Carcharodon carcharias isolate sCarCar2 chromosome 25, sCarCar2.pri, whole genome shotgun sequence.
Carcharodon carcharias (great white shark)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Lamniformes; Alopiidae; Carcharodon.
REFSEQ INFORMATION: The reference sequence is identical to\nCM029989.1.\nAssembly name: sCarCar2.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2021/03/30. The original whole-genome shotgun project has the\naccession JAGDEE000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 05-FEB-2021\nAssembly Method :: FALCON v. DX 2.0.1; FALCON-Unzip v. DX\n 1.2.1; purge_dups v. DX 19-08-10;\n scaff10X v. DX 2.0.3; bionano Solve v. DX\n 3.4.0; Salsa2 HiC v. DX 2.2.0; Arrow\n polishing and gap filling v. DX 7.0.1.1;\n Longranger Align DX v. 2.2.2.1; freebayes\n DX v. 19-07-11; gEVAL manual curation v.\n 2021-02-05; VGP assembly pipeline v. 1.6\nAssembly Name :: sCarCar2.pri\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 66.84x\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 :: Carcharodon carcharias Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.6\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.
sialic acid-binding Ig-like lectin 12, 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
sialic acid-binding Ig-like lectin 12, transcript variant X2
sialic acid-binding Ig-like lectin 12 isoform X1
sialic acid-binding Ig-like lectin 12 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins
myb/SANT-like DNA-binding domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
beta-galactosidase-1-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
beta-galactosidase-1-like protein 2, 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 4 samples with support for all annotated introns
beta-galactosidase-1-like protein 2, 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 3 samples with support for all annotated introns
beta-galactosidase-1-like protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
beta-galactosidase-1-like protein 2 isoform X2
beta-galactosidase-1-like protein 2 isoform X1
beta-galactosidase-1-like protein 2 isoform X4
beta-galactosidase-1-like protein 2 isoform X3
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
potassium-transporting ATPase alpha chain 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 233 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
sodium channel, voltage-gated, type III, beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel, voltage-gated, type III, beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel subunit beta-3 isoform X1
sodium channel subunit beta-3 isoform X2
GRAM domain containing 1Ba, 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
GRAM domain containing 1Ba, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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.
CXADR-like membrane protein, 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 3 samples with support for all annotated introns
CXADR-like membrane protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mth938 domain-containing protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mth938 domain-containing protein-like, transcript variant X1
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 4 samples with support for all annotated introns
mth938 domain-containing protein-like, transcript variant X4
mth938 domain-containing protein-like, transcript variant X3
mth938 domain-containing protein-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
small fragment nuclease, 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 4 samples with support for all annotated introns
small fragment nuclease, transcript variant 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
nuclear cap-binding protein subunit 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
junctional adhesion molecule 3b, 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
junctional adhesion molecule 3b, 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 4 samples with support for all annotated introns
non-SMC condensin II complex, subunit D3, 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 3 samples with support for all annotated introns
non-SMC condensin II complex, subunit D3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
non-SMC condensin II complex, subunit D3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
condensin-2 complex subunit D3 isoform X1
condensin-2 complex subunit D3 isoform X3
condensin-2 complex subunit D3 isoform X2
vacuolar protein sorting-associated protein 26B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
anaphase promoting complex subunit 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
anaphase promoting complex subunit 13, transcript variant X2
anaphase-promoting complex subunit 13 isoform X1
anaphase promoting complex subunit 13, transcript variant X3
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 4 samples with support for all annotated introns
anaphase-promoting complex subunit 13 isoform X2
nicotinamide N-methyltransferase-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 1 sample with support for all annotated introns
nicotinamide N-methyltransferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nicotinamide N-methyltransferase-like isoform X2
nicotinamide N-methyltransferase-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 3 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X1
neural cell adhesion molecule 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X3
neural cell adhesion molecule 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X8
neural cell adhesion molecule 1-like, transcript variant X4
neural cell adhesion molecule 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X5
neural cell adhesion molecule 1-like, transcript variant X14
neural cell adhesion molecule 1-like, transcript variant X16
neural cell adhesion molecule 1-like, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X11
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 1 sample with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X12
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
neural cell adhesion molecule 1-like, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 1-like, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neural cell adhesion molecule 1-like isoform X1
neural cell adhesion molecule 1-like isoform X2
neural cell adhesion molecule 1-like isoform X3
neural cell adhesion molecule 1-like isoform X6
neural cell adhesion molecule 1-like isoform X8
neural cell adhesion molecule 1-like isoform X4
neural cell adhesion molecule 1-like isoform X7
neural cell adhesion molecule 1-like isoform X9
neural cell adhesion molecule 1-like isoform X5
neural cell adhesion molecule 1-like isoform X14
neural cell adhesion molecule 1-like isoform X16
neural cell adhesion molecule 1-like isoform X15
neural cell adhesion molecule 1-like isoform X11
neural cell adhesion molecule 1-like isoform X10
neural cell adhesion molecule 1-like isoform X12
neural cell adhesion molecule 1-like isoform X13
neural cell adhesion molecule 1-like isoform X18
neural cell adhesion molecule 1-like isoform X17
zinc finger and BTB domain-containing protein 44-like, transcript variant X1
zinc finger and BTB domain-containing protein 44-like, transcript variant X2
zinc finger and BTB domain-containing protein 44-like isoform X1
zinc finger and BTB domain-containing protein 44-like isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 8-like, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 8-like isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 8-like isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
sorting nexin 19b, transcript variant X1
sorting nexin 19b, 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 4 samples with support for all annotated introns
uncharacterized LOC121269550, transcript variant X3
uncharacterized LOC121269550, transcript variant X4
uncharacterized LOC121269550, transcript variant X5
uncharacterized LOC121269550, transcript variant X2
uncharacterized LOC121269550, transcript variant X1
uncharacterized protein LOC121269550 isoform X1
uncharacterized protein LOC121269550 isoform X2
uncharacterized protein LOC121269550 isoform X3
uncharacterized LOC121269550, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 751 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00016
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 467 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: heat shock cognate 71 kDa protein-like
uncharacterized LOC121269555, transcript variant X2
uncharacterized LOC121269555, transcript variant X1
cytotoxic and regulatory T-cell molecule, transcript variant X3
cytotoxic and regulatory T-cell molecule, transcript variant X2
cytotoxic and regulatory T-cell molecule, transcript variant X1
cytotoxic and regulatory T-cell molecule, transcript variant X4
cytotoxic and regulatory T-cell molecule isoform X3
cytotoxic and regulatory T-cell molecule isoform X2
cytotoxic and regulatory T-cell molecule isoform X1
cytotoxic and regulatory T-cell molecule isoform X4
uncharacterized LOC121269556, transcript variant X2
uncharacterized LOC121269556, transcript variant X1
uncharacterized LOC121269556, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
cytochrome c oxidase subunit 7B, mitochondrial-like
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
cell adhesion molecule 1-like, transcript variant X5
cell adhesion molecule 1-like, 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 3 samples with support for all annotated introns
cell adhesion molecule 1-like, 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 3 samples with support for all annotated introns
cell adhesion molecule 1-like, transcript variant X2
cell adhesion molecule 1-like isoform X1
cell adhesion molecule 1-like isoform X3
cell adhesion molecule 1-like isoform X2
cell adhesion molecule 1-like isoform X5
cell adhesion molecule 1-like, transcript variant X4
cell adhesion molecule 1-like isoform X4
NKAP domain containing 1, transcript variant X7
NKAP domain containing 1, transcript variant X6
NKAP domain containing 1, transcript variant X5
NKAP domain containing 1, transcript variant X3
NKAP domain containing 1, transcript variant X2
uncharacterized protein NKAPD1 isoform X4
uncharacterized protein NKAPD1 isoform X2
uncharacterized protein NKAPD1 isoform X3
NKAP domain containing 1, transcript variant X1
NKAP domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein NKAPD1 isoform X1
PIH1 domain containing 2, transcript variant X3
PIH1 domain containing 2, 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 3 samples with support for all annotated introns
PIH1 domain containing 2, transcript variant X2
dihydrolipoamide S-acetyltransferase (E2 component of pyruvate dehydrogenase complex)
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121269736, transcript variant X2
uncharacterized LOC121269736, transcript variant X1
uncharacterized LOC121269736, transcript variant X4
uncharacterized LOC121269736, transcript variant X3
uncharacterized protein LOC121269736 isoform X1
uncharacterized protein LOC121269736 isoform X2
uncharacterized protein C11orf52 homolog, transcript variant X1
uncharacterized protein C11orf52 homolog, transcript variant X2
uncharacterized protein C11orf52 homolog
heat shock protein, alpha-crystallin-related, b2, transcript variant X2
heat shock protein, alpha-crystallin-related, b2, 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
heat shock protein, alpha-crystallin-related, b2, transcript variant X3
ferredoxin-fold anticodon binding domain containing 1, transcript variant X2
ferredoxin-fold anticodon binding domain containing 1, transcript variant X1
ferredoxin-fold anticodon-binding domain-containing protein 1
ALG9 alpha-1,2-mannosyltransferase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ALG9 alpha-1,2-mannosyltransferase, transcript variant X7
ALG9 alpha-1,2-mannosyltransferase, transcript variant X11
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
ALG9 alpha-1,2-mannosyltransferase, 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 2 samples with support for all annotated introns
ALG9 alpha-1,2-mannosyltransferase, transcript variant X2
ALG9 alpha-1,2-mannosyltransferase, transcript variant X4
ALG9 alpha-1,2-mannosyltransferase, transcript variant X10
ALG9 alpha-1,2-mannosyltransferase, transcript variant X5
ALG9 alpha-1,2-mannosyltransferase, transcript variant X9
ALG9 alpha-1,2-mannosyltransferase, transcript variant X12
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
ALG9 alpha-1,2-mannosyltransferase, transcript variant X8
ALG9 alpha-1,2-mannosyltransferase, transcript variant X14
ALG9 alpha-1,2-mannosyltransferase, transcript variant X13
alpha-1,2-mannosyltransferase ALG9 isoform X6
alpha-1,2-mannosyltransferase ALG9 isoform X8
alpha-1,2-mannosyltransferase ALG9 isoform X1
alpha-1,2-mannosyltransferase ALG9 isoform X2
alpha-1,2-mannosyltransferase ALG9 isoform X4
alpha-1,2-mannosyltransferase ALG9 isoform X5
alpha-1,2-mannosyltransferase ALG9 isoform X9
alpha-1,2-mannosyltransferase ALG9 isoform X7
alpha-1,2-mannosyltransferase ALG9 isoform X10
ALG9 alpha-1,2-mannosyltransferase, transcript variant X3
alpha-1,2-mannosyltransferase ALG9 isoform X3
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
protein phosphatase 2, regulatory subunit A, beta a
salt-inducible kinase 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
salt-inducible kinase 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase SIK2a isoform X2
serine/threonine-protein kinase SIK2a isoform X1
trafficking protein particle complex subunit 4
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
coiled-coil domain-containing protein 84
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 4 samples with support for all annotated introns
proprotein convertase subtilisin/kexin type 7, transcript variant X1
proprotein convertase subtilisin/kexin type 7, transcript variant X3
proprotein convertase subtilisin/kexin type 7, 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 1 sample with support for all annotated introns
proprotein convertase subtilisin/kexin type 7, transcript variant X4
proprotein convertase subtilisin/kexin type 7, transcript variant X5
proprotein convertase subtilisin/kexin type 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
palmitoyl-protein thioesterase ABHD10, mitochondrial-like, 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 2 samples with support for all annotated introns
palmitoyl-protein thioesterase ABHD10, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
palmitoyl-protein thioesterase ABHD10, mitochondrial-like, transcript variant X3
palmitoyl-protein thioesterase ABHD10, mitochondrial-like
SID1 transmembrane family, member 2, transcript variant X1
SID1 transmembrane family, member 2, transcript variant X3
SID1 transmembrane family, member 2, transcript variant X2
SID1 transmembrane family member 2 isoform X1
SID1 transmembrane family member 2 isoform X2
SID1 transmembrane family member 2 isoform X3
platelet-activating factor acetylhydrolase IB subunit alpha2-like, transcript variant X1
platelet-activating factor acetylhydrolase IB subunit alpha2-like, 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 3 samples with support for all annotated introns
platelet-activating factor acetylhydrolase IB subunit alpha2-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
SIK family kinase 3, transcript variant X1
SIK family kinase 3, transcript variant X3
SIK family kinase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase SIK3 homolog isoform X1
serine/threonine-protein kinase SIK3 homolog isoform X3
serine/threonine-protein kinase SIK3 homolog isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
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
chromosome 25 C11orf53 homolog, 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 1 sample with support for all annotated introns
uncharacterized protein C11orf53 homolog isoform X2
chromosome 25 C11orf53 homolog, transcript variant X1
uncharacterized protein C11orf53 homolog isoform X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC553749 homolog
uncharacterized LOC121269651, transcript variant X2
uncharacterized LOC121269651, transcript variant X1
uncharacterized LOC121269651, transcript variant X3
uncharacterized protein LOC121269651 isoform X1
uncharacterized protein LOC121269651 isoform X2
dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)
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
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
histone H4 transcription factor, transcript variant X2
histone H4 transcription factor, transcript variant X1
histone H4 transcription factor, transcript variant X3
phospholipid transfer protein C2CD2L isoform X1
phospholipid transfer protein C2CD2L isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein 1 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein 1 homolog, transcript variant X3
Down syndrome cell adhesion molecule-like protein 1 homolog isoform X1
Down syndrome cell adhesion molecule-like protein 1 homolog isoform X2
Down syndrome cell adhesion molecule-like protein 1 homolog isoform X3
centrosomal protein of 164 kDa-like, transcript variant X4
centrosomal protein of 164 kDa-like, transcript variant X3
centrosomal protein of 164 kDa-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
centrosomal protein of 164 kDa-like, transcript variant X1
centrosomal protein of 164 kDa-like, transcript variant X5
centrosomal protein of 164 kDa-like, transcript variant X6
centrosomal protein of 164 kDa-like isoform X4
centrosomal protein of 164 kDa-like isoform X3
centrosomal protein of 164 kDa-like isoform X2
centrosomal protein of 164 kDa-like isoform X1
centrosomal protein of 164 kDa-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 214, transcript variant X1
ring finger protein 214, transcript variant X2
ring finger protein 214, transcript variant X3
ring finger protein 214, transcript variant X6
ring finger protein 214, transcript variant X4
ring finger protein 214, transcript variant X5
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X1
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X2
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X4
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X3
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X5
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X6
ATP-binding cassette sub-family G member 4 isoform X2
ATP-binding cassette sub-family G member 4 isoform X1
ATP-binding cassette sub-family G member 4 isoform X3
ATP-binding cassette sub-family G member 4 isoform X4
grass carp reovirus (GCRV)-induced gene 2o
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
G protein-activated inward rectifier potassium channel 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins
centromere/kinetochore protein zw10 homolog
D(2) dopamine receptor A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
D(2) dopamine receptor A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
D(2) dopamine receptor A-like isoform X2
D(2) dopamine receptor A-like isoform X1
transmembrane protease serine 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protease serine 5-like, transcript variant X2
transmembrane protease serine 5-like isoform X1
transmembrane protease serine 5-like isoform X2
ankyrin repeat and protein kinase domain-containing protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ankyrin repeat and protein kinase domain-containing protein 1-like
tetratricopeptide repeat domain 12, transcript variant X3
tetratricopeptide repeat domain 12, transcript variant X2
tetratricopeptide repeat domain 12, 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 4 samples with support for all annotated introns
tetratricopeptide repeat domain 12, transcript variant X4
tetratricopeptide repeat domain 12, transcript variant X5
tetratricopeptide repeat protein 12 isoform X2
tetratricopeptide repeat protein 12 isoform X1
tetratricopeptide repeat protein 12 isoform X3
ubiquitin specific peptidase 28, transcript variant X3
ubiquitin specific peptidase 28, transcript variant X2
ubiquitin specific peptidase 28, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 28 isoform X3
ubiquitin carboxyl-terminal hydrolase 28 isoform X2
ubiquitin carboxyl-terminal hydrolase 28 isoform X1
5-hydroxytryptamine (serotonin) receptor 3B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxytryptamine (serotonin) receptor 3A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
zinc finger and BTB domain containing 16a, transcript variant X2
zinc finger and BTB domain containing 16a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger and BTB domain containing 16a, transcript variant X1
zinc finger and BTB domain containing 16a, transcript variant X3
zinc finger and BTB domain containing 16a, transcript variant X4
zinc finger and BTB domain-containing protein 16-A isoform X2
zinc finger and BTB domain-containing protein 16-A isoform X1
uncharacterized LOC121269645, transcript variant X1
uncharacterized LOC121269645, transcript variant X2
uncharacterized protein LOC121269645 isoform X1
uncharacterized protein LOC121269645 isoform X2
beta-carotene oxygenase 2a, transcript variant X1
beta-carotene oxygenase 2a, 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 2 samples with support for all annotated introns
beta-carotene oxygenase 2a, transcript variant X3
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 1 sample with support for all annotated introns
beta,beta-carotene 9',10'-oxygenase isoform X1
beta,beta-carotene 9',10'-oxygenase isoform X2
beta,beta-carotene 9',10'-oxygenase isoform X3
glucuronokinase with putative uridyl pyrophosphorylase, transcript variant X2
glucuronokinase with putative uridyl pyrophosphorylase, transcript variant X1
glucuronokinase with putative uridyl pyrophosphorylase isoform X2
glucuronokinase with putative uridyl pyrophosphorylase isoform X1
glucuronokinase with putative uridyl pyrophosphorylase, transcript variant X3
glucuronokinase with putative uridyl pyrophosphorylase isoform X3
glucuronokinase with putative uridyl pyrophosphorylase, transcript variant X4
glucuronokinase with putative uridyl pyrophosphorylase isoform X4
glucuronokinase with putative uridyl pyrophosphorylase, transcript variant X7
glucuronokinase with putative uridyl pyrophosphorylase, transcript variant X5
glucuronokinase with putative uridyl pyrophosphorylase, transcript variant X6
glucuronokinase with putative uridyl pyrophosphorylase isoform X5
glucuronokinase with putative uridyl pyrophosphorylase isoform X6
sodium channel, voltage-gated, type II, beta
sodium channel, voltage-gated, type IV, beta a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane serine protease 4a, 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 2 samples with support for all annotated introns
transmembrane serine protease 4a, transcript variant X3
transmembrane serine protease 4a, transcript variant X2
transmembrane protease serine 4a isoform X1
transmembrane protease serine 4a isoform X2
small integral membrane protein 35-like, transcript variant X2
small integral membrane protein 35-like, transcript variant X1
uncharacterized protein LOC121269501 isoform X2
small integral membrane protein 35-like isoform X1
interleukin-20 receptor subunit alpha-like
marginal zone B- and B1-cell-specific protein-like, transcript variant X1
marginal zone B- and B1-cell-specific protein-like, transcript variant X2
marginal zone B- and B1-cell-specific protein-like
FXYD domain containing ion transport regulator 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
FXYD domain-containing ion transport regulator 6
transmembrane protein 25, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 25, transcript variant X4
transmembrane protein 25, transcript variant X2
transmembrane protein 25, transcript variant X5
transmembrane protein 25, transcript variant X6
transmembrane protein 25, transcript variant X1
transmembrane protein 25, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lysine (K)-specific methyltransferase 2A, transcript variant X2
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 1 sample with support for all annotated introns
lysine (K)-specific methyltransferase 2A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lysine (K)-specific methyltransferase 2A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histone-lysine N-methyltransferase 2A isoform X2
histone-lysine N-methyltransferase 2A isoform X3
histone-lysine N-methyltransferase 2A isoform X1
ATP synthase subunit g, mitochondrial-like
ubiquitination factor E4A (UFD2 homolog, yeast)
Na(+)/H(+) exchange regulatory cofactor NHE-RF3-like
pleckstrin homology-like domain family B member 1, transcript variant X1
pleckstrin homology-like domain family B member 1, transcript variant X4
pleckstrin homology-like domain family B member 1, transcript variant X2
pleckstrin homology-like domain family B member 1, transcript variant X5
pleckstrin homology-like domain family B member 1, transcript variant X6
pleckstrin homology-like domain family B member 1, transcript variant X3
pleckstrin homology-like domain family B member 1, transcript variant X7
pleckstrin homology-like domain family B member 1, transcript variant X8
pleckstrin homology-like domain family B member 1 isoform X5
pleckstrin homology-like domain family B member 1 isoform X4
pleckstrin homology-like domain family B member 1 isoform X2
pleckstrin homology-like domain family B member 1 isoform X1
pleckstrin homology-like domain family B member 1 isoform X3
pleckstrin homology-like domain family B member 1 isoform X6
pleckstrin homology-like domain family B member 1 isoform X7
uncharacterized LOC121269647, transcript variant X4
uncharacterized LOC121269647, transcript variant X6
uncharacterized protein LOC121269647 isoform X4
uncharacterized LOC121269647, transcript variant X3
uncharacterized LOC121269647, transcript variant X5
uncharacterized LOC121269647, transcript variant X1
uncharacterized LOC121269647, transcript variant X2
uncharacterized protein LOC121269647 isoform X3
uncharacterized protein LOC121269647 isoform X1
uncharacterized protein LOC121269647 isoform X2
uncharacterized LOC121269647, transcript variant X7
uncharacterized protein LOC121269647 isoform X5
coatomer subunit delta, transcript variant X1
coatomer subunit delta, transcript variant X2
succinate dehydrogenase complex, subunit D, integral membrane protein b
succinate dehydrogenase [ubiquinone] cytochrome b small subunit B, mitochondrial
uncharacterized LOC121269483, transcript variant X3
uncharacterized LOC121269483, transcript variant X1
uncharacterized LOC121269483, transcript variant X2
uncharacterized protein LOC121269483 isoform X2
uncharacterized protein LOC121269483 isoform X1
ubiquitin-associated and SH3 domain-containing protein B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
sortilin-related receptor, L(DLR class) A repeats containing
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
uncharacterized LOC121269508, transcript variant X1
uncharacterized LOC121269508, transcript variant X2
uncharacterized LOC121269687, transcript variant X2
uncharacterized LOC121269687, transcript variant X1
TEN1 subunit of CST complex, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TEN1 subunit of CST complex, transcript variant X2
TEN1 subunit of CST complex, transcript variant X1
TEN1 subunit of CST complex, transcript variant X3
nectin cell adhesion molecule 1b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nectin cell adhesion molecule 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nectin cell adhesion molecule 1b isoform X3
nectin cell adhesion molecule 1b isoform X1
nectin cell adhesion molecule 1b, transcript variant X2
nectin cell adhesion molecule 1b isoform 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 2 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 1 sample with support for all annotated introns
B-cell CLL/lymphoma 9-like protein isoform X1
B-cell CLL/lymphoma 9-like protein isoform X5
B-cell CLL/lymphoma 9-like protein isoform X3
B-cell CLL/lymphoma 9-like protein isoform X2
B-cell CLL/lymphoma 9-like protein isoform X4
C-X-C chemokine receptor type 5, transcript variant X1
C-X-C chemokine receptor type 5, transcript variant X2
C-X-C chemokine receptor type 5 isoform X1
C-X-C chemokine receptor type 5 isoform X2
probable ATP-dependent RNA helicase ddx6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
probable ATP-dependent RNA helicase ddx6, 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 3 samples with support for all annotated introns
probable ATP-dependent RNA helicase ddx6
trehalase (brush-border membrane glycoprotein)
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 5 bases at 5 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
hypoxia up-regulated 1, transcript variant X1
hypoxia up-regulated 1, transcript variant X2
hypoxia up-regulated 1, transcript variant X3
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 2 samples with support for all annotated introns
hypoxia up-regulated protein 1 isoform X1
hypoxia up-regulated protein 1 isoform X2
hypoxia up-regulated protein 1 isoform X3
VPS11 core subunit of CORVET and HOPS complexes, transcript variant X1
VPS11 core subunit of CORVET and HOPS complexes, transcript variant X2
vacuolar protein sorting-associated protein 11 homolog isoform X1
vacuolar protein sorting-associated protein 11 homolog isoform X2
intraflagellar transport 46 homolog (Chlamydomonas), 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 4 samples with support for all annotated introns
intraflagellar transport protein 46 homolog isoform X1
intraflagellar transport 46 homolog (Chlamydomonas), transcript variant X2
intraflagellar transport 46 homolog (Chlamydomonas), transcript variant X3
intraflagellar transport protein 46 homolog isoform X2
intraflagellar transport protein 46 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 153
Cbl proto-oncogene, E3 ubiquitin protein ligase
basal cell adhesion molecule-like, transcript variant X4
basal cell adhesion molecule-like, transcript variant X6
basal cell adhesion molecule-like, transcript variant X5
basal cell adhesion molecule-like, transcript variant X1
basal cell adhesion molecule-like, transcript variant X2
basal cell adhesion molecule-like isoform X1
basal cell adhesion molecule-like isoform X4
basal cell adhesion molecule-like isoform X2
basal cell adhesion molecule-like, transcript variant X3
basal cell adhesion molecule-like isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 2-like isoform X1
ubiquitin carboxyl-terminal hydrolase 2-like isoform X2
ubiquitin carboxyl-terminal hydrolase 2-like isoform X4
ubiquitin carboxyl-terminal hydrolase 2-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida-like domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
hydroxymethylbilane synthase, b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
hydroxymethylbilane synthase, b, transcript variant X5
hydroxymethylbilane synthase, b, transcript variant X2
hydroxymethylbilane synthase, b, transcript variant X4
hydroxymethylbilane synthase, b, transcript variant X1
hydroxymethylbilane synthase, b isoform X3
hydroxymethylbilane synthase, b isoform X2
hydroxymethylbilane synthase, b isoform X1
hydroxymethylbilane synthase, b isoform X4
uncharacterized LOC121269527, transcript variant X1
uncharacterized LOC121269527, transcript variant X2
uncharacterized LOC121269527, transcript variant X3
uncharacterized LOC121269527, transcript variant X4
uncharacterized LOC121269527, transcript variant X5
uncharacterized protein LOC121269527 isoform X1
uncharacterized protein LOC121269527 isoform X2
uncharacterized protein LOC121269527 isoform X3
uncharacterized protein LOC121269527 isoform X4
uncharacterized protein LOC121269527 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
apolipoprotein A-IV-like, transcript variant X1
apolipoprotein A-IV-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X5
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X8
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X2
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X3
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X9
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X7
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X1
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X6
T-cell surface glycoprotein CD3 delta chain-like, transcript variant X4
T-cell surface glycoprotein CD3 delta chain-like isoform X4
uncharacterized protein LOC121269479 isoform X6
T-cell surface glycoprotein CD3 delta chain-like isoform X2
T-cell surface glycoprotein CD3 delta chain-like isoform X3
uncharacterized protein LOC121269479 isoform X7
T-cell surface glycoprotein CD3 delta chain-like isoform X5
T-cell surface glycoprotein CD3 delta chain-like isoform X1
T-cell surface glycoprotein CD3 epsilon chain-like
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
myelin protein zero-like protein 3, transcript variant X1
myelin protein zero-like protein 3, transcript variant X2
myelin protein zero-like protein 3 isoform X1
myelin protein zero-like protein 3 isoform X2
POU class 2 homeobox 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POU class 2 homeobox 3, transcript variant X1
POU class 2 homeobox 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POU class 2 homeobox 3, transcript variant X4
POU domain, class 2, transcription factor 3 isoform X3
POU domain, class 2, transcription factor 3 isoform X1
POU domain, class 2, transcription factor 3 isoform X2
POU domain, class 2, transcription factor 3 isoform X4
POU class 2 homeobox 3, transcript variant X5
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
POU domain, class 2, transcription factor 3 isoform X5
TLC domain-containing protein 5-like, transcript variant X3
TLC domain-containing protein 5-like, transcript variant X1
TLC domain-containing protein 5-like, transcript variant X2
uncharacterized protein LOC121269727 isoform X1
TLC domain-containing protein 5-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 12-like, transcript variant X5
rho guanine nucleotide exchange factor 12-like, transcript variant X1
rho guanine nucleotide exchange factor 12-like, transcript variant X4
rho guanine nucleotide exchange factor 12-like, transcript variant X3
rho guanine nucleotide exchange factor 12-like isoform X1
rho guanine nucleotide exchange factor 12-like isoform X5
rho guanine nucleotide exchange factor 12-like isoform X4
rho guanine nucleotide exchange factor 12-like isoform X3
rho guanine nucleotide exchange factor 12-like, transcript variant X2
rho guanine nucleotide exchange factor 12-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
tubulin folding cofactor E-like b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tubulin-specific chaperone cofactor E-like protein
tubulin folding cofactor E-like b, transcript variant X2
glutamate receptor, ionotropic, kainate 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 4
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
uncharacterized LOC121269484, transcript variant X3
uncharacterized LOC121269484, transcript variant X1
uncharacterized LOC121269484, transcript variant X2
uncharacterized protein LOC121269484 isoform X2
uncharacterized protein LOC121269484 isoform X1
opioid-binding protein/cell adhesion molecule-like, transcript variant X4
opioid-binding protein/cell adhesion molecule-like, transcript variant X3
opioid-binding protein/cell adhesion molecule-like, transcript variant X1
opioid-binding protein/cell adhesion molecule-like, transcript variant X5
opioid-binding protein/cell adhesion molecule-like, transcript variant X2
opioid-binding protein/cell adhesion molecule-like, transcript variant X7
opioid-binding protein/cell adhesion molecule-like, transcript variant X6
opioid-binding protein/cell adhesion molecule-like isoform X4
opioid-binding protein/cell adhesion molecule-like isoform X5
opioid-binding protein/cell adhesion molecule-like isoform X2
opioid-binding protein/cell adhesion molecule-like isoform X3
opioid-binding protein/cell adhesion molecule-like isoform X1
opioid-binding protein/cell adhesion molecule-like isoform X7
opioid-binding protein/cell adhesion molecule homolog isoform X6
V-set and immunoglobulin domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
endothelial cell-selective adhesion molecule-like, transcript variant X3
endothelial cell-selective adhesion molecule-like, transcript variant X1
endothelial cell-selective adhesion molecule-like, transcript variant X2
endothelial cell-selective adhesion molecule-like isoform X2
endothelial cell-selective adhesion molecule-like isoform X1
endothelial cell-selective adhesion molecule-like isoform X3
myb/SANT-like DNA-binding domain-containing protein 2, transcript variant X2
myb/SANT-like DNA-binding domain-containing protein 2, transcript variant X3
myb/SANT-like DNA-binding domain-containing protein 2, transcript variant X1
myb/SANT-like DNA-binding domain-containing protein 2 isoform X3
myb/SANT-like DNA-binding domain-containing protein 2 isoform X2
myb/SANT-like DNA-binding domain-containing protein 2 isoform X1
roundabout, axon guidance receptor, homolog 3 (Drosophila), transcript variant X1
roundabout, axon guidance receptor, homolog 3 (Drosophila), transcript variant X2
roundabout, axon guidance receptor, homolog 3 (Drosophila), transcript variant X3
roundabout, axon guidance receptor, homolog 3 (Drosophila), transcript variant X4
roundabout, axon guidance receptor, homolog 4 (Drosophila), transcript variant X1
roundabout, axon guidance receptor, homolog 4 (Drosophila), transcript variant X2
ATP synthase-coupling factor 6, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
pbx/knotted 1 homeobox 2, transcript variant X8
pbx/knotted 1 homeobox 2, transcript variant X5
pbx/knotted 1 homeobox 2, transcript variant X2
pbx/knotted 1 homeobox 2, transcript variant X13
pbx/knotted 1 homeobox 2, transcript variant X6
pbx/knotted 1 homeobox 2, transcript variant X7
pbx/knotted 1 homeobox 2, transcript variant X4
pbx/knotted 1 homeobox 2, transcript variant X3
pbx/knotted 1 homeobox 2, transcript variant X12
pbx/knotted 1 homeobox 2, transcript variant X1
pbx/knotted 1 homeobox 2, transcript variant X9
pbx/knotted 1 homeobox 2, transcript variant X11
pbx/knotted 1 homeobox 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins
transmembrane protein 218, transcript variant X2
transmembrane protein 218, transcript variant X1
high affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 37 member 2, transcript variant X2
solute carrier family 37 member 2, transcript variant X1
solute carrier family 37 member 2, transcript variant X3
glucose-6-phosphate exchanger SLC37A2 isoform X2
glucose-6-phosphate exchanger SLC37A2 isoform X1
glucose-6-phosphate exchanger SLC37A2 isoform X3
coiled-coil domain containing 15, transcript variant X3
coiled-coil domain containing 15, transcript variant X1
coiled-coil domain containing 15, transcript variant X2
coiled-coil domain-containing protein 15 isoform X3
coiled-coil domain-containing protein 15 isoform X1
coiled-coil domain-containing protein 15 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
arginyl-tRNA--protein transferase 1-like, transcript variant X2
arginyl-tRNA--protein transferase 1-like, transcript variant X1
arginyl-tRNA--protein transferase 1-like, transcript variant X3
arginyl-tRNA--protein transferase 1-like isoform X2
arginyl-tRNA--protein transferase 1-like isoform X1
arginyl-tRNA--protein transferase 1-like isoform X3
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fasciculation and elongation protein zeta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
EI24 autophagy associated transmembrane protein
STT3 oligosaccharyltransferase complex catalytic subunit A, transcript variant X2
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 4 samples with support for all annotated introns
STT3 oligosaccharyltransferase complex catalytic subunit A, transcript variant X1
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
cell adhesion associated, oncogene regulated, transcript variant X4
cell adhesion associated, oncogene regulated, 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 3 samples with support for all annotated introns
cell adhesion associated, oncogene regulated, transcript variant X1
cell adhesion associated, oncogene regulated, transcript variant X3
cell adhesion molecule-related/down-regulated by oncogenes isoform X2
cell adhesion molecule-related/down-regulated by oncogenes isoform X1
cell adhesion molecule-related/down-regulated by oncogenes isoform X3
V-set and immunoglobulin domain-containing protein 10-like 2
ilvB (bacterial acetolactate synthase)-like, transcript variant X2
ilvB (bacterial acetolactate synthase)-like, transcript variant X1
family with sequence similarity 118 member B, transcript variant X1
family with sequence similarity 118 member B, transcript variant X7
family with sequence similarity 118 member B, transcript variant X8
family with sequence similarity 118 member B, transcript variant X4
family with sequence similarity 118 member B, transcript variant X3
family with sequence similarity 118 member B, transcript variant X6
family with sequence similarity 118 member B, transcript variant X2
family with sequence similarity 118 member B, transcript variant X5
SRP receptor subunit alpha, transcript variant X2
SRP receptor subunit alpha, transcript variant X1
signal recognition particle receptor subunit alpha isoform X2
signal recognition particle receptor subunit alpha isoform X1
FAD-dependent oxidoreductase domain containing 1, transcript variant X1
FAD-dependent oxidoreductase domain containing 1, transcript variant X2
FAD-dependent oxidoreductase domain-containing protein 1 isoform X1
FAD-dependent oxidoreductase domain-containing protein 1 isoform X2
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
toll/interleukin-1 receptor domain-containing adapter protein isoform X1
toll-interleukin 1 receptor (TIR) domain containing adaptor protein, transcript variant X2
toll/interleukin-1 receptor domain-containing adapter protein isoform X2
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X6
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X1
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X5
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
small cysteine and glycine repeat-containing protein 6-like
ST3 beta-galactoside alpha-2,3-sialyltransferase 4, transcript variant X2
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4 isoform X1
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4 isoform X3
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4 isoform X2
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like, transcript variant X4
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like, transcript variant X2
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like isoform X1
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 4-like isoform X2
kirre like nephrin family adhesion molecule 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 150 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 143 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 Proteins
ferritin heavy chain, oocyte isoform-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ferritin heavy chain, oocyte isoform-like
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X3
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X8
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X4
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X2
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X7
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X5
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X6
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X9
Fli-1 proto-oncogene, ETS transcription factor, transcript variant X1
Friend leukemia integration 1 transcription factor isoform X2
Friend leukemia integration 1 transcription factor isoform X3
Friend leukemia integration 1 transcription factor isoform X1
Friend leukemia integration 1 transcription factor isoform X4
Friend leukemia integration 1 transcription factor isoform X5
v-ets avian erythroblastosis virus E26 oncogene homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
v-ets avian erythroblastosis virus E26 oncogene homolog 1, transcript variant X2
v-ets avian erythroblastosis virus E26 oncogene homolog 1, transcript variant X3
ATP-sensitive inward rectifier potassium channel 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins
G protein-activated inward rectifier potassium channel 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G protein-activated inward rectifier potassium channel 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 4-like
rho GTPase-activating protein 32-like, transcript variant X6
rho GTPase-activating protein 32-like, transcript variant X2
rho GTPase-activating protein 32-like, transcript variant X5
rho GTPase-activating protein 32-like, transcript variant X3
rho GTPase-activating protein 32-like, transcript variant X4
rho GTPase-activating protein 32-like, transcript variant X1
rho GTPase-activating protein 32-like, transcript variant X7
rho GTPase-activating protein 32-like isoform X1
rho GTPase-activating protein 32-like isoform X2
rho GTPase-activating protein 32-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
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 X5
thymocyte expressed, positive selection associated 1, transcript variant X2
thymocyte expressed, positive selection associated 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
baculoviral IAP repeat-containing protein 5b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 107 like, transcript variant X3
transmembrane protein 107 like, transcript variant X4
transmembrane protein 107 like, transcript variant X2
transmembrane protein 107 like, transcript variant X1
transmembrane protein 107 like isoform X2
transmembrane protein 107 like isoform X1
acyl-CoA dehydrogenase family, member 8, transcript variant X1
acyl-CoA dehydrogenase family, member 8, transcript variant X2
acyl-CoA dehydrogenase family, member 8, transcript variant X3
isobutyryl-CoA dehydrogenase, mitochondrial isoform X1
isobutyryl-CoA dehydrogenase, mitochondrial isoform X2
isobutyryl-CoA dehydrogenase, mitochondrial isoform X3
suppressor of tumorigenicity 14 protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
suppressor of tumorigenicity 14 protein homolog, transcript variant X2
suppressor of tumorigenicity 14 protein homolog isoform X1
suppressor of tumorigenicity 14 protein homolog isoform X2
amyloid beta (A4) precursor-like protein 2, transcript variant X2
amyloid beta (A4) precursor-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
amyloid beta (A4) precursor-like protein 2, transcript variant X3
amyloid beta (A4) precursor-like protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PR domain containing 10, transcript variant X2
PR domain containing 10, transcript variant X1
nuclear factor related to kappaB binding protein, transcript variant X1
nuclear factor related to kappaB binding protein, transcript variant X2
nuclear factor related to kappaB binding protein, transcript variant X3
nuclear factor related to kappaB binding protein, transcript variant X4
nuclear factor related to kappa-B-binding protein isoform X1
nuclear factor related to kappa-B-binding protein isoform X2
nuclear factor related to kappa-B-binding protein isoform X3
nuclear factor related to kappa-B-binding protein isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns