Protopterus annectens isolate FY-2018-M chromosome 6.part1, PAN1.0, whole genome shotgun sequence.
Protopterus annectens (West African lungfish)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Dipnomorpha; Ceratodontiformes; Lepidosirenoidei; Protopteridae; Protopterus.
African lungfish genome sheds light on the vertebrate water-to-land transition
REFSEQ INFORMATION: The reference sequence is identical to\nCM033086.1.\nAssembly name: PAN1.0\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Northwestern Polytechnical\nUniversity on 2021/07/20. The original whole-genome shotgun project\nhas the accession JAGYFI000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Northwestern Polytechnical University\nAssembly Method :: wtdbg v. huge\nAssembly Name :: PAN1.0\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 50.0x\nSequencing Technology :: Oxford Nanopore\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Protopterus annectens Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
RNA binding motif protein 45, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
RNA binding motif protein 45, 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 10 samples with support for all annotated introns
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 12 samples with support for all annotated introns
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 12 samples with support for all annotated introns
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 14 samples with support for all annotated introns
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01039151.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 100 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 100 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
endoplasmic reticulum junction formation protein lunapark
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
heterogeneous nuclear ribonucleoprotein A3-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein A3-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein A3-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein A3-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein A3-like, transcript variant X5
heterogeneous nuclear ribonucleoprotein A3-like isoform X1
heterogeneous nuclear ribonucleoprotein A3 homolog 2-like isoform X3
heterogeneous nuclear ribonucleoprotein A3-like isoform X4
heterogeneous nuclear ribonucleoprotein A3-like isoform X2
heterogeneous nuclear ribonucleoprotein A3 homolog 1-like isoform X5
similar to RNA sequence (same species):INSD:GGXP01034682.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 155 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; added 155 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nuclear factor erythroid 2-related factor 2
leucine-rich repeat flightless-interacting protein 2
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
NADH:ubiquinone oxidoreductase subunit B3, transcript variant X1
NADH:ubiquinone oxidoreductase subunit B3, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3
mitogen-activated protein kinase kinase kinase kinase 2-like, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 2-like, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 2-like isoform X2
mitogen-activated protein kinase kinase kinase kinase 2-like isoform X1
28S ribosomal protein S36, mitochondrial
centromere protein H, transcript variant X1
centromere protein H, transcript variant X3
centromere protein H, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
leucine-rich repeat flightless-interacting protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
leucine zipper transcription factor-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00213
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
DnaJ heat shock protein family (Hsp40) member C5 gamma, transcript variant X1
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 10 samples with support for all annotated introns
DnaJ heat shock protein family (Hsp40) member C5 gamma, 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 13 samples with support for all annotated introns
dnaJ homolog subfamily C member 5G isoform X1
dnaJ homolog subfamily C member 5G isoform X2
carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase
similar to RNA sequence (same species):INSD:GGXP01006603.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 130 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 130 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
intraflagellar transport 172, transcript variant X1
intraflagellar transport 172, transcript variant X2
intraflagellar transport protein 172 homolog isoform X1
intraflagellar transport protein 172 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
tripartite motif containing 54, 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 2 samples with support for all annotated introns
tripartite motif containing 54, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tripartite motif-containing protein 54 isoform X1
tripartite motif-containing protein 54 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial inner membrane protein MPV17, transcript variant X5
mitochondrial inner membrane protein MPV17, transcript variant X1
mitochondrial inner membrane protein MPV17, transcript variant X2
mitochondrial inner membrane protein MPV17, transcript variant X4
mitochondrial inner membrane protein MPV17, transcript variant X3
mitochondrial inner membrane protein MPV17, transcript variant X6
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor IIIC subunit 2
general transcription factor 3C polypeptide 2
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 28 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
tyrosine-protein phosphatase non-receptor type substrate 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
adhesion G protein-coupled receptor E5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
low-density lipoprotein receptor-related protein 2
sphingolipid transporter 1 (putative), transcript variant X2
sphingolipid transporter 1 (putative), transcript variant X1
sphingolipid transporter 1 (putative), transcript variant X3
coiled-coil domain-containing protein 89-like
ATP synthase subunit beta, mitochondrial
COORDINATES: nucleotide motif:Rfam:12.0:RF00273
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
FAST kinase domain-containing protein 1, mitochondrial
peptidylprolyl isomerase G, transcript variant X1
peptidylprolyl isomerase G, transcript variant X2
peptidyl-prolyl cis-trans isomerase G isoform X1
peptidyl-prolyl cis-trans isomerase G isoform X2
cilia and flagella associated protein 210, transcript variant X1
cilia and flagella associated protein 210, transcript variant X2
coiled-coil domain-containing protein 173 isoform X1
coiled-coil domain-containing protein 173 isoform X2
phosphatase, orphan 2, 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 17 samples with support for all annotated introns
phosphatase, orphan 2, 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 7 samples with support for all annotated introns
pyridoxal phosphate phosphatase PHOSPHO2
small RNA binding exonuclease protection factor La
methyltransferase 5, N6-adenosine, transcript variant X3
methyltransferase 5, N6-adenosine, transcript variant X4
methyltransferase 5, N6-adenosine, transcript variant X1
methyltransferase 5, N6-adenosine, transcript variant X2
rRNA N6-adenosine-methyltransferase METTL5 isoform X2
rRNA N6-adenosine-methyltransferase METTL5 isoform X1
ubiquitin protein ligase E3 component n-recognin 3, transcript variant X1
ubiquitin protein ligase E3 component n-recognin 3, transcript variant X2
ubiquitin protein ligase E3 component n-recognin 3, transcript variant X3
ubiquitin protein ligase E3 component n-recognin 3, transcript variant X4
E3 ubiquitin-protein ligase UBR3 isoform X1
E3 ubiquitin-protein ligase UBR3 isoform X2
E3 ubiquitin-protein ligase UBR3 isoform X3
E3 ubiquitin-protein ligase UBR3 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 18 samples with support for all annotated introns
glutamate decarboxylase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
glutamate decarboxylase 1, transcript variant X2
glutamate decarboxylase 1, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
golgi reassembly stacking protein 2, 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 16 samples with support for all annotated introns
golgi reassembly stacking protein 2, transcript variant X2
golgi reassembly stacking protein 2, transcript variant X1
Golgi reassembly-stacking protein 2 isoform X1
Golgi reassembly-stacking protein 2 isoform X2
Golgi reassembly-stacking protein 2 isoform X3
similar to RNA sequence (same species):INSD:GGXP01013307.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 172 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 172 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
serine/threonine-protein kinase tousled-like 1
methyltransferase 8, methylcytidine, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
methyltransferase 8, methylcytidine, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
methyltransferase 8, methylcytidine, 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 6 samples with support for all annotated introns
methyltransferase 8, methylcytidine, transcript variant X1
mRNA N(3)-methylcytidine methyltransferase METTL8
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
plasma membrane ascorbate-dependent reductase CYBRD1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
plasma membrane ascorbate-dependent reductase CYBRD1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
plasma membrane ascorbate-dependent reductase CYBRD1 isoform X2
plasma membrane ascorbate-dependent reductase CYBRD1 isoform X1
dynein cytoplasmic 1 intermediate chain 2, transcript variant X1
dynein cytoplasmic 1 intermediate chain 2, transcript variant X3
dynein cytoplasmic 1 intermediate chain 2, transcript variant X2
dynein cytoplasmic 1 intermediate chain 2, transcript variant X4
cytoplasmic dynein 1 intermediate chain 2 isoform X1
cytoplasmic dynein 1 intermediate chain 2 isoform X3
cytoplasmic dynein 1 intermediate chain 2 isoform X2
cytoplasmic dynein 1 intermediate chain 2 isoform X4
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
histone acetyltransferase type B catalytic subunit
methionyl aminopeptidase type 1D, mitochondrial, transcript variant X1
methionyl aminopeptidase type 1D, mitochondrial, transcript variant X3
methionine aminopeptidase 1D, mitochondrial isoform X1
methionine aminopeptidase 1D, mitochondrial isoform X3
methionyl aminopeptidase type 1D, mitochondrial, transcript variant X2
methionine aminopeptidase 1D, mitochondrial isoform X2
integrin subunit alpha 6, transcript variant X1
integrin subunit alpha 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
pyruvate dehydrogenase kinase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
pyruvate dehydrogenase kinase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
pyruvate dehydrogenase kinase 1, transcript variant X1
pyruvate dehydrogenase kinase 1, transcript variant X2
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 1, mitochondrial isoform X1
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 1, mitochondrial isoform X5
pyruvate dehydrogenase kinase 1, transcript variant X4
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 1, mitochondrial isoform X2
pyruvate dehydrogenase kinase 1, transcript variant X3
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 1, mitochondrial isoform X3
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 1, mitochondrial isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
rap guanine nucleotide exchange factor 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01052197.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 15 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 15 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
cell division cycle-associated protein 7
mitogen-activated protein kinase kinase kinase 20, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 20, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 20 isoform X1
mitogen-activated protein kinase kinase kinase 20 isoform X2
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
G protein-coupled receptor 155, 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 5 samples with support for all annotated introns
integral membrane protein GPR155 isoform X2
G protein-coupled receptor 155, 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 9 samples with support for all annotated introns
integral membrane protein GPR155 isoform X1
G protein-coupled receptor 155, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
integral membrane protein GPR155 isoform X3
WAS/WASL interacting protein family member 1
WAS/WASL-interacting protein family member 1
cholinergic receptor nicotinic alpha 1 subunit
activating transcription factor 2, 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 3 samples with support for all annotated introns
activating transcription factor 2, 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 7 samples with support for all annotated introns
activating transcription factor 2, transcript variant X4
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
cyclic AMP-dependent transcription factor ATF-2 isoform X1
cyclic AMP-dependent transcription factor ATF-2 isoform X3
activating transcription factor 2, 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, including 8 samples with support for all annotated introns
cyclic AMP-dependent transcription factor ATF-2 isoform X2
uncharacterized LOC122805433, transcript variant X2
uncharacterized LOC122805433, transcript variant X1
ATP synthase membrane subunit c locus 3, transcript variant X1
ATP synthase membrane subunit c locus 3, transcript variant X2
ATP synthase F(0) complex subunit C3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 9-like, transcript variant X10
dehydrogenase/reductase SDR family member 9-like, transcript variant X8
dehydrogenase/reductase SDR family member 9-like, transcript variant X1
dehydrogenase/reductase SDR family member 9-like, transcript variant X5
dehydrogenase/reductase SDR family member 9-like, transcript variant X6
dehydrogenase/reductase SDR family member 9-like, transcript variant X3
dehydrogenase/reductase SDR family member 9-like, transcript variant X4
dehydrogenase/reductase SDR family member 9-like, transcript variant X7
dehydrogenase/reductase SDR family member 9-like, transcript variant X2
dehydrogenase/reductase SDR family member 9-like, transcript variant X9
dehydrogenase/reductase SDR family member 9-like
ATP binding cassette subfamily B member 11
glucose-6-phosphatase catalytic subunit 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
glucose-6-phosphatase catalytic subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
glucose-6-phosphatase catalytic subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
SPC25 component of NDC80 kinetochore complex, transcript variant X3
SPC25 component of NDC80 kinetochore complex, transcript variant X2
SPC25 component of NDC80 kinetochore complex, transcript variant X1
ceramide synthase 6, transcript variant X1
ceramide synthase 6, transcript variant X2
serine/threonine kinase 39, transcript variant X1
serine/threonine kinase 39, transcript variant X2
STE20/SPS1-related proline-alanine-rich protein kinase isoform X1
STE20/SPS1-related proline-alanine-rich protein kinase isoform X2
beta-1,3-galactosyltransferase 1, transcript variant X5
beta-1,3-galactosyltransferase 1, transcript variant X4
beta-1,3-galactosyltransferase 1, transcript variant X1
beta-1,3-galactosyltransferase 1, transcript variant X3
beta-1,3-galactosyltransferase 1, transcript variant X2
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
xin actin binding repeat containing 2, transcript variant X3
xin actin-binding repeat-containing protein 2 isoform X3
xin actin binding repeat containing 2, 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 7 samples with support for all annotated introns
xin actin binding repeat containing 2, transcript variant X2
xin actin-binding repeat-containing protein 2 isoform X1
xin actin-binding repeat-containing protein 2 isoform X2
cysteine and serine rich nuclear protein 3
polypeptide N-acetylgalactosaminyltransferase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
transmembrane BAX inhibitor motif containing 1, transcript variant X4
transmembrane BAX inhibitor motif containing 1, transcript variant X1
transmembrane BAX inhibitor motif containing 1, transcript variant X2
transmembrane BAX inhibitor motif containing 1, transcript variant X5
transmembrane BAX inhibitor motif containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
microtubule affinity regulating kinase 2, transcript variant X1
microtubule affinity regulating kinase 2, transcript variant X3
microtubule affinity regulating kinase 2, transcript variant X4
microtubule affinity regulating kinase 2, transcript variant X5
microtubule affinity regulating kinase 2, transcript variant X6
microtubule affinity regulating kinase 2, transcript variant X7
microtubule affinity regulating kinase 2, transcript variant X2
serine/threonine-protein kinase MARK2 isoform X1
serine/threonine-protein kinase MARK2 isoform X3
serine/threonine-protein kinase MARK2 isoform X4
serine/threonine-protein kinase MARK2 isoform X5
serine/threonine-protein kinase MARK2 isoform X6
serine/threonine-protein kinase MARK2 isoform X7
serine/threonine-protein kinase MARK2 isoform X2
N-alpha-acetyltransferase 40, NatD catalytic subunit, transcript variant X1
N-alpha-acetyltransferase 40, NatD catalytic subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
OTU deubiquitinase, ubiquitin aldehyde binding 1, transcript variant X1
OTU deubiquitinase, ubiquitin aldehyde binding 1, transcript variant X5
OTU deubiquitinase, ubiquitin aldehyde binding 1, transcript variant X4
OTU deubiquitinase, ubiquitin aldehyde binding 1, transcript variant X3
OTU deubiquitinase, ubiquitin aldehyde binding 1, transcript variant X2
citrate synthase lysine methyltransferase, transcript variant X1
citrate synthase lysine methyltransferase, transcript variant X2
citrate synthase-lysine N-methyltransferase CSKMT, mitochondrial isoform X1
citrate synthase lysine methyltransferase, transcript variant X3
citrate synthase-lysine N-methyltransferase CSKMT, mitochondrial isoform X2
ubiquinol-cytochrome-c reductase complex assembly factor 3-like
UBX domain protein 1, transcript variant X1
UBX domain protein 1, transcript variant X2
coiled-coil domain-containing protein 69
platelet-derived growth factor receptor-like protein
cationic amino acid transporter 2-like, transcript variant X2
cationic amino acid transporter 2-like, transcript variant X1
cationic amino acid transporter 2-like, transcript variant X3
cationic amino acid transporter 2-like isoform X2
cationic amino acid transporter 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-3
adenylosuccinate synthetase isozyme 2-like
heterogeneous nuclear ribonucleoprotein U like 2
similar to RNA sequence (same species):INSD:GGXP01054809.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 195 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% 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: added 195 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
heterogeneous nuclear ribonucleoprotein U-like protein 2
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 33 samples with support for all annotated introns
tetratricopeptide repeat protein 9C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
dapper homolog 2-like, transcript variant X2
dapper homolog 2-like, transcript variant X1
dapper homolog 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated proteins 1A/1B light chain 3C-like
zinc finger and BTB domain-containing protein 3
5'-3' exonuclease PLD3-like, transcript variant X1
5'-3' exonuclease PLD3-like, transcript variant X2
5'-3' exonuclease PLD3-like, transcript variant X3
RNA polymerase II subunit G, transcript variant X1
RNA polymerase II subunit G, transcript variant X2
DNA-directed RNA polymerase II subunit RPB7 isoform X1
DNA-directed RNA polymerase II subunit RPB7 isoform X2
eukaryotic translation elongation factor 1 gamma
similar to RNA sequence (same species):INSD:GGXP01010608.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 33 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 12 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 11 bases in 10 codons; deleted 4 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 11 bases in 10 codons; deleted 4 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: neuroblast differentiation-associated protein AHNAK
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
COORDINATES: nucleotide motif:Rfam:12.0:RF02543
fibronectin leucine rich transmembrane protein 1
leucine-rich repeat transmembrane protein FLRT1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
phosphomethylethanolamine N-methyltransferase-like, transcript variant X3
phosphomethylethanolamine N-methyltransferase-like, transcript variant X1
phosphomethylethanolamine N-methyltransferase-like, transcript variant X2
phosphomethylethanolamine N-methyltransferase-like isoform X1
phosphomethylethanolamine N-methyltransferase-like isoform X2
breast cancer metastasis-suppressor 1-like protein
mediator complex subunit 18, transcript variant X3
mediator complex subunit 18, transcript variant X1
mediator complex subunit 18, transcript variant X2
mediator of RNA polymerase II transcription subunit 18
cornichon family AMPA receptor auxiliary protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Yip1 interacting factor homolog A, membrane trafficking protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
N-acetylated alpha-linked acidic dipeptidase like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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: 1 Protein, and 61% coverage of the annotated genomic feature by RNAseq alignments
ADP ribosylation factor like GTPase 2, transcript variant X1
ADP ribosylation factor like GTPase 2, transcript variant X2
ADP-ribosylation factor-like protein 2 isoform X2
ADP-ribosylation factor-like protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 40 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 22% coverage of the annotated genomic feature by RNAseq alignments
putative methyltransferase DDB_G0268948, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative methyltransferase DDB_G0268948, 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 5 samples with support for all annotated introns
putative methyltransferase DDB_G0268948 isoform X1
phthiotriol/phenolphthiotriol dimycocerosates methyltransferase-like isoform 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ubiquitin conjugating enzyme E2 F (putative), transcript variant X2
NEDD8-conjugating enzyme UBE2F isoform X2
ubiquitin conjugating enzyme E2 F (putative), transcript variant X1
NEDD8-conjugating enzyme UBE2F isoform X1
receptor activity modifying protein 1, transcript variant X2
receptor activity modifying protein 1, transcript variant X1
receptor activity-modifying protein 1 isoform X2
receptor activity-modifying protein 1 isoform X1
transient receptor potential cation channel subfamily M member 2-like
family with sequence similarity 126 member B, transcript variant X2
family with sequence similarity 126 member B, transcript variant X1
family with sequence similarity 126 member B, transcript variant X3
carbamoyl-phosphate synthase [ammonia], mitochondrial
erb-b2 receptor tyrosine kinase 4, transcript variant X2
erb-b2 receptor tyrosine kinase 4, transcript variant X1
receptor tyrosine-protein kinase erbB-4 isoform X2
receptor tyrosine-protein kinase erbB-4 isoform X1
IKAROS family zinc finger 2, transcript variant X1
IKAROS family zinc finger 2, transcript variant X3
IKAROS family zinc finger 2, transcript variant X2
sperm associated antigen 16, transcript variant X2
sperm associated antigen 16, transcript variant X1
sperm-associated antigen 16 protein isoform X1
sperm-associated antigen 16 protein isoform X2
sperm associated antigen 16, transcript variant X3
sperm-associated antigen 16 protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
von Willebrand factor C domain containing 2 like, transcript variant X5
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 9 samples with support for all annotated introns
von Willebrand factor C domain containing 2 like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
von Willebrand factor C domain containing 2 like, transcript variant X1
von Willebrand factor C domain containing 2 like, transcript variant X3
von Willebrand factor C domain containing 2 like, transcript variant X4
von Willebrand factor C domain containing 2 like, transcript variant X2
von Willebrand factor C domain-containing protein 2-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 1 sample with support for all annotated introns
ATP binding cassette subfamily A member 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
glucosylceramide transporter ABCA12-like
5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase
bifunctional purine biosynthesis protein ATIC
uncharacterized LOC122805522, transcript variant X2
uncharacterized LOC122805522, transcript variant X1
uncharacterized LOC122805522, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00087
COORDINATES: nucleotide motif:Rfam:12.0:RF00099
COORDINATES: nucleotide motif:Rfam:12.0:RF00070
COORDINATES: nucleotide motif:Rfam:12.0:RF00088
COORDINATES: nucleotide motif:Rfam:12.0:RF00089
transforming growth factor beta-2 proprotein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uridine diphosphate glucose pyrophosphatase NUDT22
DnaJ heat shock protein family (Hsp40) member C4, transcript variant X1
DnaJ heat shock protein family (Hsp40) member C4, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C4, transcript variant X4
DnaJ heat shock protein family (Hsp40) member C4, transcript variant X3
vascular endothelial growth factor B, transcript variant X1
vascular endothelial growth factor B, transcript variant X2
vascular endothelial growth factor B isoform X1
vascular endothelial growth factor B isoform X2
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122805531, transcript variant X1
uncharacterized LOC122805531, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC122805531 isoform X1
uncharacterized protein LOC122805531 isoform X2
family with sequence similarity 89 member B
T cell receptor alpha variable 26-2-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 12 samples with support for all annotated introns
DNA polymerase alpha 2, accessory subunit
protein phosphatase 1 regulatory inhibitor subunit 14B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 14B isoform X2
protein phosphatase 1 regulatory inhibitor subunit 14B, 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
protein phosphatase 1 regulatory subunit 14B isoform 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 20 samples with support for all annotated introns
peptidyl-prolyl cis-trans isomerase FKBP2
similar to RNA sequence (same species):INSD:GGXP01071281.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 102 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 102 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X4
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X2
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X5
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X3
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X1
potassium channel subfamily K member 13-like
terminal uridylyl transferase 1, U6 snRNA-specific
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
speckle targeted PIP5K1A-regulated poly(A) polymerase
similar to RNA sequence (same species):INSD:GGXP01001769.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 72 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 99% 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: added 72 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
echinoderm microtubule-associated protein-like 3
retinal outer segment membrane protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
gastrula zinc finger protein XlCGF57.1-like
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
transcriptional-regulating factor 1-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 4 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01047307.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 181 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 79% 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: added 181 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00191
integrator complex subunit 5, transcript variant X2
integrator complex subunit 5, transcript variant X1
phospholipase A and acyltransferase 2-like
phospholipase A and acyltransferase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
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
serine/threonine-protein kinase MRCK gamma
atypical kinase COQ8A, mitochondrial-like
atypical kinase COQ8A, mitochondrial-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 8 samples with support for all annotated introns
atypical kinase COQ8A, mitochondrial-like, 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 11 samples with support for all annotated introns
atypical kinase COQ8A, mitochondrial-like isoform X2
atypical kinase COQ8A, mitochondrial-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
inositol-trisphosphate 3-kinase B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
inositol-trisphosphate 3-kinase B-like, transcript variant X2
inositol-trisphosphate 3-kinase B-like, transcript variant X3
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
general transcription factor II-I repeat domain-containing protein 2A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
general transcription factor II-I repeat domain-containing protein 2A-like, transcript variant X2
general transcription factor II-I repeat domain-containing protein 2-like isoform X2
general transcription factor II-I repeat domain-containing protein 2A-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
protein phosphatase 2 regulatory subunit B'beta
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit beta isoform
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
membrane anchored junction protein, 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 2 samples with support for all annotated introns
membrane anchored junction protein, transcript variant X2
membrane-anchored junction protein isoform X1
membrane-anchored junction protein isoform X2
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
basic leucine zipper ATF-like transcription factor 2
basic leucine zipper transcriptional factor ATF-like 2
similar to RNA sequence (same species):INSD:GGXP01020028.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 71 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 71 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
solute carrier family 25 member 45-like, transcript variant X2
solute carrier family 25 member 45-like isoform X2
solute carrier family 25 member 45-like, transcript variant X1
solute carrier family 25 member 45-like, transcript variant X3
solute carrier family 25 member 45-like isoform X1
solute carrier family 25 member 45-like isoform X3
uncharacterized LOC122805566, transcript variant X2
uncharacterized LOC122805566, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC122805566, transcript variant X3
GATA zinc finger domain-containing protein 21-like
sodium/calcium exchanger 1-like, transcript variant X2
sodium/calcium exchanger 1-like, transcript variant X1
phospholipase C beta 3, transcript variant X1
phospholipase C beta 3, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-3 isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-3 isoform X1
CCAAT/enhancer-binding protein beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
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: CCAAT/enhancer-binding protein beta-like
solute carrier family 22 member 6-B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
solute carrier family 22 member 6-A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
CDC42 effector protein 2, transcript variant X1
CDC42 effector protein 2, transcript variant X2
double PHD fingers 2, transcript variant X1
double PHD fingers 2, transcript variant X2
double PHD fingers 2, transcript variant X3
double PHD fingers 2, transcript variant X4
BCL2 associated agonist of cell death, transcript variant X2
BCL2 associated agonist of cell death, transcript variant X1
G protein-coupled receptor 137, transcript variant X3
G protein-coupled receptor 137, 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 10 samples with support for all annotated introns
G protein-coupled receptor 137, transcript variant X1
integral membrane protein GPR137 isoform X1
integral membrane protein GPR137 isoform X2
integral membrane protein GPR137 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium two pore domain channel subfamily K member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
tRNA methyltransferase activator subunit 11-2
multifunctional methyltransferase subunit TRM112-like protein
similar to RNA sequence (same species):INSD:GGXP01034451.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 999 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 999 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
vacuolar protein sorting-associated protein 51 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC122805592, transcript variant X1
uncharacterized LOC122805592, transcript variant X2
uncharacterized protein LOC122805592 isoform X1
uncharacterized protein LOC122805592 isoform X2
splicing factor 1, transcript variant X2
splicing factor 1, transcript variant X1
CASP8 and FADD like apoptosis regulator, transcript variant X1
CASP8 and FADD like apoptosis regulator, transcript variant X2
galactose-3-O-sulfotransferase 3, transcript variant X1
galactose-3-O-sulfotransferase 3, transcript variant X4
galactose-3-O-sulfotransferase 3, transcript variant X5
galactose-3-O-sulfotransferase 3, transcript variant X3
galactose-3-O-sulfotransferase 3, transcript variant X2
galactose-3-O-sulfotransferase 3 isoform X1
galactose-3-O-sulfotransferase 3 isoform X2
probable basic-leucine zipper transcription factor C
similar to RNA sequence (same species):INSD:GGXP01063202.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 83 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 83 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins
transmembrane 7 superfamily member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane 7 superfamily member 2, 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 14 samples with support for all annotated introns
delta(14)-sterol reductase TM7SF2 isoform X1
delta(14)-sterol reductase TM7SF2 isoform X2
ubiquitin-like protein FUBI, transcript variant X1
ubiquitin-like protein FUBI, transcript variant X2
ubiquitin-like protein FUBI, transcript variant X3
ubiquitin-like protein FUBI, transcript variant X4
39S ribosomal protein L49, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01003256.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 698 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 483 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
E3 ubiquitin-protein ligase synoviolin isoform X1
E3 ubiquitin-protein ligase synoviolin isoform X2
speedy/RINGO cell cycle regulator family member C, transcript variant X1
speedy/RINGO cell cycle regulator family member C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 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, and 92% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01024152.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 212 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 212 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
mammalian ependymin-related protein 1-like
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3-like, transcript variant X4
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3-like, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3-like, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3-like, transcript variant X3
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3-like isoform X3
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3-like isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3-like isoform X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 3-like isoform X4
BTB/POZ domain-containing protein KCTD3-like, transcript variant X1
BTB/POZ domain-containing protein KCTD3-like, transcript variant X2
BTB/POZ domain-containing protein KCTD3-like isoform X1
BTB/POZ domain-containing protein KCTD3-like isoform X2
latent-transforming growth factor beta-binding protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
latent-transforming growth factor beta-binding protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
leucine-rich repeat-containing protein 15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase core subunit S1
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial
protein tyrosine phosphatase receptor type N, transcript variant X1
protein tyrosine phosphatase receptor type N, transcript variant X2
receptor-type tyrosine-protein phosphatase-like N isoform X1
receptor-type tyrosine-protein phosphatase-like N isoform X2
DnaJ heat shock protein family (Hsp40) member B2, transcript variant X1
DnaJ heat shock protein family (Hsp40) member B2, transcript variant X3
DnaJ heat shock protein family (Hsp40) member B2, transcript variant X2
DnaJ heat shock protein family (Hsp40) member B2, transcript variant X4
dnaJ homolog subfamily B member 2 isoform X1
dnaJ homolog subfamily B member 2 isoform X3
dnaJ homolog subfamily B member 2 isoform X2
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
striated muscle enriched protein kinase, transcript variant X1
striated muscle preferentially expressed protein kinase isoform X1
striated muscle enriched protein kinase, transcript variant X2
striated muscle preferentially expressed protein kinase isoform X2
GDP-mannose pyrophosphorylase A, transcript variant X1
GDP-mannose pyrophosphorylase A, transcript variant X2
mannose-1-phosphate guanyltransferase alpha isoform X1
mannose-1-phosphate guanyltransferase alpha isoform X2
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
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122805620, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC122805620, transcript variant X2
uncharacterized LOC122805620, transcript variant X3
acid sensing ion channel subunit family member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
basic leucine zipper and W2 domains 1, transcript variant X1
basic leucine zipper and W2 domains 1, transcript variant X2
basic leucine zipper and W2 domain-containing protein 1
thioredoxin domain-containing protein 6-like
vacuolar protein sorting-associated protein 8 homolog
chromosome chr6.part1 C3orf70 homolog, transcript variant X3
chromosome chr6.part1 C3orf70 homolog, transcript variant X1
chromosome chr6.part1 C3orf70 homolog, transcript variant X2
chromosome chr6.part1 C3orf70 homolog, transcript variant X4
enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase, transcript variant X2
enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase, transcript variant X3
enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase, transcript variant X1
peroxisomal bifunctional enzyme isoform X2
peroxisomal bifunctional enzyme isoform X1
peroxisomal bifunctional enzyme isoform X3
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phosphofurin acidic cluster sorting protein 1
similar to RNA sequence (same species):INSD:GGXP01039770.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 81 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 81 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
similar to RNA sequence (same species):INSD:GGXP01040734.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 96 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 96 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
oocyte zinc finger protein XlCOF26-like, transcript variant X2
oocyte zinc finger protein XlCOF26-like, transcript variant X3
oocyte zinc finger protein XlCOF26-like, transcript variant X1
oocyte zinc finger protein XlCOF6-like, transcript variant X2
oocyte zinc finger protein XlCOF6-like, transcript variant X1
zinc finger protein 850-like, transcript variant X2
zinc finger protein 850-like, transcript variant X1
zinc finger protein 850-like, transcript variant X3
zinc finger protein 850-like, transcript variant X4
collagen type XVIII alpha 1 chain, transcript variant X4
collagen alpha-1(XVIII) chain isoform X4
collagen type XVIII alpha 1 chain, transcript variant X1
collagen type XVIII alpha 1 chain, transcript variant X2
collagen alpha-1(XVIII) chain isoform X1
collagen alpha-1(XVIII) chain isoform X2
collagen type XVIII alpha 1 chain, transcript variant X3
collagen alpha-1(XVIII) chain isoform X3
solute carrier family 19 member 1, transcript variant X2
solute carrier family 19 member 1, transcript variant X1
solute carrier family 19 member 1, transcript variant X4
solute carrier family 19 member 1, transcript variant X3
poly(rC) binding protein 3, transcript variant X9
poly(rC) binding protein 3, transcript variant X10
poly(rC) binding protein 3, transcript variant X2
poly(rC) binding protein 3, transcript variant X5
poly(rC) binding protein 3, transcript variant X4
poly(rC) binding protein 3, transcript variant X6
poly(rC) binding protein 3, transcript variant X3
poly(rC) binding protein 3, transcript variant X1
poly(rC) binding protein 3, transcript variant X8
poly(rC) binding protein 3, transcript variant X7
poly(rC) binding protein 3, transcript variant X12
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 21 samples with support for all annotated introns
poly(rC) binding protein 3, transcript variant X11
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 21 samples with support for all annotated introns
collagen type VI alpha 1 chain, transcript variant X2
collagen type VI alpha 1 chain, transcript variant X1
collagen type VI alpha 2 chain, transcript variant X2
collagen type VI alpha 2 chain, transcript variant X1
heterogeneous nuclear ribonucleoprotein L-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein L-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein L-like isoform X2
heterogeneous nuclear ribonucleoprotein L-like isoform X1
tigger transposable element derived 3, transcript variant X4
tigger transposable element derived 3, transcript variant X3
tigger transposable element derived 3, transcript variant X2
tigger transposable element derived 3, transcript variant X1
tigger transposable element derived 3, transcript variant X5
tigger transposable element-derived protein 3 isoform X1
tigger transposable element-derived protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein DDB_G0271974
transmembrane protein 41A, transcript variant X2
transmembrane protein 41A, transcript variant X1
mitogen-activated protein kinase kinase kinase 13
myosin light chain 1, transcript variant X1
myosin light chain 1/3, skeletal muscle isoform isoform X1
myosin light chain 1, transcript variant X2
myosin light chain 1/3, skeletal muscle isoform isoform X2
acyl-CoA dehydrogenase long chain, 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 27 samples with support for all annotated introns
long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1
acyl-CoA dehydrogenase long chain, 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 6 samples with support for all annotated introns
long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2
isocitrate dehydrogenase (NADP(+)) 1, transcript variant X2
isocitrate dehydrogenase (NADP(+)) 1, transcript variant X1
isocitrate dehydrogenase [NADP] cytoplasmic
phosphoinositide kinase, FYVE-type zinc finger containing
LOW QUALITY PROTEIN: 1-phosphatidylinositol 3-phosphate 5-kinase
transformer 2 beta homolog, transcript variant X2
transformer 2 beta homolog, transcript variant X3
transformer 2 beta homolog, transcript variant X1
transformer-2 protein homolog beta isoform X3
transformer-2 protein homolog beta isoform X2
transformer-2 protein homolog beta isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 165 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
insulin like growth factor 2 mRNA binding protein 2, transcript variant X2
insulin like growth factor 2 mRNA binding protein 2, transcript variant X1
insulin like growth factor 2 mRNA binding protein 2, transcript variant X4
insulin like growth factor 2 mRNA binding protein 2, transcript variant X3
insulin like growth factor 2 mRNA binding protein 2, transcript variant X5
insulin-like growth factor 2 mRNA-binding protein 2 isoform X4
insulin-like growth factor 2 mRNA-binding protein 2 isoform X3
insulin-like growth factor 2 mRNA-binding protein 2 isoform X2
insulin-like growth factor 2 mRNA-binding protein 2 isoform X1
insulin-like growth factor 2 mRNA-binding protein 2 isoform X5
par-3 family cell polarity regulator beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
gamma-crystallin M2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
gamma-crystallin M2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
gamma-crystallin M2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 188 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 173 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
methenyltetrahydrofolate synthetase, transcript variant X5
methenyltetrahydrofolate synthetase, transcript variant X1
methenyltetrahydrofolate synthetase, transcript variant X2
methenyltetrahydrofolate synthetase, transcript variant X3
methenyltetrahydrofolate synthetase, transcript variant X4
RNA-binding protein 4-like, transcript variant X2
RNA-binding protein 4-like, transcript variant X1
RNA-binding protein 4-like, transcript variant X3
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 27 samples with support for all annotated introns
SLX9 ribosome biogenesis factor, transcript variant X1
SLX9 ribosome biogenesis factor, transcript variant X3
SLX9 ribosome biogenesis factor, transcript variant X2
SLX9 ribosome biogenesis factor, transcript variant X5
SLX9 ribosome biogenesis factor, transcript variant X4
SLX9 ribosome biogenesis factor, transcript variant X6
adenosine deaminase RNA specific B1, transcript variant X2
double-stranded RNA-specific editase 1 isoform X2
adenosine deaminase RNA specific B1, transcript variant X1
double-stranded RNA-specific editase 1 isoform X1
adenosine deaminase RNA specific B1, transcript variant X3
double-stranded RNA-specific editase 1 isoform X3
protein O-fucosyltransferase 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 8 samples with support for all annotated introns
protein O-fucosyltransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
GDP-fucose protein O-fucosyltransferase 2 isoform X2
GDP-fucose protein O-fucosyltransferase 2 isoform X1
copper chaperone for superoxide dismutase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neurexin-2-beta-like, transcript variant X4
neurexin-2-beta-like, transcript variant X5
neurexin-2-beta-like, transcript variant X1
neurexin-2-beta-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
neurexin-2-beta-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
RAS guanyl releasing protein 2, transcript variant X3
RAS guanyl releasing protein 2, transcript variant X2
RAS guanyl releasing protein 2, transcript variant X1
RAS guanyl releasing protein 2, transcript variant X6
RAS guanyl releasing protein 2, transcript variant X7
RAS guanyl releasing protein 2, transcript variant X4
RAS guanyl releasing protein 2, transcript variant X5
RAS guanyl-releasing protein 2 isoform X2
RAS guanyl-releasing protein 2 isoform X1
zinc finger protein 501-like, transcript variant X4
zinc finger protein 501-like, transcript variant X6
zinc finger protein 501-like, transcript variant X5
zinc finger protein 501-like, transcript variant X3
zinc finger protein 501-like, transcript variant X1
zinc finger protein 501-like, transcript variant X2
zinc finger DBF-type containing 2, transcript variant X4
zinc finger DBF-type containing 2, transcript variant X1
zinc finger DBF-type containing 2, transcript variant X3
zinc finger DBF-type containing 2, transcript variant X2
DBF4-type zinc finger-containing protein 2 isoform X1
zinc finger DBF-type containing 2, transcript variant X5
DBF4-type zinc finger-containing protein 2 isoform X2
ADAM metallopeptidase domain 23, transcript variant X1
ADAM metallopeptidase domain 23, transcript variant X2
ADAM metallopeptidase domain 23, transcript variant X3
disintegrin and metalloproteinase domain-containing protein 23 isoform X3
disintegrin and metalloproteinase domain-containing protein 23 isoform X1
disintegrin and metalloproteinase domain-containing protein 23 isoform X2