Protopterus annectens isolate FY-2018-M chromosome 1.part2, 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\nCM033075.1.\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: tRNAscan-SE.
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.
EGF containing fibulin extracellular matrix protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
EGF containing fibulin extracellular matrix protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
EGF containing fibulin extracellular matrix protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
EGF containing fibulin extracellular matrix protein 1, transcript variant X1
EGF containing fibulin extracellular matrix protein 1, transcript variant X3
EGF-containing fibulin-like extracellular matrix protein 1 isoform X1
EGF-containing fibulin-like extracellular matrix protein 1 isoform X2
COORDINATES: polyA evidence [ECO:0006239]
coiled-coil domain-containing protein 85A
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
transfer RNA leucine (anticodon UAA); 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: 28 Proteins
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
similar to RNA sequence (same species):INSD:GGXP01073918.1
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 98 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 98 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
VRK serine/threonine kinase 2, transcript variant X3
VRK serine/threonine kinase 2, transcript variant X1
VRK serine/threonine kinase 2, transcript variant X2
serine/threonine-protein kinase VRK2 isoform X3
serine/threonine-protein kinase VRK2 isoform X1
serine/threonine-protein kinase VRK2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
BAF chromatin remodeling complex subunit BCL11A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01065610.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 120 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 120 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
proto-oncogene c-Rel-like, transcript variant X1
proto-oncogene c-Rel-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
proto-oncogene c-Rel-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
proto-oncogene c-Rel-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
pseudouridine synthase 10, transcript variant X2
pseudouridine synthase 10, transcript variant X1
tRNA pseudouridine synthase Pus10 isoform X2
tRNA pseudouridine synthase Pus10 isoform X1
golgin subfamily A member 6-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein KIAA1841 homolog
ankyrin repeat and SOCS box containing 3
ChaC glutathione specific gamma-glutamylcyclotransferase 2
glutathione-specific gamma-glutamylcyclotransferase 2
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
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 15 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translational initiation factor 2
similar to RNA sequence (same species):INSD:GGXP01053429.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 121 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 121 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
translation initiation factor IF-2, mitochondrial
clathrin heavy chain linker domain containing 1, transcript variant X1
clathrin heavy chain linker domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
clathrin heavy chain linker domain-containing protein 1
polyribonucleotide nucleotidyltransferase 1
polyribonucleotide nucleotidyltransferase 1, mitochondrial
protein phosphatase 4 regulatory subunit 3B, transcript variant X1
protein phosphatase 4 regulatory subunit 3B, transcript variant X2
protein phosphatase 4 regulatory subunit 3B, transcript variant X5
protein phosphatase 4 regulatory subunit 3B, transcript variant X3
protein phosphatase 4 regulatory subunit 3B, transcript variant X4
serine/threonine-protein phosphatase 4 regulatory subunit 3B isoform X1
serine/threonine-protein phosphatase 4 regulatory subunit 3B isoform X2
serine/threonine-protein phosphatase 4 regulatory subunit 3B isoform X3
serine/threonine-protein phosphatase 4 regulatory subunit 3B isoform X5
serine/threonine-protein phosphatase 4 regulatory subunit 3B isoform X4
cilia and flagella associated protein 36
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 26 samples with support for all annotated introns
cilia- and flagella-associated protein 36
coiled-coil domain containing 88A, transcript variant X2
coiled-coil domain containing 88A, transcript variant X1
coiled-coil domain containing 88A, transcript variant X3
coiled-coil domain containing 88A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
prolyl-tRNA synthetase associated domain-containing protein 1-like
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
follicle-stimulating hormone receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
protein phosphatase 1 regulatory subunit 21, transcript variant X2
protein phosphatase 1 regulatory subunit 21, transcript variant X1
protein phosphatase 1 regulatory subunit 21, transcript variant X3
protein phosphatase 1 regulatory subunit 21 isoform X2
protein phosphatase 1 regulatory subunit 21 isoform X1
protein phosphatase 1 regulatory subunit 21 isoform X3
Bardet-Biedl syndrome 10, transcript variant X1
Bardet-Biedl syndrome 10 protein isoform X1
Bardet-Biedl syndrome 10, transcript variant X2
Bardet-Biedl syndrome 10 protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 2 regulatory subunit B'alpha
similar to RNA sequence (same species):INSD:GGXP01030033.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 93 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 93 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform
cyclic AMP-dependent transcription factor ATF-3
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
basic leucine zipper ATF-like transcription factor 3, transcript variant X1
basic leucine zipper ATF-like transcription factor 3, transcript variant X3
basic leucine zipper ATF-like transcription factor 3, transcript variant X2
basic leucine zipper transcriptional factor ATF-like 3 isoform X1
basic leucine zipper transcriptional factor ATF-like 3 isoform X3
basic leucine zipper transcriptional factor ATF-like 3 isoform X2
NSL1 component of MIS12 kinetochore complex
similar to RNA sequence (same species):INSD:GGXP01036550.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 55 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 55 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
kinetochore-associated protein NSL1 homolog
TatD DNase domain containing 3, transcript variant X1
TatD DNase domain containing 3, transcript variant X2
TatD DNase domain containing 3, transcript variant X3
putative deoxyribonuclease TATDN3 isoform X1
putative deoxyribonuclease TATDN3 isoform X2
putative deoxyribonuclease TATDN3 isoform X3
TatD DNase domain containing 3, transcript variant X4
putative deoxyribonuclease TATDN3 isoform 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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
feline leukemia virus subgroup C receptor-related protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein S6 kinase C1, transcript variant X1
ribosomal protein S6 kinase C1, transcript variant X3
ribosomal protein S6 kinase delta-1 isoform X1
ribosomal protein S6 kinase delta-1 isoform X3
ribosomal protein S6 kinase C1, transcript variant X2
ribosomal protein S6 kinase delta-1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
EH domain binding protein 1, transcript variant X1
EH domain binding protein 1, transcript variant X2
EH domain binding protein 1, transcript variant X3
EH domain binding protein 1, transcript variant X4
orthodenticle homeobox 1, transcript variant X1
orthodenticle homeobox 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
WD repeat containing planar cell polarity effector
WD repeat-containing and planar cell polarity effector protein fritz homolog
malate dehydrogenase 1, transcript variant X2
malate dehydrogenase 1, transcript variant X1
malate dehydrogenase, cytoplasmic isoform X1
malate dehydrogenase, cytoplasmic isoform X2
similar to RNA sequence (same species):INSD:GGXP01052668.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 198 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 198 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
UTP--glucose-1-phosphate uridylyltransferase
vacuolar protein sorting-associated protein 54
E3 ubiquitin-protein ligase pellino homolog 1
ABC transporter G family member 23-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
ABC transporter G family member 23-like, transcript variant X3
ABC transporter G family member 23-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
ABC transporter G family member 23-like isoform X2
ABC transporter G family member 20-like isoform X1
SERTA domain containing 2, transcript variant X1
SERTA domain containing 2, transcript variant X4
SERTA domain containing 2, transcript variant X2
SERTA domain containing 2, transcript variant X3
SERTA domain-containing protein 2 isoform X1
SERTA domain-containing protein 2 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
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: neutral amino acid transporter A
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 10 samples with support for all annotated introns
N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase- like, transcript variant X2
N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase- like, transcript variant X1
N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase- like isoform X2
N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase- like isoform X1
actin related protein 2, transcript variant X1
actin related protein 2, transcript variant X2
sprouty related EVH1 domain containing 2
sprouty-related, EVH1 domain-containing protein 2
zona pellucida sperm-binding protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transfer RNA lysine (anticodon UUU); 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 11% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF02543
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
ETAA1 activator of ATR kinase, transcript variant X1
ETAA1 activator of ATR kinase, transcript variant X2
ewing's tumor-associated antigen 1 isoform X1
ewing's tumor-associated antigen 1 isoform X2
transfer RNA serine (anticodon AGA); 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: 6 Proteins
C1D nuclear receptor corepressor, transcript variant X3
C1D nuclear receptor corepressor, transcript variant X2
C1D nuclear receptor corepressor, transcript variant X4
C1D nuclear receptor corepressor, transcript variant X1
nuclear nucleic acid-binding protein C1D isoform X1
nuclear nucleic acid-binding protein C1D isoform X2
nuclear nucleic acid-binding protein C1D isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01055659.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 33 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 33 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein phosphatase 3 regulatory subunit B, alpha
cannabinoid receptor interacting protein 1
CB1 cannabinoid receptor-interacting protein 1
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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
prokineticin receptor 1, transcript variant X2
prokineticin receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
proprotein convertase subtilisin/kexin type 2, transcript variant X2
proprotein convertase subtilisin/kexin type 2, transcript variant X1
small nuclear ribonucleoprotein polypeptide B2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
interferon regulatory factor 2 binding protein 2
interferon regulatory factor 2-binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
fibronectin leucine rich transmembrane protein 3
leucine-rich repeat transmembrane protein FLRT3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase complex assembly factor 5, transcript variant X1
NADH:ubiquinone oxidoreductase complex assembly factor 5, transcript variant X2
arginine-hydroxylase NDUFAF5, mitochondrial isoform X2
arginine-hydroxylase NDUFAF5, mitochondrial isoform X1
ESF1 nucleolar pre-rRNA processing protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
serine palmitoyltransferase long chain base subunit 3
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
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
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
hepatocyte nuclear factor 3-beta isoform X1
hepatocyte nuclear factor 3-beta isoform X2
GDNF-inducible zinc finger protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
GDNF-inducible zinc finger protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
GDNF-inducible zinc finger protein 1-like isoform X1
GDNF-inducible zinc finger protein 1-like isoform X2
GDNF inducible zinc finger protein 1, transcript variant X2
GDNF inducible zinc finger protein 1, transcript variant X1
glycerophosphocholine phosphodiesterase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycerophosphocholine phosphodiesterase GPCPD1
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
tRNA methyltransferase 6 non-catalytic subunit
tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6
minichromosome maintenance 8 homologous recombination repair factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
THAP domain-containing protein 6-like, transcript variant X2
THAP domain-containing protein 6-like, transcript variant X1
THAP domain-containing protein 6-like isoform X2
THAP domain-containing protein 6-like isoform X1
cardiolipin synthase 1, transcript variant X1
cardiolipin synthase 1, transcript variant X3
cardiolipin synthase 1, transcript variant X2
cardiolipin synthase (CMP-forming) isoform X1
cardiolipin synthase (CMP-forming) isoform X3
cardiolipin synthase (CMP-forming) isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 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: 2 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin related transmembrane protein 4
thioredoxin-related transmembrane protein 4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1
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
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-4
lysosomal associated membrane protein family member 5
lysosome-associated membrane glycoprotein 5
p21 (RAC1) activated kinase 5, transcript variant X1
p21 (RAC1) activated kinase 5, transcript variant X2
p21 (RAC1) activated kinase 5, transcript variant X3
p21 (RAC1) activated kinase 5, transcript variant X4
serine/threonine-protein kinase PAK 5 isoform X2
serine/threonine-protein kinase PAK 5 isoform X3
serine/threonine-protein kinase PAK 5 isoform X1
serine/threonine-protein kinase PAK 5 isoform X4
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ankyrin repeat and EF-hand domain containing 1
ankyrin repeat and EF-hand domain-containing protein 1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like
synaptosome associated protein 25, transcript variant X2
synaptosome associated protein 25, transcript variant X1
synaptosomal-associated protein 25 isoform X2
synaptosomal-associated protein 25 isoform X1
McKusick-Kaufman/Bardet-Biedl syndromes putative chaperonin-like, transcript variant X1
McKusick-Kaufman/Bardet-Biedl syndromes putative chaperonin-like isoform X1
McKusick-Kaufman/Bardet-Biedl syndromes putative chaperonin-like, 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 21 samples with support for all annotated introns
McKusick-Kaufman/Bardet-Biedl syndromes putative chaperonin-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein SLX4IP-like, transcript variant X1
protein SLX4IP-like, transcript variant X2
protein SLX4IP-like, transcript variant X3
uncharacterized protein LOC122789371 isoform X2
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
synapse differentiation inducing 1, transcript variant X1
synapse differentiation inducing 1, transcript variant X2
synapse differentiation-inducing gene protein 1
transfer RNA serine (anticodon ACU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
similar to RNA sequence (same species):INSD:GGXP01024212.1
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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
lysine acetyltransferase 14, transcript variant X2
similar to RNA sequence (same species):INSD:GGXP01046531.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 116 bases not found in genome assembly
lysine acetyltransferase 14, transcript variant X1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 116 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
cysteine-rich protein 2-binding protein isoform X1
cysteine-rich protein 2-binding protein isoform X2
mitochondrial genome maintenance exonuclease 1, transcript variant X5
mitochondrial genome maintenance exonuclease 1, transcript variant X6
mitochondrial genome maintenance exonuclease 1, transcript variant X2
mitochondrial genome maintenance exonuclease 1, transcript variant X1
mitochondrial genome maintenance exonuclease 1, transcript variant X3
mitochondrial genome maintenance exonuclease 1, transcript variant X4
mitochondrial genome maintenance exonuclease 1 isoform X1
mitochondrial genome maintenance exonuclease 1 isoform X2
double zinc ribbon and ankyrin repeat domains 1
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
double zinc ribbon and ankyrin repeat-containing protein 1
DNA-directed RNA polymerase III subunit RPC6
SEC23 homolog B, COPII coat complex component, transcript variant X1
protein transport protein Sec23B isoform X1
SEC23 homolog B, COPII coat complex component, transcript variant X2
protein transport protein Sec23B isoform X2
Ras and Rab interactor 2, transcript variant X2
Ras and Rab interactor 2, transcript variant X1
Ras and Rab interactor 2, transcript variant X5
Ras and Rab interactor 2, transcript variant X4
Ras and Rab interactor 2, transcript variant X3
Ras and Rab interactor 2, transcript variant X6
Ras and Rab interactor 2, transcript variant X7
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 20, NatB catalytic subunit
cilia and flagella associated protein 61
cilia- and flagella-associated protein 61
Ral GTPase activating protein catalytic subunit alpha 2
ral GTPase-activating protein subunit alpha-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
bifunctional protein GlmU-like, transcript variant X2
bifunctional protein GlmU-like isoform X2
bifunctional protein GlmU-like, transcript variant X3
bifunctional protein GlmU-like, transcript variant X1
bifunctional protein GlmU-like isoform X3
bifunctional protein GlmU-like isoform X1
kizuna centrosomal protein, transcript variant X1
kizuna centrosomal protein, transcript variant X2
kizuna centrosomal protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122789745, transcript variant X1
uncharacterized LOC122789745, transcript variant X2
uncharacterized LOC122789768, transcript variant X1
uncharacterized LOC122789768, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
BUB1 mitotic checkpoint serine/threonine kinase, transcript variant X1
BUB1 mitotic checkpoint serine/threonine kinase, transcript variant X2
mitotic checkpoint serine/threonine-protein kinase BUB1 isoform X1
mitotic checkpoint serine/threonine-protein kinase BUB1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122789850, transcript variant X3
uncharacterized LOC122789850, transcript variant X2
uncharacterized LOC122789850, 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 9 samples with support for all annotated introns
myelin and lymphocyte protein-like isoform 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 8 samples with support for all annotated introns
myelin and lymphocyte protein-like, transcript variant X2
myelin and lymphocyte protein-like isoform X2
myelin and lymphocyte protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 8 member A1, transcript variant X1
solute carrier family 8 member A1, transcript variant X4
solute carrier family 8 member A1, transcript variant X5
solute carrier family 8 member A1, transcript variant X6
solute carrier family 8 member A1, transcript variant X7
solute carrier family 8 member A1, transcript variant X2
solute carrier family 8 member A1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 8% coverage of the annotated genomic feature by RNAseq alignments
DExH-box helicase 57, transcript variant X1
DExH-box helicase 57, transcript variant X4
DExH-box helicase 57, transcript variant X3
DExH-box helicase 57, transcript variant X2
putative ATP-dependent RNA helicase DHX57 isoform X1
putative ATP-dependent RNA helicase DHX57 isoform X3
putative ATP-dependent RNA helicase DHX57 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
CAP-Gly domain-containing linker protein 1-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
heterogeneous nuclear ribonucleoprotein L like
heterogeneous nuclear ribonucleoprotein L-like
galactose mutarotase, transcript variant X2
galactose mutarotase, transcript variant X1
galactose mutarotase, transcript variant X3
serine and arginine rich splicing factor 7
similar to RNA sequence (same species):INSD:GGXP01050066.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 181 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 181 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 64 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: zinc finger protein 99-like
zinc finger protein 501-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01043986.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1193 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 864 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
transmembrane protein 178A, transcript variant X1
transmembrane protein 178A, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X4
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 3, transcript variant X5
mitogen-activated protein kinase kinase kinase kinase 3 isoform X1
mitogen-activated protein kinase kinase kinase kinase 3 isoform X3
mitogen-activated protein kinase kinase kinase kinase 3 isoform X4
mitogen-activated protein kinase kinase kinase kinase 3 isoform X2
mitogen-activated protein kinase kinase kinase kinase 3 isoform X5
eukaryotic translation initiation factor 4A3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
GINS complex subunit 1, transcript variant X2
GINS complex subunit 1, transcript variant X1
DNA replication complex GINS protein PSF1 isoform X1
DNA replication complex GINS protein PSF1 isoform X2
lysophosphatidylserine lipase ABHD12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
atlastin GTPase 2, transcript variant X1
atlastin GTPase 2, transcript variant X2
atlastin GTPase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ectonucleoside triphosphate diphosphohydrolase 6, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 6, transcript variant X2
ectonucleoside triphosphate diphosphohydrolase 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
acyl-CoA synthetase short chain family member 1
acetyl-coenzyme A synthetase 2-like, mitochondrial
adipocyte plasma membrane associated protein, transcript variant X1
adipocyte plasma membrane-associated protein isoform X1
adipocyte plasma membrane associated protein, transcript variant X2
adipocyte plasma membrane-associated protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial amidoxime reducing component 2-like
ribosomally synthesized cyclic peptide ustiloxin B precursosr-like
chromosome chr1.part2 C1orf115 homolog, transcript variant X1
chromosome chr1.part2 C1orf115 homolog, transcript variant X2
uncharacterized protein C1orf115 homolog
ADP-ribosylation factor-like protein 6-interacting protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 89% 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: 86% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
mitochondrial amidoxime reducing component 2
H2.0 like homeobox, transcript variant X1
H2.0 like homeobox, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TATA-box binding protein associated factor, RNA polymerase I subunit A
TATA box-binding protein-associated factor RNA polymerase I subunit A
transport and Golgi organization protein 1 homolog
axin interactor, dorsalization associated, transcript variant X3
axin interactor, dorsalization associated, transcript variant X1
axin interactor, dorsalization associated, transcript variant X2
axin interactor, dorsalization-associated protein isoform X2
axin interactor, dorsalization-associated protein isoform X3
axin interactor, dorsalization-associated protein isoform X1
BRO1 domain and CAAX motif containing, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BRO1 domain and CAAX motif containing, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
family with sequence similarity 177 member B, transcript variant X1
family with sequence similarity 177 member B, transcript variant X2
protein dispatched homolog 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein dispatched homolog 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein dispatched homolog 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
dispatched RND transporter family member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
regulator of microtubule dynamics protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 66% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerase I subunit RPA2
NLR family CARD domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01021160.1
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.
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
regulator of G protein signaling 7, transcript variant X3
regulator of G protein signaling 7, transcript variant X1
regulator of G protein signaling 7, transcript variant X2
regulator of G-protein signaling 7 isoform X2
regulator of G-protein signaling 7 isoform X1
regulator of G-protein signaling 7 isoform X3
toll-like receptor 5, transcript variant X2
toll-like receptor 5, transcript variant X1
toll-like receptor 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
saccharopine dehydrogenase-like oxidoreductase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122790554, transcript variant X1
uncharacterized LOC122790554, transcript variant X2
uncharacterized LOC122790554, transcript variant X3
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
kinesin family member 26B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
kinesin family member 26B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein U
cytochrome c oxidase assembly protein COX20, mitochondrial, transcript variant X2
cytochrome c oxidase assembly protein COX20, mitochondrial, transcript variant X1
cytochrome c oxidase assembly protein COX20, mitochondrial isoform X2
cytochrome c oxidase assembly protein COX20, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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 94% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 22 member 6-B-like
catsper channel auxiliary subunit epsilon
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
cation channel sperm-associated protein subunit epsilon
centrosomal protein 170, transcript variant X5
centrosomal protein 170, transcript variant X3
centrosomal protein 170, transcript variant X8
centrosomal protein 170, transcript variant X7
centrosomal protein 170, transcript variant X6
centrosomal protein 170, transcript variant X4
centrosomal protein 170, transcript variant X1
centrosomal protein 170, transcript variant X2
centrosomal protein of 170 kDa isoform X4
centrosomal protein of 170 kDa isoform X2
centrosomal protein of 170 kDa isoform X7
centrosomal protein of 170 kDa isoform X6
centrosomal protein of 170 kDa isoform X5
centrosomal protein of 170 kDa isoform X3
centrosomal protein of 170 kDa isoform X1
SHH signaling and ciliogenesis regulator SDCCAG8
serologically defined colon cancer antigen 8
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
RAC-gamma serine/threonine-protein kinase
zinc finger and BTB domain containing 18, transcript variant X2
zinc finger and BTB domain containing 18, transcript variant X1
zinc finger and BTB domain-containing protein 18 isoform X1
zinc finger and BTB domain-containing protein 18 isoform X2
phospholipase D family member 5, transcript variant X1
phospholipase D family member 5, transcript variant X2
microtubule associated protein 1 light chain 3 gamma
microtubule-associated proteins 1A/1B light chain 3C
similar to RNA sequence (same species):INSD:GGXP01054772.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 97 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 97 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
baculoviral IAP repeat containing 6, transcript variant X1
baculoviral IAP repeat containing 6, transcript variant X7
baculoviral IAP repeat containing 6, transcript variant X5
baculoviral IAP repeat containing 6, transcript variant X2
baculoviral IAP repeat containing 6, transcript variant X6
baculoviral IAP repeat containing 6, transcript variant X3
baculoviral IAP repeat containing 6, transcript variant X4
baculoviral IAP repeat containing 6, transcript variant X8
baculoviral IAP repeat-containing protein 6 isoform X1
baculoviral IAP repeat-containing protein 6 isoform X7
baculoviral IAP repeat-containing protein 6 isoform X5
baculoviral IAP repeat-containing protein 6 isoform X2
baculoviral IAP repeat-containing protein 6 isoform X6
baculoviral IAP repeat-containing protein 6 isoform X3
baculoviral IAP repeat-containing protein 6 isoform X4
baculoviral IAP repeat-containing protein 6 isoform X8
tetratricopeptide repeat domain 27, transcript variant X2
tetratricopeptide repeat domain 27, transcript variant X1
G patch domain-containing protein 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
HEAT repeat containing 5B, transcript variant X2
HEAT repeat containing 5B, transcript variant X1
HEAT repeat containing 5B, transcript variant X3
HEAT repeat-containing protein 5B isoform X1
HEAT repeat-containing protein 5B isoform X2
dpy-30 histone methyltransferase complex regulatory subunit, transcript variant X2
dpy-30 histone methyltransferase complex regulatory subunit, transcript variant X1
G2/M phase-specific E3 ubiquitin-protein ligase-like
similar to RNA sequence (same species):INSD:GGXP01040096.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 321 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 255 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
similar to RNA sequence (same species):INSD:GGXP01024265.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 939 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 793 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC122790942, transcript variant X2
uncharacterized LOC122790942, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
steroid 5 alpha-reductase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
3-oxo-5-alpha-steroid 4-dehydrogenase 2 isoform X2
steroid 5 alpha-reductase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
3-oxo-5-alpha-steroid 4-dehydrogenase 2 isoform X1
AT-hook containing transcription factor 1
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon GUU); 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: 6 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: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01071227.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 114 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 114 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
probable ATP-dependent RNA helicase DDX46
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
nuclear valosin-containing protein-like isoform X1
nuclear valosin-containing protein-like isoform X2
cornichon family AMPA receptor auxiliary protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 315 Proteins
WD repeat domain 26, transcript variant X2
WD repeat domain 26, transcript variant X8
WD repeat domain 26, transcript variant X4
WD repeat domain 26, transcript variant X3
WD repeat domain 26, transcript variant X7
WD repeat domain 26, transcript variant X6
WD repeat domain 26, transcript variant X1
WD repeat domain 26, transcript variant X5
WD repeat-containing protein 26 isoform X8
WD repeat-containing protein 26 isoform X6
WD repeat-containing protein 26 isoform X2
WD repeat-containing protein 26 isoform X4
WD repeat-containing protein 26 isoform X3
WD repeat-containing protein 26 isoform X1
WD repeat-containing protein 26 isoform X7
WD repeat-containing protein 26 isoform X5
cornichon family AMPA receptor auxiliary protein 3
gap junction alpha-4 protein-like, transcript variant X1
gap junction alpha-4 protein-like, transcript variant X3
gap junction alpha-4 protein-like, transcript variant X2
gap junction alpha-4 protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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 13 samples with support for all annotated introns
CAP-Gly domain containing linker protein family member 4
CAP-Gly domain-containing linker protein 4
dehydrogenase/reductase SDR family member 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122791131, transcript variant X2
uncharacterized LOC122791131, transcript variant X1
uncharacterized LOC122791131, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
cysteine rich transmembrane BMP regulator 1, transcript variant X2
cysteine rich transmembrane BMP regulator 1, transcript variant X1
cysteine-rich motor neuron 1 protein isoform X2
cysteine-rich motor neuron 1 protein isoform X1
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01025527.1
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 38 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
RAS guanyl releasing protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
RAS guanyl releasing protein 3, 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 6 samples with support for all annotated introns
ras guanyl-releasing protein 3 isoform X1
ras guanyl-releasing protein 3 isoform X2
latent transforming growth factor beta binding protein 1, transcript variant X3
latent transforming growth factor beta binding protein 1, transcript variant X1
latent transforming growth factor beta binding protein 1, transcript variant X2
latent transforming growth factor beta binding protein 1, transcript variant X5
latent transforming growth factor beta binding protein 1, transcript variant X4
latent-transforming growth factor beta-binding protein 1 isoform X2
latent-transforming growth factor beta-binding protein 1 isoform X3
latent-transforming growth factor beta-binding protein 1 isoform X1
latent-transforming growth factor beta-binding protein 1 isoform X5
latent-transforming growth factor beta-binding protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
fasciculation and elongation protein zeta 2, transcript variant X1
fasciculation and elongation protein zeta 2, transcript variant X2
fasciculation and elongation protein zeta-2 isoform X1
fasciculation and elongation protein zeta-2 isoform X2
5-methyltetrahydrofolate-homocysteine methyltransferase, transcript variant X2
5-methyltetrahydrofolate-homocysteine methyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
HEAT repeat containing 1, transcript variant X1
HEAT repeat containing 1, transcript variant X2
HEAT repeat-containing protein 1 isoform X1
HEAT repeat-containing protein 1 isoform X2
ribosomal oxygenase 1, transcript variant X2
ribosomal oxygenase 1, transcript variant X3
ribosomal oxygenase 1, transcript variant X1
cholinergic receptor muscarinic 3, transcript variant X6
cholinergic receptor muscarinic 3, transcript variant X1
cholinergic receptor muscarinic 3, transcript variant X2
cholinergic receptor muscarinic 3, transcript variant X3
cholinergic receptor muscarinic 3, transcript variant X4
cholinergic receptor muscarinic 3, transcript variant X5
coiled-coil domain-containing protein 177-like
gremlin 2, DAN family BMP antagonist, transcript variant X2
gremlin 2, DAN family BMP antagonist, transcript variant 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 1 sample 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 1 sample with support for all annotated introns
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
small integral membrane protein 12, transcript variant X1
small integral membrane protein 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122792481, transcript variant X1
uncharacterized LOC122792481, transcript variant X2
platelet-activating factor receptor-like, transcript variant X1
platelet-activating factor receptor-like, transcript variant X2
platelet-activating factor receptor-like
interferon alpha-inducible protein 27-like protein 2A
zinc finger MYM-type containing 4, transcript variant X4
zinc finger MYM-type containing 4, transcript variant X5
zinc finger MYM-type containing 4, transcript variant X7
zinc finger MYM-type containing 4, transcript variant X6
zinc finger MYM-type containing 4, transcript variant X2
zinc finger MYM-type containing 4, transcript variant X1
zinc finger MYM-type containing 4, transcript variant X9
zinc finger MYM-type containing 4, transcript variant X3
zinc finger MYM-type protein 4 isoform X6
zinc finger MYM-type protein 4 isoform X5
zinc finger MYM-type protein 4 isoform X2
zinc finger MYM-type protein 4 isoform X1
zinc finger MYM-type protein 4 isoform X3
zinc finger MYM-type protein 4 isoform X4
zinc finger MYM-type containing 4, transcript variant X8
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
zinc finger MYM-type protein 4 isoform X7
splicing factor proline and glutamine rich, transcript variant X3
splicing factor proline and glutamine rich, transcript variant X1
splicing factor proline and glutamine rich, transcript variant X2
splicing factor, proline- and glutamine-rich isoform X1
splicing factor, proline- and glutamine-rich isoform X2
similar to RNA sequence (same species):INSD:GGXP01011022.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 38 bases not found in genome assembly
coiled-coil domain-containing protein 107
transmembrane protein 35B, transcript variant X1
transmembrane protein 35B, transcript variant X2
dyslexia-associated protein KIAA0319-like protein homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
dyslexia-associated protein KIAA0319-like protein homolog isoform X2
transcription factor AP-2 epsilon, transcript variant X1
transcription factor AP-2 epsilon, transcript variant X3
transcription factor AP-2-epsilon isoform X1
transcription factor AP-2-epsilon isoform X3
transcription factor AP-2 epsilon, transcript variant X2
transcription factor AP-2 epsilon, transcript variant X4
transcription factor AP-2-epsilon isoform X2
transcription factor AP-2-epsilon isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
CDC42 binding protein kinase alpha, transcript variant X1
CDC42 binding protein kinase alpha, transcript variant X2
serine/threonine-protein kinase MRCK alpha isoform X1
serine/threonine-protein kinase MRCK alpha isoform X2
stum, mechanosensory transduction mediator homolog, transcript variant X2
stum, mechanosensory transduction mediator homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
replication stress response regulator SDE2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
CSC1-like protein 2, transcript variant X2
CSC1-like protein 2, transcript variant X3
CSC1-like protein 2, transcript variant X10
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
CSC1-like protein 2, transcript variant X11
CSC1-like protein 2, transcript variant X6
CSC1-like protein 2, transcript variant X1
uncharacterized protein LOC122791769 isoform X6
CSC1-like protein 2, transcript variant X4
CSC1-like protein 2, transcript variant X12
CSC1-like protein 2, transcript variant X7
CSC1-like protein 2, transcript variant X5
CSC1-like protein 2, transcript variant X8
CSC1-like protein 2, transcript variant X9
CSC1-like protein 2, transcript variant X13
similar to RNA sequence (same species):INSD:GGXP01052131.1
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.
signal recognition particle 9 kDa protein
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ENAH actin regulator, transcript variant X1
ENAH actin regulator, transcript variant X2
ENAH actin regulator, transcript variant X3
ENAH actin regulator, transcript variant X8
ENAH actin regulator, transcript variant X6
ENAH actin regulator, transcript variant X7
ENAH actin regulator, transcript variant X9
ENAH actin regulator, transcript variant X4
ENAH actin regulator, transcript variant X5
COORDINATES: nucleotide motif:Rfam:12.0:RF00607
delta(14)-sterol reductase LBR isoform X1
delta(14)-sterol reductase LBR isoform X2
delta(14)-sterol reductase LBR isoform X3
LOW QUALITY PROTEIN: dynein axonemal heavy chain 14
gap junction beta-4 protein-like, transcript variant X4
gap junction beta-4 protein-like, transcript variant X2
gap junction beta-4 protein-like, transcript variant X3
gap junction beta-4 protein-like, transcript variant X1
gap junction beta-4 protein-like, transcript variant X7
gap junction beta-4 protein-like, transcript variant X5
gap junction beta-4 protein-like, transcript variant X6
gap junction beta-4 protein-like, transcript variant X8
gap junction beta-3 protein-like, transcript variant X2
gap junction beta-3 protein-like, transcript variant X3
gap junction beta-3 protein-like, transcript variant X1
TOG array regulator of axonemal microtubules 2
TOG array regulator of axonemal microtubules protein 2
COORDINATES: nucleotide motif:Rfam:12.0:RF00325
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
tRNA (adenine(58)-N(1))-methyltransferase, mitochondrial
ribonucleoside-diphosphate reductase subunit M2-like, transcript variant X2
ribonucleoside-diphosphate reductase subunit M2-like, transcript variant X1
ribonucleoside-diphosphate reductase subunit M2-like isoform X1
ribonucleoside-diphosphate reductase subunit M2-like isoform X2
speedy/RINGO cell cycle regulator family member A, transcript variant X2
speedy/RINGO cell cycle regulator family member A, transcript variant X1
protein phosphatase 1 catalytic subunit beta, transcript variant X1
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X1
protein phosphatase 1 catalytic subunit beta, transcript variant X2
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X2
protein phosphatase 1 catalytic subunit beta, transcript variant X3
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X3
protein phosphatase 1 catalytic subunit beta, transcript variant X4
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X4
microtubule-actin cross-linking factor 1-like
similar to RNA sequence (same species):INSD:GGXP01026337.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 723 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 723 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: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
polyadenylate-binding protein 4-like, transcript variant X1
polyadenylate-binding protein 4-like isoform X1
polyadenylate-binding protein 4-like, transcript variant X2
polyadenylate-binding protein 4-like isoform X2
hairy/enhancer-of-split related with YRPW motif protein 2-like, transcript variant X1
hairy/enhancer-of-split related with YRPW motif-like protein isoform X1
hairy/enhancer-of-split related with YRPW motif protein 2-like, transcript variant X2
hairy/enhancer-of-split related with YRPW motif protein 2-like isoform X2
NADH:ubiquinone oxidoreductase subunit S5, transcript variant X1
NADH:ubiquinone oxidoreductase subunit S5, transcript variant X2
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5
antizyme inhibitor 2-like, transcript variant X2
antizyme inhibitor 2-like, transcript variant X1
adenylate kinase 2, transcript variant X1
adenylate kinase 2, transcript variant X2
adenylate kinase 2, mitochondrial isoform X2
adenylate kinase 2, mitochondrial isoform X1
ring finger protein 19B, transcript variant X1
ring finger protein 19B, transcript variant X2
transmembrane protein 54, transcript variant X1
transmembrane protein 54, transcript variant X2
transmembrane protein 54, transcript variant X3
neuron-specific calcium-binding protein hippocalcin
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tumor necrosis factor alpha-induced protein 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein K02A2.6-like
fibronectin type III domain containing 5
fibronectin type III domain-containing protein 5
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tyrosine--tRNA ligase, cytoplasmic-like, transcript variant X1
tyrosine--tRNA ligase, cytoplasmic-like, transcript variant X2
KIAA1522 ortholog, transcript variant X1
KIAA1522 ortholog, transcript variant X2
KIAA1522 ortholog, transcript variant X3
uncharacterized protein KIAA1522 homolog isoform X1
uncharacterized protein KIAA1522 homolog isoform X2
uncharacterized protein KIAA1522 homolog isoform X3
baculoviral IAP repeat-containing protein 5.1-like
syncoilin, intermediate filament protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
trafficking protein particle complex subunit 3, transcript variant X1
trafficking protein particle complex subunit 3, transcript variant X2
trafficking protein particle complex subunit 3 isoform X2
trafficking protein particle complex subunit 3 isoform X1
zinc finger and BTB domain containing 8 opposite strand, transcript variant X1
zinc finger and BTB domain containing 8 opposite strand, transcript variant X2
RB binding protein 4, chromatin remodeling factor
LOW QUALITY PROTEIN: histone-binding protein RBBP4
collagen type VIII alpha 2 chain, transcript variant X3
collagen type VIII alpha 2 chain, transcript variant X2
collagen type VIII alpha 2 chain, transcript variant X1
collagen type VIII alpha 2 chain, transcript variant X4
collagen type VIII alpha 2 chain, transcript variant X5
ADP-ribosylserine hydrolase, transcript variant X1
ADP-ribose glycohydrolase ARH3 isoform X1
ADP-ribosylserine hydrolase, transcript variant X2
ADP-ribose glycohydrolase ARH3 isoform X2
protein argonaute-1, transcript variant X1
protein argonaute-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01013877.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 133 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 133 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
zinc finger BED domain-containing protein 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
chromosome chr1.part2 C1orf216 homolog, transcript variant X2
chromosome chr1.part2 C1orf216 homolog, transcript variant X1
chromosome chr1.part2 C1orf216 homolog, transcript variant X3
general transcription factor II-I repeat domain-containing protein 2B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
stromal membrane-associated protein 2 isoform X1
stromal membrane-associated protein 2 isoform X2
regulating synaptic membrane exocytosis 3
regulating synaptic membrane exocytosis protein 3
CUB and sushi domain-containing protein 1-like
CUB and sushi domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transcription elongation factor A protein 3-like, transcript variant X3
transcription elongation factor A protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription elongation factor A protein 3-like, transcript variant X4
transcription elongation factor A protein 3-like, transcript variant X1
transcription elongation factor A protein 3-like isoform X3
transcription elongation factor A protein 3-like isoform X2
transcription elongation factor A protein 3-like isoform X4
transcription elongation factor A protein 3-like isoform X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3-like, transcript variant X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3-like isoform X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
methionine sulfoxide reductase A, transcript variant X1
methionine sulfoxide reductase A, transcript variant X2
mitochondrial peptide methionine sulfoxide reductase isoform X2
mitochondrial peptide methionine sulfoxide reductase isoform X1
YTH N6-methyladenosine RNA binding protein 2
glucocorticoid modulatory element binding protein 1, transcript variant X1
glucocorticoid modulatory element binding protein 1, transcript variant X4
glucocorticoid modulatory element binding protein 1, transcript variant X3
glucocorticoid modulatory element binding protein 1, transcript variant X2
glucocorticoid modulatory element-binding protein 1 isoform X4
glucocorticoid modulatory element-binding protein 1 isoform X3
glucocorticoid modulatory element-binding protein 1 isoform X2
glucocorticoid modulatory element-binding protein 1 isoform X1
discoidin, CUB and LCCL domain-containing protein 1-like
TATA-box binding protein associated factor 12
transcription initiation factor TFIID subunit 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
small nucleolar RNA SNORA16B/SNORA16A family
COORDINATES: nucleotide motif:Rfam:12.0:RF00190
COORDINATES: nucleotide motif:Rfam:12.0:RF00608
cbp/p300-interacting transactivator 3-like
COORDINATES: nucleotide motif:Rfam:12.0:RF01960
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
phosphatase and actin regulator 4-like, transcript variant X4
phosphatase and actin regulator 4-like, transcript variant X1
phosphatase and actin regulator 4-like, transcript variant X2
phosphatase and actin regulator 4-like, transcript variant X3
phosphatase and actin regulator 4-like isoform X3
phosphatase and actin regulator 4-like isoform X1
phosphatase and actin regulator 4-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01053739.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 452 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 452 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
interferon alpha-inducible protein 6-like
solute carrier family 22 member 13-like, transcript variant X1
solute carrier family 22 member 13-like, transcript variant X2
solute carrier family 22 member 13-like isoform X2
solute carrier family 22 member 6-B-like isoform X1
cAMP-dependent protein kinase inhibitor beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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 8 samples with support for all annotated introns
CD2-associated protein-like, transcript variant X2
CD2-associated protein-like, transcript variant X1
thyroid hormone receptor-associated protein 3-like
MAP7 domain-containing protein 1-like, transcript variant X2
MAP7 domain-containing protein 1-like, transcript variant X1
MAP7 domain-containing protein 1-like isoform X2
MAP7 domain-containing protein 1-like isoform X1
uncharacterized LOC122792266, transcript variant X2
uncharacterized LOC122792266, transcript variant X1
uncharacterized LOC122792266, transcript variant X3
extracellular calcium-sensing receptor-like
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
kinesin light chain 1-like, transcript variant X6
kinesin light chain 1-like, transcript variant X7
kinesin light chain 1-like, transcript variant X8
kinesin light chain 1-like, transcript variant X1
kinesin light chain 1-like, transcript variant X5
kinesin light chain 1-like, transcript variant X3
kinesin light chain 1-like, transcript variant X4
kinesin light chain 1-like, transcript variant X2
serum response factor, transcript variant X1
serum response factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
serum response factor, transcript variant X2
dual specificity phosphatase 23, transcript variant X2
dual specificity phosphatase 23, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: limb region 1 protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01049694.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 117 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 117 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
CD276 antigen-like, transcript variant X1
CD276 antigen-like, 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 11 samples with support for all annotated introns
platelet activating factor acetylhydrolase 2, transcript variant X7
platelet activating factor acetylhydrolase 2, transcript variant X6
platelet activating factor acetylhydrolase 2, transcript variant X4
platelet activating factor acetylhydrolase 2, transcript variant X1
platelet activating factor acetylhydrolase 2, transcript variant X3
platelet activating factor acetylhydrolase 2, transcript variant X2
platelet activating factor acetylhydrolase 2, transcript variant X5
platelet-activating factor acetylhydrolase 2, cytoplasmic isoform X2
platelet-activating factor acetylhydrolase 2, cytoplasmic isoform X1
putative postmeiotic segregation increased 2-like protein 3
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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
zinc transporter 2-like, transcript variant X1
zinc transporter 2-like, transcript variant X2
tripartite motif containing 63, transcript variant X1
tripartite motif containing 63, transcript variant X2
E3 ubiquitin-protein ligase TRIM63 isoform X1
E3 ubiquitin-protein ligase TRIM63 isoform X2
PDLIM1 interacting kinase 1 like, transcript variant X1
PDLIM1 interacting kinase 1 like, transcript variant X2
serine/threonine-protein kinase PDIK1L isoform X2
serine/threonine-protein kinase PDIK1L isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 41% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sperm acrosome membrane-associated protein 1
UDP-galactose-4-epimerase, transcript variant X1
UDP-galactose-4-epimerase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
hydroxymethylglutaryl-CoA lyase, mitochondrial
heterogeneous nuclear ribonucleoprotein R
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
small nucleolar RNA Z195/SNORD33/SNORD32 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00133
COORDINATES: nucleotide motif:Rfam:12.0:RF00147
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ATP synthase inhibitory factor subunit 1
low density lipoprotein receptor adaptor protein 1
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 13 samples with support for all annotated introns
low density lipoprotein receptor adapter protein 1
zinc finger C2HC-type containing 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger C2HC-type containing 1B, transcript variant X3
zinc finger C2HC-type containing 1B, transcript variant X1
zinc finger C2HC domain-containing protein 1B isoform X3
zinc finger C2HC domain-containing protein 1B isoform X2
zinc finger C2HC domain-containing protein 1B isoform X1
phosphatase and actin regulator 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
phosphatase and actin regulator 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
phosphatase and actin regulator 2-like isoform X2
phosphatase and actin regulator 2-like isoform X1
UTP11 small subunit processome component
probable U3 small nucleolar RNA-associated protein 11
transmembrane protein 50A, transcript variant X2
transmembrane protein 50A, transcript variant X1
arginine and serine rich protein 1, transcript variant X1
arginine and serine rich protein 1, transcript variant X2
arginine and serine rich protein 1, transcript variant X3
arginine and serine rich protein 1, transcript variant X5
arginine and serine rich protein 1, transcript variant X4
arginine/serine-rich protein 1 isoform X1
arginine/serine-rich protein 1 isoform X3
arginine/serine-rich protein 1 isoform X2
arginine and serine rich protein 1, transcript variant X6
arginine and serine rich protein 1, transcript variant X7
arginine/serine-rich protein 1 isoform X4
replication protein A2, transcript variant X4
replication protein A2, transcript variant X6
replication protein A2, transcript variant X2
replication protein A2, transcript variant X1
replication protein A2, transcript variant X5
replication protein A2, transcript variant X3
replication protein A 32 kDa subunit isoform X2
replication protein A 32 kDa subunit isoform X4
replication protein A 32 kDa subunit isoform X6
replication protein A 32 kDa subunit isoform X1
replication protein A 32 kDa subunit isoform X3
replication protein A 32 kDa subunit isoform X5
sphingomyelin phosphodiesterase acid like 3B
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 11 samples with support for all annotated introns
acid sphingomyelinase-like phosphodiesterase 3b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
EYA transcriptional coactivator and phosphatase 3, transcript variant X3
EYA transcriptional coactivator and phosphatase 3, transcript variant X2
EYA transcriptional coactivator and phosphatase 3, transcript variant X1
serine/threonine-protein kinase Sgk1-like
mitochondrial fission regulator 1 like, transcript variant X1
mitochondrial fission regulator 1 like, transcript variant X2
nuclear receptor coactivator 7-like, transcript variant X1
nuclear receptor coactivator 7-like isoform X1
nuclear receptor coactivator 7-like, transcript variant X2
nuclear receptor coactivator 7-like isoform X2
similar to RNA sequence (same species):INSD:GGXP01053992.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 204 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 204 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
similar to RNA sequence (same species):INSD:GGXP01002824.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 174 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 174 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
leucine zipper protein 1, transcript variant X1
leucine zipper protein 1, transcript variant X2
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein phosphatase 1 regulatory subunit 8
nuclear inhibitor of protein phosphatase 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00553
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns