Protopterus annectens isolate FY-2018-M chromosome 17.part0, 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\nCM033099.1.\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.
PH and SEC7 domain-containing protein 3-like
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon UCC); 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: 98% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
chondroitin sulfate N-acetylgalactosaminyltransferase 1, transcript variant X2
chondroitin sulfate N-acetylgalactosaminyltransferase 1, transcript variant X6
chondroitin sulfate N-acetylgalactosaminyltransferase 1, transcript variant X4
chondroitin sulfate N-acetylgalactosaminyltransferase 1, transcript variant X5
chondroitin sulfate N-acetylgalactosaminyltransferase 1, transcript variant X1
chondroitin sulfate N-acetylgalactosaminyltransferase 1, transcript variant X3
chondroitin sulfate N-acetylgalactosaminyltransferase 1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
integrator complex subunit 10, transcript variant X1
integrator complex subunit 10, transcript variant X2
integrator complex subunit 10 isoform X1
integrator complex subunit 10 isoform X2
heparan-alpha-glucosaminide N-acetyltransferase
similar to RNA sequence (same species):INSD:GGXP01033585.1
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 277 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 277 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein O-mannose kinase, transcript variant X2
protein O-mannose kinase, transcript variant X1
farnesyltransferase, CAAX box, alpha, transcript variant X2
protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha isoform X2
farnesyltransferase, CAAX box, alpha, 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 34 samples with support for all annotated introns
protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha isoform X1
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mitochondrial ribosomal protein S18C, transcript variant X1
mitochondrial ribosomal protein S18C, transcript variant X2
28S ribosomal protein S18c, mitochondrial isoform X1
28S ribosomal protein S18c, mitochondrial isoform X2
abraxas 1, BRCA1 A complex subunit, transcript variant X1
abraxas 1, BRCA1 A complex subunit, transcript variant X2
BRCA1-A complex subunit Abraxas 1 isoform X1
BRCA1-A complex subunit Abraxas 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
WD repeat and FYVE domain-containing protein 3
probable isoprenylcysteine alpha-carbonyl methylesterase ICMEL2
Rho GTPase activating protein 24, transcript variant X2
Rho GTPase activating protein 24, transcript variant X3
Rho GTPase activating protein 24, transcript variant X1
rho GTPase-activating protein 24 isoform X1
rho GTPase-activating protein 24 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 12 samples with support for all annotated introns
Rho GTPase activating protein 24, transcript variant X5
rho GTPase-activating protein 24 isoform X4
Rho GTPase activating protein 24, transcript variant X4
rho GTPase-activating protein 24 isoform X3
Rho GTPase activating protein 24, transcript variant X7
rho GTPase-activating protein 24 isoform X6
Rho GTPase activating protein 24, transcript variant X6
rho GTPase-activating protein 24 isoform X5
mitogen-activated protein kinase 10, transcript variant X3
mitogen-activated protein kinase 10, transcript variant X1
mitogen-activated protein kinase 10, transcript variant X2
mitogen-activated protein kinase 10, 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 18 samples with support for all annotated introns
mitogen-activated protein kinase 10 isoform X3
mitogen-activated protein kinase 10 isoform X2
mitogen-activated protein kinase 10 isoform X1
mitogen-activated protein kinase 10, transcript variant X6
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 9 samples with support for all annotated introns
mitogen-activated protein kinase 10, transcript variant X5
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 13 samples with support for all annotated introns
mitogen-activated protein kinase 10 isoform X4
mitogen-activated protein kinase 10 isoform X5
uncharacterized LOC122791758, transcript variant X1
uncharacterized LOC122791758, 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 28 samples with support for all annotated introns
tyrosine-protein phosphatase non-receptor type 9-like
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
RNA binding protein, mRNA processing factor, transcript variant X2
RNA binding protein, mRNA processing factor, 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 25 samples with support for all annotated introns
RNA-binding protein with multiple splicing
peptidyl-prolyl cis-trans isomerase NIMA-interacting 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor IIE subunit 2
transcription initiation factor IIE subunit beta
store-operated calcium entry associated regulatory factor
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 40 samples with support for all annotated introns
store-operated calcium entry-associated regulatory factor
leptin receptor overlapping transcript like 1, transcript variant X3
leptin receptor overlapping transcript like 1, transcript variant X1
leptin receptor overlapping transcript-like 1 isoform X1
leptin receptor overlapping transcript like 1, transcript variant X2
leptin receptor overlapping transcript-like 1 isoform X2
leptin receptor overlapping transcript-like 1 isoform X3
signal recognition particle subunit SRP72
theg spermatid protein like, transcript variant X1
theg spermatid protein 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 17 samples with support for all annotated introns
testicular haploid expressed gene protein-like isoform X2
testicular haploid expressed gene protein-like isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF02543
neuronal acetylcholine receptor subunit alpha-7-like
neuronal acetylcholine receptor subunit beta-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase
similar to RNA sequence (same species):INSD:GGXP01015410.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 162 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 162 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
zinc finger CCHC domain-containing protein 7
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glyoxylate reductase/hydroxypyruvate reductase-like
zinc finger and BTB domain containing 5, 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 9 samples with support for all annotated introns
zinc finger and BTB domain containing 5, 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 8 samples with support for all annotated introns
zinc finger and BTB domain containing 5, transcript variant X4
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 19 samples with support for all annotated introns
zinc finger and BTB domain containing 5, transcript variant X3
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 32 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 5 isoform X1
zinc finger and BTB domain-containing protein 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
RNA polymerase I subunit E, transcript variant X1
RNA polymerase I subunit E, transcript variant X2
DNA-directed RNA polymerase I subunit RPA49 isoform X1
DNA-directed RNA polymerase I subunit RPA49 isoform X2
translocase of outer mitochondrial membrane 5
mitochondrial import receptor subunit TOM5 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
FERM and PDZ domain-containing protein 1
solute carrier family 25 member 51, transcript variant X1
solute carrier family 25 member 51, transcript variant X2
solute carrier family 25 member 51, transcript variant X3
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51
thymosin beta-10-like, transcript variant X1
thymosin beta-10-like, transcript variant X2
solute carrier family 49 member 3, 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
solute carrier family 49 member A3 isoform X2
solute carrier family 49 member 3, transcript variant X1
solute carrier family 49 member A3 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
purine-rich element-binding protein gamma
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: Werner syndrome ATP-dependent helicase
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
testis expressed 15, meiosis and synapsis associated
protein phosphatase 2 catalytic subunit beta
serine/threonine-protein phosphatase 2A catalytic subunit beta isoform
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
potassium channel modulatory factor 1, transcript variant X1
potassium channel modulatory factor 1, transcript variant X3
potassium channel modulatory factor 1, transcript variant X2
potassium channel modulatory factor 1, transcript variant X4
E3 ubiquitin-protein ligase KCMF1 isoform X1
E3 ubiquitin-protein ligase KCMF1 isoform X3
E3 ubiquitin-protein ligase KCMF1 isoform X4
E3 ubiquitin-protein ligase KCMF1 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 10 samples with support for all annotated introns
endosomal/lysosomal potassium channel TMEM175
S-adenosylmethionine synthase-like, transcript variant X2
S-adenosylmethionine synthase-like, transcript variant X3
S-adenosylmethionine synthase-like, transcript variant X1
S-adenosylmethionine synthase-like isoform X1
S-adenosylmethionine synthase-like isoform X3
S-adenosylmethionine synthase-like isoform X2
solute carrier family 20 member 2, transcript variant X1
solute carrier family 20 member 2, transcript variant X4
solute carrier family 20 member 2, transcript variant X2
solute carrier family 20 member 2, transcript variant X3
solute carrier family 20 member 2, transcript variant X5
sodium-dependent phosphate transporter 2 isoform X1
solute carrier family 20 member 2, transcript variant X6
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 9 samples with support for all annotated introns
sodium-dependent phosphate transporter 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerase II subunit RPB2
insulin like growth factor binding protein 7, transcript variant X2
insulin like growth factor binding protein 7, transcript variant X1
insulin-like growth factor-binding protein 7 isoform X2
insulin-like growth factor-binding protein 7 isoform X1
insulin like growth factor binding protein like 1
insulin-like growth factor-binding protein-like 1
17-beta-hydroxysteroid dehydrogenase 13-like
low-density lipoprotein receptor-related protein 2-like
FK506-binding protein 4-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
FK506-binding protein 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cell division cycle 14B, transcript variant X1
cell division cycle 14B, transcript variant X5
cell division cycle 14B, transcript variant X6
dual specificity protein phosphatase CDC14B isoform X4
dual specificity protein phosphatase CDC14B isoform X1
dual specificity protein phosphatase CDC14B isoform X3
cell division cycle 14B, transcript variant X4
cell division cycle 14B, transcript variant X3
cell division cycle 14B, transcript variant X2
dual specificity protein phosphatase CDC14B isoform X2
aminopeptidase O (putative), transcript variant X5
aminopeptidase O (putative), transcript variant X2
aminopeptidase O (putative), transcript variant X1
aminopeptidase O (putative), transcript variant X3
aminopeptidase O (putative), transcript variant X4
FA complementation group C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
FA complementation group C, 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 14 samples with support for all annotated introns
FA complementation group C, transcript variant X3
Fanconi anemia group C protein isoform X2
Fanconi anemia group C protein isoform X1
Fanconi anemia group C protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
similar to RNA sequence (same species):INSD:GGXP01043013.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 201 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 201 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transfer RNA valine (anticodon CAC); 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: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
DNA excision repair protein ERCC-6-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 35 member D2, 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 15 samples with support for all annotated introns
solute carrier family 35 member D2, transcript variant X2
solute carrier family 35 member D2, transcript variant X1
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter isoform X1
UDP-N-acetylglucosamine/UDP-glucose/GDP-mannose transporter isoform X2
hyaluronan binding protein 4, transcript variant X2
hyaluronan binding protein 4, transcript variant X1
intracellular hyaluronan-binding protein 4 isoform X1
intracellular hyaluronan-binding protein 4 isoform X2
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fucosyltransferase 10, transcript variant X2
fucosyltransferase 10, transcript variant X1
adaptor related protein complex 3 subunit sigma 1, 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 36 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
adaptor related protein complex 3 subunit sigma 1, transcript variant X2
transmembrane emp24 domain-containing protein 7
TIR domain-containing adapter molecule 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 1 sample with support for all annotated introns
coiled-coil domain-containing protein 112
tripartite motif containing 36, transcript variant X1
E3 ubiquitin-protein ligase TRIM36 isoform X1
tripartite motif containing 36, transcript variant X2
E3 ubiquitin-protein ligase TRIM36 isoform X2
potassium calcium-activated channel subfamily N member 2, transcript variant X1
potassium calcium-activated channel subfamily N member 2, transcript variant X2
small conductance calcium-activated potassium channel protein 2 isoform X2
small conductance calcium-activated potassium channel protein 2 isoform X1
potassium calcium-activated channel subfamily N member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
small conductance calcium-activated potassium channel protein 2 isoform X3
fructose-1,6-bisphosphatase isozyme 2-like
ADP ribosylation factor like GTPase 14 effector protein like, transcript variant X3
ADP ribosylation factor like GTPase 14 effector protein like, transcript variant X2
ADP ribosylation factor like GTPase 14 effector protein like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
probable WRKY transcription factor protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 30% 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein K02A2.6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
pro-neuregulin-1, membrane-bound isoform isoform X3
pro-neuregulin-1, membrane-bound isoform isoform X2
pro-neuregulin-1, membrane-bound isoform isoform X1
peroxisomal multifunctional enzyme type 2
TNF alpha induced protein 8, transcript variant X3
TNF alpha induced protein 8, transcript variant X2
TNF alpha induced protein 8, transcript variant X1
tumor necrosis factor alpha-induced protein 8 isoform X2
tumor necrosis factor alpha-induced protein 8 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 15% coverage of the annotated genomic feature by RNAseq alignments
DTW domain containing 2, transcript variant X2
DTW domain containing 2, transcript variant X1
tRNA-uridine aminocarboxypropyltransferase 2 isoform X1
tRNA-uridine aminocarboxypropyltransferase 2 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
sodium-coupled monocarboxylate transporter 2
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
NME/NM23 nucleoside diphosphate kinase 6, transcript variant X5
nucleoside diphosphate kinase 6 isoform X4
NME/NM23 nucleoside diphosphate kinase 6, transcript variant X2
nucleoside diphosphate kinase 6 isoform X2
NME/NM23 nucleoside diphosphate kinase 6, transcript variant X4
NME/NM23 nucleoside diphosphate kinase 6, transcript variant X3
NME/NM23 nucleoside diphosphate kinase 6, transcript variant X1
nucleoside diphosphate kinase 6 isoform X3
nucleoside diphosphate kinase 6 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 2 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01071276.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 142 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 142 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
coiled-coil domain-containing protein 34
leucine rich repeat containing G protein-coupled receptor 4
leucine-rich repeat-containing G-protein coupled receptor 4
lin-7 homolog C, crumbs cell polarity complex component
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
brain derived neurotrophic factor, transcript variant X1
brain derived neurotrophic factor, transcript variant X3
brain derived neurotrophic factor, transcript variant X4
brain derived neurotrophic factor, transcript variant X2
brain-derived neurotrophic factor isoform X1
brain-derived neurotrophic factor isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
12S rRNA N4-methylcytidine (m4C) methyltransferase
uncharacterized LOC122791328, transcript variant X1
uncharacterized LOC122791328, transcript variant X2
potassium voltage-gated channel subfamily A member 4
potassium voltage-gated channel subfamily A member 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 156 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
potassium voltage-gated channel subfamily A member 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 156 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel subfamily A member 2-like
ADP ribosylation factor like GTPase 14 effector protein
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
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: ARL14 effector protein
eukaryotic translation initiation factor 3 subunit M, transcript variant X1
eukaryotic translation initiation factor 3 subunit M, transcript variant X2
eukaryotic translation initiation factor 3 subunit M isoform X1
eukaryotic translation initiation factor 3 subunit M isoform X2
WT1 transcription factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
WT1 transcription factor, 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
WT1 transcription factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
doublecortin domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
DnaJ heat shock protein family (Hsp40) member C24
inner mitochondrial membrane peptidase subunit 1, transcript variant X2
inner mitochondrial membrane peptidase subunit 1, transcript variant X3
inner mitochondrial membrane peptidase subunit 1, transcript variant X1
inner mitochondrial membrane peptidase subunit 1, transcript variant X4
mitochondrial inner membrane protease subunit 1
elongator acetyltransferase complex subunit 4, transcript variant X1
elongator acetyltransferase complex subunit 4, transcript variant X3
elongator acetyltransferase complex subunit 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
metallophosphoesterase domain containing 2
proline rich and Gla domain 4, 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 7 samples with support for all annotated introns
proline rich and Gla domain 4, 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 10 samples with support for all annotated introns
proline rich and Gla domain 4, 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 6 samples with support for all annotated introns
transmembrane gamma-carboxyglutamic acid protein 4 isoform X1
transmembrane gamma-carboxyglutamic acid protein 4 isoform X2
transfer RNA glutamine (anticodon CUG); 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: 94% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
cat eye syndrome critical region protein 2 homolog, 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 25 samples with support for all annotated introns
cat eye syndrome critical region protein 2 homolog
cat eye syndrome critical region protein 2 homolog, transcript variant X2
bromodomain-containing protein DDB_G0280777-like
transfer RNA threonine (anticodon AGU); 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: 17 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutamine amidotransferase class 1 domain containing 1, 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 32 samples with support for all annotated introns
glutamine amidotransferase-like class 1 domain-containing protein 1 isoform X1
glutamine amidotransferase class 1 domain containing 1, 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 32 samples with support for all annotated introns
glutamine amidotransferase-like class 1 domain-containing protein 1 isoform X2
transmembrane protein 138, transcript variant X1
transmembrane protein 138, transcript variant X3
transmembrane protein 138, 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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: 27 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 10B
protein phosphatase 1 regulatory subunit 32, transcript variant X1
protein phosphatase 1 regulatory subunit 32, transcript variant X2
protein phosphatase 1 regulatory subunit 32
succinate dehydrogenase complex assembly factor 2
succinate dehydrogenase assembly factor 2, mitochondrial
cleavage and polyadenylation specific factor 7
similar to RNA sequence (same species):INSD:GGXP01028379.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 154 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 154 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
cleavage and polyadenylation specificity factor subunit 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
diacylglycerol lipase alpha, transcript variant X4
diacylglycerol lipase alpha, 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 5 samples with support for all annotated introns
diacylglycerol lipase alpha, 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 5 samples with support for all annotated introns
diacylglycerol lipase alpha, transcript variant X2
diacylglycerol lipase alpha, transcript variant X3
diacylglycerol lipase alpha, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
diacylglycerol lipase alpha, 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 3 samples with support for all annotated introns
TMEM9 domain family member B, transcript variant X1
TMEM9 domain family member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 11
signal peptide, CUB and EGF-like domain-containing protein 2
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
forkhead box protein M1-like, transcript variant X2
forkhead box protein M1-like, transcript variant X1
forkhead box protein M1-like, transcript variant X3
uncharacterized protein LOC122791688 isoform 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 9 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00283
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2, transcript variant X1
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2, transcript variant X2
Hermansky-Pudlak syndrome 5 protein isoform X1
Hermansky-Pudlak syndrome 5 protein isoform X2
general transcription factor IIH subunit 1
tumor susceptibility 101, transcript variant X1
tumor susceptibility 101, transcript variant X2
tumor susceptibility gene 101 protein isoform X2
tumor susceptibility gene 101 protein isoform X1
ras association domain-containing protein 8-like, transcript variant X4
ras association domain-containing protein 8-like, transcript variant X2
ras association domain-containing protein 8-like, transcript variant X5
ras association domain-containing protein 8-like, transcript variant X1
ras association domain-containing protein 8-like, transcript variant X3
ras association domain-containing protein 8-like isoform X2
ras association domain-containing protein 8-like isoform X1
leucine rich repeat containing 56, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine rich repeat containing 56, transcript variant X2
leucine-rich repeat-containing protein 56 isoform X1
leucine-rich repeat-containing protein 56 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 120 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
PHD and RING finger domain-containing protein 1-like
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, including 30 samples with support for all annotated introns
PHD and ring finger domains 1, transcript variant X3
PHD and ring finger domains 1, transcript variant X2
PHD and ring finger domains 1, transcript variant X4
PHD and ring finger domains 1, transcript variant X1
PHD and RING finger domain-containing protein 1 isoform X3
PHD and RING finger domain-containing protein 1 isoform X2
PHD and RING finger domain-containing protein 1 isoform X4
PHD and RING finger domain-containing protein 1 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 11 samples with support for all annotated introns
malignant fibrous histiocytoma-amplified sequence 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
interferon regulatory factor 3-like, transcript variant X2
interferon regulatory factor 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
interferon regulatory factor 3-like isoform X2
interferon regulatory factor 3-like isoform X1
interferon regulatory factor 3-like, transcript variant X3
uncharacterized protein LOC122791286 isoform X2
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
synaptotagmin-A-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 4 samples with support for all annotated introns
synaptotagmin-A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01055288.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 109 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 109 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
transient receptor potential cation channel subfamily M member 5
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
potassium voltage-gated channel subfamily Q member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
potassium voltage-gated channel subfamily KQT member 1
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 13 samples with support for all annotated introns
pleckstrin homology like domain family A member 2
pleckstrin homology-like domain family A member 2
oxysterol binding protein like 5, transcript variant X7
oxysterol binding protein like 5, transcript variant X1
oxysterol binding protein like 5, transcript variant X5
oxysterol binding protein like 5, transcript variant X10
oxysterol binding protein like 5, transcript variant X2
oxysterol binding protein like 5, transcript variant X6
oxysterol binding protein like 5, transcript variant X8
oxysterol binding protein like 5, transcript variant X3
oxysterol binding protein like 5, transcript variant X4
oxysterol binding protein like 5, transcript variant X9
oxysterol-binding protein-related protein 5 isoform X1
oxysterol-binding protein-related protein 5 isoform X2
tumor necrosis factor receptor superfamily member 1A-like, transcript variant X1
tumor necrosis factor receptor superfamily member 1A-like isoform X1
tumor necrosis factor receptor superfamily member 1A-like, transcript variant X2
tumor necrosis factor receptor superfamily member 1A-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00430
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
TEA domain transcription factor 1, transcript variant X2
TEA domain transcription factor 1, transcript variant X5
TEA domain transcription factor 1, transcript variant X1
TEA domain transcription factor 1, transcript variant X4
TEA domain transcription factor 1, transcript variant X3
transcriptional enhancer factor TEF-1 isoform X3
transcriptional enhancer factor TEF-1 isoform X1
transcriptional enhancer factor TEF-1 isoform X2
ras association domain-containing protein 10
aryl hydrocarbon receptor nuclear translocator like
aryl hydrocarbon receptor nuclear translocator-like protein 1
BTB domain containing 10, transcript variant X1
BTB domain containing 10, transcript variant X5
BTB domain containing 10, transcript variant X2
BTB domain containing 10, transcript variant X4
BTB domain containing 10, transcript variant X3
BTB/POZ domain-containing protein 10 isoform X1
BTB/POZ domain-containing protein 10 isoform X3
BTB/POZ domain-containing protein 10 isoform X2
BTB/POZ domain-containing protein 10 isoform X4
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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine protease inhibitor Kazal-type 1-like
serine protease inhibitor Kazal-type 1-like, transcript variant X2
serine protease inhibitor Kazal-type 1-like, transcript variant X1
serine protease inhibitor Kazal-type 1-like isoform X2
serine protease inhibitor Kazal-type 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transcriptional enhancer factor TEF-1-like, transcript variant X1
transcriptional enhancer factor TEF-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transcriptional enhancer factor TEF-1-like isoform X1
transcriptional enhancer factor TEF-1-like isoform X2
mediator complex subunit 25, transcript variant X1
mediator complex subunit 25, transcript variant X2
mediator of RNA polymerase II transcription subunit 25 isoform X1
mediator of RNA polymerase II transcription subunit 25 isoform X2
protein kinase C and casein kinase substrate in neurons protein 1-like, transcript variant X1
protein kinase C and casein kinase substrate in neurons protein 1-like, transcript variant X2
protein kinase C and casein kinase substrate in neurons protein 1-like isoform X1
protein kinase C and casein kinase substrate in neurons protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
uncharacterized LOC122791606, transcript variant X1
uncharacterized LOC122791606, transcript variant X3
uncharacterized LOC122791606, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00604
acid phosphatase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
acid phosphatase 4, transcript variant X1
nuclear receptor subfamily 1 group H member 2, transcript variant X1
nuclear receptor subfamily 1 group H member 2, transcript variant X3
nuclear receptor subfamily 1 group H member 2, transcript variant X2
mitochondrial mRNA pseudouridine synthase Trub2-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
uncharacterized LOC122791360, 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 14 samples with support for all annotated introns
uncharacterized LOC122791360, transcript variant X1
ER membrane protein complex subunit 10, transcript variant X1
ER membrane protein complex subunit 10, 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 19 samples with support for all annotated introns
ER membrane protein complex subunit 10 isoform X1
ER membrane protein complex subunit 10 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
DNA polymerase delta 1, catalytic subunit
similar to RNA sequence (same species):INSD:GGXP01065757.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 126 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 126 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Spi-B transcription factor, transcript variant X1
Spi-B transcription factor, transcript variant X2
Spi-B transcription factor, transcript variant X3
Spi-B transcription factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122791358, transcript variant X2
uncharacterized LOC122791358, transcript variant X1
leucine rich repeat containing 4C, transcript variant X2
leucine rich repeat containing 4C, transcript variant X3
leucine rich repeat containing 4C, transcript variant X1
leucine-rich repeat-containing protein 4C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tyrosine (anticodon AUA); 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: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat-containing protein 4B
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 59% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein C19orf81 homolog
SH3 and multiple ankyrin repeat domains 1
SH3 and multiple ankyrin repeat domains protein 1
fuzzy planar cell polarity protein, 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 10 samples with support for all annotated introns
fuzzy planar cell polarity protein, 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 15 samples with support for all annotated introns
napsin A aspartic peptidase, transcript variant X1
napsin A aspartic peptidase, transcript variant X2
potassium voltage-gated channel subfamily C member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 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: 23 Proteins
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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
proline-rich AKT1 substrate 1 isoform X1
proline-rich AKT1 substrate 1 isoform X2
galactoside alpha-(1,2)-fucosyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 113 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Josephin domain containing 2, transcript variant X1
Josephin domain containing 2, transcript variant X2
aspartate dehydrogenase domain containing, transcript variant X2
aspartate dehydrogenase domain containing, transcript variant X1
putative L-aspartate dehydrogenase isoform X1
putative L-aspartate dehydrogenase isoform X2
cell adhesion molecule 3, transcript variant X1
cell adhesion molecule 3, transcript variant X2
cell adhesion molecule 3, transcript variant X3
ATP-sensitive inward rectifier potassium channel 11-like, transcript variant X2
ATP-sensitive inward rectifier potassium channel 11-like, transcript variant X1
ATP-sensitive inward rectifier potassium channel 11-like, transcript variant X3
ATP-sensitive inward rectifier potassium channel 11-like
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ras-related protein R-Ras2-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 30 samples with support for all annotated introns
ras-related protein R-Ras2-like, transcript variant X1
ras-related protein R-Ras2-like isoform X1
ras-related protein R-Ras2-like isoform X2
sodium-dependent neutral amino acid transporter B(0)AT2-like, transcript variant X1
sodium-dependent neutral amino acid transporter B(0)AT2-like, transcript variant X3
sodium-dependent neutral amino acid transporter B(0)AT2-like, transcript variant X2
sodium-dependent neutral amino acid transporter B(0)AT2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 112 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 112 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 112 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: 24 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
galactoside alpha-(1,2)-fucosyltransferase 2-like, transcript variant X4
galactoside alpha-(1,2)-fucosyltransferase 2-like isoform X1
galactoside alpha-(1,2)-fucosyltransferase 2-like isoform X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
toll-interacting protein, transcript variant X1
toll-interacting protein, transcript variant X2
BR serine/threonine kinase 2, transcript variant X1
BR serine/threonine kinase 2, transcript variant X3
BR serine/threonine kinase 2, transcript variant X7
BR serine/threonine kinase 2, transcript variant X5
BR serine/threonine kinase 2, transcript variant X9
BR serine/threonine kinase 2, transcript variant X10
BR serine/threonine kinase 2, transcript variant X2
BR serine/threonine kinase 2, transcript variant X4
BR serine/threonine kinase 2, transcript variant X6
BR serine/threonine kinase 2, transcript variant X8
serine/threonine-protein kinase BRSK2 isoform X9
serine/threonine-protein kinase BRSK2 isoform X10
serine/threonine-protein kinase BRSK2 isoform X1
serine/threonine-protein kinase BRSK2 isoform X3
serine/threonine-protein kinase BRSK2 isoform X7
serine/threonine-protein kinase BRSK2 isoform X5
serine/threonine-protein kinase BRSK2 isoform X2
serine/threonine-protein kinase BRSK2 isoform X4
serine/threonine-protein kinase BRSK2 isoform X6
serine/threonine-protein kinase BRSK2 isoform X8
MOB kinase activator 2, transcript variant X5
MOB kinase activator 2, transcript variant X4
MOB kinase activator 2, transcript variant X3
MOB kinase activator 2, transcript variant X2
MOB kinase activator 2, transcript variant X1
dual specificity phosphatase 8, transcript variant X1
dual specificity phosphatase 8, transcript variant X2
dual specificity phosphatase 8, transcript variant X3
dual specificity phosphatase 8, transcript variant X4
dual specificity protein phosphatase 8 isoform X1
dual specificity protein phosphatase 8 isoform X2
dual specificity protein phosphatase 8 isoform 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 7 samples with support for all annotated introns
synaptotagmin-2-like, transcript variant X1
synaptotagmin-2-like, transcript variant X5
synaptotagmin-2-like, transcript variant X3
synaptotagmin-2-like, transcript variant X4
synaptotagmin-2-like, transcript variant X2
non-muscle caldesmon-like, transcript variant X2
non-muscle caldesmon-like, transcript variant X1
non-muscle caldesmon-like, transcript variant X3
troponin T3, fast skeletal type, transcript variant X7
troponin T3, fast skeletal type, transcript variant X1
troponin T3, fast skeletal type, transcript variant X2
troponin T3, fast skeletal type, transcript variant X3
troponin T3, fast skeletal type, transcript variant X4
troponin T3, fast skeletal type, transcript variant X5
troponin T3, fast skeletal type, transcript variant X6
troponin T, fast skeletal muscle isoform X1
troponin T, fast skeletal muscle isoform X3
troponin T, fast skeletal muscle isoform X5
troponin T, fast skeletal muscle isoform X2
troponin T, fast skeletal muscle isoform X4
troponin T, fast skeletal muscle isoform X6
troponin T, fast skeletal muscle isoform X7
39S ribosomal protein L23, mitochondrial-like
insulin-like growth factor II, transcript variant X1
insulin-like growth factor II, transcript variant X2
insulin-like growth factor II isoform X1
insulin-like growth factor II isoform 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 3 samples with support for all annotated introns
transfer RNA glutamic acid (anticodon UUC); 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: 91% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 665-like, 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 14 samples with support for all annotated introns
zinc finger protein 665-like, 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 11 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 98% coverage of the annotated genomic feature by RNAseq alignments
troponin T1, slow skeletal type, transcript variant X2
troponin T1, slow skeletal type, transcript variant X4
troponin T1, slow skeletal type, transcript variant X6
troponin T, slow skeletal muscle isoform X2
troponin T, slow skeletal muscle isoform X4
troponin T, slow skeletal muscle isoform X6
troponin T1, slow skeletal type, transcript variant X1
troponin T1, slow skeletal type, transcript variant X3
troponin T1, slow skeletal type, transcript variant X5
troponin T, slow skeletal muscle isoform X1
troponin T, slow skeletal muscle isoform X3
troponin T, slow skeletal muscle isoform X5
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
NACHT, LRR and PYD domains-containing protein 3-like
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
protein phosphatase 1 regulatory subunit 12C
similar to RNA sequence (same species):INSD:GGXP01058796.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 95 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 95 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: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like protein 1
uncharacterized LOC122791629, transcript variant X2
uncharacterized LOC122791629, transcript variant X1
protein tyrosine phosphatase receptor type H
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
receptor-type tyrosine-protein phosphatase H
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
BR serine/threonine kinase 1, transcript variant X8
BR serine/threonine kinase 1, transcript variant X7
BR serine/threonine kinase 1, transcript variant X9
BR serine/threonine kinase 1, transcript variant X5
BR serine/threonine kinase 1, transcript variant X4
BR serine/threonine kinase 1, transcript variant X6
BR serine/threonine kinase 1, transcript variant X3
BR serine/threonine kinase 1, transcript variant X2
BR serine/threonine kinase 1, transcript variant X1
serine/threonine-protein kinase BRSK1 isoform X8
serine/threonine-protein kinase BRSK1 isoform X7
serine/threonine-protein kinase BRSK1 isoform X9
serine/threonine-protein kinase BRSK1 isoform X5
serine/threonine-protein kinase BRSK1 isoform X4
serine/threonine-protein kinase BRSK1 isoform X6
serine/threonine-protein kinase BRSK1 isoform X3
serine/threonine-protein kinase BRSK1 isoform X2
serine/threonine-protein kinase BRSK1 isoform X1
charged multivesicular body protein 2A, transcript variant X5
charged multivesicular body protein 2A, transcript variant X4
charged multivesicular body protein 2A, transcript variant X2
charged multivesicular body protein 2A, transcript variant X3
charged multivesicular body protein 2A, transcript variant X1
tripartite motif containing 28, transcript variant X2
tripartite motif containing 28, transcript variant X1
transcription intermediary factor 1-beta isoform X2
transcription intermediary factor 1-beta isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 45, transcript variant X1
zinc finger and BTB domain containing 45, transcript variant X2
zinc finger and BTB domain-containing protein 45
HSPA (Hsp70) binding protein 1, transcript variant X4
HSPA (Hsp70) binding protein 1, transcript variant X1
HSPA (Hsp70) binding protein 1, transcript variant X3
HSPA (Hsp70) binding protein 1, transcript variant X2
protein phosphatase 6 regulatory subunit 1
serine/threonine-protein phosphatase 6 regulatory subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase KMT5C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 150B, transcript variant X1
modulator of macroautophagy TMEM150B isoform X1
transmembrane protein 150B, transcript variant X2
modulator of macroautophagy TMEM150B isoform 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
dual specificity protein kinase splB-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 24 samples with support for all annotated introns
uncharacterized protein LOC122791850 isoform X2
dual specificity protein kinase splB-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 40 samples with support for all annotated introns
dual specificity protein kinase splB-like isoform X1
speedy protein 1-B-like, transcript variant X2
speedy protein 1-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 43 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
IgA receptor-like, transcript variant X3
IgA receptor-like, transcript variant X1
IgA receptor-like, transcript variant X2
stress response protein NST1-like isoform X1
stress response protein NST1-like isoform X2
myb-like protein X, transcript variant X2
myb-like protein X, transcript variant X1
myb-like protein X, transcript variant X4
myb-like protein X, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
extracellular calcium-sensing receptor-like
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: 19 Proteins
deformed epidermal autoregulatory factor 1 homolog
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
epidermal growth factor receptor kinase substrate 8-like protein 2
similar to RNA sequence (same species):INSD:GGXP01036903.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 199 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 199 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: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
lysosomal membrane ascorbate-dependent ferrireductase CYB561A3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
lysosomal membrane ascorbate-dependent ferrireductase CYB561A3, transcript variant X1
lysosomal membrane ascorbate-dependent ferrireductase CYB561A3 isoform X1
lysosomal membrane ascorbate-dependent ferrireductase CYB561A3 isoform X2
triokinase and FMN cyclase, transcript variant X3
triokinase and FMN cyclase, transcript variant X2
triokinase and FMN cyclase, transcript variant X1
protein phosphatase 1 regulatory subunit 12A-like
transfer RNA serine (anticodon ACU); 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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor C and EGF domain-containing protein
uncharacterized LOC122791780, transcript variant X1
uncharacterized protein LOC122791780 isoform X1
uncharacterized LOC122791780, transcript variant X2
uncharacterized LOC122791780, transcript variant X3
uncharacterized protein LOC122791780 isoform X2
circularly permutated Ras protein 1-like
similar to RNA sequence (same species):INSD:GGXP01039214.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 917 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 917 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: 1 Protein, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
RNA binding protein fox-1 homolog 3-like
endoplasmic reticulum-Golgi intermediate compartment protein 2-like, transcript variant X2
endoplasmic reticulum-Golgi intermediate compartment protein 2-like, transcript variant X1
endoplasmic reticulum-Golgi intermediate compartment protein 2-like isoform X2
endoplasmic reticulum-Golgi intermediate compartment protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 3% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01034722.1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
chromosome chr17.part0 C11orf91 homolog, transcript variant X1
uncharacterized protein C11orf91 homolog
chromosome chr17.part0 C11orf91 homolog, transcript variant X2
chromosome chr17.part0 C11orf91 homolog, transcript variant X3
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 3 samples with support for all annotated introns
upstream transcription factor 1, transcript variant X2
upstream transcription factor 1, transcript variant X1
upstream transcription factor 1, transcript variant X3
upstream stimulatory factor 1 isoform X1
upstream stimulatory factor 1 isoform X2
upstream stimulatory factor 1 isoform X3
Rho GTPase activating protein 30, transcript variant X1
Rho GTPase activating protein 30, transcript variant X2
rho GTPase-activating protein 30 isoform X2
rho GTPase-activating protein 30 isoform X1
nectin cell adhesion molecule 4, transcript variant X2
nectin cell adhesion molecule 4, 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 5 samples with support for all annotated introns
cytochrome c oxidase subunit 7A-related protein, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
intelectin-1a-like, transcript variant X1
intelectin-1a-like, transcript variant X2
thiosulfate sulfurtransferase like domain containing 1
thiosulfate:glutathione sulfurtransferase
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
galanin peptides-like, transcript variant X1
galanin peptides-like, transcript variant X3
galanin peptides-like, transcript variant X2
aldehyde dehydrogenase X, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
aldehyde dehydrogenase 16 family member A1
aldehyde dehydrogenase family 16 member A1
uncharacterized LOC122791844, transcript variant X9
uncharacterized LOC122791844, transcript variant X10
uncharacterized LOC122791844, transcript variant X2
uncharacterized LOC122791844, transcript variant X1
uncharacterized LOC122791844, transcript variant X8
uncharacterized LOC122791844, transcript variant X4
uncharacterized LOC122791844, transcript variant X11
uncharacterized LOC122791844, transcript variant X3
uncharacterized LOC122791844, transcript variant X6
uncharacterized protein LOC122791844 isoform X1
uncharacterized protein LOC122791844 isoform X4
uncharacterized protein LOC122791844 isoform X5
uncharacterized protein LOC122791844 isoform X6
uncharacterized protein LOC122791844 isoform X7
uncharacterized LOC122791844, transcript variant X5
uncharacterized LOC122791844, transcript variant X7
uncharacterized protein LOC122791844 isoform X3
uncharacterized protein LOC122791844 isoform X2
excitatory amino acid transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122791664, transcript variant X2
uncharacterized LOC122791664, transcript variant X3
uncharacterized LOC122791664, transcript variant X1
uncharacterized protein LOC122791664 isoform X2
uncharacterized protein LOC122791664 isoform X3
uncharacterized protein LOC122791664 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00211
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like
cilia and flagella associated protein 126
succinate dehydrogenase complex subunit C, transcript variant X1
succinate dehydrogenase complex subunit C, transcript variant X2
succinate dehydrogenase cytochrome b560 subunit, mitochondrial isoform X1
succinate dehydrogenase cytochrome b560 subunit, mitochondrial isoform X2
uncharacterized LOC122791701, transcript variant X1
uncharacterized LOC122791701, transcript variant X2
nuclear receptor subfamily 1 group I member 3-like
nuclear receptor subfamily 1 group I member 3-like, transcript variant X2
nuclear receptor subfamily 1 group I member 3-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 4 samples with support for all annotated introns
nuclear receptor subfamily 1 group I member 3-like, transcript variant X1
nuclear receptor subfamily 1 group I member 3-like isoform X1
nuclear receptor subfamily 1 group I member 2-like isoform X2
translocase of outer mitochondrial membrane 40 like
mitochondrial import receptor subunit TOM40B
ubiquitin-fold modifier conjugating enzyme 1
ubiquitin-fold modifier-conjugating enzyme 1
eukaryotic translation initiation factor 3 subunit F
potassium inwardly rectifying channel subfamily J member 10
ATP-sensitive inward rectifier potassium channel 10
potassium inwardly rectifying channel subfamily J member 9, transcript variant X1
potassium inwardly rectifying channel subfamily J member 9, transcript variant X2
potassium inwardly rectifying channel subfamily J member 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
G protein-activated inward rectifier potassium channel 3 isoform X1
G protein-activated inward rectifier potassium channel 3 isoform X2
kirre like nephrin family adhesion molecule 1, 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 5 samples with support for all annotated introns
kirre like nephrin family adhesion molecule 1, 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 2 samples with support for all annotated introns
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins
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
signaling lymphocytic activation molecule-like, transcript variant X1
signaling lymphocytic activation molecule-like, transcript variant X2
signaling lymphocytic activation molecule-like isoform 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 1 sample 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 28 samples with support for all annotated introns
Rho guanine nucleotide exchange factor 11, transcript variant X5
Rho guanine nucleotide exchange factor 11, transcript variant X1
Rho guanine nucleotide exchange factor 11, transcript variant X7
Rho guanine nucleotide exchange factor 11, transcript variant X6
Rho guanine nucleotide exchange factor 11, transcript variant X4
Rho guanine nucleotide exchange factor 11, transcript variant X2
Rho guanine nucleotide exchange factor 11, transcript variant X3
rho guanine nucleotide exchange factor 11 isoform X1
rho guanine nucleotide exchange factor 11 isoform X7
rho guanine nucleotide exchange factor 11 isoform X6
rho guanine nucleotide exchange factor 11 isoform X4
rho guanine nucleotide exchange factor 11 isoform X2
rho guanine nucleotide exchange factor 11 isoform X3
rho guanine nucleotide exchange factor 11 isoform X5
sodium/potassium-transporting ATPase subunit alpha-2, transcript variant X3
sodium/potassium-transporting ATPase subunit alpha-2 isoform X3
sodium/potassium-transporting ATPase subunit alpha-2, transcript variant X4
sodium/potassium-transporting ATPase subunit alpha-2 isoform X4
sodium/potassium-transporting ATPase subunit alpha-2, transcript variant X2
sodium/potassium-transporting ATPase subunit alpha-2, transcript variant X1
sodium/potassium-transporting ATPase subunit alpha-2 isoform X2
sodium/potassium-transporting ATPase subunit alpha-2 isoform X1
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ubiquitin-conjugating enzyme E2 variant 2, transcript variant X3
ubiquitin-conjugating enzyme E2 variant 2, transcript variant X2
ubiquitin-conjugating enzyme E2 variant 2 isoform X2
ubiquitin-conjugating enzyme E2 variant 2 isoform X3
ubiquitin-conjugating enzyme E2 variant 2, transcript variant X1
ubiquitin-conjugating enzyme E2 variant 2, transcript variant X4
ubiquitin-conjugating enzyme E2 variant 2 isoform X1
ubiquitin-conjugating enzyme E2 variant 2 isoform X4
GRB2 associated regulator of MAPK1 subtype 1
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 23 samples with support for all annotated introns
GRB2-associated and regulator of MAPK protein 1
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCG); 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: 4 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
SLAM family member 9-like, transcript variant X1
SLAM family member 9-like, transcript variant X2
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/threonine-protein kinase PINK1, mitochondrial
nucleobindin-2-like, transcript variant X1
nucleobindin-2-like, transcript variant X2
pleckstrin homology domain containing A4, transcript variant X4
pleckstrin homology domain containing A4, transcript variant X1
pleckstrin homology domain containing A4, transcript variant X3
pleckstrin homology domain containing A4, transcript variant X5
pleckstrin homology domain containing A4, transcript variant X6
pleckstrin homology domain containing A4, transcript variant X2
pleckstrin homology domain-containing family A member 4 isoform X1
pleckstrin homology domain-containing family A member 4 isoform X2
pleckstrin homology domain-containing family A member 4 isoform X4
pleckstrin homology domain-containing family A member 4 isoform X3
pleckstrin homology domain-containing family A member 4 isoform X5
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X4
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X1
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X2
branched-chain-amino-acid aminotransferase, cytosolic-like isoform X1
branched-chain-amino-acid aminotransferase, cytosolic-like isoform X4
branched-chain-amino-acid aminotransferase, cytosolic-like isoform X2
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X3
branched-chain-amino-acid aminotransferase, cytosolic-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 133 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
golgin subfamily A member 6-like protein 22
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: golgin subfamily A member 6-like protein 22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 128 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
proliferation and apoptosis adaptor protein 15, transcript variant X1
proliferation and apoptosis adaptor protein 15, transcript variant X2
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 6 samples with support for all annotated introns
ETS translocation variant 3-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
C1q-related factor-like, transcript variant X2
C1q-related factor-like, transcript variant X3
C1q-related factor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 125 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122791341, transcript variant X4
uncharacterized LOC122791341, transcript variant X2
uncharacterized LOC122791341, transcript variant X3
uncharacterized protein LOC122791341 isoform X3
uncharacterized protein LOC122791341 isoform X2
uncharacterized LOC122791341, transcript variant X5
uncharacterized LOC122791341, transcript variant X1
uncharacterized protein LOC122791341 isoform X1
uncharacterized protein LOC122791341 isoform X4
uncharacterized LOC122791341, transcript variant X6
uncharacterized protein LOC122791341 isoform X5
beta-1,4-galactosyltransferase 3-like, transcript variant X2
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
beta-1,4-galactosyltransferase 3-like, transcript variant X1
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 5 samples with support for all annotated introns
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
similar to RNA sequence (same species):INSD:GGXP01001006.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 147 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 147 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC122791586, transcript variant X3
uncharacterized LOC122791586, transcript variant X2
uncharacterized LOC122791586, transcript variant X4
uncharacterized LOC122791586, 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: extracellular calcium-sensing receptor-like
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: 11 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 2 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
nucleolar protein dao-5-like, transcript variant X1
nucleolar protein dao-5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
intelectin-1a-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 2 samples with support for all annotated introns
eukaryotic translation initiation factor 4 gamma 2
COORDINATES: nucleotide motif:Rfam:12.0:RF01291
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
zinc finger BED domain-containing protein 5
adenosine monophosphate deaminase 3, transcript variant X3
adenosine monophosphate deaminase 3, transcript variant X2
adenosine monophosphate deaminase 3, transcript variant X1
adenosine monophosphate deaminase 3, transcript variant X4
lymphatic vessel endothelial hyaluronan receptor 1
lymphatic vessel endothelial hyaluronic acid receptor 1
inositol 1,4,5-triphosphate receptor associated 1
CTR9 homolog, Paf1/RNA polymerase II complex component
RNA polymerase-associated protein CTR9 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
transmembrane protein 41B, transcript variant X2
transmembrane protein 41B, transcript variant X4
transmembrane protein 41B, transcript variant X1
transmembrane protein 41B, transcript variant X3
DENN domain containing 5A, transcript variant X2
DENN domain containing 5A, transcript variant X1
DENN domain-containing protein 5A isoform X2
DENN domain-containing protein 5A isoform X1
p53-induced death domain-containing protein 1
homeodomain interacting protein kinase 3
homeodomain-interacting protein kinase 3
homeodomain-interacting protein kinase 3-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