Plectropomus leopardus isolate mb chromosome 21, YSFRI_Pleo_2.0, whole genome shotgun sequence.
Plectropomus leopardus (leopard coralgrouper)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Neoteleostei; Acanthomorphata; Eupercaria; Perciformes; Serranoidei; Serranidae; Epinephelinae; Epinephelini; Plectropomus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM018428.2.\nAssembly name: YSFRI_Pleo_2.0\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Yellow Sea Fisheries Research\nInstitute, Chinese Academy of Fishery Sciences on 2020/05/27. The\noriginal whole-genome shotgun project has the accession\nVJNF00000000.2.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Yellow Sea Fisheries Research Institute,\n Chinese Academy of Fishery Sciences\nAssembly Method :: Supernova v. 1.2.4\nAssembly Name :: YSFRI_Pleo_2.0\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 381.0x\nSequencing Technology :: PacBio\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plectropomus leopardus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
ras responsive element binding protein 1a
COORDINATES: polyA evidence [ECO:0006239]
ras-responsive element-binding protein 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, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 36% 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
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: enoyl-CoA delta isomerase 2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
glutaminase liver isoform, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: succinate--hydroxymethylglutarate CoA-transferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 128 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tubulin, beta 6 class V
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
uncharacterized protein C18orf63, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C18orf63, transcript variant X2
uncharacterized protein C18orf63 isoform X1
uncharacterized protein C18orf63 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
protein phosphatase 1 regulatory subunit 3G
phenylalanyl-tRNA synthetase 2, mitochondrial
phenylalanine--tRNA ligase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
sodium channel protein type 3 subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
caspase recruitment domain-containing protein 8-like, transcript variant X1
caspase recruitment domain-containing protein 8-like, transcript variant X2
caspase recruitment domain-containing protein 8-like isoform X1
caspase recruitment domain-containing protein 8-like isoform X2
sodium channel protein type 5 subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
calponin homology domain-containing protein DDB_G0272472-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized abhydrolase domain-containing protein DDB_G0269086-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
GTPase IMAP family member 2-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 3 samples with support for all annotated introns
GTPase IMAP family member 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
GTPase IMAP family member 2-like, transcript variant X2
GTPase IMAP family member 6-like isoform X1
immune-associated nucleotide-binding protein 8-like isoform X3
GTPase IMAP family member 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
enhancer of zeste 2 polycomb repressive complex 2 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: polyhomeotic-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable cationic amino acid transporter, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable cationic amino acid transporter, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable cationic amino acid transporter
eukaryotic translation initiation factor 5A-1-like
traf2 and NCK-interacting protein kinase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
kelch-like family member 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kelch-like family member 15, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 20 Proteins, and 95% 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: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
MAP7 domain-containing protein 2-like, transcript variant X1
MAP7 domain-containing protein 2-like, transcript variant X2
MAP7 domain-containing protein 2-like, transcript variant X3
MAP7 domain-containing protein 2-like, transcript variant X4
MAP7 domain-containing protein 2-like, transcript variant X5
MAP7 domain-containing protein 2-like isoform X1
MAP7 domain-containing protein 2-like isoform X2
MAP7 domain-containing protein 2-like isoform X3
MAP7 domain-containing protein 2-like isoform X4
MAP7 domain-containing protein 2-like isoform X5
uncharacterized protein LOC503771 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tumor necrosis factor ligand superfamily member 10
neutral cholesterol ester hydrolase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: calcium-binding protein P-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase RNF31-like
LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: U6 snRNA-associated Sm-like protein LSm5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
late secretory pathway protein AVL9 homolog
kelch repeat and BTB (POZ) domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kelch repeat and BTB domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
drosha ribonuclease III, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
drosha ribonuclease III, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
drosha ribonuclease III, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cadherin 10, type 2a (T2-cadherin), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cadherin 10, type 2a (T2-cadherin), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 15% 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
enhancer of polycomb homolog 1-like, transcript variant X2
enhancer of polycomb homolog 1-like isoform X2
enhancer of polycomb homolog 1-like, transcript variant X3
enhancer of polycomb homolog 1-like, transcript variant X1
enhancer of polycomb homolog 1-like isoform X1
enhancer of polycomb homolog 1-like isoform X3
collagen alpha-1(XVIII) chain-like, transcript variant X1
collagen alpha-1(XVIII) chain-like, transcript variant X2
collagen alpha-1(XVIII) chain-like isoform X1
collagen alpha-1(XVIII) chain-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
gamma-glutamyl hydrolase (conjugase, folylpolygammaglutamyl hydrolase)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dipeptidyl aminopeptidase-like protein 6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 6 bases in 4 codons; deleted 3 bases in 2 codons; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 6 bases in 4 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: serine-rich adhesin for platelets
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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphate regulating endopeptidase homolog, X-linked, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphate regulating endopeptidase homolog, X-linked, 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 1 sample with support for all annotated introns
phosphate-regulating neutral endopeptidase PHEX isoform X1
phosphate-regulating neutral endopeptidase PHEX isoform X2
membrane-bound transcription factor peptidase, site 2
membrane-bound transcription factor site-2 protease
small muscle protein X-linked, transcript variant X2
small muscle protein X-linked, transcript variant X3
small muscle protein X-linked, 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
connector enhancer of kinase suppressor of Ras 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
connector enhancer of kinase suppressor of Ras 2a, transcript variant X1
connector enhancer of kinase suppressor of ras 2 isoform X2
connector enhancer of kinase suppressor of ras 2 isoform X1
toll-like receptor 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
toll-like receptor 13, transcript variant X2
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, including 3 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 15
SH3-domain kinase binding protein 1, transcript variant X1
SH3-domain kinase binding protein 1, transcript variant X2
SH3 domain-containing kinase-binding protein 1 isoform X2
SH3 domain-containing kinase-binding protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 84% coverage of the annotated genomic feature by RNAseq alignments
rho GTPase-activating protein 21-like, transcript variant X4
rho GTPase-activating protein 21-like, transcript variant X3
rho GTPase-activating protein 21-like, transcript variant X2
rho GTPase-activating protein 21-like, transcript variant X1
rho GTPase-activating protein 21-like, transcript variant X5
rho GTPase-activating protein 21-like isoform X4
rho GTPase-activating protein 21-like isoform X3
rho GTPase-activating protein 21-like isoform X2
rho GTPase-activating protein 21-like isoform X1
rho GTPase-activating protein 21-like isoform X5
phosphoribosyl transferase domain containing 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphoribosyltransferase domain-containing protein 1
enkurin, TRPC channel interacting protein
patched domain-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
hydroxyacyl-coenzyme A dehydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tripartite motif-containing protein 16-like
glutamate decarboxylase 2, transcript variant X2
glutamate decarboxylase 2, transcript variant X1
amyloid beta (A4) precursor protein-binding, family B, member 1 interacting protein
amyloid beta A4 precursor protein-binding family B member 1-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
prenyl (decaprenyl) diphosphate synthase, subunit 1
decaprenyl-diphosphate synthase subunit 1
abl-interactor 1a, transcript variant X8
abl-interactor 1a, transcript variant X7
abl-interactor 1a, transcript variant X4
abl-interactor 1a, transcript variant X6
abl-interactor 1a, transcript variant X2
abl-interactor 1a, transcript variant X3
abl-interactor 1a, transcript variant X1
abl-interactor 1a, transcript variant X5
acyl-CoA-binding domain-containing protein 5A
uncharacterized LOC121960677, transcript variant X1
uncharacterized LOC121960677, transcript variant X2
microtubule associated serine/threonine kinase-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, including 3 samples with support for all annotated introns
serine/threonine-protein kinase greatwall
ATP-dependent zinc metalloprotease YME1L1-like, transcript variant X1
ATP-dependent zinc metalloprotease YME1L1-like, transcript variant X2
ATP-dependent zinc metalloprotease YME1L1-like isoform X1
ATP-dependent zinc metalloprotease YME1L1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
highly reducing polyketide synthase cm3B
highly reducing polyketide synthase pks5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
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
RNA-binding Raly-like protein, 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 2 samples with support for all annotated introns
RNA-binding Raly-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RNA-binding Raly-like protein isoform X2
RNA-binding Raly-like protein isoform X1
uncharacterized protein LOC553663 homolog, transcript variant X4
v-ral simian leukemia viral oncogene homolog Aa (ras related), transcript variant X2
v-ral simian leukemia viral oncogene homolog Aa (ras related), transcript variant X1
uncharacterized protein LOC553663 homolog, transcript variant X3
mediator of RNA polymerase II transcription subunit 1 isoform X3
uncharacterized protein LOC553663 homolog, transcript variant X2
uncharacterized protein LOC553663 homolog, transcript variant X1
mediator of RNA polymerase II transcription subunit 1 isoform X1
mediator of RNA polymerase II transcription subunit 1 isoform X2
mediator of RNA polymerase II transcription subunit 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
cadherin 19, type 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cadherin 19, type 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pre-mRNA processing factor 4Bb, transcript variant X1
pre-mRNA processing factor 4Bb, transcript variant X2
pre-mRNA processing factor 4Bb isoform X1
pre-mRNA processing factor 4Bb isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine zipper transcription factor-like 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 2 samples with support for all annotated introns
leucine zipper transcription factor-like protein 1
dnaJ homolog subfamily C member 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dnaJ homolog subfamily C member 13, transcript variant X1
dnaJ homolog subfamily C member 13, transcript variant X3
dnaJ homolog subfamily C member 13, transcript variant X4
dnaJ homolog subfamily C member 13, transcript variant X5
dnaJ homolog subfamily C member 13, transcript variant X6
dnaJ homolog subfamily C member 13, transcript variant X7
dnaJ homolog subfamily C member 13 isoform X1
dnaJ homolog subfamily C member 13 isoform X2
dnaJ homolog subfamily C member 13 isoform X3
dnaJ homolog subfamily C member 13 isoform X4
dnaJ homolog subfamily C member 13 isoform X5
dnaJ homolog subfamily C member 13 isoform X6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DNA topoisomerase 2-binding protein 1
carnitine deficiency-associated gene expressed in ventricle 3, transcript variant X1
carnitine deficiency-associated gene expressed in ventricle 3, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: protein scribble homolog
poly(U)-binding-splicing factor PUF60-like, transcript variant X3
poly(U)-binding-splicing factor PUF60-like, transcript variant X8
poly(U)-binding-splicing factor PUF60-like, transcript variant X6
poly(U)-binding-splicing factor PUF60-like, transcript variant X7
poly(U)-binding-splicing factor PUF60-like, transcript variant X5
poly(U)-binding-splicing factor PUF60-like, transcript variant X2
poly(U)-binding-splicing factor PUF60-like, transcript variant X1
poly(U)-binding-splicing factor PUF60-like, transcript variant X4
poly(U)-binding-splicing factor PUF60-like isoform X7
poly(U)-binding-splicing factor PUF60-like isoform X5
poly(U)-binding-splicing factor PUF60-like isoform X6
poly(U)-binding-splicing factor PUF60-like isoform X4
poly(U)-binding-splicing factor PUF60-like isoform X2
poly(U)-binding-splicing factor PUF60-like isoform X1
poly(U)-binding-splicing factor PUF60-like isoform X3
uncharacterized protein LOC100536977 homolog
uncharacterized protein si:ch1073-406l10.2
solute carrier family 4 member 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 4 member 2b, transcript variant X1
solute carrier family 4 member 2b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier family 4 member 2b, transcript variant X3
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 1 sample with support for all annotated introns
solute carrier family 4 member 2b, transcript variant X4
uncharacterized protein si:ch73-173p19.1
ATP-binding cassette sub-family F member 2
chondroitin sulfate glucuronyltransferase
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3b, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3b, transcript variant X5
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3b, transcript variant X1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3b, transcript variant X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3b isoform X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3b isoform X6
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3b isoform X5
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3b isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3b isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3b isoform X4
nuclear transcription factor, X-box binding 1
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1b, transcript variant X3
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1b, transcript variant X1
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1b, transcript variant X4
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1b, transcript variant X2
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1b, transcript variant X5
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X3
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X4
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
family with sequence similarity 49 member Bb, transcript variant X1
family with sequence similarity 49 member Bb, transcript variant X2
transcriptional regulator Myc-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcriptional regulator Myc-like, transcript variant X1
OTU deubiquitinase with linear linkage specificity a
LOW QUALITY PROTEIN: OTU deubiquitinase with linear linkage specificity a
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
POU domain, class 6, transcription factor 2
VPS41 subunit of HOPS complex, transcript variant X1
VPS41 subunit of HOPS complex, transcript variant X2
vacuolar protein sorting-associated protein 41 homolog isoform X1
vacuolar protein sorting-associated protein 41 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
39S ribosomal protein L15, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myosin regulatory light chain 2, smooth muscle minor isoform
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
structural maintenance of chromosomes flexible hinge domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes flexible hinge domain-containing protein 1
N(6)-adenine-specific methyltransferase METTL4
adenylate cyclase activating polypeptide 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 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: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc transporter ZIP12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc transporter ZIP12-like, transcript variant X2
calcium channel, voltage-dependent, beta 2a, transcript variant X1
voltage-dependent L-type calcium channel subunit beta-2a isoform X1
calcium channel, voltage-dependent, beta 2a, transcript variant X2
voltage-dependent L-type calcium channel subunit beta-2a isoform X2
NOP2/Sun RNA methyltransferase 6, transcript variant X1
NOP2/Sun RNA methyltransferase 6, transcript variant X2
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6
ADP-ribosylation factor-like 8, transcript variant X1
ADP-ribosylation factor-like 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADP-ribosylation factor-like 8 isoform X1
ADP-ribosylation factor-like 8 isoform X2
MAF1 homolog, negative regulator of RNA polymerase III b
transfer RNA arginine (anticodon CCG); 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MAM and LDL receptor class A domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
MAM and LDL-receptor class A domain-containing protein 1
leucine-rich repeat-containing protein 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
cytoplasmic dynein 2 intermediate chain 1
non-SMC condensin II complex, subunit G2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: condensin-2 complex subunit G2
protein tyrosine phosphatase receptor type N2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase N2
DnaJ heat shock protein family (Hsp40) member B6b, transcript variant X1
DnaJ heat shock protein family (Hsp40) member B6b, transcript variant X2
motor neuron and pancreas homeobox protein 1
nucleolar MIF4G domain-containing protein 1
ring finger protein 32, transcript variant X1
ring finger protein 32, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RNA binding motif protein 33a, transcript variant X2
RNA binding motif protein 33a, transcript variant X3
RNA binding motif protein 33a, transcript variant X1
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: 22 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: homeobox protein engrailed-2a
5-hydroxytryptamine (serotonin) receptor 5A, genome duplicate b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
discs, large (Drosophila) homolog-associated protein 1b
sickle tail protein, transcript variant X6
sickle tail protein, transcript variant X1
sickle tail protein, transcript variant X5
sickle tail protein, transcript variant X2
sickle tail protein, transcript variant X4
sickle tail protein, transcript variant X3
sickle tail protein, transcript variant X9
sickle tail protein, transcript variant X7
sickle tail protein, transcript variant X8
uracil nucleotide/cysteinyl leukotriene receptor
ubiquitin-like modifier activating enzyme 5
ubiquitin-like modifier-activating enzyme 5
acyl-CoA dehydrogenase family, member 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA dehydrogenase family, member 11, transcript variant X2
acyl-CoA dehydrogenase family member 11 isoform X1
acyl-CoA dehydrogenase family member 11 isoform X2
U2 snRNP-associated SURP domain containing, transcript variant X2
U2 snRNP-associated SURP domain containing, transcript variant X1
U2 snRNP-associated SURP motif-containing protein isoform X1
U2 snRNP-associated SURP motif-containing protein isoform X2
transient receptor potential cation channel, subfamily C, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
short transient receptor potential channel 1
carbohydrate (N-acetylglucosamine-6-O) sulfotransferase 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2
procollagen-lysine,2-oxoglutarate 5-dioxygenase 2
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
zic family member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zic family member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zic family member 1 (odd-paired homolog, Drosophila), 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 2 samples with support for all annotated introns
zic family member 1 (odd-paired homolog, Drosophila), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
glycogenin-1-like, transcript variant X1
glycogenin-1-like, transcript variant X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like
NCK adaptor protein 1b, transcript variant X1
NCK adaptor protein 1b, transcript variant X2
Golgi reassembly-stacking protein 1-like, transcript variant X2
Golgi reassembly-stacking protein 1-like, transcript variant X1
Golgi reassembly-stacking protein 1-like isoform X2
Golgi reassembly-stacking protein 1-like isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
cysteine-serine-rich nuclear protein 1b, transcript variant X2
cysteine-serine-rich nuclear protein 1b, transcript variant X1
cysteine/serine-rich nuclear protein 1b isoform X1
cysteine/serine-rich nuclear protein 1b isoform X2
xin actin-binding repeat-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
LIM domain-containing protein isoform X2
xin actin-binding repeat-containing protein 1, transcript variant X1
LIM domain-containing protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
oxidative stress responsive kinase 1b, transcript variant X2
oxidative stress responsive kinase 1b, transcript variant X1
serine/threonine-protein kinase OSR1b isoform X2
serine/threonine-protein kinase OSR1b isoform X1
MYD88 innate immune signal transduction adaptor
myeloid differentiation primary response protein MyD88
mitogen-activated protein kinase kinase kinase 22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DLEC1 cilia and flagella associated protein
deleted in lung and esophageal cancer protein 1
phospholipase C, delta 1a, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1a isoform X2
phospholipase C, delta 1a, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1a isoform X1
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase-like a, 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 2 samples with support for all annotated introns
CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase-like a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase-like a isoform X2
CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase-like a isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: glycine--tRNA ligase-like
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF01229
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and BTB domain containing 47b
zinc finger and BTB domain-containing protein 47
LOW QUALITY PROTEIN: NK-tumor recognition protein
SEC22 homolog C, vesicle trafficking protein, transcript variant X2
SEC22 homolog C, vesicle trafficking protein, transcript variant X1
vesicle-trafficking protein SEC22c isoform X1
vesicle-trafficking protein SEC22c isoform X2
vasoactive intestinal peptide receptor 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
vasoactive intestinal polypeptide receptor 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 59% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein si:ch211-161h7.5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
family with sequence similarity 162 member A, transcript variant X2
family with sequence similarity 162 member A, transcript variant X1
mitochondrial matrix import factor 23, transcript variant X1
mitochondrial matrix import factor 23, transcript variant X2
uncharacterized LOC121960835, transcript variant X2
uncharacterized LOC121960835, transcript variant X1
leukocyte cysteine proteinase inhibitor 1-like
thiosulfate:glutathione sulfurtransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X2
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X2
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 191
zinc finger DHHC-type palmitoyltransferase 23b
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
V-type proton ATPase catalytic subunit A
N-alpha-acetyltransferase 50, NatE catalytic subunit, transcript variant X1
N-alpha-acetyltransferase 50, NatE catalytic subunit, transcript variant X2
basic helix-loop-helix domain-containing protein USF3
BOC cell adhesion associated, oncogene regulated
spindle and centriole associated protein 1, transcript variant X2
spindle and centriole associated protein 1, transcript variant X1
spindle and centriole-associated protein 1 isoform X2
spindle and centriole-associated protein 1 isoform X1
ATPase phospholipid transporting 8A2, transcript variant X2
ATPase phospholipid transporting 8A2, transcript variant X3
ATPase phospholipid transporting 8A2, transcript variant X1
phospholipid-transporting ATPase IB isoform X2
phospholipid-transporting ATPase IB isoform X3
phospholipid-transporting ATPase IB isoform X1
wiskott-Aldrich syndrome protein family member 3b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 12A
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 3 samples with support for all annotated introns
ureidoimidazoline (2-oxo-4-hydroxy-4-carboxy-5-) decarboxylase
2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase
receptor-type tyrosine-protein kinase FLT3
poly(A) specific ribonuclease subunit PAN3
PAN2-PAN3 deadenylation complex subunit PAN3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vascular endothelial growth factor receptor 1
suppressor of tumorigenicity 14 protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis associated 13, transcript variant X1
spermatogenesis associated 13, transcript variant X2
spermatogenesis-associated protein 13 isoform X1
spermatogenesis-associated protein 13 isoform X2
complement C1q and tumor necrosis factor-related protein 9A
abhydrolase domain containing 10, depalmitoylase b
YTH N(6)-methyladenosine RNA binding protein 3
basic helix-loop-helix family, member e22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
class E basic helix-loop-helix protein 22
armadillo repeat containing 1, transcript variant X3
armadillo repeat containing 1, transcript variant X2
armadillo repeat containing 1, transcript variant X1
phosphodiesterase 7A, transcript variant X3
phosphodiesterase 7A, transcript variant X2
phosphodiesterase 7A, transcript variant X1
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X2
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X1
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X3
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tripartite motif containing 55b, transcript variant X1
tripartite motif containing 55b, transcript variant X2
tripartite motif-containing protein 55b isoform X1
tripartite motif-containing protein 55b isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ribosome biogenesis regulatory protein homolog
v-myb avian myeloblastosis viral oncogene homolog-like 1, transcript variant X2
v-myb avian myeloblastosis viral oncogene homolog-like 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
v-myb avian myeloblastosis viral oncogene homolog-like 1, transcript variant X1
serum/glucocorticoid regulated kinase family member 3
minichromosome maintenance domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase Sgk3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein phosphatase 1, regulatory subunit 42
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1 regulatory subunit 42
centrosome and spindle pole-associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor guanine nucleotide-exchange factor 1 (brefeldin A-inhibited), transcript variant X2
ADP-ribosylation factor guanine nucleotide-exchange factor 1 (brefeldin A-inhibited), transcript variant X1
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X2
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol-3,4, 5-trisphosphate-dependent Rac exchange factor 2
phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
extracellular sulfatase Sulf-1 isoform X5
extracellular sulfatase Sulf-1 isoform X1
extracellular sulfatase Sulf-1 isoform X3
extracellular sulfatase Sulf-1 isoform X2
extracellular sulfatase Sulf-1 isoform X4
solute carrier organic anion transporter family member 5A1, transcript variant X1
solute carrier organic anion transporter family member 5A1, transcript variant X2
solute carrier organic anion transporter family member 5A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
nuclear receptor coactivator 2, transcript variant X2
nuclear receptor coactivator 2, transcript variant X3
nuclear receptor coactivator 2, transcript variant X1
nuclear receptor coactivator 2 isoform X2
nuclear receptor coactivator 2 isoform X1
translocation associated membrane protein 1
translocating chain-associated membrane protein 1
XK, Kell blood group complex subunit-related family, member 9
EYA transcriptional coactivator and phosphatase 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 1 sample with support for all annotated introns
EYA transcriptional coactivator and phosphatase 1, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
EYA transcriptional coactivator and phosphatase 1, transcript variant X12
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
EYA transcriptional coactivator and phosphatase 1, transcript variant X13
EYA transcriptional coactivator and phosphatase 1, transcript variant X11
EYA transcriptional coactivator and phosphatase 1, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
EYA transcriptional coactivator and phosphatase 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
EYA transcriptional coactivator and phosphatase 1, transcript variant X6
EYA transcriptional coactivator and phosphatase 1, transcript variant X5
EYA transcriptional coactivator and phosphatase 1, transcript variant X8
EYA transcriptional coactivator and phosphatase 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
EYA transcriptional coactivator and phosphatase 1, transcript variant X4
EYA transcriptional coactivator and phosphatase 1, transcript variant X1
EYA transcriptional coactivator and phosphatase 1, transcript variant X3
EYA transcriptional coactivator and phosphatase 1, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transient receptor potential cation channel, subfamily A, member 1b
transient receptor potential cation channel subfamily A member 1b
potassium voltage-gated channel subfamily B member 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily B member 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel subfamily B member 2
telomeric repeat binding factor (NIMA-interacting) 1
somatomedin-B and thrombospondin type-1 domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein si:ch211-171b20.3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
myosin VIIA and Rab interacting protein b, transcript variant X6
myosin VIIA and Rab interacting protein b, 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 1 sample with support for all annotated introns
myosin VIIA and Rab interacting protein b, transcript variant X5
myosin VIIA and Rab interacting protein b, transcript variant X4
myosin VIIA and Rab interacting protein b, transcript variant X7
myosin VIIA and Rab interacting protein b, transcript variant X1
myosin VIIA and Rab interacting protein b, transcript variant X2
NADH:ubiquinone oxidoreductase subunit B4
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4
phosphate cytidylyltransferase 1B, choline a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
choline-phosphate cytidylyltransferase B isoform X1
phosphate cytidylyltransferase 1B, choline a, 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 1 sample with support for all annotated introns
choline-phosphate cytidylyltransferase B isoform X2
pyruvate dehydrogenase kinase, isozyme 3a
pyruvate dehydrogenase (acetyl-transferring) kinase isozyme 3, mitochondrial
organic solute transporter subunit alpha
arylamine N-acetyltransferase, pineal gland isozyme NAT-10-like
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
E3 ubiquitin-protein ligase MARCHF6-like
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase MARCHF6-like
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
carboxymethylenebutenolidase homolog (Pseudomonas)
chaperonin containing TCP1, subunit 5 (epsilon)
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X2
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
methionine synthase reductase isoform X1
methionine synthase reductase isoform X2
uncharacterized LOC121960673, transcript variant X2
uncharacterized LOC121960673, transcript variant X1
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A, transcript variant X1
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A, transcript variant X2
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein si:dkey-118j18.2
translocase of inner mitochondrial membrane 21
mitochondrial import inner membrane translocase subunit Tim21-like
neuropilin (NRP) and tolloid (TLL)-like 1, like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: suppressor of cytokine signaling 6
docking protein 6, transcript variant X2
docking protein 6, transcript variant X1
cysteine-rich secretory protein LCCL domain containing 1a
cysteine-rich secretory protein LCCL domain-containing 1
peptidase inhibitor 15a, transcript variant X1
peptidase inhibitor 15a, transcript variant X2
ganglioside induced differentiation associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ganglioside-induced differentiation-associated protein 1
ubiquitin-conjugating enzyme E2 W, transcript variant X2
ubiquitin-conjugating enzyme E2 W isoform X2
ubiquitin-conjugating enzyme E2 W, transcript variant X1
ubiquitin-conjugating enzyme E2 W isoform X1
staufen double-stranded RNA binding protein 2
double-stranded RNA-binding protein Staufen homolog 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00581
ranBP-type and C3HC4-type zinc finger-containing protein 1-like
LOW QUALITY PROTEIN: ranBP-type and C3HC4-type zinc finger-containing protein 1-like
protein phosphatase 1, regulatory subunit 16A, transcript variant X1
protein phosphatase 1, regulatory subunit 16A, transcript variant X2
protein phosphatase 1 regulatory subunit 16A
protein disulfide isomerase family A, member 4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 60% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: polycystic kidney disease 1 like 1
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X1
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X2
LOW QUALITY PROTEIN: uncharacterized protein LOC121960983
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol-5-phosphate 4-kinase, type II, alpha a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphatidylinositol-5-phosphate 4-kinase, type II, alpha a, transcript variant X1
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X2
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
methionine-R-sulfoxide reductase B2, mitochondrial
complement component 8, gamma polypeptide
complement C1q tumor necrosis factor-related protein 3-like
thiamin pyrophosphokinase 1, transcript variant X1
thiamin pyrophosphokinase 1, transcript variant X4
thiamin pyrophosphokinase 1, transcript variant X3
thiamin pyrophosphokinase 1, transcript variant X2
uncharacterized protein LOC553712 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC100150965 homolog, transcript variant X2
uncharacterized protein LOC100150965 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tumor necrosis factor receptor superfamily, member 11a, NFKB activator
tumor necrosis factor receptor superfamily member 11A
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X4
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X3
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X2
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X1
RAB11-binding protein RELCH homolog isoform X4
RAB11-binding protein RELCH homolog isoform X3
RAB11-binding protein RELCH homolog isoform X2
RAB11-binding protein RELCH homolog isoform X1
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X5
phosphatidylinositol glycan anchor biosynthesis, class N, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis, class N, transcript variant X2
GPI ethanolamine phosphate transferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
peroxisomal biogenesis factor 2, transcript variant X3
peroxisomal biogenesis factor 2, transcript variant X4
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 3 samples with support for all annotated introns
peroxisomal biogenesis factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
peroxisome biogenesis factor 2 isoform X2
peroxisome biogenesis factor 2 isoform X3
peroxisome biogenesis factor 2 isoform X4
peroxisomal biogenesis factor 2, transcript variant X1
peroxisome biogenesis factor 2 isoform X1
LOW QUALITY PROTEIN: zinc finger homeobox protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
rhophilin associated tail protein 1-like, transcript variant X2
rhophilin associated tail protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat domain-containing protein 33B
catenin (cadherin-associated protein), delta 2a
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121960805, transcript variant X2
uncharacterized LOC121960805, transcript variant X1
zinc finger, C2HC-type containing 1A, transcript variant X2
zinc finger, C2HC-type containing 1A, transcript variant X1
zinc finger C2HC domain-containing protein 1A isoform X2
zinc finger C2HC domain-containing protein 1A isoform X1
cAMP-dependent protein kinase inhibitor alpha, transcript variant X1
cAMP-dependent protein kinase inhibitor alpha, transcript variant X2
cAMP-dependent protein kinase inhibitor alpha
pleckstrin homology-like domain, family B, member 2b, transcript variant X2
pleckstrin homology-like domain, family B, member 2b, transcript variant X3
pleckstrin homology-like domain, family B, member 2b, transcript variant X1
pleckstrin homology-like domain, family B, member 2b, transcript variant X4
pleckstrin homology-like domain family B member 1 isoform X2
pleckstrin homology-like domain family B member 2 isoform X3
pleckstrin homology-like domain family B member 2 isoform X1
pleckstrin homology-like domain family B member 2 isoform X4
phosphatidylinositol-specific phospholipase C, X domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
male germ cell-associated kinase, transcript variant X3
male germ cell-associated kinase, transcript variant X1
male germ cell-associated kinase, transcript variant X5
male germ cell-associated kinase, transcript variant X4
serine/threonine-protein kinase MAK isoform X3
serine/threonine-protein kinase MAK isoform X1
male germ cell-associated kinase, transcript variant X2
serine/threonine-protein kinase MAK isoform X2
transcription factor AP-2 alpha, transcript variant X2
transcription factor AP-2-alpha isoform X2
transcription factor AP-2 alpha, transcript variant X1
transcription factor AP-2-alpha isoform X1
transcription factor AP-2 alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription factor AP-2-alpha isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 7% coverage of the annotated genomic feature by RNAseq alignments
adenosine 3'-phospho 5'-phosphosulfate transporter 2
eukaryotic translation elongation factor 1 epsilon 1
eukaryotic translation elongation factor 1 epsilon-1
biogenesis of lysosomal organelles complex-1, subunit 5, muted, transcript variant X2
biogenesis of lysosomal organelles complex-1, subunit 5, muted, transcript variant X1
biogenesis of lysosome-related organelles complex 1 subunit 5
uncharacterized protein LOC449822 homolog
LOW QUALITY PROTEIN: probable enoyl-CoA hydratase
programmed cell death 6, transcript variant X1
programmed cell death 6, transcript variant X2
programmed cell death protein 6 isoform X2
programmed cell death protein 6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC556372 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein si:ch211-196f5.2
LOW QUALITY PROTEIN: sialic acid-binding Ig-like lectin 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphoenolpyruvate carboxykinase 2 (mitochondrial)
phosphoenolpyruvate carboxykinase [GTP], mitochondrial
fat storage-inducing transmembrane protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thiamine triphosphatase, transcript variant X2
thiamine triphosphatase, transcript variant X1
zinc finger homeobox 2, transcript variant X2
zinc finger homeobox protein 3 isoform X2
zinc finger homeobox 2, transcript variant X1
zinc finger homeobox protein 3 isoform X1
poly(A) binding protein, nuclear 1, transcript variant X1
poly(A) binding protein, nuclear 1, transcript variant X2
polyadenylate-binding protein 2 isoform X1
polyadenylate-binding protein 2 isoform X2
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon CGA); 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: 215 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
receptor activity-modifying protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
matrix metalloproteinase-16-like, transcript variant X1
matrix metalloproteinase-16-like, transcript variant X2
matrix metalloproteinase-16-like isoform X1
matrix metalloproteinase-16-like isoform X2
cyclic nucleotide-gated cation channel beta-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
neutral sphingomyelinase (N-SMase) activation associated factor
transmembrane protein 241, transcript variant X1
transmembrane protein 241, transcript variant X4
transmembrane protein 241, transcript variant X3
transmembrane protein 241, transcript variant X2
transmembrane protein 241, transcript variant X5
retinoblastoma binding protein 8, transcript variant X2
retinoblastoma binding protein 8, transcript variant X1
family with sequence similarity 168 member B, transcript variant X2
family with sequence similarity 168 member B, transcript variant X1
family with sequence similarity 168 member B, transcript variant X3
myelin-associated neurite-outgrowth inhibitor
negative regulator of reactive oxygen species
transforming growth factor beta activator LRRC33
crystallin J1A-like, transcript variant X1
crystallin J1A-like, transcript variant 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; deleted 1 base in 1 codon
LOW QUALITY PROTEIN: guanine nucleotide exchange factor VAV3
RNA-binding region (RNP1, RRM) containing 3, transcript variant X1
RNA-binding region (RNP1, RRM) containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121960449, transcript variant X2
uncharacterized LOC121960449, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retinal-specific phospholipid-transporting ATPase ABCA4-like
LOW QUALITY PROTEIN: retinal-specific phospholipid-transporting ATPase ABCA4-like
Rho GTPase activating protein 29a, transcript variant X2
Rho GTPase activating protein 29a, transcript variant X1
Rho GTPase activating protein 29a, transcript variant X3
Rho GTPase activating protein 29a, transcript variant X4
rho GTPase-activating protein 29 isoform X2
rho GTPase-activating protein 29 isoform X1
rho GTPase-activating protein 29 isoform X3
rho GTPase-activating protein 29 isoform X4
protein kinase, DNA-activated, catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
DNA-dependent protein kinase catalytic subunit
GRB2-associated and regulator of MAPK protein 1
neutrophil cytosolic factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neutrophil cytosolic factor 2, transcript variant X2
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2
mitochondrial calcium uniporter regulator 1
regulator of G protein signaling 9 binding protein
regulator of G-protein signaling 9-binding protein
regulator of G-protein signaling 9-binding protein B-like
COORDINATES: nucleotide motif:Rfam:12.0:RF01277
ankyrin repeat and SAM domain-containing protein 6-like, transcript variant X2
ankyrin repeat and SAM domain-containing protein 6-like, transcript variant X1
ankyrin repeat and SAM domain-containing protein 6-like
aryl-hydrocarbon receptor repressor a, transcript variant X1
aryl-hydrocarbon receptor repressor a isoform X1
aryl-hydrocarbon receptor repressor a, transcript variant X3
aryl-hydrocarbon receptor repressor a, transcript variant X2
aryl-hydrocarbon receptor repressor a isoform X2
phosphatidylinositol glycan anchor biosynthesis, class M
serpin peptidase inhibitor, clade B (ovalbumin), member 1, like 3, transcript variant X1
serpin peptidase inhibitor, clade B (ovalbumin), member 1, like 3, transcript variant X3
serpin peptidase inhibitor, clade B (ovalbumin), member 1, like 3, transcript variant X4
serpin peptidase inhibitor, clade B (ovalbumin), member 1, like 3, transcript variant X2
serpin peptidase inhibitor, clade B (ovalbumin), member 1, like 3 isoform X2
serpin peptidase inhibitor, clade B (ovalbumin), member 1, like 3 isoform X1
agouti-signaling protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
agouti-signaling protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
agouti-signaling protein-like isoform X1
agouti-signaling protein-like isoform X2
NEDD4-like E3 ubiquitin-protein ligase WWP1, transcript variant X2
NEDD4-like E3 ubiquitin-protein ligase WWP1, transcript variant X1
NEDD4-like E3 ubiquitin-protein ligase WWP1
regulator of microtubule dynamics protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
isopentenyl-diphosphate delta isomerase 1
isopentenyl-diphosphate Delta-isomerase 1
WD repeat-containing protein 37-like, transcript variant X3
WD repeat-containing protein 37-like, transcript variant X1
WD repeat-containing protein 37-like, transcript variant X2
adenosine deaminase RNA specific B2 (inactive)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
phosphofructokinase, platelet a, transcript variant X6
phosphofructokinase, platelet a, transcript variant X3
phosphofructokinase, platelet a, transcript variant X7
phosphofructokinase, platelet a, transcript variant X2
phosphofructokinase, platelet a, transcript variant X4
phosphofructokinase, platelet a, transcript variant X1
phosphofructokinase, platelet a, transcript variant X5
ATP-dependent 6-phosphofructokinase, platelet type isoform X6
ATP-dependent 6-phosphofructokinase, platelet type isoform X3
ATP-dependent 6-phosphofructokinase, platelet type isoform X7
ATP-dependent 6-phosphofructokinase, platelet type isoform X2
ATP-dependent 6-phosphofructokinase, platelet type isoform X4
ATP-dependent 6-phosphofructokinase, platelet type isoform X1
ATP-dependent 6-phosphofructokinase, platelet type isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 2F2-like, transcript variant X3
cytochrome P450 2F2-like, transcript variant X2
cytochrome P450 2F2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
partitioning defective 3 homolog, transcript variant X1
partitioning defective 3 homolog, transcript variant X3
partitioning defective 3 homolog, transcript variant X2
partitioning defective 3 homolog, transcript variant X4
partitioning defective 3 homolog isoform X1
partitioning defective 3 homolog isoform X3
partitioning defective 3 homolog isoform X2
partitioning defective 3 homolog isoform X4
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
integrin beta-1-like, transcript variant X1
integrin beta-1-like, transcript variant X2
outer dynein arm docking complex subunit 2
outer dynein arm-docking complex subunit 2
membrane palmitoylated protein 7a, transcript variant X1
membrane palmitoylated protein 7a, transcript variant X2
WW domain containing adaptor with coiled-coil a, transcript variant X2
WW domain containing adaptor with coiled-coil a, transcript variant X1
WW domain-containing adapter protein with coiled-coil isoform X2
WW domain-containing adapter protein with coiled-coil isoform X1
BMP and activin membrane-bound inhibitor (Xenopus laevis) homolog a
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
junctional cadherin 5 associated a, transcript variant X1
junctional cadherin 5 associated a, transcript variant X2
junctional protein associated with coronary artery disease
mitogen-activated protein kinase kinase kinase 8
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 438, transcript variant X1
zinc finger protein 438, transcript variant X2
Rho GTPase activating protein 12b, transcript variant X10
Rho GTPase activating protein 12b, transcript variant X9
Rho GTPase activating protein 12b, transcript variant X8
Rho GTPase activating protein 12b, transcript variant X5
Rho GTPase activating protein 12b, transcript variant X7
Rho GTPase activating protein 12b, transcript variant X6
Rho GTPase activating protein 12b, transcript variant X4
Rho GTPase activating protein 12b, transcript variant X3
Rho GTPase activating protein 12b, transcript variant X2
Rho GTPase activating protein 12b, transcript variant X1
rho GTPase-activating protein 12b isoform X10
rho GTPase-activating protein 12b isoform X9
rho GTPase-activating protein 12b isoform X8
rho GTPase-activating protein 12b isoform X5
rho GTPase-activating protein 12b isoform X7
rho GTPase-activating protein 12b isoform X6
rho GTPase-activating protein 12b isoform X4
rho GTPase-activating protein 12b isoform X3
rho GTPase-activating protein 12b isoform X2
rho GTPase-activating protein 12b isoform X1
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: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: kinesin-1 heavy chain-like
glucose-fructose oxidoreductase domain containing 1
glucose-fructose oxidoreductase domain-containing protein 1
solute carrier family 12 member 7b, transcript variant X5
solute carrier family 12 member 7b, transcript variant X3
solute carrier family 12 member 7b, transcript variant X2
solute carrier family 12 member 7b, transcript variant X1
solute carrier family 12 member 7b, transcript variant X4
solute carrier family 12 member 7 isoform X5
solute carrier family 12 member 7 isoform X3
solute carrier family 12 member 7 isoform X2
solute carrier family 12 member 7 isoform X1
solute carrier family 12 member 7 isoform X4
amiloride-sensitive amine oxidase [copper-containing]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, subfamily H (eag-related), member 2b
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: potassium voltage-gated channel subfamily H member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
intraflagellar transport 74, transcript variant X2
intraflagellar transport 74, transcript variant X1
intraflagellar transport protein 74 homolog
zinc finger, CCHC domain containing 2, transcript variant X3
zinc finger CCHC domain-containing protein 2 isoform X3
zinc finger, CCHC domain containing 2, transcript variant X5
zinc finger, CCHC domain containing 2, transcript variant X4
zinc finger CCHC domain-containing protein 2 isoform X4
zinc finger, CCHC domain containing 2, transcript variant X2
zinc finger, CCHC domain containing 2, transcript variant X1
zinc finger CCHC domain-containing protein 2 isoform X2
zinc finger CCHC domain-containing protein 2 isoform X1
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: collagen alpha-1(XXI) chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
V-set and transmembrane domain containing 2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
V-set and transmembrane domain-containing protein 2A
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase HECW1-like
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
vesicular, overexpressed in cancer, prosurvival protein 1
LanC lantibiotic synthetase component C-like 2 (bacterial)
transforming growth factor, beta receptor 1 b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 143 Proteins
reversion-inducing cysteine-rich protein with Kazal motifs-like
LOW QUALITY PROTEIN: reversion-inducing cysteine-rich protein with Kazal motifs-like
polypyrimidine tract-binding protein 2-like, transcript variant X1
polypyrimidine tract-binding protein 2-like, transcript variant X2
polypyrimidine tract-binding protein 2-like, transcript variant X3
polypyrimidine tract-binding protein 2-like isoform X1
polypyrimidine tract-binding protein 2-like isoform X2
polypyrimidine tract-binding protein 2-like isoform X3
LOW QUALITY PROTEIN: sorting nexin-7-like
phospholipid phosphatase-related protein type 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
2-lysophosphatidate phosphatase PLPPR4-like
tRNA (cytosine(38)-C(5))-methyltransferase
complement component 1, q subcomponent-like 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins
phosphodiesterase 1C, calmodulin-dependent a
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A
protein phosphatase 1 regulatory subunit 17
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, including 1 sample with support for all annotated introns
protein phosphatase 1, regulatory subunit 17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: neurogenic differentiation factor 6-A
cubilin (intrinsic factor-cobalamin receptor)
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 15
ATP-binding cassette, sub-family D (ALD), member 3a
ATP-binding cassette sub-family D member 3a
ALG14 UDP-N-acetylglucosaminyltransferase subunit
UDP-N-acetylglucosamine transferase subunit ALG14 homolog
coiled-coil-helix-coiled-coil-helix domain containing 7
coiled-coil-helix-coiled-coil-helix domain-containing protein 7
v-mos Moloney murine sarcoma viral oncogene homolog
proto-oncogene serine/threonine-protein kinase mos
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: 31 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: metalloreductase STEAP2-like
rho guanine nucleotide exchange factor 4-like, transcript variant X4
rho guanine nucleotide exchange factor 4-like, transcript variant X1
rho guanine nucleotide exchange factor 4-like, transcript variant X2
rho guanine nucleotide exchange factor 4-like, transcript variant X3
rho guanine nucleotide exchange factor 4-like isoform X1
rho guanine nucleotide exchange factor 4-like isoform X2
rho guanine nucleotide exchange factor 4-like isoform X3
rho guanine nucleotide exchange factor 4-like isoform X4
CBY1-interacting BAR domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
zinc finger BED domain-containing protein 4-like