Gallus gallus isolate bGalGal1 chromosome 34, bGalGal1.mat.broiler.GRCg7b, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Galloanserae; Galliformes; Phasianidae; Phasianinae; Gallus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM028515.1.\nAssembly name: bGalGal1.mat.broiler.GRCg7b\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2021/01/19. The original whole-genome shotgun project has the\naccession JAENSK000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 22-JUL-2020\nAssembly Method :: TrioCanu v. 1.8; purge_dups v. 1.0.0;\n Scaff 10x v. 4.1.0; Bionano solve v.\n 3.2.1_04122018; Salsa2 HiC v. 2.2; Arrow\n polishing and gap filling v.\n SMRTLink7.0.1; Freebayes v. 1.3.1; gEVAL\n manual curation v. 2020-07-22; VGP trio\n assembly pipeline v. 1.6\nAssembly Name :: bGalGal1.mat.broiler.GRCg7b\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 102.01x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Gallus gallus Annotation Release 106\nAnnotation Version :: 106\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##
Wnt family member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
COORDINATES: ab initio prediction:SignalP:4.0
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: cap analysis [ECO:0007248] and polyA evidence [ECO:0006239]
peptidyl-prolyl cis-trans isomerase FKBP11
coiled-coil domain containing 65, transcript variant X2
coiled-coil domain containing 65, transcript variant X1
dynein regulatory complex subunit 2 isoform X1
dynein regulatory complex subunit 2 isoform X2
DEAD-box helicase 23, transcript variant X1
DEAD-box helicase 23, transcript variant X2
probable ATP-dependent RNA helicase DDX23 isoform X1
probable ATP-dependent RNA helicase DDX23 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DDX23
COORDINATES: polyA evidence [ECO:0006239]
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable ATP-dependent RNA helicase DDX23
serine/arginine repetitive matrix protein 1-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like, transcript variant X1
serine/arginine repetitive matrix protein 1-like, transcript variant X4
serine/arginine repetitive matrix protein 1-like, transcript variant X3
voltage-dependent L-type calcium channel subunit beta-3 isoform X2
voltage-dependent L-type calcium channel subunit beta-3 isoform X1
voltage-dependent L-type calcium channel subunit beta-3 isoform X4
voltage-dependent L-type calcium channel subunit beta-3 isoform X3
adenylate cyclase type 6-like, transcript variant X1
adenylate cyclase type 6-like, transcript variant X2
KAT8 regulatory NSL complex subunit 2, transcript variant X2
KAT8 regulatory NSL complex subunit 2, transcript variant X1
KAT8 regulatory NSL complex subunit 2, transcript variant X4
KAT8 regulatory NSL complex subunit 2, transcript variant X3
KAT8 regulatory NSL complex subunit 2 isoform X1
KAT8 regulatory NSL complex subunit 2 isoform X3
KAT8 regulatory NSL complex subunit 2 isoform X2
NCK associated protein 5 like, transcript variant X1
LOW QUALITY PROTEIN: nck-associated protein 5-like isoform X1
transmembrane BAX inhibitor motif containing 6, transcript variant X1
transmembrane BAX inhibitor motif containing 6, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: formin-like protein 3
formin-like protein 3, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 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: formin-like protein 3 isoform X1
autophagy related 101, transcript variant X4
autophagy related 101, transcript variant X2
autophagy related 101, transcript variant X3
autophagy related 101, transcript variant X1
autophagy related 101, transcript variant X8
autophagy related 101, transcript variant X6
autophagy related 101, transcript variant X7
autophagy related 101, transcript variant X5
autophagy-related protein 101 isoform X4
autophagy-related protein 101 isoform X2
autophagy-related protein 101 isoform X3
autophagy-related protein 101 isoform X1
autophagy-related protein 101 isoform X8
autophagy-related protein 101 isoform X6
autophagy-related protein 101 isoform X7
autophagy-related protein 101 isoform X5
nuclear receptor subfamily 4 group A member 1, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nuclear receptor subfamily 4 group A member 1
general receptor for phosphoinositides 1 associated scaffold protein
activin A receptor type 1B, transcript variant X1
activin A receptor type 1B, transcript variant X3
activin A receptor type 1B, transcript variant X2
activin A receptor like type 1, transcript variant X2
activin A receptor like type 1, transcript variant X1
serine/threonine-protein kinase receptor R3 isoform X1
serine/threonine-protein kinase receptor R3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121106464, transcript variant X2
uncharacterized LOC121106464, transcript variant X1
transmembrane and death domain protein 1
sodium voltage-gated channel alpha subunit 8, transcript variant X4
sodium voltage-gated channel alpha subunit 8, transcript variant X2
sodium voltage-gated channel alpha subunit 8, transcript variant X1
sodium voltage-gated channel alpha subunit 8, transcript variant X3
sodium voltage-gated channel alpha subunit 8, transcript variant X6
sodium voltage-gated channel alpha subunit 8, transcript variant X5
sodium channel protein type 8 subunit alpha isoform X2
sodium channel protein type 8 subunit alpha isoform X1
sodium channel protein type 8 subunit alpha isoform X3
activating transcription factor 1, transcript variant X9
activating transcription factor 1, transcript variant X5
activating transcription factor 1, transcript variant X7
activating transcription factor 1, transcript variant X3
activating transcription factor 1, transcript variant X6
activating transcription factor 1, transcript variant X2
activating transcription factor 1, transcript variant X1
activating transcription factor 1, transcript variant X4
activating transcription factor 1, transcript variant X10
activating transcription factor 1, transcript variant X8
cyclic AMP-dependent transcription factor ATF-1 isoform X2
cyclic AMP-dependent transcription factor ATF-1 isoform X1
cyclic AMP-dependent transcription factor ATF-1 isoform X3
cyclic AMP-dependent transcription factor ATF-1 isoform X4
cyclic AMP-dependent transcription factor ATF-1 isoform X5
cyclic AMP-dependent transcription factor ATF-1 isoform X6
disco interacting protein 2 homolog B, transcript variant X2
disco interacting protein 2 homolog B, transcript variant X1
disco-interacting protein 2 homolog B isoform X2
disco-interacting protein 2 homolog B isoform X1
microRNA 1668; Derived by automated computational analysis using gene prediction method: BestRefSeq.
La ribonucleoprotein domain family member 4; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
La ribonucleoprotein domain family member 4
similar to RNA sequence, mRNA (same species):RefSeq:NM_001395973.1
annotated by transcript or proteomic data
The RefSeq transcript has 26 substitutions, 7 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
La ribonucleoprotein domain family member 4, transcript variant X2
La ribonucleoprotein domain family member 4, transcript variant X1
La ribonucleoprotein domain family member 4, transcript variant X4
La ribonucleoprotein domain family member 4, transcript variant X3
similar to AA sequence (same species):RefSeq:NP_001382902.1
The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC121108085, transcript variant X1
uncharacterized LOC121108085, transcript variant X5
uncharacterized LOC121108085, transcript variant X4
uncharacterized LOC121108085, transcript variant X2
uncharacterized LOC121108085, transcript variant X3
LIM domain and actin binding 1, transcript variant X3
LIM domain and actin binding 1, transcript variant X9
LIM domain and actin binding 1, transcript variant X4
LIM domain and actin binding 1, transcript variant X5
LIM domain and actin binding 1, transcript variant X6
LIM domain and actin binding 1, transcript variant X1
LIM domain and actin binding 1, transcript variant X7
LIM domain and actin binding 1, transcript variant X2
LIM domain and actin binding 1, transcript variant X8
LIM domain and actin-binding protein 1 isoform X1
LIM domain and actin-binding protein 1 isoform X2
ceramide synthase 5, transcript variant X1
ceramide synthase 5, transcript variant X2
ceramide synthase 5, transcript variant X4
ceramide synthase 5, transcript variant X5
ceramide synthase 5, transcript variant X3
COX14, cytochrome c oxidase assembly factor; Derived by automated computational analysis using gene prediction method: BestRefSeq.
COX14, cytochrome c oxidase assembly factor
cytochrome c oxidase assembly homolog 14
glycerol-3-phosphate dehydrogenase 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 1
acid sensing ion channel subunit 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
acid sensing ion channel subunit 1, transcript variant X4
acid sensing ion channel subunit 1, transcript variant X3
acid sensing ion channel subunit 1, transcript variant X2
acid sensing ion channel subunit 1, transcript variant X1
WAS/WASL-interacting protein family member 3-like
WAS/WASL-interacting protein family member 3
similar to RNA sequence, mRNA (same species):RefSeq:NM_001040467.1
The RefSeq transcript has 5 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
propagated from UniProtKB/Swiss-Prot (Q1XA76.1); transmembrane region
Important for channel gating; propagated from UniProtKB/Swiss-Prot (Q1XA76.1); other site
Important for channel desensitizing; propagated from UniProtKB/Swiss-Prot (Q1XA76.1); other site
N-linked (GlcNAc...) asparagine. /evidence=ECO:0000269|PubMed:17882215, ECO:0000269|PubMed:22760635, ECO:0000269|PubMed:22842900; propagated from UniProtKB/Swiss-Prot (Q1XA76.1); glycosylation site
propagated from UniProtKB/Swiss-Prot (Q1XA76.1); Region: Selectivity filter. /evidence=ECO:0000305
Rac GTPase activating protein 1, transcript variant X4
Rac GTPase activating protein 1, transcript variant X6
Rac GTPase activating protein 1, transcript variant X3
Rac GTPase activating protein 1, transcript variant X1
Rac GTPase activating protein 1, transcript variant X2
rac GTPase-activating protein 1 isoform X2
Rac GTPase activating protein 1, transcript variant X5
rac GTPase-activating protein 1 isoform X1
histone deacetylase 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001031402.2
The RefSeq transcript has 11 substitutions, 1 frameshift, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001026573.1
The RefSeq protein has 1 frameshift compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Twist homlog 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001103214.1
The RefSeq transcript has 11 substitutions, 13 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
solute carrier family 48 member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
solute carrier family 48 member 1, transcript variant X3
solute carrier family 48 member 1, transcript variant X2
solute carrier family 48 member 1, transcript variant X1
propagated from UniProtKB/Swiss-Prot (Q5ZHU0.1); transmembrane region
propagated from UniProtKB/Swiss-Prot (Q5ZHU0.1); Region: Di-leucine motif
Rap guanine nucleotide exchange factor 3, transcript variant X1
rap guanine nucleotide exchange factor 3 isoform X1
Rap guanine nucleotide exchange factor 3, transcript variant X2
rap guanine nucleotide exchange factor 3 isoform X2
Rap guanine nucleotide exchange factor 3, transcript variant X3
rap guanine nucleotide exchange factor 3 isoform X3
neuronal differentiation 4; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
neuronal differentiation 4, transcript variant X1
similar to RNA sequence, mRNA (same species):RefSeq:NM_205076.1
The RefSeq transcript has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_990407.1
propagated from UniProtKB/Swiss-Prot (P79766.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
propagated from UniProtKB/Swiss-Prot (P79766.1); Region: Nuclear localization signal. /evidence=ECO:0000255
propagated from UniProtKB/Swiss-Prot (P79766.1); Region: Leucine-zipper
neurogenic differentiation factor 4 isoform X1
thymocyte expressed, positive selection associated 1, transcript variant X7
thymocyte expressed, positive selection associated 1, transcript variant X5
thymocyte expressed, positive selection associated 1, transcript variant X4
thymocyte expressed, positive selection associated 1, transcript variant X3
thymocyte expressed, positive selection associated 1, transcript variant X2
thymocyte expressed, positive selection associated 1, transcript variant X1
thymocyte expressed, positive selection associated 1, transcript variant X6
protein phosphatase 1 regulatory inhibitor subunit 1A
protein phosphatase 1 regulatory subunit 1A
phosphodiesterase 1B, transcript variant X1
phosphodiesterase 1B, transcript variant X2
phosphodiesterase 1B, transcript variant X3
phosphodiesterase 1B, transcript variant X4
calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B isoform X1
calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B isoform X2
calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B isoform X3
NCK associated protein 1 like; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
NCK associated protein 1 like, transcript variant X1
nck-associated protein 1-like isoform X1
gametocyte specific factor 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
gametocyte specific factor 2, transcript variant X5
gametocyte specific factor 2, transcript variant X17
gametocyte specific factor 2, transcript variant X18
gametocyte specific factor 2, transcript variant X16
gametocyte specific factor 2, transcript variant X20
gametocyte specific factor 2, transcript variant X15
gametocyte specific factor 2, transcript variant X6
gametocyte specific factor 2, transcript variant X19
gametocyte specific factor 2, transcript variant X7
gametocyte specific factor 2, transcript variant X13
gametocyte specific factor 2, transcript variant X3
gametocyte specific factor 2, transcript variant X4
gametocyte specific factor 2, transcript variant X11
gametocyte specific factor 2, transcript variant X12
gametocyte specific factor 2, transcript variant X9
gametocyte specific factor 2, transcript variant X8
gametocyte specific factor 2, transcript variant X14
gametocyte specific factor 2, transcript variant X10
gametocyte specific factor 2, transcript variant X2
gametocyte specific factor 2, transcript variant X1
gametocyte specific factor 2, transcript variant X22
gametocyte specific factor 2, transcript variant X21
integrin, alpha 5 (fibronectin receptor, alpha polypeptide), transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 4 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 4 codons; deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: integrin alpha-5 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons
LOW QUALITY PROTEIN: zinc finger protein 385A
coatomer protein complex subunit zeta 1, transcript variant X1
coatomer protein complex subunit zeta 1, transcript variant X2
microRNA mir-148b; Derived by automated computational analysis using gene prediction method: BestRefSeq.
heterogeneous nuclear ribonucleoprotein A1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
heterogeneous nuclear ribonucleoprotein A1, transcript variant X4
heterogeneous nuclear ribonucleoprotein A1, transcript variant X5
heterogeneous nuclear ribonucleoprotein A1, transcript variant X2
heterogeneous nuclear ribonucleoprotein A1 isoform X4
heterogeneous nuclear ribonucleoprotein A1 isoform X2
heterogeneous nuclear ribonucleoprotein A1, transcript variant X6
heterogeneous nuclear ribonucleoprotein A1, transcript variant X3
heterogeneous nuclear ribonucleoprotein A1
heterogeneous nuclear ribonucleoprotein A1, transcript variant X1
heterogeneous nuclear ribonucleoprotein A1 isoform X3
heterogeneous nuclear ribonucleoprotein A1 isoform X1
heterogeneous nuclear ribonucleoprotein A1 isoform X5
single-strand-selective monofunctional uracil-DNA glycosylase 1, transcript variant X1
single-strand selective monofunctional uracil DNA glycosylase
uncharacterized LOC112530920, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
homeobox C8; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_204893.3
The RefSeq transcript has 1 frameshift compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_990224.1
propagated from UniProtKB/Swiss-Prot (Q9YH13.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
propagated from UniProtKB/Swiss-Prot (Q9YH13.1); Region: Antp-type hexapeptide
homeobox C9; Derived by automated computational analysis using gene prediction method: BestRefSeq.
microRNA 196a-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
homeobox C10; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC107055410, transcript variant X1
uncharacterized LOC107055410, transcript variant X2
ATP synthase, H+ transporting, mitochondrial Fo complex subunit C2 (subunit 9)
ATP synthase F(0) complex subunit C2, mitochondrial
activating transcription factor 7, transcript variant X9
activating transcription factor 7, transcript variant X3
activating transcription factor 7, transcript variant X7
activating transcription factor 7, transcript variant X1
activating transcription factor 7, transcript variant X2
activating transcription factor 7, transcript variant X4
activating transcription factor 7, transcript variant X5
microRNA 2130; Derived by automated computational analysis using gene prediction method: BestRefSeq.
cyclic AMP-dependent transcription factor ATF-7 isoform X1
activating transcription factor 7, transcript variant X8
activating transcription factor 7, transcript variant X6
cyclic AMP-dependent transcription factor ATF-7 isoform X2
microRNA 7477; Derived by automated computational analysis using gene prediction method: BestRefSeq.
TARBP2, RISC loading complex RNA binding subunit, transcript variant X2
TARBP2, RISC loading complex RNA binding subunit, transcript variant X1
RISC-loading complex subunit TARBP2 isoform X2
RISC-loading complex subunit TARBP2 isoform X1
mitogen-activated protein kinase kinase kinase 12, transcript variant X1
mitogen-activated protein kinase kinase kinase 12 isoform X1
mitogen-activated protein kinase kinase kinase 12, 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 43 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 12 isoform X2
poly(rC) binding protein 2, transcript variant X11
poly(rC) binding protein 2, transcript variant X10
poly(rC) binding protein 2, transcript variant X9
poly(rC) binding protein 2, transcript variant X8
poly(rC) binding protein 2, transcript variant X7
poly(rC) binding protein 2, transcript variant X5
poly(rC) binding protein 2, transcript variant X4
poly(rC) binding protein 2, transcript variant X3
poly(rC) binding protein 2, transcript variant X1
poly(rC) binding protein 2, transcript variant X6
poly(rC) binding protein 2, transcript variant X2
anti-Mullerian hormone receptor type 2, transcript variant X1
anti-Muellerian hormone type-2 receptor isoform X1
Sp1 transcription factor; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
Sp1 transcription factor, transcript variant X1
formin-like protein 16, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 88% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor Sp7
vitamin D (1,25- dihydroxyvitamin D3) receptor; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X1
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X11
vitamin D (1,25- dihydroxyvitamin D3) receptor
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X4
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X2
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X8
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X7
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X6
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X5
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X3
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X9
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X10
vitamin D (1,25- dihydroxyvitamin D3) receptor, transcript variant X12
propagated from UniProtKB/Swiss-Prot (O42392.1); Region: Hinge
propagated from UniProtKB/Swiss-Prot (O42392.1); Region: Vitamin D3 binding. /evidence=ECO:0000250
propagated from UniProtKB/Swiss-Prot (O42392.1); Region: Interaction with coactivator LXXLL motif. /evidence=ECO:0000250
propagated from UniProtKB/Swiss-Prot (O42392.1); Region: 9aaTAD. /evidence=ECO:0000250|UniProtKB:P11473
transmembrane protein 106C, transcript variant X5
transmembrane protein 106C, transcript variant X3
transmembrane protein 106C, transcript variant X1
transmembrane protein 106C, transcript variant X4
transmembrane protein 106C, transcript variant X2
collagen type II alpha 1 chain; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_204426.2
The RefSeq transcript has 26 substitutions, 1 frameshift, 2 non-frameshifting indels and aligns at 7% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_989757.2
The RefSeq protein has 12 substitutions, 1 frameshift and aligns at 3% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SUMO specific peptidase 1, transcript variant X1
LOW QUALITY PROTEIN: sentrin-specific protease 1 isoform X1
phosphofructokinase, muscle; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
phosphofructokinase, muscle, transcript variant X1
ATP-dependent 6-phosphofructokinase, muscle type isoform X1
similar to RNA sequence, mRNA (same species):RefSeq:NM_204223.2
The RefSeq transcript has 1 substitution, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP-dependent 6-phosphofructokinase, muscle type
ankyrin repeat and SOCS box containing 8; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ankyrin repeat and SOCS box containing 8, transcript variant X1
ankyrin repeat and SOCS box containing 8
ankyrin repeat and SOCS box protein 8 isoform X1
zinc finger protein 853-like, transcript variant X3
zinc finger protein 853-like, transcript variant X2
zinc finger protein 853-like, transcript variant X1
zinc finger protein 853, transcript variant X2
zinc finger protein 853, transcript variant X3
zinc finger protein 853, transcript variant X1
extra spindle pole bodies like 1, separase, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 10 bases in 9 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 10 bases in 9 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
interferon-induced guanylate-binding protein 1-like, transcript variant X1
cysteine acid decarboxylase, transcript variant X2
cysteine acid decarboxylase, transcript variant X1
cysteine acid decarboxylase, transcript variant X3
cysteine acid decarboxylase, transcript variant X4
cysteine sulfinic acid decarboxylase isoform X2
cysteine sulfinic acid decarboxylase isoform X1
cysteine sulfinic acid decarboxylase isoform X3
cysteine sulfinic acid decarboxylase isoform X4
microRNA mir-12287; Derived by automated computational analysis using gene prediction method: BestRefSeq.
zinc finger protein 740, transcript variant X2
zinc finger protein 740, transcript variant X1
zinc finger protein 740, transcript variant X3
zinc finger protein 740, transcript variant X4
integrin beta-7-like, transcript variant X2
integrin beta-7-like, transcript variant X1
retinoic acid receptor gamma-like, transcript variant X1
LOW QUALITY PROTEIN: retinoic acid receptor gamma isoform X1
major facilitator superfamily domain containing 5, transcript variant X3
major facilitator superfamily domain containing 5, transcript variant X1
major facilitator superfamily domain containing 5, transcript variant X2
SPRY domain containing 3, transcript variant X2
SPRY domain containing 3, transcript variant X1
SPRY domain-containing protein 3 isoform X1
SPRY domain-containing protein 3 isoform X2
proline-rich proteoglycan 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
protein kinase AMP-activated non-catalytic subunit gamma 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
protein kinase AMP-activated non-catalytic subunit gamma 1, transcript variant X2
protein kinase AMP-activated non-catalytic subunit gamma 1, transcript variant X1
protein kinase AMP-activated non-catalytic subunit gamma 1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001034827.2
The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
5'-AMP-activated protein kinase subunit gamma-1
5'-AMP-activated protein kinase subunit gamma-1 isoform X1
5'-AMP-activated protein kinase subunit gamma-1 isoform X2
lysine methyltransferase 2D, transcript variant X3
lysine methyltransferase 2D, transcript variant X6
lysine methyltransferase 2D, transcript variant X1
lysine methyltransferase 2D, transcript variant X5
lysine methyltransferase 2D, transcript variant X4
lysine methyltransferase 2D, transcript variant X2
histone-lysine N-methyltransferase 2D isoform X3
histone-lysine N-methyltransferase 2D isoform X1
histone-lysine N-methyltransferase 2D isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
limb development membrane protein 1 like, transcript variant X1
limb development membrane protein 1 like, transcript variant X2
tubulin alpha 1a; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305272.2
similar to AA sequence (same species):RefSeq:NP_001292201.2
tubulin alpha-1C chain-like, transcript variant X1
PYM homolog 1, exon junction complex associated factor
diacylglycerol kinase alpha, transcript variant X1
premelanosome protein; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
premelanosome protein, transcript variant X4
premelanosome protein, transcript variant X3
premelanosome protein, transcript variant X2
premelanosome protein, transcript variant X1
N-linked (GlcNAc...) asparagine. /evidence=ECO:0000255; propagated from UniProtKB/Swiss-Prot (Q98917.3); glycosylation site
propagated from UniProtKB/Swiss-Prot (Q98917.3); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
propagated from UniProtKB/Swiss-Prot (Q98917.3); Region: 4 X 24 AA approximate tandem repeats of T-[AD]-[EG]-D-[AV]-[AV]-[AG]-[AP]-T-[AP]-[AG]-A-T-A-[AE]- [DS]-[IV]-A-[DV]-[DP]-T-A-G-A
cyclin dependent kinase 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
RAB5B, member RAS oncogene family; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
RAB5B, member RAS oncogene family, transcript variant X2
RAB5B, member RAS oncogene family, transcript variant X1
propagated from UniProtKB/Swiss-Prot (Q5ZHW4.1); Region: Effector region. /evidence=ECO:0000255
propagated from UniProtKB/Swiss-Prot (Q5ZHW4.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
sulfite oxidase; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
IKAROS family zinc finger 4, transcript variant X3
IKAROS family zinc finger 4, transcript variant X1
IKAROS family zinc finger 4, transcript variant X2
IKAROS family zinc finger 4, transcript variant X4
erb-b2 receptor tyrosine kinase 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001044669.1
The RefSeq transcript has 23 substitutions, 1 frameshift, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
erb-b2 receptor tyrosine kinase 3, transcript variant X1
erb-b2 receptor tyrosine kinase 3, transcript variant X2
similar to AA sequence (same species):RefSeq:NP_001038134.1
The RefSeq protein has 2 substitutions, 1 frameshift compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
receptor tyrosine-protein kinase erbB-3 precursor
receptor tyrosine-protein kinase erbB-3 isoform X1
receptor tyrosine-protein kinase erbB-3 isoform X2
proliferation-associated 2G4, 38kDa, transcript variant X1
proliferation-associated protein 2G4 isoform X1
zinc finger CCCH domain-containing protein 10
extended synaptotagmin 1, transcript variant X1
myosin, light chain 6, alkali, smooth muscle and non-muscle; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
myosin, light chain 6, alkali, smooth muscle and non-muscle, transcript variant X1
myosin, light chain 6, alkali, smooth muscle and non-muscle
N-acetylcysteine. /evidence=ECO:0000269|PubMed:6870825; propagated from UniProtKB/Swiss-Prot (P02607.3); acetylation site
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X6
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X5
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X1
SWI/SNF complex subunit SMARCC2 isoform X5
SWI/SNF complex subunit SMARCC2 isoform X4
SWI/SNF complex subunit SMARCC2 isoform X2
SWI/SNF complex subunit SMARCC2 isoform X3
SWI/SNF complex subunit SMARCC2 isoform X1
SWI/SNF complex subunit SMARCC2 isoform X6
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.
ring finger protein 41, transcript variant X2
ring finger protein 41, transcript variant X1
nucleic acid binding protein 2, transcript variant X3
nucleic acid binding protein 2, transcript variant X1
nucleic acid binding protein 2, transcript variant X2
ankyrin repeat domain 52; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ankyrin repeat domain 52, transcript variant X3
ankyrin repeat domain 52, transcript variant X2
ankyrin repeat domain 52, transcript variant X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 1
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 2
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 3
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 4
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 5
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 6
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 7
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 8
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 9
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 10
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 11
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 12
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 13
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 14
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 15
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 16
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 17
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 18
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 19
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 20
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 21
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 22
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 23
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 24
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 25
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 26
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 27
propagated from UniProtKB/Swiss-Prot (Q5ZLC8.1); Region: ANK 28
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C isoform X3
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C isoform X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C isoform X2
coenzyme Q-binding protein COQ10 homolog A, mitochondrial isoform X2
coenzyme Q-binding protein COQ10 homolog A, mitochondrial isoform X3
coenzyme Q-binding protein COQ10 homolog A, mitochondrial isoform X1
citrate synthase, mitochondrial isoform X2
citrate synthase, mitochondrial isoform X1
citrate synthase, mitochondrial isoform X4
citrate synthase, mitochondrial isoform X3
PAN2 poly(A) specific ribonuclease subunit; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
PAN2 poly(A) specific ribonuclease subunit, transcript variant X1
PAN2 poly(A) specific ribonuclease subunit
PAN2-PAN3 deadenylation complex catalytic subunit PAN2
propagated from UniProtKB/Swiss-Prot (Q5F450.1); Region: WD 1. /evidence=ECO:0000255|HAMAP-Rule:MF_03182
propagated from UniProtKB/Swiss-Prot (Q5F450.1); Region: WD 2. /evidence=ECO:0000255|HAMAP-Rule:MF_03182
propagated from UniProtKB/Swiss-Prot (Q5F450.1); Region: WD 3. /evidence=ECO:0000255|HAMAP-Rule:MF_03182
propagated from UniProtKB/Swiss-Prot (Q5F450.1); Region: WD 4. /evidence=ECO:0000255|HAMAP-Rule:MF_03182
propagated from UniProtKB/Swiss-Prot (Q5F450.1); Region: Linker. /evidence=ECO:0000255|HAMAP-Rule:MF_03182
propagated from UniProtKB/Swiss-Prot (Q5F450.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X1
signal transducer and activator of transcription 2, transcript variant X3
signal transducer and activator of transcription 2, transcript variant X2
signal transducer and activator of transcription 2, transcript variant X1
signal transducer and activator of transcription 2, transcript variant X7
signal transducer and activator of transcription 2 isoform X1
signal transducer and activator of transcription 2 isoform X3
signal transducer and activator of transcription 2, transcript variant X6
signal transducer and activator of transcription 2, transcript variant X5
signal transducer and activator of transcription 2, transcript variant X4
signal transducer and activator of transcription 2 isoform X2
LOW QUALITY PROTEIN: protein timeless homolog
major intrinsic protein of lens fiber; Derived by automated computational analysis using gene prediction method: BestRefSeq.
propagated from UniProtKB/Swiss-Prot (P28238.2); transmembrane region
propagated from UniProtKB/Swiss-Prot (P28238.2); Region: NPA 1
propagated from UniProtKB/Swiss-Prot (P28238.2); Region: NPA 2
propagated from UniProtKB/Swiss-Prot (P28238.2); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
RNA binding motif single stranded interacting protein 2, transcript variant X1
RNA binding motif single stranded interacting protein 2, transcript variant X2
RNA binding motif single stranded interacting protein 2, transcript variant X3
RNA binding motif single stranded interacting protein 2, transcript variant X4
RNA-binding motif, single-stranded-interacting protein 2 isoform X1
RNA-binding motif, single-stranded-interacting protein 2 isoform X2
RNA-binding motif, single-stranded-interacting protein 2 isoform X3
RNA-binding motif, single-stranded-interacting protein 2 isoform X4
bromodomain adjacent to zinc finger domain 2A, transcript variant X7
bromodomain adjacent to zinc finger domain 2A, transcript variant X2
bromodomain adjacent to zinc finger domain 2A, transcript variant X6
bromodomain adjacent to zinc finger domain 2A, transcript variant X1
bromodomain adjacent to zinc finger domain 2A, transcript variant X5
bromodomain adjacent to zinc finger domain 2A, transcript variant X3
bromodomain adjacent to zinc finger domain 2A, transcript variant X4
bromodomain adjacent to zinc finger domain protein 2A isoform X2
bromodomain adjacent to zinc finger domain protein 2A isoform X1
bromodomain adjacent to zinc finger domain protein 2A isoform X3
ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide; Derived by automated computational analysis using gene prediction method: BestRefSeq.
ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide
ATP synthase subunit beta, mitochondrial precursor
Mitochondrion. /evidence=ECO:0000250|UniProtKB:P00829; propagated from UniProtKB/Swiss-Prot (Q5ZLC5.1)
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00273
prostaglandin E synthase 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
prostaglandin E synthase 3, transcript variant X1
prostaglandin E synthase 3, transcript variant X2
nascent polypeptide-associated complex alpha subunit; Derived by automated computational analysis using gene prediction method: BestRefSeq.
nascent polypeptide-associated complex alpha subunit
nascent polypeptide-associated complex subunit alpha
retinol dehydrogenase 7-like, transcript variant X1
G protein-coupled receptor 182, transcript variant X1
G protein-coupled receptor 182, transcript variant X2
zinc finger and BTB domain-containing protein 39 isoform X1
myosin IA; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
propagated from UniProtKB/Swiss-Prot (P47807.2); Region: Actin-binding. /evidence=ECO:0000255
nuclear envelope integral membrane protein 1, transcript variant X4
nuclear envelope integral membrane protein 1, transcript variant X2
nuclear envelope integral membrane protein 1, transcript variant X3
nuclear envelope integral membrane protein 1, transcript variant X6
nuclear envelope integral membrane protein 1, transcript variant X1
nuclear envelope integral membrane protein 1, transcript variant X5
nuclear envelope integral membrane protein 1 isoform X4
nuclear envelope integral membrane protein 1 isoform X2
nuclear envelope integral membrane protein 1 isoform X3
nuclear envelope integral membrane protein 1 isoform X1
nuclear envelope integral membrane protein 1 isoform X5
nuclear envelope integral membrane protein 1, transcript variant X7
nuclear envelope integral membrane protein 1 isoform X6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
microRNA mir-12267; Derived by automated computational analysis using gene prediction method: BestRefSeq.
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NGFI-A-binding protein 2 isoform X1
signal transducer and activator of transcription 6, transcript variant X5
signal transducer and activator of transcription 6, transcript variant X4
signal transducer and activator of transcription 6, transcript variant X3
signal transducer and activator of transcription 6, transcript variant X2
signal transducer and activator of transcription 6, transcript variant X1
signal transducer and activator of transcription 6, transcript variant X6
signal transducer and activator of transcription 6 isoform X2
signal transducer and activator of transcription 6 isoform X1
signal transducer and activator of transcription 6 isoform X3
signal transducer and activator of transcription 6 isoform X4
LDL receptor related protein 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_205242.3
The RefSeq transcript has 8 substitutions, 1 frameshift compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_990573.3
low-density lipoprotein receptor-related protein 1 precursor
N-linked (GlcNAc...) asparagine. /evidence=ECO:0000255; propagated from UniProtKB/Swiss-Prot (P98157.1); glycosylation site
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 1
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 2
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 3
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 4
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 5
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 6
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 7
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 8
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 9
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 10
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 11
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 12
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 13
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 14
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 15
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 16
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 17
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 18
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 19
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 20
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 21
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 22
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 23
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 24
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 25
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 26
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 27
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 28
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 29
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 30
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 31
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: Recognition site for proteolytical processing. /evidence=ECO:0000255
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 32
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 33
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: LDL-receptor class B 34
propagated from UniProtKB/Swiss-Prot (P98157.1); transmembrane region
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: NPXY motif
propagated from UniProtKB/Swiss-Prot (P98157.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
microRNA 6619; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SH3 and cysteine-rich domain-containing protein 3-like, transcript variant X1
similar to RNA sequence, mRNA (same species):INSD:KY501151.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 371 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 371 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
SH3 and cysteine-rich domain-containing protein 3 isoform X1
R3H domain containing 2, transcript variant X1
LOW QUALITY PROTEIN: R3H domain-containing protein 2 isoform X1
inhibin beta C chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
inhibin beta E subunit, transcript variant X1
GLI family zinc finger 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
GLI family zinc finger 1, transcript variant X3
GLI family zinc finger 1, transcript variant X1
GLI family zinc finger 1, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C14, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C14, transcript variant X1
ORMDL sphingolipid biosynthesis regulator 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ORMDL sphingolipid biosynthesis regulator 2
ORMDL sphingolipid biosynthesis regulator 2, transcript variant X1
propagated from UniProtKB/Swiss-Prot (Q5ZIU0.1); transmembrane region
SAP domain containing ribonucleoprotein; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
SAP domain containing ribonucleoprotein, transcript variant 1
SAP domain containing ribonucleoprotein, transcript variant 2
SAP domain containing ribonucleoprotein, transcript variant X1
isoform 1 is encoded by transcript variant 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SAP domain-containing ribonucleoprotein isoform 1
isoform 2 is encoded by transcript variant 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
SAP domain-containing ribonucleoprotein isoform 2
inositol polyphosphate-1-phosphatase, transcript variant X1
inositol polyphosphate 1-phosphatase isoform X1
inositol polyphosphate-1-phosphatase, transcript variant X2
inositol polyphosphate-1-phosphatase, transcript variant X3
inositol polyphosphate 1-phosphatase isoform X2
retinol dehydrogenase 5; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
retinol dehydrogenase 5, transcript variant X1
biogenesis of lysosomal organelles complex 1 subunit 1
biogenesis of lysosome-related organelles complex 1 subunit 1
integrin subunit alpha 7, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: integrin alpha-7 isoform X1
microspherule protein 1, transcript variant X1
spermatogenesis associated serine rich 2, transcript variant X2
spermatogenesis associated serine rich 2, transcript variant X1
spermatogenesis associated serine rich 2, transcript variant X4
spermatogenesis associated serine rich 2, transcript variant X3
spermatogenesis-associated serine-rich protein 2
DnaJ heat shock protein family (Hsp40) member C22, transcript variant X3
DnaJ heat shock protein family (Hsp40) member C22, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C22, transcript variant X1
pH-response regulator protein palI/RIM9-like
eukaryotic translation initiation factor 4B, transcript variant X6
eukaryotic translation initiation factor 4B, transcript variant X5
eukaryotic translation initiation factor 4B, transcript variant X2
eukaryotic translation initiation factor 4B, transcript variant X7
eukaryotic translation initiation factor 4B, transcript variant X4
eukaryotic translation initiation factor 4B, transcript variant X3
eukaryotic translation initiation factor 4B, transcript variant X1
eukaryotic translation initiation factor 4B isoform X6
eukaryotic translation initiation factor 4B isoform X5
eukaryotic translation initiation factor 4B isoform X2
eukaryotic translation initiation factor 4B isoform X7
eukaryotic translation initiation factor 4B isoform X4
eukaryotic translation initiation factor 4B isoform X3
eukaryotic translation initiation factor 4B isoform X1
keratin, type I cytoskeletal 18 isoform X1
keratin, type I cytoskeletal 18 isoform X2
keratin, type II cytoskeletal 8 isoform X1
keratin, type II cytoskeletal 8 isoform X2
768880 KRT75L1 keratin, type II cytoskeletal 75-like 2
keratin, type II cytoskeletal 79-like, transcript variant X2
keratin, type II cytoskeletal 79-like, transcript variant X3
keratin, type II cytoskeletal 79-like, transcript variant X4
keratin, type II cytoskeletal 79-like, transcript variant X1
uncharacterized PE-PGRS family protein PE_PGRS54 isoform X2
uncharacterized PE-PGRS family protein PE_PGRS54 isoform X3
uncharacterized PE-PGRS family protein PE_PGRS54 isoform X4
keratin, type II cytoskeletal 1 isoform X1
keratin, type II cytoskeletal 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 long SRA reads, 108 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
keratin, type II cytoskeletal 7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 32 long SRA reads, 108 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
keratin, type II cytoskeletal 4 isoform X2
keratin, type II cytoskeletal 7 isoform X1
keratin, type II cytoskeletal 73-like, transcript variant X1
keratin, type II cytoskeletal 73-like, transcript variant X2
keratin, type II cytoskeletal 4-like isoform X1
keratin, type II cytoskeletal 4-like isoform X2
keratin 5; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin 6A; Derived by automated computational analysis using gene prediction method: BestRefSeq.
keratin 75; Derived by automated computational analysis using gene prediction method: BestRefSeq.
uncharacterized LOC112530948, transcript variant X1
keratin, type II cuticular Hb4-like, transcript variant X1
keratin, type II cuticular Hb4-like, transcript variant X2
keratin, type II cytoskeletal cochleal isoform X1
keratin, type II cytoskeletal cochleal isoform X2
keratin 7; Derived by automated computational analysis using gene prediction method: BestRefSeq.
propagated from UniProtKB/Swiss-Prot (O93532.1); Region: Head
propagated from UniProtKB/Swiss-Prot (O93532.1); Region: Coil 1A
propagated from UniProtKB/Swiss-Prot (O93532.1); Region: Linker 1
propagated from UniProtKB/Swiss-Prot (O93532.1); Region: Coil 1B
propagated from UniProtKB/Swiss-Prot (O93532.1); Region: Linker 12
propagated from UniProtKB/Swiss-Prot (O93532.1); Region: Coil 2
propagated from UniProtKB/Swiss-Prot (O93532.1); Region: Tail
BCDIN3 domain containing RNA methyltransferase, transcript variant X3
BCDIN3 domain containing RNA methyltransferase, transcript variant X4
BCDIN3 domain containing RNA methyltransferase, transcript variant X1
BCDIN3 domain containing RNA methyltransferase, transcript variant X2
RNA 5'-monophosphate methyltransferase isoform X1
RNA 5'-monophosphate methyltransferase isoform X2
Fas apoptotic inhibitory molecule 2, transcript variant X1
Fas apoptotic inhibitory molecule 2, transcript variant X2
aquaporin 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
solute carrier family 4 member 8, transcript variant X2
solute carrier family 4 member 8, transcript variant X1
solute carrier family 4 member 8, transcript variant X3
solute carrier family 4 member 8, transcript variant X4
solute carrier family 4 member 8, transcript variant X5
electroneutral sodium bicarbonate exchanger 1 isoform X2
electroneutral sodium bicarbonate exchanger 1 isoform X1
electroneutral sodium bicarbonate exchanger 1 isoform X3
electroneutral sodium bicarbonate exchanger 1 isoform X4
uncharacterized LOC121108096, transcript variant X1
TRAF family member-associated NF-kappa-B activator-like, transcript variant X3
TRAF family member-associated NF-kappa-B activator-like, transcript variant X1
TRAF family member-associated NF-kappa-B activator-like, transcript variant X2
uncharacterized protein LOC100858973 isoform X1
uncharacterized protein LOC100858973 isoform X2
polypeptide N-acetylgalactosaminyltransferase 6; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
polypeptide N-acetylgalactosaminyltransferase 6
polypeptide N-acetylgalactosaminyltransferase 6, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 6, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 6 isoform X1
chymotrypsin like elastase family member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
chymotrypsin like elastase family member 1
chymotrypsin like elastase family member 1, transcript variant X1
chymotrypsin-like elastase family member 1 precursor
chymotrypsin-like elastase family member 1 isoform X1
bridging integrator 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
propagated from UniProtKB/Swiss-Prot (Q5ZKL7.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
small cell adhesion glycoprotein, transcript variant X5
small cell adhesion glycoprotein, transcript variant X1
small cell adhesion glycoprotein, transcript variant X2
small cell adhesion glycoprotein, transcript variant X3
small cell adhesion glycoprotein, transcript variant X4
small cell adhesion glycoprotein, transcript variant X6
DAZ associated protein 2, transcript variant X1
LOW QUALITY PROTEIN: POU domain, class 6, transcription factor 1
transcription factor CP2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
transcription factor CP2, transcript variant X4
transcription factor CP2, transcript variant X1
transcription factor CP2, transcript variant X2
transcription factor CP2, transcript variant X3
transcription factor CP2, transcript variant 2
transcription factor CP2, transcript variant 1
propagated from UniProtKB/Swiss-Prot (Q7T2U9.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite
propagated from UniProtKB/Swiss-Prot (Q7T2U9.1); Region: DNA-binding. /evidence=ECO:0000250
cysteine and serine rich nuclear protein 2, transcript variant X2
cysteine and serine rich nuclear protein 2, transcript variant X1
cysteine/serine-rich nuclear protein 2 isoform X1
cysteine/serine-rich nuclear protein 2 isoform X2
probable serine/threonine-protein kinase DDB_G0272254
solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2, transcript variant 1
solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2, transcript variant X1
solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2, transcript variant 2
natural resistance-associated macrophage protein 2 isoform 1
natural resistance-associated macrophage protein 2 isoform X1
natural resistance-associated macrophage protein 2 isoform 2
solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2, transcript variant X2
natural resistance-associated macrophage protein 2 isoform X2
uncharacterized LOC101751319, transcript variant X1
uncharacterized protein LOC101751319 isoform X1
dynactin subunit 2; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
dynactin subunit 2, transcript variant X5
dynactin subunit 2, transcript variant X2
dynactin subunit 2, transcript variant X4
dynactin subunit 2, transcript variant X3
dynactin subunit 2, transcript variant X1
LOW QUALITY PROTEIN: kinesin heavy chain
phosphatidylinositol-5-phosphate 4-kinase type 2 gamma
LOW QUALITY PROTEIN: phosphatidylinositol 5-phosphate 4-kinase type-2 gamma
serine/arginine repetitive matrix protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC121108100 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 81-like 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
maestro heat-like repeat-containing protein family member 2A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
maestro heat-like repeat-containing protein family member 2A isoform X1
coiled-coil domain-containing protein 81-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 81-like, transcript variant X2
coiled-coil domain-containing protein 81-like isoform X2
coiled-coil domain-containing protein 81-like, transcript variant X1
uncharacterized LOC112530913, transcript variant X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC107049856, transcript variant X1
uncharacterized LOC107049856, transcript variant X2
uncharacterized LOC107049856, transcript variant X3
uncharacterized LOC107049856, transcript variant X4
maestro heat-like repeat-containing protein family member 2A isoform X2
maestro heat-like repeat-containing protein family member 2A isoform X3
maestro heat-like repeat-containing protein family member 2A isoform X4
uncharacterized LOC107049599, transcript variant X1
uncharacterized LOC107049599, transcript variant X3
uncharacterized LOC107049599, transcript variant X2
uncharacterized protein LOC107049599 isoform X1
uncharacterized protein LOC107049599 isoform X3
uncharacterized LOC101749099, transcript variant X5
uncharacterized LOC101749099, transcript variant X4
uncharacterized LOC101749099, transcript variant X2
uncharacterized LOC101749099, transcript variant X3
uncharacterized LOC101749099, transcript variant X1
uncharacterized LOC121108062, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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 27 samples with support for all annotated introns
maestro heat-like repeat-containing protein family member 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC121108060 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121108106, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC121108106 isoform X1
uncharacterized LOC121108107, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC121108107 isoform X1
uncharacterized protein LOC121108064 isoform X1
uncharacterized protein LOC121108064 isoform X2
uncharacterized LOC121108065, transcript variant X1
uncharacterized LOC121108065, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC121108065, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121112422, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
maestro heat-like repeat-containing protein family member 2A
uncharacterized LOC121108067, transcript variant X2
uncharacterized LOC121108067, transcript variant X1
uncharacterized protein LOC121108067 isoform X2
uncharacterized protein LOC121108067 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121108075, transcript variant X1
uncharacterized LOC112530932, transcript variant X4
uncharacterized LOC112530932, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC112530932, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC112530932, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC112530932, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC112530932, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC112530932, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC107049479, transcript variant X1
uncharacterized protein LOC107049479 isoform X1
uncharacterized LOC107050557, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC107050557 isoform X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 65% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC107050377, transcript variant X1
uncharacterized LOC121108081, transcript variant X1
uncharacterized LOC121108081, transcript variant X2
uncharacterized LOC121108081, transcript variant X4
uncharacterized LOC121108081, transcript variant X3
uncharacterized LOC121108081, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC121106503 isoform X1
uncharacterized LOC107049478, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC107049478 isoform X1
uncharacterized LOC121108113, transcript variant X1
ADP-ribosylarginine hydrolase-like, transcript variant X2
ADP-ribosylarginine hydrolase-like, transcript variant X3
ADP-ribosylarginine hydrolase-like, transcript variant X1
ADP-ribosylarginine hydrolase-like, transcript variant X7
ADP-ribosylarginine hydrolase-like, transcript variant X6
ADP-ribosylarginine hydrolase-like, transcript variant X5
ADP-ribosylarginine hydrolase-like, transcript variant X4
protein ADP-ribosylarginine hydrolase isoform X2
protein ADP-ribosylarginine hydrolase isoform X3
protein ADP-ribosylarginine hydrolase isoform X1
protein ADP-ribosylarginine hydrolase isoform X6
protein ADP-ribosylarginine hydrolase isoform X5
protein ADP-ribosylarginine hydrolase isoform X4
microRNA mir-12286; Derived by automated computational analysis using gene prediction method: BestRefSeq.
methionyl-tRNA synthetase; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001257372.2
The RefSeq transcript has 1 substitution, 1 frameshift and aligns at 40% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001244301.2
The RefSeq protein has 1 substitution, 1 frameshift and aligns at 40% coverage compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 46% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121108117, transcript variant X1