinase domain 2B isoform X1
divergent protein kinase domain 2B isoform X2
uncharacterized LOC121554750, transcript variant X2
uncharacterized LOC121554750, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
coiled-coil domain-containing protein 80
solute carrier family 35 member A5, transcript variant X1
solute carrier family 35 member A5, transcript variant X2
probable UDP-sugar transporter protein SLC35A5 isoform X1
probable UDP-sugar transporter protein SLC35A5 isoform X2
coagulation factor V, transcript variant X1
coagulation factor V, transcript variant X2
regulator of cell cycle, transcript variant X1
regulator of cell cycle, transcript variant X2
von Willebrand factor A domain containing 8
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 27 samples with support for all annotated introns
von Willebrand factor A domain-containing protein 8
diacylglycerol kinase, eta, transcript variant X3
diacylglycerol kinase, eta, transcript variant X4
diacylglycerol kinase, eta, transcript variant X5
diacylglycerol kinase, eta, transcript variant X1
diacylglycerol kinase, eta, transcript variant X2
diacylglycerol kinase, eta, transcript variant X6
uncharacterized LOC121556385, transcript variant X1
uncharacterized LOC121556385, transcript variant X2
uncharacterized LOC121556385, transcript variant X3
uncharacterized protein LOC121556385 isoform X1
uncharacterized protein LOC121556385 isoform X2
uncharacterized protein LOC121556385 isoform X3
calcitonin gene-related peptide type 1 receptor
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
tissue factor pathway inhibitor, transcript variant X2
tissue factor pathway inhibitor, transcript variant X1
tissue factor pathway inhibitor isoform X2
tissue factor pathway inhibitor isoform X1
PTB domain-containing engulfment adapter protein 1, transcript variant X4
PTB domain-containing engulfment adapter protein 1, transcript variant X5
PTB domain-containing engulfment adapter protein 1, transcript variant X6
PTB domain-containing engulfment adapter protein 1, transcript variant X2
PTB domain-containing engulfment adapter protein 1, transcript variant X3
PTB domain-containing engulfment adapter protein 1, transcript variant X1
PTB domain-containing engulfment adapter protein 1, transcript variant X8
PTB domain-containing engulfment adapter protein 1, transcript variant X7
PTB domain-containing engulfment adapter protein 1 isoform X1
PTB domain-containing engulfment adapter protein 1 isoform X5
PTB domain-containing engulfment adapter protein 1 isoform X3
PTB domain-containing engulfment adapter protein 1 isoform X6
PTB domain-containing engulfment adapter protein 1 isoform X2
PTB domain-containing engulfment adapter protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns