Clupea harengus chromosome 24, Ch_v2.0.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Clupei; Clupeiformes; Clupeoidei; Clupeidae; Clupea.
REFSEQ INFORMATION: The reference sequence is identical to\nLR535880.1.\nAssembly name: Ch_v2.0.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the UPPSALA UNIVERISTY on\n2019/04/16. The original whole-genome shotgun project has the\naccession CAADHV000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Clupea harengus Annotation Release\n 102\nAnnotation Version :: 102\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
interferon-induced protein 44-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interferon-induced protein 44-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
interferon-induced protein 44-like isoform X2
interferon-induced protein 44-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% 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 7 samples with support for all annotated introns
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, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
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 4 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
deleted in malignant brain tumors 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
microfibril-associated glycoprotein 4-like
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
scavenger receptor cysteine-rich type 1 protein M130-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% 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
deleted in malignant brain tumors 1 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% 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: 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
intraflagellar transport 27 homolog (Chlamydomonas)
intraflagellar transport protein 27 homolog
voltage-dependent calcium channel gamma-2 subunit
eukaryotic translation initiation factor 3, subunit D
eukaryotic translation initiation factor 3 subunit D
protein CutA homolog, transcript variant X2
protein CutA homolog, transcript variant X3
protein CutA homolog, transcript variant X4
protein CutA homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GRB2 related adaptor protein 2b, transcript variant X3
GRB2 related adaptor protein 2b, transcript variant X2
GRB2 related adaptor protein 2b, transcript variant X1
voltage-dependent T-type calcium channel subunit alpha-1I-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 1 sample with support for all annotated introns
uncharacterized protein LOC436988 homolog
arf-GAP with dual PH domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
lectin, galactoside-binding, soluble, 2b
GTP-binding protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
GTP-binding protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
GTP-binding protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GTP-binding protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 87% coverage of the annotated genomic feature by RNAseq alignments
tRNA (guanine(26)-N(2))-dimethyltransferase-like
E3 ubiquitin/ISG15 ligase TRIM25-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin/ISG15 ligase TRIM25-like, transcript variant X1
E3 ubiquitin/ISG15 ligase TRIM25-like isoform X2
E3 ubiquitin/ISG15 ligase TRIM25-like isoform X1
beta-1,3-N-acetylglucosaminyltransferase manic fringe
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 12 samples with support for all annotated introns
tripartite motif-containing protein 14-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tripartite motif-containing protein 14-like, transcript variant X2
tripartite motif-containing protein 14-like
tRNA methyltransferase 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tRNA methyltransferase 1, transcript variant X7
tRNA methyltransferase 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 6 samples with support for all annotated introns
tRNA methyltransferase 1, transcript variant X5
tRNA methyltransferase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tRNA methyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tRNA methyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tRNA methyltransferase 1, transcript variant X3
tRNA (guanine(26)-N(2))-dimethyltransferase isoform X2
tRNA (guanine(26)-N(2))-dimethyltransferase isoform X1
tRNA (guanine(26)-N(2))-dimethyltransferase isoform X3
tRNA (guanine(26)-N(2))-dimethyltransferase isoform X4
nucleus accumbens associated 1, BEN and BTB (POZ) domain containing b, 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 5 samples with support for all annotated introns
nucleus accumbens associated 1, BEN and BTB (POZ) domain containing b, 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 7 samples with support for all annotated introns
nucleus accumbens associated 1, BEN and BTB (POZ) domain containing b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nucleus accumbens associated 1, BEN and BTB (POZ) domain containing b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
nucleus accumbens-associated protein 1 isoform X1
nucleus accumbens-associated protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X5
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X2
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X12
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
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X9
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X6
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
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X4
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
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X8
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b, transcript variant X1
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X11
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X12
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X10
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X9
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X7
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X5
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X6
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X4
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X3
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X2
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform X8
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b isoform 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: WD repeat domain-containing protein 83
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; 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: inserted 4 bases in 3 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 97% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette sub-family C member 10-like, transcript variant X2
ATP-binding cassette sub-family C member 10-like, transcript variant X1
ATP-binding cassette sub-family C member 10-like
group XIIB secretory phospholipase A2-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein
ATP-binding cassette sub-family C member 10
neuroblast differentiation-associated protein AHNAK
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
WAS/WASL interacting protein family, member 2a, transcript variant X1
WAS/WASL interacting protein family, member 2a, transcript variant X2
WAS/WASL-interacting protein family member 2
B-cell receptor CD22-like, transcript variant X3
B-cell receptor CD22-like, transcript variant X1
B-cell receptor CD22-like, transcript variant X2
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 LOC116219211, transcript variant X1
uncharacterized LOC116219211, transcript variant X2
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X7
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 5 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X9
NACHT, LRR and PYD domains-containing protein 12-like isoform X2
NACHT, LRR and PYD domains-containing protein 12-like isoform X6
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X5
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
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X6
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X8
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X4
NACHT, LRR and PYD domains-containing protein 12-like isoform X1
NACHT, LRR and PYD domains-containing protein 12-like isoform X4
NACHT, LRR and PYD domains-containing protein 12-like isoform X5
NLR family CARD domain-containing protein 3-like isoform X7
NACHT, LRR and PYD domains-containing protein 12-like isoform X3
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 X3
serine/arginine repetitive matrix protein 1-like isoform X3
uncharacterized protein LOC105911238 isoform X1
uncharacterized protein DDB_G0284459-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X1
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X2
phosphatidylinositol 5-phosphate 4-kinase type-2 beta isoform X2
phosphatidylinositol 5-phosphate 4-kinase type-2 beta isoform X1
CDGSH iron-sulfur domain-containing protein 3, mitochondrial
CDGSH iron-sulfur domain-containing protein 3, mitochondrial-like
CWC25 spliceosome associated protein homolog
uncharacterized protein LOC570444 homolog
insulin-like growth factor-binding protein 4, transcript variant X1
insulin-like growth factor-binding protein 4, transcript variant X2
insulin-like growth factor-binding protein 4 isoform X1
insulin-like growth factor-binding protein 4 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1 isoform X1
keratin, type I cytoskeletal 18 isoform X1
keratin, type I cytoskeletal 18 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 23 Proteins
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
junction plakoglobin a, transcript variant X1
junction plakoglobin a, transcript variant X3
junction plakoglobin a, transcript variant X2
uncharacterized LOC122128807, transcript variant X2
uncharacterized LOC122128807, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
TOG array regulator of axonemal microtubules protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC116219027, transcript variant X2
uncharacterized LOC116219027, transcript variant X1
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
TOG array regulator of axonemal microtubules protein 2-like, transcript variant X2
TOG array regulator of axonemal microtubules protein 2-like, transcript variant X3
TOG array regulator of axonemal microtubules protein 2-like
TOG array regulator of axonemal microtubules protein 2-like, transcript variant X1
coiled-coil domain containing 88Aa, transcript variant X1
coiled-coil domain containing 88Aa, transcript variant X2
centrosomal protein 170Ab, transcript variant X5
centrosomal protein 170Ab, transcript variant X6
centrosomal protein 170Ab, transcript variant X1
centrosomal protein 170Ab, transcript variant X2
centrosomal protein 170Ab, transcript variant X3
centrosomal protein 170Ab, transcript variant X4
centrosomal protein of 170 kDa isoform X2
centrosomal protein of 170 kDa isoform X3
centrosomal protein of 170 kDa isoform X1
BAF chromatin remodeling complex subunit BCL11A b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SEC23 homolog B, coat complex II component
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: 6 Proteins, and 93% 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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein transport protein Sec23B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sodium/potassium/calcium exchanger 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ras and Rab interactor 2
eukaryotic translation elongation factor 1 alpha 1b, transcript variant X3
eukaryotic translation elongation factor 1 alpha 1b, transcript variant X1
eukaryotic translation elongation factor 1 alpha 1b, transcript variant X4
eukaryotic translation elongation factor 1 alpha 1b, transcript variant X5
eukaryotic translation elongation factor 1 alpha 1b, transcript variant X2
potassium voltage-gated channel, KQT-like subfamily, member 5b
potassium voltage-gated channel subfamily KQT member 5
regulating synaptic membrane exocytosis 1b, transcript variant X1
regulating synaptic membrane exocytosis 1b, transcript variant X4
regulating synaptic membrane exocytosis 1b, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis 1b, transcript variant X5
regulating synaptic membrane exocytosis 1b, transcript variant X2
regulating synaptic membrane exocytosis 1b, transcript variant X6
regulating synaptic membrane exocytosis 1b, transcript variant X10
regulating synaptic membrane exocytosis 1b, transcript variant X8
regulating synaptic membrane exocytosis 1b, transcript variant X13
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
regulating synaptic membrane exocytosis 1b, transcript variant X3
regulating synaptic membrane exocytosis 1b, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulating synaptic membrane exocytosis 1b, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulating synaptic membrane exocytosis 1b, transcript variant X11
regulating synaptic membrane exocytosis protein 1 isoform X4
regulating synaptic membrane exocytosis protein 1 isoform X12
regulating synaptic membrane exocytosis protein 1 isoform X13
regulating synaptic membrane exocytosis protein 1 isoform X7
regulating synaptic membrane exocytosis protein 1 isoform X5
regulating synaptic membrane exocytosis protein 1 isoform X2
regulating synaptic membrane exocytosis protein 1 isoform X6
regulating synaptic membrane exocytosis protein 1 isoform X10
regulating synaptic membrane exocytosis protein 1 isoform X9
regulating synaptic membrane exocytosis protein 1 isoform X8
regulating synaptic membrane exocytosis protein 1 isoform X3
regulating synaptic membrane exocytosis protein 1 isoform X1
regulating synaptic membrane exocytosis protein 1 isoform X11
myosin heavy chain, fast skeletal muscle-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% 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; Derived by automated computational analysis using gene prediction method: Gnomon.
centromere protein K, transcript variant X1
centromere protein K, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 31% coverage of the annotated genomic feature by RNAseq alignments
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, including 3 samples with support for all annotated introns
solute carrier family 2 member 15b, transcript variant X1
solute carrier family 2 member 15b, transcript variant X2
solute carrier family 2 member 15b isoform X1
solute carrier family 2 member 15b isoform X2
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 5 samples with support for all annotated introns
deleted in primary ciliary dyskinesia homolog (mouse)
cyclin and CBS domain divalent metal cation transport mediator 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cyclin and CBS domain divalent metal cation transport mediator 2b, transcript variant X2
5'-nucleotidase, cytosolic IIb, transcript variant X1
5'-nucleotidase, cytosolic IIb, transcript variant X2
5'-nucleotidase, cytosolic IIb, transcript variant X3
cytosolic purine 5'-nucleotidase isoform X1
cytosolic purine 5'-nucleotidase isoform X2
internexin neuronal intermediate filament protein, alpha b
TAF5 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 5
ATP synthase membrane subunit DAPIT, mitochondrial
uncharacterized protein LOC557610 homolog
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 5 samples with support for all annotated introns
inositol 1,4,5-trisphosphate receptor-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 12% coverage of the annotated genomic feature by RNAseq alignments
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
STE20-like serine/threonine-protein kinase
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 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: STE20-like serine/threonine-protein kinase
STN1 subunit of CST complex, transcript variant X2
STN1 subunit of CST complex, transcript variant X1
SH3 and PX domains 2Aa, transcript variant X1
SH3 and PX domains 2Aa, transcript variant X2
SH3 and PX domains 2Aa, transcript variant X5
SH3 and PX domains 2Aa, transcript variant X3
SH3 and PX domains 2Aa, transcript variant X4
SH3 and PX domain-containing protein 2A isoform X1
SH3 and PX domain-containing protein 2A isoform X2
SH3 and PX domain-containing protein 2A isoform X5
SH3 and PX domain-containing protein 2A isoform X3
SH3 and PX domain-containing protein 2A isoform X4
neuralized E3 ubiquitin protein ligase 1Aa, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neuralized E3 ubiquitin protein ligase 1Aa, 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 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEURL1 isoform X1
E3 ubiquitin-protein ligase NEURL1 isoform X2
cilia and flagella associated protein 58, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
cilia and flagella associated protein 58, 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
cilia- and flagella-associated protein 58 isoform X2
cilia- and flagella-associated protein 58 isoform X1
sortilin related VPS10 domain containing receptor 3
LOW QUALITY PROTEIN: VPS10 domain-containing receptor SorCS1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
calcyon neuron-specific vesicular protein, transcript variant X2
calcyon neuron-specific vesicular protein, 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
calcyon neuron-specific vesicular protein isoform X1
calcyon neuron-specific vesicular protein 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, including 1 sample with support for all annotated introns
patatin-like phospholipase domain containing 6, transcript variant X2
patatin-like phospholipase domain containing 6, transcript variant X7
patatin-like phospholipase domain containing 6, transcript variant X3
patatin-like phospholipase domain containing 6, transcript variant X1
patatin-like phospholipase domain containing 6, transcript variant X4
patatin-like phospholipase domain containing 6, transcript variant X5
patatin-like phospholipase domain containing 6, transcript variant X6
patatin-like phospholipase domain containing 6, transcript variant X8
patatin-like phospholipase domain-containing protein 6 isoform X2
patatin-like phospholipase domain-containing protein 6 isoform X1
patatin-like phospholipase domain-containing protein 6 isoform X3
patatin-like phospholipase domain-containing protein 6 isoform X4
patatin-like phospholipase domain-containing protein 6 isoform X5
patatin-like phospholipase domain-containing protein 6 isoform X6
R3H domain and coiled-coil containing 1-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 8 samples with support for all annotated introns
R3H domain and coiled-coil containing 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
coiled-coil domain-containing protein R3HCC1L
ERO1-like protein beta, transcript variant X2
ERO1-like protein beta, 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 13 samples 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: 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 84% 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
endoplasmic reticulum oxidoreductase 1 beta, transcript variant X1
endoplasmic reticulum oxidoreductase 1 beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tubulin-specific chaperone E, transcript variant X2
tubulin-specific chaperone E, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
breast cancer anti-estrogen resistance protein 3 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
interferon regulatory factor 2 binding protein 2b
interferon regulatory factor 2-binding protein 2-B
microtubule-associated protein 1 light chain 3 gamma
microtubule-associated proteins 1A/1B light chain 3C
striatin, calmodulin binding protein, transcript variant X4
striatin, calmodulin binding protein, transcript variant X2
striatin, calmodulin binding protein, transcript variant X1
striatin, calmodulin binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00150
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kinesin-like protein KIF19, transcript variant X2
kinesin-like protein KIF19, transcript variant X1
eukaryotic translation initiation factor 3 subunit B
BRCA1-associated ATM activator 1, transcript variant X3
BRCA1-associated ATM activator 1, transcript variant X1
BRCA1-associated ATM activator 1, transcript variant X2
BRCA1-associated ATM activator 1 isoform X1
BRCA1-associated ATM activator 1 isoform X2
BRCA1-associated ATM activator 1 isoform X3
guanine nucleotide-binding protein subunit alpha-12, transcript variant X2
guanine nucleotide-binding protein subunit alpha-12, transcript variant X1
guanine nucleotide-binding protein subunit alpha-12 isoform X2
guanine nucleotide-binding protein subunit alpha-12 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
B-cell receptor CD22-like, transcript variant X4
B-cell receptor CD22-like, transcript variant X5
B-cell receptor CD22-like, transcript variant X7
B-cell receptor CD22-like, transcript variant X6
uncharacterized LOC116219158, transcript variant X1
uncharacterized LOC116219158, 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 5 samples with support for all annotated introns
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X1
basement membrane-specific heparan sulfate proteoglycan core protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 113 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 3A30-like, transcript variant X3
cytochrome P450 3A30-like, transcript variant X1
cytochrome P450 3A30-like, transcript variant X2
cytochrome P450 3A30-like, transcript variant X4
G patch domain and ankyrin repeat-containing protein 1
alpha-N-acetylgalactosamine-specific lectin-like, transcript variant X2
alpha-N-acetylgalactosamine-specific lectin-like, transcript variant X1
alpha-N-acetylgalactosamine-specific lectin-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
gastrula zinc finger protein XlCGF26.1-like
mitochondrial translational initiation factor 2, transcript variant X2
mitochondrial translational initiation factor 2, transcript variant X1
translation initiation factor IF-2, mitochondrial isoform X1
translation initiation factor IF-2, mitochondrial isoform X2
echinoderm microtubule-associated protein-like 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
reticulon-3-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
reticulon-3-B-like, transcript variant X3
reticulon-3-B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
spectrin, beta, non-erythrocytic 1, transcript variant X1
spectrin, beta, non-erythrocytic 1, transcript variant X2
spectrin beta chain, non-erythrocytic 1 isoform X1
spectrin beta chain, non-erythrocytic 1 isoform X2
sulfotransferase 6B1-like, transcript variant X2
sulfotransferase 6B1-like, transcript variant X1
sulfotransferase 6B1-like, transcript variant X3
vasoactive intestinal peptide b, transcript variant X2
vasoactive intestinal peptide b, transcript variant X1
solute carrier family 29 member 1b, transcript variant X5
solute carrier family 29 member 1b, transcript variant X3
solute carrier family 29 member 1b, transcript variant X4
solute carrier family 29 member 1b, transcript variant X2
solute carrier family 29 member 1b, transcript variant X1
CSC1-like protein 2, transcript variant X1
CSC1-like protein 2, transcript variant X4
CSC1-like protein 2, transcript variant X3
CSC1-like protein 2, transcript variant X2
transcription elongation factor 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 353 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: 510 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: 126 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: 360 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 223 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: 20 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: 140 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: 348 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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
collagen alpha-1(X) chain-like, transcript variant X2
collagen alpha-1(X) chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
NLR family CARD domain-containing protein 3-like
EMI domain-containing protein 1-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
EMI domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pulmonary surfactant-associated protein D-like isoform X2
EMI domain-containing protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
GTPase IMAP family member 8-like, transcript variant X5
GTPase IMAP family member 8-like, transcript variant X4
GTPase IMAP family member 8-like, transcript variant X7
GTPase IMAP family member 8-like, transcript variant X2
GTPase IMAP family member 8-like, transcript variant X6
GTPase IMAP family member 8-like, transcript variant X8
GTPase IMAP family member 8-like, transcript variant X1
GTPase IMAP family member 8-like, transcript variant X3
GTPase IMAP family member 8-like isoform X3
GTPase IMAP family member 8-like isoform X1
GTPase IMAP family member 8-like isoform X2
kinesin light chain 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
kinesin light chain 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
kinesin light chain 1-like, transcript variant X3
phosphofurin acidic cluster sorting protein 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: phosphofurin acidic cluster sorting protein 2-like
ribosomal RNA processing protein 36 homolog
signal-induced proliferation-associated 1 like 2, transcript variant X3
signal-induced proliferation-associated 1 like 2, transcript variant X4
signal-induced proliferation-associated 1 like 2, transcript variant X1
signal-induced proliferation-associated 1 like 2, transcript variant X2
signal-induced proliferation-associated 1-like protein 2 isoform X1
signal-induced proliferation-associated 1-like protein 2 isoform X2
myosin heavy chain, fast skeletal muscle
myosin heavy chain, skeletal muscle-like
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 13 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 70% coverage of the annotated genomic feature by RNAseq alignments
TAF5-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor, transcript variant X1
TAF5-like RNA polymerase II, p300/CBP-associated factor (PCAF)-associated factor, transcript variant X2
TAF5-like RNA polymerase II p300/CBP-associated factor-associated factor 65 kDa subunit 5L
LTV1 ribosome biogenesis factor, transcript variant X1
LTV1 ribosome biogenesis factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
BTB (POZ) domain containing 3a, transcript variant X2
BTB (POZ) domain containing 3a, transcript variant X1
ESF1, nucleolar pre-rRNA processing protein, homolog (S. cerevisiae)
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 10 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase complex assembly factor 5
arginine-hydroxylase NDUFAF5, mitochondrial
kinesin family member 16Ba, transcript variant X8
kinesin family member 16Ba, transcript variant X5
kinesin family member 16Ba, transcript variant X2
kinesin family member 16Ba, transcript variant X4
kinesin family member 16Ba, transcript variant X3
kinesin family member 16Ba, transcript variant X1
kinesin family member 16Ba, transcript variant X7
kinesin family member 16Ba, transcript variant X6
small nuclear ribonucleoprotein polypeptide B2
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: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: prokineticin receptor 1a
aprataxin and PNK-like factor, 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 9 samples with support for all annotated introns
aprataxin and PNK-like factor, transcript variant X3
aprataxin and PNK-like factor, transcript variant X1
aprataxin and PNK-like factor isoform X2
aprataxin and PNK-like factor isoform X1
F-box only protein 48, transcript variant X1
F-box only protein 48, transcript variant X2
F-box only protein 48, transcript variant X3
cannabinoid receptor interacting protein 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
CB1 cannabinoid receptor-interacting protein 1a
protein phosphatase 3 (formerly 2B), regulatory s1ubunit B, alpha isoform, b, transcript variant X2
calcineurin subunit B type 1b isoform X2
protein phosphatase 3 (formerly 2B), regulatory s1ubunit B, alpha isoform, b, transcript variant X1
calcineurin subunit B type 1b isoform X1
ETAA1 activator of ATR kinase a, transcript variant X2
ETAA1 activator of ATR kinase a, transcript variant X1
ewing's tumor-associated antigen 1 isoform X2
ewing's tumor-associated antigen 1 isoform X1
Meis homeobox 1 a, 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 3 samples with support for all annotated introns
Meis homeobox 1 a, 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 7 samples with support for all annotated introns
sprouty related EVH1 domain containing 2a
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 12 samples with support for all annotated introns
sprouty-related, EVH1 domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 300 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
serine hydrolase like, transcript variant X2
serine hydrolase like, transcript variant X3
serine hydrolase like, transcript variant X5
serine hydrolase like, transcript variant X4
serine hydrolase like, transcript variant X1
activating transcription factor 7 interacting protein, transcript variant X6
activating transcription factor 7 interacting protein, transcript variant X1
activating transcription factor 7 interacting protein, transcript variant X4
activating transcription factor 7 interacting protein, transcript variant X5
activating transcription factor 7 interacting protein, transcript variant X2
activating transcription factor 7 interacting protein, transcript variant X3
activating transcription factor 7-interacting protein 1 isoform X1
activating transcription factor 7-interacting protein 1 isoform X4
activating transcription factor 7-interacting protein 1 isoform X2
activating transcription factor 7-interacting protein 1 isoform X3
glutamate receptor, ionotropic, N-methyl D-aspartate 2B, genome duplicate b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC100151507 homolog
uncharacterized protein si:ch211-243a20.3
uncharacterized si:ch211-243a20.4, transcript variant X1
uncharacterized si:ch211-243a20.4, transcript variant X2
uncharacterized protein si:ch211-243a20.4 isoform X1
uncharacterized protein si:ch211-243a20.4 isoform X2
coagulation factor VIII associated, transcript variant X1
coagulation factor VIII associated, transcript variant X2
40-kDa huntingtin-associated protein isoform X1
40-kDa huntingtin-associated protein isoform X2
epithelial membrane protein 1, transcript variant X1
epithelial membrane protein 1, transcript variant X2
epithelial membrane protein 1 isoform X1
epithelial membrane protein 1 isoform X2
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
ecotropic viral integration site 5 like, transcript variant X4
ecotropic viral integration site 5 like, transcript variant X3
ecotropic viral integration site 5 like, transcript variant X2
ecotropic viral integration site 5 like, transcript variant X1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 39Aa
heparan sulfate glucosamine 3-O-sulfotransferase 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 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: 357 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: 123 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: 205 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: 226 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: 358 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: 130 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: 206 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: 37 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: 352 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: 522 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: 222 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
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 356 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: 129 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: 509 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: 31 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: 354 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: 125 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: 55 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 355 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: 225 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: 43 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: 135 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: 349 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 34
exportin 1 (CRM1 homolog, yeast) a, transcript variant X2
exportin 1 (CRM1 homolog, yeast) a, transcript variant X1
chaperonin containing TCP1, subunit 4 (delta), transcript variant X1
T-complex protein 1 subunit delta isoform X1
chaperonin containing TCP1, subunit 4 (delta), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
T-complex protein 1 subunit delta isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
pseudouridine synthase 10, transcript variant X3
pseudouridine synthase 10, transcript variant X1
pseudouridine synthase 10, transcript variant X2
putative tRNA pseudouridine synthase Pus10
v-akt murine thymoma viral oncogene homolog 3b
RAC-gamma serine/threonine-protein kinase
small integral membrane protein 28, transcript variant X2
small integral membrane protein 28, transcript variant X1
glutamyl-tRNA synthetase 2, mitochondrial
probable glutamate--tRNA ligase, mitochondrial
ADP-ribosylation factor-binding protein GGA3, transcript variant X2
ADP-ribosylation factor-binding protein GGA3, transcript variant X1
ADP-ribosylation factor-binding protein GGA3 isoform X1
ADP-ribosylation factor-binding protein GGA3 isoform X2
cAMP-specific 3',5'-cyclic phosphodiesterase 4B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
cell division cycle 37 homolog (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA exonuclease 5, transcript variant X3
RNA exonuclease 5, transcript variant X1
RNA exonuclease 5, transcript variant X2
RNA exonuclease 5, transcript variant X4
poly(A)-specific ribonuclease (deadenylation nuclease), transcript variant X2
poly(A)-specific ribonuclease (deadenylation nuclease), transcript variant X1
poly(A)-specific ribonuclease PARN isoform X2
poly(A)-specific ribonuclease PARN isoform X1
bifunctional apoptosis regulator, transcript variant X3
bifunctional apoptosis regulator, transcript variant X1
bifunctional apoptosis regulator, 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 6 samples with support for all annotated introns
thioredoxin domain-containing protein 11
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48% coverage of the annotated genomic feature by RNAseq alignments
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
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
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 2 samples with support for all annotated introns
copper metabolism (Murr1) domain containing 1
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2-like, transcript variant X2
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2-like
uncharacterized protein LOC393502 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
malate dehydrogenase 1Aa, NAD (soluble), transcript variant X1
malate dehydrogenase 1Aa, NAD (soluble) isoform X1
malate dehydrogenase 1Aa, NAD (soluble), transcript variant X2
malate dehydrogenase 1Aa, NAD (soluble) isoform X2
UDP-glucose pyrophosphorylase 2a, transcript variant X3
UDP-glucose pyrophosphorylase 2a, transcript variant X4
UDP-glucose pyrophosphorylase 2a, transcript variant X2
UDP-glucose pyrophosphorylase 2a, transcript variant X1
UDP-glucose pyrophosphorylase 2a isoform X1
UDP-glucose pyrophosphorylase 2a isoform X2
UDP-glucose pyrophosphorylase 2a isoform X3
dpy-30 histone methyltransferase complex regulatory subunit, transcript variant X1
dpy-30 histone methyltransferase complex regulatory subunit, transcript variant X3
dpy-30 histone methyltransferase complex regulatory subunit, transcript variant X2
steroid-5-alpha-reductase, alpha polypeptide 2a
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 12 samples with support for all annotated introns
3-oxo-5-alpha-steroid 4-dehydrogenase 2a
cadherin EGF LAG seven-pass G-type receptor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protocadherin-like wing polarity protein stan, transcript variant X2
protocadherin-like wing polarity protein stan, transcript variant X1
protocadherin-like wing polarity protein stan isoform X2
protocadherin-like wing polarity protein stan isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC116219348, transcript variant X1
uncharacterized LOC116219348, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
polyunsaturated fatty acid lipoxygenase ALOX15B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
arachidonate 12-lipoxygenase, 12R-type-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 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: 30 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 117 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: 11 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: 227 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: 39 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: 131 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: 350 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: 236 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: 37 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
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 7 samples with support for all annotated introns
uncharacterized LOC122128795, transcript variant X2
uncharacterized LOC122128795, transcript variant X1
uncharacterized protein LOC122128795 isoform X1
uncharacterized protein LOC122128795 isoform X2
adhesion G protein-coupled receptor E5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
adhesion G protein-coupled receptor E3-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 9 samples with support for all annotated introns
gastrula zinc finger protein XlCGF17.1-like
uncharacterized protein LOC561073 homolog
glycine N-acyltransferase, transcript variant X1
glycine N-acyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC796649 homolog
uncharacterized protein si:ch211-114l13.9
polymerase (RNA) III (DNA directed) polypeptide F
DNA-directed RNA polymerase III subunit RPC6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 109 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 151 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: 240 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: 239 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: 43 Proteins, and 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: 520 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: 27 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: 231 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: 521 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: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida sperm-binding protein 3-like, transcript variant X3
zona pellucida sperm-binding protein 3-like, transcript variant X2
zona pellucida sperm-binding protein 3-like, transcript variant X1
zona pellucida sperm-binding protein 3-like isoform X3
zona pellucida sperm-binding protein 3-like isoform X2
zona pellucida sperm-binding protein 3-like isoform 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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 221 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: 38 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: 351 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: 114 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: 195 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: 292 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: 514 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: 34 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 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: 502 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: 70 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: 42 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: 132 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
double zinc ribbon and ankyrin repeat domains 1
double zinc ribbon and ankyrin repeat-containing protein 1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein PET117 homolog, mitochondrial, transcript variant X2
cysteine-rich protein 2-binding protein isoform X2
protein PET117 homolog, mitochondrial, 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 13 samples with support for all annotated introns
protein PET117 homolog, mitochondrial isoform X1
structural maintenance of chromosomes protein 5-like, transcript variant X1
structural maintenance of chromosomes protein 5-like, transcript variant X2
structural maintenance of chromosomes protein 5-like isoform X1
structural maintenance of chromosomes protein 5-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ribosome-binding protein 1b
alanine--tRNA ligase, mitochondrial-like, transcript variant X1
alanine--tRNA ligase, mitochondrial-like, transcript variant X2
alanine--tRNA ligase, mitochondrial-like, transcript variant X3
alanine--tRNA ligase, mitochondrial-like isoform X1
alanine--tRNA ligase, mitochondrial-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 487 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
guanylate-binding protein 1-like, transcript variant X2
guanylate-binding protein 1-like, transcript variant X3
guanylate-binding protein 1-like, transcript variant X4
guanylate-binding protein 1-like isoform X2
guanylate-binding protein 1-like isoform X3
guanylate-binding protein 1-like, transcript variant X5
guanylate-binding protein 1-like, transcript variant X1
guanylate-binding protein 1-like isoform X4
guanylate-binding protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 107 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: 420 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: 45 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: 291 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
guanylate-binding protein 1-like, transcript variant X6
guanylate-binding protein 1-like isoform X5
uncharacterized protein DDB_G0271670-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
serine-aspartate repeat-containing protein I-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 394 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: zinc finger protein 585A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 236 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 117 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: zinc finger protein 658B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 124 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 189 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
calpain-1 catalytic subunit-like, 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 9 samples with support for all annotated introns
calpain-1 catalytic subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
calpain-1 catalytic subunit-like isoform X1
calpain-1 catalytic subunit-like isoform X2
zona pellucida sperm-binding protein 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zona pellucida sperm-binding protein 3-like isoform X4
zona pellucida sperm-binding protein 3-like, transcript variant X5
zona pellucida sperm-binding protein 3-like isoform X5
tetraspanin-16-like, transcript variant X1
tetraspanin-16-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
RAD23 homolog A, nucleotide excision repair protein a
guided entry of tail-anchored proteins factor 3, ATPase
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 13 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 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 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: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger BED domain-containing protein 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 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: 27 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP11, transcript variant X2
protein mono-ADP-ribosyltransferase PARP11, transcript variant X3
protein mono-ADP-ribosyltransferase PARP11, transcript variant X1
protein mono-ADP-ribosyltransferase PARP11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: NACHT, LRR and PYD domains-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
CMRF35-like molecule 1, transcript variant X2
CMRF35-like molecule 1, transcript variant X1
CMRF35-like molecule 1, transcript variant X3
low-density lipoprotein receptor class A domain-containing protein 3-like, transcript variant X1
low-density lipoprotein receptor class A domain-containing protein 3-like, transcript variant X2
low-density lipoprotein receptor class A domain-containing protein 3-like isoform X1
uncharacterized protein LOC116219252 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sialoadhesin-like, transcript variant X2
sialoadhesin-like, transcript variant X1
uncharacterized protein LOC116219295 isoform X1
uncharacterized LOC122128796, transcript variant X4
uncharacterized LOC122128796, transcript variant X3
uncharacterized LOC122128796, transcript variant X2
uncharacterized LOC122128796, transcript variant X1
uncharacterized protein LOC122128796 isoform X2
uncharacterized protein LOC122128796 isoform X1
uncharacterized protein LOC122128796 isoform X3
CMRF35-like molecule 6, transcript variant X3
CMRF35-like molecule 6, transcript variant X1
CMRF35-like molecule 6, transcript variant X4
uncharacterized protein LOC105908987 isoform X3
uncharacterized protein LOC105908987 isoform X4
CMRF35-like molecule 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
trem-like transcript 4 protein, transcript variant X1
trem-like transcript 4 protein, transcript variant X2
trem-like transcript 4 protein isoform X2
polymeric immunoglobulin receptor-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
advanced glycosylation end product-specific receptor-like
polymeric immunoglobulin receptor-like, transcript variant X4
polymeric immunoglobulin receptor-like, transcript variant X2
polymeric immunoglobulin receptor-like, transcript variant X1
polymeric immunoglobulin receptor-like, transcript variant X3
polymeric immunoglobulin receptor-like isoform X3
polymeric immunoglobulin receptor-like isoform X2
uncharacterized LOC122128803, transcript variant X1
uncharacterized LOC122128803, transcript variant X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 57% 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
CMRF35-like molecule 9, transcript variant X1
CMRF35-like molecule 9, transcript variant X2
uncharacterized protein LOC116219248 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
CMRF35-like molecule 8, transcript variant X2
CMRF35-like molecule 8, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 190 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: 97% 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 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% 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: 6 Proteins
uncharacterized LOC116219242, transcript variant X2
uncharacterized LOC116219242, transcript variant X3
uncharacterized LOC116219242, transcript variant X1
uncharacterized protein LOC116219242 isoform X2
uncharacterized protein LOC116219242 isoform X3
uncharacterized protein LOC116219242 isoform X1
caspase recruitment domain-containing protein 8-like
uncharacterized protein LOC100003596 homolog
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-5
histone-arginine methyltransferase CARM1-like, transcript variant X1
histone-arginine methyltransferase CARM1-like, transcript variant X2
histone-arginine methyltransferase CARM1-like isoform X2
histone-arginine methyltransferase CARM1-like isoform X1
afadin- and alpha-actinin-binding protein
uncharacterized LOC105908557, transcript variant X1
uncharacterized LOC105908557, transcript variant X2
uncharacterized protein LOC105908557 isoform X1
uncharacterized protein LOC105908557 isoform X2
coiled-coil and C2 domain-containing protein 1A
methylthioribose-1-phosphate isomerase 1
leydig cell tumor 10 kDa protein homolog
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
calcium-binding mitochondrial carrier protein SCaMC-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122128787, transcript variant X1
uncharacterized LOC122128787, transcript variant X3
uncharacterized LOC122128787, transcript variant X2
uncharacterized protein LOC122128787 isoform X1
uncharacterized protein LOC122128787 isoform X2
KH-type splicing regulatory protein, 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 5 samples with support for all annotated introns
KH-type splicing regulatory protein, transcript variant X2
KH-type splicing regulatory protein, transcript variant X4
KH-type splicing regulatory protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
KH-type splicing regulatory protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
far upstream element-binding protein 2 isoform X1
far upstream element-binding protein 2 isoform X2
far upstream element-binding protein 2 isoform X3
far upstream element-binding protein 2 isoform X4
far upstream element-binding protein 2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
eukaryotic translation initiation factor 4A3
uncharacterized protein LOC563864 homolog
EGF-containing fibulin-like extracellular matrix protein 1
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
apoptosis-stimulating of p53 protein 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: apoptosis-stimulating of p53 protein 2-like
neoverrucotoxin subunit beta-like, transcript variant X4
neoverrucotoxin subunit beta-like, transcript variant X1
neoverrucotoxin subunit beta-like, transcript variant X2
neoverrucotoxin subunit beta-like, transcript variant X3
neoverrucotoxin subunit beta-like, transcript variant X5
neoverrucotoxin subunit beta-like isoform X3
neoverrucotoxin subunit beta-like isoform X1
neoverrucotoxin subunit beta-like isoform X4
neoverrucotoxin subunit beta-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 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: 7 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 25% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X4
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like isoform X1
NACHT, LRR and PYD domains-containing protein 3-like isoform X3
NACHT, LRR and PYD domains-containing protein 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
stonustoxin subunit beta-like, transcript variant X3
stonustoxin subunit beta-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
stonustoxin subunit beta-like, transcript variant X1
stonustoxin subunit beta-like isoform X1
stonustoxin subunit beta-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 48% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 11% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 26% coverage of the annotated genomic feature by RNAseq alignments
GTPase IMAP family member 9-like, transcript variant X1
GTPase IMAP family member 9-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dexamethasone-induced Ras-related protein 1-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 3 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 6-like, transcript variant X3
NACHT, LRR and PYD domains-containing protein 6-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 6-like, transcript variant X1
NACHT, LRR and PYD domains-containing protein 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 19% 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 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: 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 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: 9 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 35% 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 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 81% 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: 3 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial dicarboxylate carrier-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NLR family CARD domain-containing protein 3-like, transcript variant X1
NLR family CARD domain-containing protein 3-like, transcript variant X3
NLR family CARD domain-containing protein 3-like, transcript variant X4
NLR family CARD domain-containing protein 3-like, transcript variant X2
NLR family CARD domain-containing protein 3-like isoform X1
NLR family CARD domain-containing protein 3-like isoform X2
NACHT, LRR and PYD domains-containing protein 14-like
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, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
putative adhesion G protein-coupled receptor E4P
adhesion G protein-coupled receptor E4-like
putative adhesion G protein-coupled receptor E4P, transcript variant X2
putative adhesion G protein-coupled receptor E4P isoform X2
putative adhesion G protein-coupled receptor E4P, transcript variant X1
putative adhesion G protein-coupled receptor E4P isoform X1
adhesion G protein-coupled receptor E1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61% coverage of the annotated genomic feature by RNAseq alignments
DnaJ heat shock protein family (Hsp40) member B1b
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 12 samples with support for all annotated introns
trans-2,3-enoyl-CoA reductase b, transcript variant X2
trans-2,3-enoyl-CoA reductase b isoform X2
trans-2,3-enoyl-CoA reductase b, transcript variant X1
trans-2,3-enoyl-CoA reductase b isoform X1
NADH:ubiquinone oxidoreductase subunit B7
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 7
sterile alpha motif domain containing 1b
protein kinase, cAMP-dependent, catalytic, alpha, genome duplicate b, transcript variant X3
protein kinase, cAMP-dependent, catalytic, alpha, genome duplicate b, transcript variant X1
protein kinase, cAMP-dependent, catalytic, alpha, genome duplicate b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cAMP-dependent protein kinase catalytic subunit alpha isoform X2
cAMP-dependent protein kinase catalytic subunit alpha isoform X1
cAMP-dependent protein kinase catalytic subunit alpha isoform X3
anti-silencing function 1Bb histone chaperone
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 13 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00271
complement C3-like, transcript variant X2
complement C3-like, transcript variant X1
DENN domain containing 1C, transcript variant X2
DENN domain containing 1C, transcript variant X1
DENN domain-containing protein 1B isoform X2
DENN domain-containing protein 1B isoform X1
uncharacterized protein LOC335798 homolog
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 10 samples with support for all annotated introns
GDP-L-fucose synthase, transcript variant X1
GDP-L-fucose synthase, transcript variant X2
collagen beta(1-O)galactosyltransferase 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
adhesion G protein-coupled receptor L1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% 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: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% 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: 86% coverage of the annotated genomic feature by RNAseq alignments
basement membrane-specific heparan sulfate proteoglycan core protein-like
adhesion G protein-coupled receptor E5, transcript variant X4
adhesion G protein-coupled receptor E5, transcript variant X3
adhesion G protein-coupled receptor E5, transcript variant X7
adhesion G protein-coupled receptor E5, transcript variant X2
adhesion G protein-coupled receptor E5, transcript variant X6
adhesion G protein-coupled receptor E5, transcript variant X9
adhesion G protein-coupled receptor E5, transcript variant X5
adhesion G protein-coupled receptor E5, transcript variant X1
adhesion G protein-coupled receptor E5, transcript variant X8
adhesion G protein-coupled receptor E5, transcript variant X10
adhesion G protein-coupled receptor E5, transcript variant X11
adhesion G protein-coupled receptor E1 isoform X3
adhesion G protein-coupled receptor E1 isoform X2
adhesion G protein-coupled receptor E1 isoform X5
adhesion G protein-coupled receptor E1 isoform X7
adhesion G protein-coupled receptor E1 isoform X1
adhesion G protein-coupled receptor E5 isoform X4
adhesion G protein-coupled receptor E1 isoform X6
adhesion G protein-coupled receptor E1 isoform X8
adhesion G protein-coupled receptor E5 isoform X9
adhesion G protein-coupled receptor E5, transcript variant X12
long-chain fatty acid transport protein 1
tumor necrosis factor ligand superfamily member 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
52 kDa repressor of the inhibitor of the protein kinase
transmembrane p24 trafficking protein 1b
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 13 samples with support for all annotated introns
transmembrane emp24 domain-containing protein 1b
pre-B-cell leukemia transcription factor 1-like, transcript variant X2
pre-B-cell leukemia transcription factor 1-like, transcript variant X1
pre-B-cell leukemia transcription factor 1-like
uncharacterized LOC116219138, transcript variant X1
uncharacterized LOC116219138, transcript variant X2
lysophosphatidic acid receptor 2b, transcript variant X3
lysophosphatidic acid receptor 2b, transcript variant X1
lysophosphatidic acid receptor 2b, transcript variant X4
lysophosphatidic acid receptor 2b, transcript variant X2
lysophosphatidic acid receptor 2b isoform X1
lysophosphatidic acid receptor 2b isoform X2
calmodulin-regulated spectrin-associated protein 3, 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 1 sample with support for all annotated introns
calmodulin-regulated spectrin-associated protein 3, transcript variant X4
calmodulin-regulated spectrin-associated protein 3, transcript variant X3
calmodulin-regulated spectrin-associated protein 3, transcript variant X2
calmodulin-regulated spectrin-associated protein 3, transcript variant X5
calmodulin-regulated spectrin-associated protein 3 isoform X1
calmodulin-regulated spectrin-associated protein 3 isoform X4
calmodulin-regulated spectrin-associated protein 3 isoform X3
calmodulin-regulated spectrin-associated protein 3 isoform X2
calmodulin-regulated spectrin-associated protein 3 isoform X5
keratin, type I cytoskeletal 9-like, transcript variant X1
keratin, type I cytoskeletal 9-like, transcript variant X3
keratin, type I cytoskeletal 9-like, transcript variant X2
keratin, type I cytoskeletal 9-like, transcript variant X4
keratin, type I cytoskeletal 9-like isoform X1
keratin, type I cytoskeletal 9-like isoform X3
keratin, type I cytoskeletal 9-like isoform X2
keratin, type I cytoskeletal 9-like isoform X4
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, 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 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
microfibril-associated glycoprotein 4-like, transcript variant X2
microfibril-associated glycoprotein 4-like isoform X2
microfibril-associated glycoprotein 4-like, transcript variant X1
microfibril-associated glycoprotein 4-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 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: 31 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: 26 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cdc42-interacting protein 4 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cdc42-interacting protein 4 homolog, 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 8 samples with support for all annotated introns
cdc42-interacting protein 4 homolog isoform X1
cdc42-interacting protein 4 homolog isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: breast cancer anti-estrogen resistance protein 3 homolog
peptidylprolyl cis/trans isomerase, NIMA-interacting 1
peptidyl-prolyl cis-trans isomerase NIMA-interacting 1
gastrula zinc finger protein XlCGF17.1-like, transcript variant X2
gastrula zinc finger protein XlCGF17.1-like, transcript variant X1
gastrula zinc finger protein XlCGF17.1-like, transcript variant X4
gastrula zinc finger protein XlCGF17.1-like, transcript variant X3
gastrula zinc finger protein XlCGF17.1-like, transcript variant X5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: gastrula zinc finger protein XlCGF17.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like, transcript variant X1
oocyte zinc finger protein XlCOF6-like, transcript variant X2
THUMP domain containing 1, transcript variant X1
THUMP domain containing 1, transcript variant X3
THUMP domain containing 1, transcript variant X2
general transcription factor 3C polypeptide 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments