Cottoperca gobio chromosome 2, fCotGob3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Neoteleostei; Acanthomorphata; Eupercaria; Perciformes; Notothenioidei; Bovichtidae; Cottoperca.
REFSEQ INFORMATION: The reference sequence is identical to\nLR131927.1.\nAssembly name: fCotGob3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the SC on 2019/02/06. The\noriginal whole-genome shotgun project has the accession\nCAAAFJ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Cottoperca gobio Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.2\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: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon.
coactivator associated arginine methyltransferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
histone-arginine methyltransferase CARM1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 207 member A
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
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
chloride intracellular channel protein 4-like, transcript variant X2
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
chloride intracellular channel protein 4-like, transcript variant X1
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, including 2 samples with support for all annotated introns
chloride intracellular channel protein 4-like isoform X2
chloride intracellular channel protein 4-like isoform X1
runt-related transcription factor 1-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: 52 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: runt-related transcription factor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; 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, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: rho GTPase-activating protein 1-like
ADP ribosylation factor like GTPase 6 interacting protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ADP-ribosylation factor-like protein 6-interacting protein 6
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cysteinyl-tRNA synthetase 2, mitochondrial
probable cysteine--tRNA ligase, mitochondrial
DDRGK domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DDRGK domain containing 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 2 samples with support for all annotated introns
DDRGK domain-containing protein 1 isoform X1
DDRGK domain-containing protein 1 isoform X2
sodium/potassium-transporting ATPase subunit beta-233-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cyclic nucleotide-gated channel cone photoreceptor subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 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: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DEAD-box helicase 4, transcript variant X1
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, including 1 sample with support for all annotated introns
DEAD-box helicase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 132 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable ATP-dependent RNA helicase DDX4
coiled-coil domain containing 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
coiled-coil domain containing 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain containing 14, transcript variant X3
coiled-coil domain-containing protein 14 isoform X1
coiled-coil domain-containing protein 14 isoform X2
coiled-coil domain-containing protein 14 isoform X3
coiled-coil domain containing 14, transcript variant X4
coiled-coil domain containing 14, transcript variant X5
coiled-coil domain-containing protein 14 isoform X4
coiled-coil domain-containing protein 14 isoform X5
ankyrin repeat domain-containing protein 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heat shock transcription factor 2 binding protein, transcript variant X1
heat shock transcription factor 2 binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
diacylglycerol kinase zeta-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
diacylglycerol kinase zeta-like isoform X3
diacylglycerol kinase zeta-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 2 samples with support for all annotated introns
diacylglycerol kinase zeta-like, transcript variant X2
diacylglycerol kinase zeta-like isoform X1
diacylglycerol kinase zeta-like isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
muscarinic acetylcholine receptor M4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
N-acylglucosamine 2-epimerase-like, transcript variant X1
N-acylglucosamine 2-epimerase-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 3 samples with support for all annotated introns
N-acylglucosamine 2-epimerase-like isoform X1
N-acylglucosamine 2-epimerase-like isoform 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, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
N-acylglucosamine 2-epimerase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
patatin like phospholipase domain containing 4, transcript variant X2
patatin like phospholipase domain containing 4, transcript variant X3
patatin like phospholipase domain containing 4, transcript variant X4
patatin like phospholipase domain containing 4, 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
patatin-like phospholipase domain-containing protein 4 isoform X1
patatin-like phospholipase domain-containing protein 4 isoform X2
patatin-like phospholipase domain-containing protein 4 isoform X3
patatin-like phospholipase domain-containing protein 4 isoform X4
neuroligin 4 X-linked, transcript variant X3
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
neuroligin 4 X-linked, 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
neuroligin 4 X-linked, transcript variant X2
protein kinase X-linked, transcript variant X2
protein kinase X-linked, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cAMP-dependent protein kinase catalytic subunit PRKX isoform X1
cAMP-dependent protein kinase catalytic subunit PRKX isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
immunoglobulin superfamily member 10-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: 12 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: immunoglobulin superfamily member 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CD99 antigen-like protein 2, 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 4 samples with support for all annotated introns
CD99 antigen-like protein 2, 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 4 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
dehydrogenase/reductase SDR family member on chromosome X
LOW QUALITY PROTEIN: zinc finger BED domain-containing 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: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein PLAGL2-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: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: putative Polycomb group protein ASXL1
myelin transcription factor 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myelin transcription factor 1-like, transcript variant X4
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
myelin transcription factor 1-like, transcript variant X3
myelin transcription factor 1-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 1 sample with support for all annotated introns
myelin transcription factor 1-like, transcript variant X1
myelin transcription factor 1-like isoform X5
myelin transcription factor 1-like isoform X4
myelin transcription factor 1-like isoform X3
myelin transcription factor 1-like isoform X2
myelin transcription factor 1-like isoform X1
protein-serine O-palmitoleoyltransferase porcupine-like, transcript variant X1
protein-serine O-palmitoleoyltransferase porcupine-like isoform X1
protein-serine O-palmitoleoyltransferase porcupine-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein-serine O-palmitoleoyltransferase porcupine-like, transcript variant X5
protein-serine O-palmitoleoyltransferase porcupine-like, transcript variant X4
protein-serine O-palmitoleoyltransferase porcupine-like, transcript variant X3
protein-serine O-palmitoleoyltransferase porcupine-like isoform X2
organic solute transporter subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
suppressor of variegation 3-9 homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
suppressor of variegation 3-9 homolog 1, 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 2 samples with support for all annotated introns
histone-lysine N-methyltransferase SUV39H1 isoform X2
histone-lysine N-methyltransferase SUV39H1 isoform X3
suppressor of variegation 3-9 homolog 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
suppressor of variegation 3-9 homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
suppressor of variegation 3-9 homolog 1, transcript variant X5
histone-lysine N-methyltransferase SUV39H1 isoform X1
forkhead box protein P1-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
forkhead box protein P1-B-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 1 sample with support for all annotated introns
forkhead box protein P1-B-like, transcript variant X2
forkhead box protein P1-B-like isoform X1
forkhead box protein P1-B-like isoform X2
trafficking protein particle complex subunit 6b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
putative beta-lactamase-like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
putative beta-lactamase-like 1, 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 1 sample with support for all annotated introns
putative beta-lactamase-like 1 isoform X2
putative beta-lactamase-like 1 isoform X1
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, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: paired box protein Pax-7
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: 1 Protein
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: uncharacterized protein LOC115016659
EF-hand domain family member D2, transcript variant X2
EF-hand domain family member D2, transcript variant X1
EF-hand domain family member D2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
EF-hand domain-containing protein D2 isoform X1
EF-hand domain-containing protein D2 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: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
60S ribosomal protein L22, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
60S ribosomal protein L22, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
isoprenylcysteine carboxyl methyltransferase
protein-S-isoprenylcysteine O-methyltransferase
regulator of telomere elongation helicase 1-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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: regulator of telomere elongation helicase 1-like
NADH:ubiquinone oxidoreductase subunit B11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial
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 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: coiled-coil domain-containing protein 22
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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine/threonine-protein kinase 35-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glucocorticoid modulatory element-binding protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq 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 97% 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: targeting protein for Xklp2
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1-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: 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: procollagen-lysine,2-oxoglutarate 5-dioxygenase 1-like
uncharacterized protein KIAA2013 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
receptor-type guanylate cyclase gcy-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine/threonine-protein kinase 38-like
DENN domain containing 2D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DENN domain containing 2D, transcript variant X2
DENN domain-containing protein 2D isoform X1
DENN domain-containing protein 2D isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC115018137, transcript variant X2
uncharacterized LOC115018137, 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
ligand dependent nuclear receptor interacting factor 1, transcript variant X5
ligand-dependent nuclear receptor-interacting factor 1 isoform X4
ligand dependent nuclear receptor interacting factor 1, transcript variant X3
ligand dependent nuclear receptor interacting factor 1, transcript variant X2
ligand dependent nuclear receptor interacting factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ligand-dependent nuclear receptor-interacting factor 1 isoform X1
ligand-dependent nuclear receptor-interacting factor 1 isoform X2
ligand dependent nuclear receptor interacting factor 1, transcript variant X4
ligand-dependent nuclear receptor-interacting factor 1 isoform X3
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ankyrin repeat domain-containing protein SOWAHC-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: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: ankyrin repeat domain-containing protein SOWAHC-like
E3 ubiquitin-protein ligase HECW2-like, transcript variant X3
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
E3 ubiquitin-protein ligase HECW2-like, transcript variant X2
E3 ubiquitin-protein ligase HECW2-like, transcript variant X1
E3 ubiquitin-protein ligase HECW2-like isoform X3
E3 ubiquitin-protein ligase HECW2-like isoform X2
E3 ubiquitin-protein ligase HECW2-like isoform X1
general transcription factor IIIC subunit 3, transcript variant X2
general transcription factor IIIC subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
general transcription factor 3C polypeptide 3 isoform X2
general transcription factor 3C polypeptide 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
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: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
cilia and flagella associated protein 47
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
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.
LOW QUALITY PROTEIN: cilia- and flagella-associated protein 47
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nuclear FMR1 interacting protein 1, transcript variant X2
nuclear FMR1 interacting protein 1, 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 3 samples with support for all annotated introns
nuclear fragile X mental retardation-interacting protein 1 isoform X2
nuclear fragile X mental retardation-interacting protein 1 isoform X1
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; deleted 3 bases in 3 codons; 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, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nucleolar protein 58
COORDINATES: nucleotide motif:Rfam:12.0:RF01192
islet cell autoantigen 1 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
islet cell autoantigen 1 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
islet cell autoantigen 1-like protein isoform X1
islet cell autoantigen 1-like protein isoform X2
family with sequence similarity 117 member B
bone morphogenetic protein receptor type 2
bone morphogenetic protein receptor type-2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: dedicator of cytokinesis protein 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 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: 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
sodium-driven chloride bicarbonate exchanger-like, transcript variant X1
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, including 1 sample with support for all annotated introns
sodium-driven chloride bicarbonate exchanger-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium-driven chloride bicarbonate exchanger-like, transcript variant X3
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, including 1 sample with support for all annotated introns
sodium-driven chloride bicarbonate exchanger-like isoform X1
sodium-driven chloride bicarbonate exchanger-like isoform X2
sodium-driven chloride bicarbonate exchanger-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 7-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: 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: potassium voltage-gated channel subfamily H member 7-like
sodium channel protein type 2 subunit alpha-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein type 2 subunit alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein type 2 subunit alpha-like isoform X2
sodium channel protein type 2 subunit alpha-like isoform X1
cysteine/serine-rich nuclear protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cysteine/serine-rich nuclear protein 3-like, transcript variant X1
cysteine/serine-rich nuclear protein 3-like isoform X2
cysteine/serine-rich nuclear protein 3-like isoform X1
xin actin-binding repeat-containing 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: xin actin-binding repeat-containing protein 2-like
beta-1,3-galactosyltransferase 1, 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 2 samples with support for all annotated introns
beta-1,3-galactosyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
retinol dehydrogenase 7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
retinol dehydrogenase 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATP synthase subunit beta, mitochondrial
collagen alpha-1(XXVIII) chain-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 1 sample with support for all annotated introns
collagen alpha-1(XXVIII) chain-like isoform X1
collagen alpha-1(XXVIII) chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
collagen alpha-1(XXVIII) chain-like isoform X2
collagen alpha-1(XXVIII) chain-like, transcript variant X3
collagen alpha-1(XXVIII) chain-like isoform X3
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: 13 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: kelch-like protein 41b
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
heparan-sulfate 6-O-sulfotransferase 3-B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC115020042, transcript variant X2
uncharacterized LOC115020042, transcript variant X3
uncharacterized LOC115020042, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein DZIP1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 16% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
multidrug resistance-associated protein 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
multidrug resistance-associated protein 4-like isoform X1
multidrug resistance-associated protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
multidrug resistance-associated protein 4-like isoform X2
multidrug resistance-associated protein 4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: multidrug resistance-associated protein 4-like
translocase of inner mitochondrial membrane domain containing 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: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: complex I assembly factor TIMMDC1, mitochondrial
protein O-glucosyltransferase 1, transcript variant X2
protein O-glucosyltransferase 1, transcript variant X1
protein O-glucosyltransferase 1 isoform X1
protein O-glucosyltransferase 1 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: 23 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: calsequestrin-2-like
vang-like protein 1, 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 3 samples with support for all annotated introns
vang-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
vang-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 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: 83 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
gap junction beta-6 protein-like, transcript variant X2
gap junction beta-6 protein-like, transcript variant X3
gap junction beta-6 protein-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 2 samples with support for all annotated introns
gap junction beta-6 protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gap junction beta-6 protein-like isoform X2
gap junction beta-2 protein-like isoform X1
gap junction beta-6 protein-like isoform X3
histone deacetylase complex subunit SAP18
RNA transcription, translation and transport factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RNA transcription, translation and transport factor protein
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
prostaglandin E2 receptor EP2 subtype-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
prostaglandin E2 receptor EP2 subtype-like, transcript variant X2
prostaglandin E2 receptor EP2 subtype-like, transcript variant X3
prostaglandin E2 receptor EP2 subtype-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, including 1 sample with support for all annotated introns
thioredoxin domain containing 16, transcript variant X1
thioredoxin domain-containing protein 16
thioredoxin domain containing 16, transcript variant X2
G protein-coupled receptor 137C, transcript variant X1
G protein-coupled receptor 137C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
integral membrane protein GPR137C isoform X2
integral membrane protein GPR137C isoform X1
acid phosphatase 2, lysosomal, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acid phosphatase 2, lysosomal, transcript variant X1
insulin receptor substrate 2-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
insulin receptor substrate 2-like, transcript variant X2
insulin receptor substrate 2-like isoform X1
insulin receptor substrate 2-like isoform X2
nucleotide triphosphate diphosphatase NUDT15
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: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 122
mitochondrial translation release factor 1, 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 3 samples with support for all annotated introns
mitochondrial translation release factor 1, transcript variant X2
peptide chain release factor 1, mitochondrial isoform X2
peptide chain release factor 1, mitochondrial isoform X1
mitochondrial translation release factor 1, transcript variant X3
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
peptide chain release factor 1, mitochondrial isoform X3
LOW QUALITY PROTEIN: WW domain-binding protein 4
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glycerol kinase-like, transcript variant X1
glycerol kinase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NF-kappa-B inhibitor zeta-like
jagunal homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
jagunal homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
jagunal homolog 1, transcript variant X3
filamin A-interacting protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
filamin A-interacting protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
filamin A-interacting protein 1-like isoform X3
filamin A-interacting protein 1-like isoform X1
filamin A-interacting protein 1-like, transcript variant X2
filamin A-interacting protein 1-like isoform X2
epithelial cell-transforming sequence 2 oncogene-like
coiled-coil domain containing 28A, transcript variant X2
coiled-coil domain containing 28A, transcript variant X3
coiled-coil domain containing 28A, transcript variant X1
coiled-coil domain-containing protein 28A
sodium/potassium-transporting ATPase subunit alpha-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 295 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit alpha-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 258 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium/potassium-transporting ATPase subunit alpha-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 287 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit alpha-1 isoform X1
sodium/potassium-transporting ATPase subunit alpha-1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1-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: 22 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1-like
striated muscle preferentially expressed protein kinase-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
inhibin subunit alpha, transcript variant X1
inhibin subunit alpha, transcript variant X2
inhibin subunit alpha, transcript variant X3
gap junction gamma-1 protein-like, transcript variant X5
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, including 2 samples with support for all annotated introns
gap junction gamma-1 protein-like, transcript variant X3
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, including 3 samples with support for all annotated introns
gap junction gamma-1 protein-like, transcript variant X2
gap junction gamma-1 protein-like, transcript variant X4
gap junction gamma-1 protein-like, transcript variant X1
serine/threonine kinase 11 interacting protein
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: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine/threonine-protein kinase 11-interacting protein
insulin-like growth factor-binding protein 2-A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
insulin-like growth factor-binding protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cyclin-Y-like protein 1, transcript variant X3
cyclin-Y-like protein 1, transcript variant X2
cyclin-Y-like protein 1, transcript variant X1
cyclin-Y-like protein 1, transcript variant X4
protein N-lysine methyltransferase METTL21A
cyclic AMP-responsive element-binding protein 1-like, transcript variant X1
cyclic AMP-responsive element-binding protein 1-like, transcript variant X2
cyclic AMP-responsive element-binding protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cyclic AMP-responsive element-binding protein 1-like, transcript variant X4
cyclic AMP-responsive element-binding protein 1-like isoform X2
cyclic AMP-responsive element-binding protein 1-like isoform X1
Krueppel-like factor 7, transcript variant X1
Krueppel-like factor 7, transcript variant X2
receptor activity-modifying protein 1-like
receptor tyrosine-protein kinase erbB-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
myosin light chain 3, skeletal muscle isoform-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: 115 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: myosin light chain 3, skeletal muscle isoform-like
acyl-CoA dehydrogenase long chain, transcript variant X1
long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1
acyl-CoA dehydrogenase long chain, transcript variant X2
long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2
long-chain specific acyl-CoA dehydrogenase, mitochondrial-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 2 samples with support for all annotated introns
long-chain specific acyl-CoA dehydrogenase, mitochondrial-like isoform X1
long-chain specific acyl-CoA dehydrogenase, mitochondrial-like, transcript variant X2
long-chain specific acyl-CoA dehydrogenase, mitochondrial-like isoform X2
long-chain specific acyl-CoA dehydrogenase, mitochondrial-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: 22 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: long-chain specific acyl-CoA dehydrogenase, mitochondrial-like
microtubule-associated protein 2-like, transcript variant X3
microtubule-associated protein 2-like, transcript variant X6
microtubule-associated protein 2-like, transcript variant X1
microtubule-associated protein 2-like, transcript variant X4
microtubule-associated protein 2-like, transcript variant X5
microtubule-associated protein 2-like, transcript variant X2
microtubule-associated protein 2-like isoform X1
microtubule-associated protein 2-like isoform X4
microtubule-associated protein 2-like isoform X2
microtubule-associated protein 2-like isoform X3
unc-80 homolog, NALCN channel complex subunit
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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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: deleted 1 base in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein unc-80 homolog
leukotriene-B(4) omega-hydroxylase 2-like, transcript variant X1
leukotriene-B(4) omega-hydroxylase 2-like, transcript variant X2
leukotriene-B(4) omega-hydroxylase 2-like isoform X1
leukotriene-B(4) omega-hydroxylase 2-like isoform X2
solute carrier family 19 member 1, transcript variant X1
solute carrier family 19 member 1, transcript variant X2
C-X-C chemokine receptor type 1-like, transcript variant X2
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 2 samples with support for all annotated introns
C-X-C chemokine receptor type 1-like, transcript variant X1
C-X-C chemokine receptor type 1-like isoform X2
C-X-C chemokine receptor type 1-like isoform X1
actin related protein 2/3 complex subunit 2
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 4 samples with support for all annotated introns
actin-related protein 2/3 complex subunit 2
keratin, type I cytoskeletal 18-like, transcript variant X1
keratin, type I cytoskeletal 18-like, transcript variant X2
keratin, type I cytoskeletal 18-like isoform X1
keratin, type I cytoskeletal 18-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
histone deacetylase 4-like, transcript variant X1
histone deacetylase 4-like, transcript variant X3
histone deacetylase 4-like, transcript variant X4
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
histone deacetylase 4-like, transcript variant X5
histone deacetylase 4-like, transcript variant X7
histone deacetylase 4-like, transcript variant X2
histone deacetylase 4-like, transcript variant X8
histone deacetylase 4-like, transcript variant X6
ribose-phosphate pyrophosphokinase 2, transcript variant X1
ribose-phosphate pyrophosphokinase 2 isoform X1
ribose-phosphate pyrophosphokinase 2, transcript variant X2
ribose-phosphate pyrophosphokinase 2 isoform X2
transcription elongation factor A N-terminal and central domain containing, transcript variant X1
transcription elongation factor A N-terminal and central domain containing, transcript variant X2
transcription elongation factor A N-terminal and central domain-containing protein
ras-related protein Rab-9A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras-related protein Rab-9A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras-related protein Rab-9A-like, transcript variant X2
ras-related protein Rab-9A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
gem nuclear organelle associated protein 8, transcript variant X1
gem nuclear organelle associated protein 8, transcript variant X3
gem nuclear organelle associated protein 8, transcript variant X2
uncharacterized LOC115020356, transcript variant X3
uncharacterized LOC115020356, transcript variant X1
uncharacterized LOC115020356, transcript variant X2
OX-2 membrane glycoprotein-like, transcript variant X1
OX-2 membrane glycoprotein-like, transcript variant X3
OX-2 membrane glycoprotein-like, transcript variant X4
OX-2 membrane glycoprotein-like, transcript variant X2
OX-2 membrane glycoprotein-like isoform X1
OX-2 membrane glycoprotein-like isoform X2
OX-2 membrane glycoprotein-like isoform X3
OX-2 membrane glycoprotein-like, transcript variant X5
OX-2 membrane glycoprotein-like isoform X4
OX-2 membrane glycoprotein-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
splicing factor U2AF 35 kDa subunit-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 4 samples with support for all annotated introns
splicing factor U2AF 35 kDa subunit-like isoform X2
splicing factor U2AF 35 kDa subunit-like, transcript variant X1
splicing factor U2AF 35 kDa subunit-like isoform X1
uncharacterized LOC115016849, transcript variant X1
uncharacterized LOC115016849, transcript variant X2
vascular endothelial growth factor C-like
trace amine-associated receptor 13c-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
ETS translocation variant 5-like, transcript variant X2
ETS translocation variant 5-like, transcript variant X1
ETS translocation variant 5-like isoform X2
ETS translocation variant 5-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 119 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: 52 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: 116 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: 54 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 136 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
DNA-binding protein SATB2-like, transcript variant X2
DNA-binding protein SATB2-like, transcript variant X1
DNA-binding protein SATB2-like isoform X2
DNA-binding protein SATB2-like isoform X1
potassium voltage-gated channel subfamily H member 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily H member 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily H member 8-like, transcript variant X3
potassium voltage-gated channel subfamily H member 8-like isoform X2
potassium voltage-gated channel subfamily H member 8-like isoform X1
potassium voltage-gated channel subfamily H member 8-like isoform X3
protein FAM184A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein FAM184A-like, transcript variant X1
protein FAM184A-like, transcript variant X2
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; 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
LOW QUALITY PROTEIN: T-cell surface antigen CD2-like
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 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: prostaglandin F2 receptor negative regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP-dependent RNA helicase DDX3X-like, transcript variant X1
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 1 sample with support for all annotated introns
ATP-dependent RNA helicase DDX3X-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATP-dependent RNA helicase DDX3X-like isoform X1
ATP-dependent RNA helicase DDX3X-like isoform X2
TDP-glucose 4,6-dehydratase, transcript variant X2
TDP-glucose 4,6-dehydratase, transcript variant X1
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
small integral membrane protein 11A-like
voltage-dependent L-type calcium channel subunit beta-4-like, transcript variant X1
voltage-dependent L-type calcium channel subunit beta-4-like, transcript variant X2
voltage-dependent L-type calcium channel subunit beta-4-like, transcript variant X3
voltage-dependent L-type calcium channel subunit beta-4-like isoform X2
voltage-dependent L-type calcium channel subunit beta-4-like isoform X1
voltage-dependent L-type calcium channel subunit beta-4-like isoform X3
semaphorin-5B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
semaphorin-5B-like, transcript variant X2
semaphorin-5B-like, 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 2 samples with support for all annotated introns
autophagy related 13, transcript variant X2
autophagy related 13, transcript variant X1
harbinger transposase derived 1, transcript variant X1
harbinger transposase derived 1, transcript variant X2
cAMP responsive element binding protein 3 like 1
cyclic AMP-responsive element-binding protein 3-like protein 1
ras-related and estrogen-regulated growth inhibitor-like
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial-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: 12 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial-like
unc-50 inner nuclear membrane RNA binding protein
inosine-uridine preferring nucleoside hydrolase-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: inosine-uridine preferring nucleoside hydrolase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor 7-like, transcript variant X1
rho guanine nucleotide exchange factor 7-like, 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, including 1 sample with support for all annotated introns
rho guanine nucleotide exchange factor 7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho guanine nucleotide exchange factor 7-like isoform X1
rho guanine nucleotide exchange factor 7-like isoform X2
rho guanine nucleotide exchange factor 7-like, transcript variant X4
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
probable phospholipid-transporting ATPase IH
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: probable phospholipid-transporting ATPase IH
tubulin gamma complex associated protein 3
fibroblast growth factor 14-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fibroblast growth factor 14-like, transcript variant X3
fibroblast growth factor 14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibroblast growth factor 14-like isoform X1
fibroblast growth factor 14-like isoform X2
fibroblast growth factor 14-like isoform X3
RCC1 and BTB domain-containing protein 1-like, transcript variant X2
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 4 samples with support for all annotated introns
RCC1 and BTB domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RCC1 and BTB domain-containing protein 1-like isoform X1
RCC1 and BTB domain-containing protein 1-like isoform X2
cytidine and dCMP deaminase domain containing 1
cytidine and dCMP deaminase domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
guanine nucleotide exchange factor DBS-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide exchange factor DBS-like, transcript variant X3
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 1 sample with support for all annotated introns
guanine nucleotide exchange factor DBS-like, transcript variant X4
guanine nucleotide exchange factor DBS-like, transcript variant X1
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 1 sample with support for all annotated introns
guanine nucleotide exchange factor DBS-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide exchange factor DBS-like, transcript variant X6
guanine nucleotide exchange factor DBS-like, transcript variant X2
guanine nucleotide exchange factor DBS-like, transcript variant X5
guanine nucleotide exchange factor DBS-like isoform X7
guanine nucleotide exchange factor DBS-like isoform X4
guanine nucleotide exchange factor DBS-like isoform X3
guanine nucleotide exchange factor DBS-like isoform X1
guanine nucleotide exchange factor DBS-like isoform X6
guanine nucleotide exchange factor DBS-like isoform X8
guanine nucleotide exchange factor DBS-like isoform X2
guanine nucleotide exchange factor DBS-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq 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: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: probable ribonuclease ZC3H12C
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X9
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X16
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X15
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X14
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X12
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X17
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X8
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X6
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X5
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X4
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X13
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X7
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X11
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X10
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 4 isoform X8
mitogen-activated protein kinase kinase kinase kinase 4 isoform X15
mitogen-activated protein kinase kinase kinase kinase 4 isoform X14
mitogen-activated protein kinase kinase kinase kinase 4 isoform X13
mitogen-activated protein kinase kinase kinase kinase 4 isoform X11
mitogen-activated protein kinase kinase kinase kinase 4 isoform X16
mitogen-activated protein kinase kinase kinase kinase 4 isoform X7
mitogen-activated protein kinase kinase kinase kinase 4 isoform X5
mitogen-activated protein kinase kinase kinase kinase 4 isoform X4
mitogen-activated protein kinase kinase kinase kinase 4 isoform X3
mitogen-activated protein kinase kinase kinase kinase 4 isoform X12
mitogen-activated protein kinase kinase kinase kinase 4 isoform X6
mitogen-activated protein kinase kinase kinase kinase 4 isoform X10
mitogen-activated protein kinase kinase kinase kinase 4 isoform X9
mitogen-activated protein kinase kinase kinase kinase 4 isoform X2
mitogen-activated protein kinase kinase kinase kinase 4 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: carbohydrate sulfotransferase 10
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; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger CCCH domain-containing protein 13
carboxypeptidase B2-like, transcript variant X1
carboxypeptidase B2-like, transcript variant X2
GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ras-associated and pleckstrin homology domains-containing protein 1-like
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, including 2 samples with support for all annotated introns
uncharacterized LOC115019885, transcript variant X1
uncharacterized LOC115019885, transcript variant X2
uncharacterized protein LOC115019885 isoform X1
uncharacterized protein LOC115019885 isoform X2
FAST kinase domains 2, transcript variant X1
FAST kinase domains 2, transcript variant X2
FAST kinase domain-containing protein 2, mitochondrial
reticulophagy regulator family member 2, transcript variant X2
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
reticulophagy regulator family member 2, transcript variant X1
5'-AMP-activated protein kinase subunit gamma-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; 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, including 4 samples with support for all annotated introns
ATP binding cassette subfamily B member 6 (Langereis blood group)
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: 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: ATP-binding cassette sub-family B member 6, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
partitioning defective 3 homolog B-like, transcript variant X2
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
partitioning defective 3 homolog B-like, transcript variant X1
partitioning defective 3 homolog B-like isoform X2
partitioning defective 3 homolog B-like isoform X1
zona pellucida sperm-binding protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zona pellucida sperm-binding protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zona pellucida sperm-binding protein 3-like isoform X1
zona pellucida sperm-binding protein 3-like 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: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: muscleblind-like protein 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
39S ribosomal protein L39, mitochondrial
junctional adhesion molecule 2, transcript variant X1
junctional adhesion molecule 2, transcript variant X2
junctional adhesion molecule B isoform X1
junctional adhesion molecule B isoform X2
ATP synthase peripheral stalk subunit F6
ATP synthase-coupling factor 6, mitochondrial
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: 25 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: amyloid-beta precursor protein
ADAM metallopeptidase with thrombospondin type 1 motif 1
A disintegrin and metalloproteinase with thrombospondin motifs 1
ADAM metallopeptidase with thrombospondin type 1 motif 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 5
sodium- and chloride-dependent GABA transporter 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: 70 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: sodium- and chloride-dependent GABA transporter 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: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: histone demethylase UTY-like
FUN14 domain-containing protein 1, transcript variant X1
FUN14 domain-containing protein 1, transcript variant X3
FUN14 domain-containing protein 1, transcript variant X2
FUN14 domain-containing protein 1 isoform X1
FUN14 domain-containing protein 1 isoform X3
FUN14 domain-containing protein 1 isoform X2
centromere protein L, transcript variant X2
centromere protein L, transcript variant X1
centromere protein L, transcript variant X3
calcium/calmodulin dependent serine protein kinase, transcript variant X10
calcium/calmodulin dependent serine protein kinase, transcript variant X2
calcium/calmodulin dependent serine protein kinase, transcript variant X7
calcium/calmodulin dependent serine protein kinase, transcript variant X4
calcium/calmodulin dependent serine protein kinase, transcript variant X9
calcium/calmodulin dependent serine protein kinase, transcript variant X1
calcium/calmodulin dependent serine protein kinase, transcript variant X6
calcium/calmodulin dependent serine protein kinase, transcript variant X5
calcium/calmodulin dependent serine protein kinase, transcript variant X11
calcium/calmodulin dependent serine protein kinase, transcript variant X3
calcium/calmodulin dependent serine protein kinase, transcript variant X8
peripheral plasma membrane protein CASK isoform X1
peripheral plasma membrane protein CASK isoform X2
peripheral plasma membrane protein CASK isoform X6
peripheral plasma membrane protein CASK isoform X7
peripheral plasma membrane protein CASK isoform X3
peripheral plasma membrane protein CASK isoform X8
peripheral plasma membrane protein CASK isoform X4
peripheral plasma membrane protein CASK isoform X9
peripheral plasma membrane protein CASK isoform X10
peripheral plasma membrane protein CASK isoform X5
peripheral plasma membrane protein CASK isoform X11
nuclear receptor subfamily 0 group B member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interleukin-1 receptor accessory protein-like 1, transcript variant X5
interleukin-1 receptor accessory protein-like 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interleukin-1 receptor accessory protein-like 1, transcript variant X7
interleukin-1 receptor accessory protein-like 1, transcript variant X8
interleukin-1 receptor accessory protein-like 1, transcript variant X1
interleukin-1 receptor accessory protein-like 1, transcript variant X3
interleukin-1 receptor accessory protein-like 1, transcript variant X6
interleukin-1 receptor accessory protein-like 1, transcript variant X2
interleukin-1 receptor accessory protein-like 1, transcript variant X4
interleukin-1 receptor accessory protein-like 1 isoform X4
interleukin-1 receptor accessory protein-like 1 isoform X2
interleukin-1 receptor accessory protein-like 1 isoform X3
interleukin-1 receptor accessory protein-like 1 isoform X1
uncharacterized LOC115019944, transcript variant X2
uncharacterized LOC115019944, transcript variant X1
FERM and PDZ domain-containing protein 4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: FERM and PDZ domain-containing protein 4-like
MSL complex subunit 3, transcript variant X3
MSL complex subunit 3, transcript variant X4
MSL complex subunit 3, transcript variant X1
MSL complex subunit 3, transcript variant X2
male-specific lethal 3 homolog isoform X3
male-specific lethal 3 homolog isoform X1
male-specific lethal 3 homolog isoform X2
Rho GTPase activating protein 6, transcript variant X1
Rho GTPase activating protein 6, transcript variant X2
rho GTPase-activating protein 6 isoform X1
rho GTPase-activating protein 6 isoform X2
Rho GTPase activating protein 6, transcript variant X3
rho GTPase-activating protein 6 isoform X3
E3 ubiquitin-protein ligase Midline-1-like, transcript variant X2
E3 ubiquitin-protein ligase Midline-1-like, transcript variant X1
E3 ubiquitin-protein ligase Midline-1-like, transcript variant X3
E3 ubiquitin-protein ligase Midline-1-like
SLIT and NTRK like family member 5, transcript variant X1
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
SLIT and NTRK like family member 5, transcript variant X2
SLIT and NTRK like family member 5, transcript variant X3
SLIT and NTRK like family member 6, transcript variant X3
SLIT and NTRK like family member 6, transcript variant X1
SLIT and NTRK like family member 6, transcript variant X2
protein sprouty homolog 2-like, transcript variant X7
protein sprouty homolog 2-like, transcript variant X6
protein sprouty homolog 2-like, transcript variant X5
protein sprouty homolog 2-like, transcript variant X9
protein sprouty homolog 2-like, transcript variant X8
protein sprouty homolog 2-like, transcript variant X3
protein sprouty homolog 2-like, transcript variant X2
protein sprouty homolog 2-like, transcript variant X4
protein sprouty homolog 2-like, transcript variant X11
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
protein sprouty homolog 2-like, transcript variant X10
protein sprouty homolog 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein sprouty homolog 2-like, transcript variant X12
Nedd4 family interacting protein 2, transcript variant X2
Nedd4 family interacting protein 2, transcript variant X1
NEDD4 family-interacting protein 2 isoform X1
NEDD4 family-interacting protein 2 isoform X2
gamma-aminobutyric acid receptor subunit beta-3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-3-like isoform X2
gamma-aminobutyric acid receptor subunit beta-3-like isoform X1
gamma-aminobutyric acid receptor subunit beta-3-like isoform X3
gamma-aminobutyric acid receptor subunit beta-3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-3-like isoform X4
gamma-aminobutyric acid receptor subunit alpha-5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit gamma-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia and flagella associated protein 221, transcript variant X5
cilia and flagella associated protein 221, transcript variant X4
cilia and flagella associated protein 221, transcript variant X3
cilia and flagella associated protein 221, transcript variant X1
cilia and flagella associated protein 221, transcript variant X2
cilia- and flagella-associated protein 221
vasoactive intestinal polypeptide receptor-like
acyl-CoA-binding protein-like, transcript variant X1
acyl-CoA-binding protein-like, transcript variant X2
acyl-CoA-binding protein-like isoform X2
acyl-CoA-binding protein-like isoform X1
metalloreductase STEAP3-like, transcript variant X2
metalloreductase STEAP3-like, transcript variant X1
metalloreductase STEAP3-like, transcript variant X3
metalloreductase STEAP3-like, transcript variant X5
metalloreductase STEAP3-like, transcript variant X4
complement C1q-like protein 2, transcript variant X1
complement C1q-like protein 2, transcript variant X2
complement C1q-like protein 2 isoform X1
complement C1q-like protein 2 isoform X2
homeobox protein engrailed-1-B-like, transcript variant X1
homeobox protein engrailed-1-B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
homeobox protein engrailed-1-B-like isoform X1
homeobox protein engrailed-1-B-like isoform X2
L-threonine 3-dehydrogenase, mitochondrial-like
LOW QUALITY PROTEIN: retinitis pigmentosa 1-like 1 protein
glucokinase regulator, transcript variant X2
glucokinase regulator, transcript variant X3
glucokinase regulator, transcript variant X1
glucokinase regulatory protein isoform X2
glucokinase regulatory protein isoform X3
glucokinase regulatory protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ectonucleotide pyrophosphatase/phosphodiesterase 4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: bis(5'-adenosyl)-triphosphatase ENPP4
chloride intracellular channel 5, transcript variant X1
chloride intracellular channel 5, transcript variant X2
chloride intracellular channel protein 5 isoform X1
chloride intracellular channel protein 5 isoform X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X3
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X1
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X8
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X7
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X4
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A isoform X1
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A isoform X4
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X6
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A isoform X3
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase, transcript variant X5
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A 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
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 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: DNA annealing helicase and endonuclease ZRANB3
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 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: R3H domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
methylmalonic aciduria and homocystinuria type D homolog, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; 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
LOW QUALITY PROTEIN: uncharacterized protein LOC115022049
neurobeachin like 1, transcript variant X2
neurobeachin like 1, transcript variant X1
STE20-related kinase adapter protein beta-like, transcript variant X1
STE20-related kinase adapter protein beta-like, transcript variant X2
STE20-related kinase adapter protein beta-like, transcript variant X3
STE20-related kinase adapter protein beta-like isoform X1
STE20-related kinase adapter protein beta-like isoform X2
trafficking kinesin-binding protein 2-like, transcript variant X1
trafficking kinesin-binding protein 2-like, transcript variant X2
trafficking kinesin-binding protein 2-like, transcript variant X3
trafficking kinesin-binding protein 2-like, transcript variant X4
trafficking kinesin-binding protein 2-like, transcript variant X9
trafficking kinesin-binding protein 2-like isoform X1
trafficking kinesin-binding protein 2-like isoform X2
trafficking kinesin-binding protein 2-like isoform X3
trafficking kinesin-binding protein 2-like isoform X4
trafficking kinesin-binding protein 2-like isoform X6
trafficking kinesin-binding protein 2-like, transcript variant X8
trafficking kinesin-binding protein 2-like, transcript variant X7
trafficking kinesin-binding protein 2-like, transcript variant X5
trafficking kinesin-binding protein 2-like, transcript variant X6
trafficking kinesin-binding protein 2-like isoform X5
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: 5 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: E3 ubiquitin/ISG15 ligase TRIM25-like
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
FERM, ARHGEF and pleckstrin domain-containing protein 1-like, transcript variant X3
FERM, ARHGEF and pleckstrin domain-containing protein 1-like, transcript variant X1
FERM, ARHGEF and pleckstrin domain-containing protein 1-like, transcript variant X2
FERM, ARHGEF and pleckstrin domain-containing protein 1-like isoform X1
FERM, ARHGEF and pleckstrin domain-containing protein 1-like isoform X2
FERM, ARHGEF and pleckstrin domain-containing protein 1-like isoform X3
ADP-ribosylation factor-like protein 13B
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: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: ADP-ribosylation factor-like protein 13B
neural cell adhesion molecule 2, transcript variant X1
neural cell adhesion molecule 2, transcript variant X3
neural cell adhesion molecule 2, transcript variant X2
neural cell adhesion molecule 2, transcript variant X4
neural cell adhesion molecule 2, transcript variant X6
neural cell adhesion molecule 2, transcript variant X5
neural cell adhesion molecule 2, transcript variant X7
neural cell adhesion molecule 2 isoform X3
neural cell adhesion molecule 2 isoform X6
neural cell adhesion molecule 2 isoform X7
neural cell adhesion molecule 2 isoform X1
neural cell adhesion molecule 2 isoform X2
neural cell adhesion molecule 2 isoform X4
neural cell adhesion molecule 2 isoform X5
uncharacterized LOC115018771, transcript variant X2
uncharacterized LOC115018771, transcript variant X3
uncharacterized LOC115018771, transcript variant X4
uncharacterized LOC115018771, transcript variant X1
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X1
trifunctional purine biosynthetic protein adenosine-3 isoform X1
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X3
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X2
trifunctional purine biosynthetic protein adenosine-3 isoform X2
trifunctional purine biosynthetic protein adenosine-3 isoform X3
methyltransferase N6AMT1-like, transcript variant X2
methyltransferase N6AMT1-like, transcript variant X1
methyltransferase N6AMT1-like isoform X2
methyltransferase N6AMT1-like isoform X1
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X1
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X3
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X2
calponin homology domain-containing protein DDB_G0272472-like, transcript variant X4
calponin homology domain-containing protein DDB_G0272472-like isoform X1
calponin homology domain-containing protein DDB_G0272472-like isoform X3
calponin homology domain-containing protein DDB_G0272472-like isoform X2
calponin homology domain-containing protein DDB_G0272472-like isoform X4
high-affinity choline transporter 1-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: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: high-affinity choline transporter 1-like
oxysterol-binding protein-related protein 11
glycerol-3-phosphate dehydrogenase 1-like protein
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; deleted 1 base in 1 codon; 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
LOW QUALITY PROTEIN: nck-associated protein 5-like
ly6/PLAUR domain-containing protein 1-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: 34 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: actin-related protein 3-like
POU domain, class 3, transcription factor 3-B, transcript variant X2
POU domain, class 3, transcription factor 3-B, transcript variant X1
POU domain, class 3, transcription factor 3-B isoform X1
POU domain, class 3, transcription factor 3-B isoform X2
SLAIN motif-containing protein 1-like, transcript variant X4
SLAIN motif-containing protein 1-like, transcript variant X5
SLAIN motif-containing protein 1-like, transcript variant X1
SLAIN motif-containing protein 1-like, transcript variant X2
SLAIN motif-containing protein 1-like, transcript variant X3
SLAIN motif-containing protein 1-like isoform X3
SLAIN motif-containing protein 1-like isoform X4
SLAIN motif-containing protein 1-like isoform X1
SLAIN motif-containing protein 1-like isoform X2
uncharacterized LOC115018886, transcript variant X1
uncharacterized LOC115018886, transcript variant X2
methyltransferase N6AMT1-like, transcript variant X3
methyltransferase N6AMT1-like isoform X3
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 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase ZSWIM2
calcitonin gene-related peptide type 1 receptor-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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: calcitonin gene-related peptide type 1 receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 7 Proteins
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: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: copper-transporting ATPase 2-like
fibronectin type III domain-containing protein 4-like, transcript variant X3
fibronectin type III domain-containing protein 4-like, transcript variant X9
fibronectin type III domain-containing protein 4-like, transcript variant X4
fibronectin type III domain-containing protein 4-like, transcript variant X7
fibronectin type III domain-containing protein 4-like, transcript variant X2
leucine-rich repeat-containing protein 3-like
poly(rC)-binding protein 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
poly(rC)-binding protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
poly(rC)-binding protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
poly(rC)-binding protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
fibronectin type III domain-containing protein 4-like, transcript variant X5
poly(rC)-binding protein 3-like isoform X4
poly(rC)-binding protein 3-like isoform X3
poly(rC)-binding protein 3-like isoform X2
poly(rC)-binding protein 3-like isoform X1
fibronectin type III domain-containing protein 4-like, transcript variant X6
fibronectin type III domain-containing protein 4-like, transcript variant X8
fibronectin type III domain-containing protein 4-like, transcript variant X1
fibronectin type III domain-containing protein 4-like isoform X1
fibronectin type III domain-containing protein 4-like isoform X2
glycerol-3-phosphate dehydrogenase, mitochondrial-like, transcript variant X2
glycerol-3-phosphate dehydrogenase, mitochondrial-like, transcript variant X1
glycerol-3-phosphate dehydrogenase, mitochondrial-like, transcript variant X5
glycerol-3-phosphate dehydrogenase, mitochondrial-like, transcript variant X4
glycerol-3-phosphate dehydrogenase, mitochondrial-like isoform X2
glycerol-3-phosphate dehydrogenase, mitochondrial-like isoform X1
glycerol-3-phosphate dehydrogenase, mitochondrial-like isoform X4
glycerol-3-phosphate dehydrogenase, mitochondrial-like isoform X5
glycerol-3-phosphate dehydrogenase, mitochondrial-like, transcript variant X3
glycerol-3-phosphate dehydrogenase, mitochondrial-like isoform X3
nuclear receptor subfamily 4 group A member 2-like, transcript variant X1
nuclear receptor subfamily 4 group A member 2-like, transcript variant X2
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 1 sample with support for all annotated introns
nuclear receptor subfamily 4 group A member 2-like isoform X1
nuclear receptor subfamily 4 group A member 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 481 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
inactive dipeptidyl peptidase 10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inactive dipeptidyl peptidase 10-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inactive dipeptidyl peptidase 10-like isoform X1
inactive dipeptidyl peptidase 10-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X6
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X8
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X10
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X9
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X1
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X5
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X7
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X3
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X4
type I inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X2
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X5
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X7
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X9
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X8
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X1
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X4
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X6
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X2
type I inositol 3,4-bisphosphate 4-phosphatase-like isoform X3
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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: retinol dehydrogenase 7-like
neuronal acetylcholine receptor subunit alpha-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X2
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X4
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X3
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X1
alsin Rho guanine nucleotide exchange factor ALS2, transcript variant X5
abl interactor 2, transcript variant X10
abl interactor 2, transcript variant X11
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: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: collagen alpha-1(XVIII) chain-like
NACHT, LRR and PYD domains-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
PI-PLC X domain-containing protein 1-like, transcript variant X1
PI-PLC X domain-containing protein 1-like, transcript variant X2
PI-PLC X domain-containing protein 1-like isoform X1
PI-PLC X domain-containing protein 1-like isoform X2
four and a half LIM domains protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
four and a half LIM domains protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
four and a half LIM domains protein 2-like
plakophilin-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
plakophilin-4-like, transcript variant X1
plakophilin-4-like, transcript variant X3
plakophilin-4-like, transcript variant X4
plakophilin-4-like, transcript variant X5
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 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: methyl-CpG-binding domain protein 5
origin recognition complex subunit 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
origin recognition complex subunit 4-like, transcript variant X2
origin recognition complex subunit 4-like, transcript variant X3
origin recognition complex subunit 4-like
methyl-CpG-binding domain protein 5-like
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
activin A receptor type 2A, transcript variant X2
activin A receptor type 2A, transcript variant X1
activin A receptor type 2A, transcript variant X3
zinc finger E-box binding homeobox 2, transcript variant X1
zinc finger E-box binding homeobox 2, transcript variant X4
zinc finger E-box binding homeobox 2, transcript variant X2
zinc finger E-box-binding homeobox 2 isoform X1
zinc finger E-box-binding homeobox 2 isoform X3
zinc finger E-box binding homeobox 2, transcript variant X5
zinc finger E-box binding homeobox 2, transcript variant X3
zinc finger E-box-binding homeobox 2 isoform X2
zinc finger E-box binding homeobox 2, transcript variant X6
zinc finger E-box-binding homeobox 2 isoform X4
zinc finger E-box binding homeobox 2, transcript variant X7
zinc finger E-box-binding homeobox 2 isoform X5
von Willebrand factor D and EGF domain-containing protein-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: von Willebrand factor D and EGF domain-containing protein-like
uncharacterized LOC115020887, transcript variant X4
uncharacterized LOC115020887, transcript variant X3
uncharacterized LOC115020887, transcript variant X2
uncharacterized LOC115020887, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
basic leucine zipper and W2 domain-containing protein 1-A
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: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 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: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: aldehyde oxidase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: SH3 domain-binding protein 4-A-like
uncharacterized LOC115017430, transcript variant X4
uncharacterized LOC115017430, transcript variant X1
uncharacterized LOC115017430, transcript variant X2
uncharacterized LOC115017430, transcript variant X3
uncharacterized protein LOC115017430 isoform X1
uncharacterized protein LOC115017430 isoform X2
uncharacterized protein LOC115017430 isoform X3
uncharacterized protein LOC115017430 isoform X4
aryl hydrocarbon receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aryl hydrocarbon receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
aryl hydrocarbon receptor-like, transcript variant X4
aryl hydrocarbon receptor-like, transcript variant X2
aryl hydrocarbon receptor-like isoform X1
aryl hydrocarbon receptor-like, transcript variant X5
aryl hydrocarbon receptor-like isoform X2
aryl hydrocarbon receptor-like, transcript variant X6
aryl hydrocarbon receptor-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
major facilitator superfamily domain containing 6, transcript variant X3
major facilitator superfamily domain containing 6, transcript variant X1
major facilitator superfamily domain containing 6, transcript variant X2
major facilitator superfamily domain containing 6, transcript variant X4
major facilitator superfamily domain containing 6, transcript variant X6
major facilitator superfamily domain containing 6, transcript variant X5
major facilitator superfamily domain-containing protein 6 isoform X1
major facilitator superfamily domain-containing protein 6 isoform X2
major facilitator superfamily domain-containing protein 6 isoform X3
major facilitator superfamily domain-containing protein 6 isoform X4
major facilitator superfamily domain-containing protein 6 isoform X6
major facilitator superfamily domain-containing protein 6 isoform X5
NGFI-A binding protein 1, transcript variant X1
NGFI-A binding protein 1, transcript variant X2
glutaminase kidney isoform, mitochondrial-like, transcript variant X2
glutaminase kidney isoform, mitochondrial-like, transcript variant X1
glutaminase kidney isoform, mitochondrial-like isoform X1
glutaminase kidney isoform, mitochondrial-like isoform X2
signal transducer and activator of transcription 1-alpha/beta-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: 32 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: signal transducer and activator of transcription 1-alpha/beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 120 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; 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
LOW QUALITY PROTEIN: protein Shroom2-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: 4 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase kinase 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: 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: mitogen-activated protein kinase kinase kinase 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: transmembrane protein 198-B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
aspartyl aminopeptidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
aspartyl aminopeptidase, transcript variant X4
aspartyl aminopeptidase, transcript variant X1
aspartyl aminopeptidase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aspartyl aminopeptidase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein tyrosine phosphatase receptor type N
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: receptor-type tyrosine-protein phosphatase-like N
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 601 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: 562 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: 612 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: 71% coverage of the annotated genomic feature by RNAseq alignments
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1, transcript variant X3
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1, transcript variant X4
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1, transcript variant X2
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1, transcript variant X1
ArfGAP with GTPase domain, ankyrin repeat and PH domain 1, transcript variant X5
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
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1 isoform X3
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1 isoform X4
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1 isoform X2
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1 isoform X1
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1 isoform X5
fas apoptotic inhibitory molecule 1-like
ras-related protein ralB-A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras-related protein ralB-A-like, transcript variant X1
ras-related protein ralB-A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 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: 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: 26 Proteins, and 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: 27 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments