NUP62CL (nucleoporin 62 C-terminal like) - Rat Genome Database

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Gene: NUP62CL (nucleoporin 62 C-terminal like) Homo sapiens
Analyze
Symbol: NUP62CL
Name: nucleoporin 62 C-terminal like
RGD ID: 1606555
HGNC Page HGNC:25960
Description: Predicted to be a structural constituent of nuclear pore. Predicted to be involved in nucleocytoplasmic transport and protein transport. Predicted to be located in nuclear envelope. Predicted to be part of nuclear pore.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ20130; nucleoporin 62kDa C-terminal like; nucleoporin-62 C-terminal-like protein; RP13-383K5.2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X107,123,427 - 107,206,433 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 EnsemblX107,123,427 - 107,206,433 (-)EnsemblGRCh38hg38GRCh38
GRCh37X106,366,657 - 106,449,663 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X106,253,358 - 106,336,200 (-)NCBINCBI36Build 36hg18NCBI36
CeleraX106,837,965 - 106,921,027 (-)NCBICelera
Cytogenetic MapXq22.3NCBI
HuRefX95,994,426 - 96,076,159 (-)NCBIHuRef
CHM1_1X106,277,530 - 106,360,560 (-)NCBICHM1_1
T2T-CHM13v2.0X105,559,960 - 105,642,842 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
NUP62CLHumanautistic disorder  IAGPRGD:143515258554872ClinVar Annotator: match by term: AutismClinVarPMID:21681106|PMID:30208311
NUP62CLHumanautosomal hemophilia A  IAGPRGD:4083875868554872ClinVar Annotator: match by term: AUTOSOMAL HEMOPHILIA AClinVarPMID:31690835
NUP62CLHumanCharcot-Marie-Tooth disease type X  IAGPRGD:1564504438554872ClinVar Annotator: match by term: Charcot-Marie-Tooth Neuropathy XClinVarPMID:24528855|PMID:28492532
NUP62CLHumanfactor VIII deficiency  IAGPRGD:4083875868554872ClinVar Annotator: match by term: Factor 8 deficiency, congenitalClinVarPMID:31690835
NUP62CLHumansyndromic X-linked intellectual disability Lubs type  IAGPRGD:143993378554872ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs typeClinVarPMID:25741868

1 to 20 of 70 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
NUP62CLHuman1,2-dichloroethane decreases expressionISORGD:16219896480464ethylene dichloride results in decreased expression of NUP62CL mRNACTDPMID:28960355
NUP62CLHuman2,3,7,8-tetrachlorodibenzodioxine decreases expressionISORGD:15643536480464Tetrachlorodibenzodioxin results in decreased expression of NUP62CL mRNACTDPMID:22808131
NUP62CLHuman2,3,7,8-tetrachlorodibenzodioxine increases expressionISORGD:15643536480464Tetrachlorodibenzodioxin results in increased expression of NUP62CL mRNACTDPMID:32109520
NUP62CLHuman4,4'-sulfonyldiphenol increases expressionISORGD:16219896480464bisphenol S results in increased expression of NUP62CL mRNACTDPMID:30951980
NUP62CLHuman6-propyl-2-thiouracil multiple interactionsISORGD:16219896480464[Propylthiouracil co-treated with Iodine deficiency] results in decreased expression of NUP62CL mRNACTDPMID:36706583
NUP62CLHumanaflatoxin B1 affects expressionEXP 6480464Aflatoxin B1 affects the expression of NUP62CL proteinCTDPMID:20106945
NUP62CLHumanaflatoxin B1 increases methylationEXP 6480464Aflatoxin B1 results in increased methylation of NUP62CL intronCTDPMID:30157460
NUP62CLHumanaflatoxin B1 increases expressionEXP 6480464Aflatoxin B1 results in increased expression of NUP62CL mRNACTDPMID:21632981
NUP62CLHumanall-trans-retinoic acid decreases expressionEXP 6480464Tretinoin results in decreased expression of NUP62CL mRNACTDPMID:23724009
NUP62CLHumanall-trans-retinoic acid increases expressionISORGD:16219896480464Tretinoin results in increased expression of NUP62CL mRNACTDPMID:36189433
NUP62CLHumanall-trans-retinoic acid multiple interactionsISORGD:16219896480464[mono-(2-ethylhexyl)phthalate co-treated with Tretinoin] results in increased expression of NUP62CL mRNACTDPMID:36189433
NUP62CLHumanamphetamine increases expressionISORGD:15643536480464Amphetamine results in increased expression of NUP62CL mRNACTDPMID:30779732
NUP62CLHumanarsane increases methylationEXP 6480464Arsenic results in increased methylation of NUP62CL promoterCTDPMID:21291286
NUP62CLHumanarsane multiple interactionsEXP 6480464[sodium arsenate results in increased abundance of Arsenic] which results in decreased expression of NUP62CL more ...CTDPMID:32525701
NUP62CLHumanarsenic atom increases methylationEXP 6480464Arsenic results in increased methylation of NUP62CL promoterCTDPMID:21291286
NUP62CLHumanarsenic atom multiple interactionsEXP 6480464[sodium arsenate results in increased abundance of Arsenic] which results in decreased expression of NUP62CL more ...CTDPMID:32525701
NUP62CLHumanbenzo[a]pyrene increases expressionEXP 6480464Benzo(a)pyrene results in increased expression of NUP62CL mRNACTDPMID:21632981|PMID:32234424
NUP62CLHumanbenzo[a]pyrene affects methylationEXP 6480464Benzo(a)pyrene affects the methylation of NUP62CL 5' UTRCTDPMID:27901495
NUP62CLHumanbeta-lapachone increases expressionEXP 6480464beta-lapachone results in increased expression of NUP62CL mRNACTDPMID:38218311
NUP62CLHumanbisphenol A affects expressionISORGD:15643536480464bisphenol A affects the expression of NUP62CL mRNACTDPMID:25181051

1 to 20 of 70 rows

Biological Process

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
NUP62CLHumannucleocytoplasmic transport involved_inIEAGO:0017056150520179 GOCGO_REF:0000108
NUP62CLHumanprotein transport involved_inIEAUniProtKB-KW:KW-0653150520179 UniProtGO_REF:0000043

Cellular Component

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
NUP62CLHumannuclear envelope located_inIEAARBA:ARBA00026328150520179 UniProtGO_REF:0000117
NUP62CLHumannuclear pore part_ofIEAInterPro:IPR026010150520179 InterProGO_REF:0000002

Molecular Function

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
NUP62CLHumanprotein binding enablesIPIUniProtKB:O15294|UniProtKB:O95994150520179 PMID:25416956IntActPMID:25416956
NUP62CLHumanprotein binding enablesIPIUniProtKB:O15294-3150520179 PMID:26871637IntActPMID:26871637
NUP62CLHumanprotein binding enablesIPIUniProtKB:O95295|UniProtKB:O95994|UniProtKB:P78424150520179 PMID:32296183IntActPMID:32296183
NUP62CLHumanprotein binding enablesIPIUniProtKB:Q7Z3B4150520179 PMID:31515488IntActPMID:31515488
NUP62CLHumanprotein binding enablesIPIUniProtKB:O15294|UniProtKB:Q7Z3B4150520179 PMID:33961781IntActPMID:33961781
NUP62CLHumanprotein binding enablesIPIUniProtKB:O15294150520179 PMID:16189514IntActPMID:16189514
NUP62CLHumanstructural constituent of nuclear pore enablesIEAInterPro:IPR026010150520179 InterProGO_REF:0000002

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
NUP62CLHumanAutism  IAGPRGD:143515258554872ClinVar Annotator: match by term: AutismClinVarPMID:21681106|PMID:30208311

#
Reference Title
Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
PMID:10737800   PMID:12477932   PMID:14702039   PMID:15489334   PMID:15772651   PMID:16189514   PMID:18029348   PMID:19322201   PMID:20360068   PMID:21832049   PMID:21873635   PMID:25416956  
PMID:26871637   PMID:27107012   PMID:28514442   PMID:28700943   PMID:31515488   PMID:32296183   PMID:33961781  



NUP62CL
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X107,123,427 - 107,206,433 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 EnsemblX107,123,427 - 107,206,433 (-)EnsemblGRCh38hg38GRCh38
GRCh37X106,366,657 - 106,449,663 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X106,253,358 - 106,336,200 (-)NCBINCBI36Build 36hg18NCBI36
CeleraX106,837,965 - 106,921,027 (-)NCBICelera
Cytogenetic MapXq22.3NCBI
HuRefX95,994,426 - 96,076,159 (-)NCBIHuRef
CHM1_1X106,277,530 - 106,360,560 (-)NCBICHM1_1
T2T-CHM13v2.0X105,559,960 - 105,642,842 (-)NCBIT2T-CHM13v2.0
Nup62cl
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X138,907,551 - 138,963,456 (-)NCBIGRCm39GRCm39mm39
GRCm39 EnsemblX138,907,554 - 138,963,461 (-)EnsemblGRCm39 Ensembl
GRCm38X140,006,802 - 140,062,707 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX140,006,805 - 140,062,712 (-)EnsemblGRCm38mm10GRCm38
MGSCv37X136,542,212 - 136,597,107 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36X135,354,037 - 135,408,909 (-)NCBIMGSCv36mm8
CeleraX123,269,854 - 123,324,869 (-)NCBICelera
Cytogenetic MapXF1NCBI
cM MapX61.35NCBI
Nup62cl
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8X108,457,043 - 108,513,525 (-)NCBIGRCr8
mRatBN7.2X103,668,458 - 103,724,957 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 EnsemblX103,668,455 - 103,724,081 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.0X111,333,274 - 111,390,023 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 EnsemblX111,334,252 - 111,365,849 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0353,207,455 - 53,264,220 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4X127,752,322 - 127,812,950 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera344,203,467 - 44,259,295 (+)NCBICelera
Cytogenetic MapXq32NCBI
Nup62cl
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554908,842,889 - 8,860,885 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554908,807,866 - 8,904,153 (+)NCBIChiLan1.0ChiLan1.0
NUP62CL
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2X106,605,716 - 106,722,143 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1X106,609,317 - 106,725,744 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0X96,222,802 - 96,300,219 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1X106,600,838 - 106,676,569 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 EnsemblX106,600,819 - 106,638,256 (-)Ensemblpanpan1.1panPan2
NUP62CL
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1X80,708,829 - 80,787,441 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 EnsemblX80,729,667 - 80,784,034 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_TashaX66,827,950 - 66,922,117 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0X82,352,349 - 82,446,668 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1X79,815,275 - 79,909,439 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0X81,526,810 - 81,620,971 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0X81,318,837 - 81,412,574 (-)NCBIUU_Cfam_GSD_1.0
Nup62cl
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X80,077,312 - 80,154,636 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049364997,503,475 - 7,579,453 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NUP62CL
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 EnsemblX87,601,042 - 87,630,253 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1X87,578,656 - 87,658,296 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2X101,950,958 - 102,030,618 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NUP62CL
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X94,952,017 - 95,033,089 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 EnsemblX94,951,636 - 94,998,052 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366606520,032,182 - 20,116,664 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nup62cl
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248039,424,628 - 9,487,626 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248039,391,282 - 9,487,066 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

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Variants in NUP62CL
18 total Variants

Predicted Target Of
Summary Value
Count of predictions:1861
Count of miRNA genes:588
Interacting mature miRNAs:659
Transcripts:ENST00000372461, ENST00000372466, ENST00000421752, ENST00000432145, ENST00000484614
Prediction methods:Miranda, Pita, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 10 of 18 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
596979989GWAS1099508_Hmemory performance, sex interaction measurement QTL GWAS1099508 (human)0.000004memory performance, sex interaction measurementX107161677107161678Human
597064951GWAS1161025_Halcoholic pancreatitis QTL GWAS1161025 (human)2e-17alcoholic pancreatitisX107123872107123873Human
596979991GWAS1099510_Hmemory performance, sex interaction measurement QTL GWAS1099510 (human)0.000009memory performance, sex interaction measurementX107191031107191032Human
597064949GWAS1161023_Halcoholic pancreatitis QTL GWAS1161023 (human)1e-32alcoholic pancreatitisX107131628107131629Human
597199957GWAS1296031_Hmemory performance, sex interaction measurement QTL GWAS1296031 (human)0.000004memory performance, sex interaction measurementX107191425107191426Human
597064952GWAS1161026_Halcoholic pancreatitis QTL GWAS1161026 (human)1e-08alcoholic pancreatitisX107158099107158100Human
597199958GWAS1296032_Hmemory performance, sex interaction measurement QTL GWAS1296032 (human)0.000004memory performance, sex interaction measurementX107191031107191032Human
597224918GWAS1320992_HCOVID-19 QTL GWAS1320992 (human)0.000001COVID-19X107192186107192187Human
597135526GWAS1231600_Hmemory performance, sex interaction measurement QTL GWAS1231600 (human)0.000004memory performance, sex interaction measurementX107129640107129641Human
596984295GWAS1103814_Hmemory performance, sex interaction measurement QTL GWAS1103814 (human)0.000009memory performance, sex interaction measurementX107129640107129641Human

1 to 10 of 18 rows
AL035123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X106,420,644 - 106,420,889UniSTSGRCh37
Build 36X106,307,300 - 106,307,545RGDNCBI36
CeleraX106,891,955 - 106,892,200RGD
Cytogenetic MapXq22.3UniSTS
HuRefX96,047,479 - 96,047,724UniSTS
DXS1504  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X106,391,354 - 106,391,414UniSTSGRCh37
Build 36X106,278,010 - 106,278,070RGDNCBI36
CeleraX106,862,662 - 106,862,722RGD
Cytogenetic MapXq22.3UniSTS
HuRefX96,019,203 - 96,019,263UniSTS
stbA92F23T7  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X106,412,698 - 106,412,834UniSTSGRCh37
Build 36X106,299,354 - 106,299,490RGDNCBI36
CeleraX106,884,008 - 106,884,144RGD
Cytogenetic MapXq22.3UniSTS
HuRefX96,039,614 - 96,039,750UniSTS
L77251  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X106,412,508 - 106,412,599UniSTSGRCh37
Build 36X106,299,164 - 106,299,255RGDNCBI36
CeleraX106,883,818 - 106,883,909RGD
Cytogenetic MapXq22.3UniSTS
HuRefX96,039,424 - 96,039,515UniSTS
DXS6972E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X106,374,999 - 106,375,173UniSTSGRCh37
Build 36X106,261,655 - 106,261,829RGDNCBI36
CeleraX106,846,307 - 106,846,481RGD
Cytogenetic Map6q21UniSTS
Cytogenetic MapXq22.3UniSTS
HuRefX96,002,769 - 96,002,943UniSTS
GeneMap99-GB4 RH MapX293.07UniSTS




adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
1159 2383 2486 2056 4808 1713 2327 5 613 1700 455 2188 6609 5970 39 3613 1 844 1728 1604 172


1 to 18 of 18 rows
RefSeq Transcripts NG_021315 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001433614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_017681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_033676 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024452393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AI702317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000137 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL390039 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF805909 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX105515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB448067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178655 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU178656 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 18 of 18 rows

Ensembl Acc Id: ENST00000372466   ⟹   ENSP00000361544
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblX107,123,427 - 107,206,433 (-)Ensembl
Ensembl Acc Id: ENST00000421752   ⟹   ENSP00000405906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblX107,153,292 - 107,206,433 (-)Ensembl
Ensembl Acc Id: ENST00000432145   ⟹   ENSP00000408612
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblX107,124,148 - 107,154,234 (-)Ensembl
Ensembl Acc Id: ENST00000484614   ⟹   ENSP00000433269
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 EnsemblX107,123,472 - 107,206,433 (-)Ensembl
RefSeq Acc Id: NM_017681   ⟹   NP_060151
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X107,123,427 - 107,206,433 (-)NCBI
GRCh37X106,366,657 - 106,449,670 (-)RGD
Build 36X106,253,358 - 106,336,200 (-)NCBI Archive
CeleraX106,837,965 - 106,921,027 (-)RGD
HuRefX95,994,426 - 96,076,159 (-)RGD
CHM1_1X106,277,530 - 106,360,560 (-)NCBI
T2T-CHM13v2.0X105,559,960 - 105,642,842 (-)NCBI
Sequence:
RefSeq Acc Id: NR_033676
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X107,123,427 - 107,206,433 (-)NCBI
GRCh37X106,366,657 - 106,449,670 (-)RGD
CeleraX106,837,965 - 106,921,027 (-)RGD
HuRefX95,994,426 - 96,076,159 (-)RGD
CHM1_1X106,277,530 - 106,360,560 (-)NCBI
T2T-CHM13v2.0X105,559,960 - 105,642,842 (-)NCBI
Sequence:
RefSeq Acc Id: NP_060151   ⟸   NM_017681
- UniProtKB: Q8WVL6 (UniProtKB/Swiss-Prot),   D3DUX4 (UniProtKB/Swiss-Prot),   Q9NXP2 (UniProtKB/Swiss-Prot),   Q9H1M0 (UniProtKB/Swiss-Prot),   A0A0S2Z5E8 (UniProtKB/TrEMBL),   A0A0S2Z5B5 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000361544   ⟸   ENST00000372466
Ensembl Acc Id: ENSP00000433269   ⟸   ENST00000484614
Ensembl Acc Id: ENSP00000408612   ⟸   ENST00000432145
Ensembl Acc Id: ENSP00000405906   ⟸   ENST00000421752
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H1M0-F1-model_v2 AlphaFold Q9H1M0 1-184 view protein structure

RGD ID:6808614
Promoter ID:HG_KWN:67701
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid
Transcripts:ENST00000336387,   ENST00000372461,   ENST00000372465,   NM_001169154,   NM_173494,   NR_033676,   OTTHUMT00000057828,   OTTHUMT00000057830,   UC004END.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36X106,335,616 - 106,336,317 (+)MPROMDB
RGD ID:13627798
Promoter ID:EPDNEW_H29174
Type:initiation region
Name:NUP62CL_1
Description:nucleoporin 62 C-terminal like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H29177  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38X107,206,433 - 107,206,493EPDNEW


1 to 30 of 30 rows
Database
Acc Id
Source(s)
COSMIC NUP62CL COSMIC
Ensembl Genes ENSG00000198088 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000372466 ENTREZGENE
  ENST00000372466.8 UniProtKB/Swiss-Prot
  ENST00000484614 ENTREZGENE
  ENST00000484614.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.5.170 UniProtKB/Swiss-Prot
GTEx ENSG00000198088 GTEx
HGNC ID HGNC:25960 ENTREZGENE
Human Proteome Map NUP62CL Human Proteome Map
InterPro NSP1/NUP62 UniProtKB/Swiss-Prot
  Nucleoporin_NSP1_C UniProtKB/Swiss-Prot
KEGG Report hsa:54830 UniProtKB/Swiss-Prot
NCBI Gene 54830 ENTREZGENE
PANTHER NUCLEOPORIN 62 C-TERMINAL LIKE UniProtKB/Swiss-Prot
  PTHR12084 UniProtKB/Swiss-Prot
Pfam Nsp1_C UniProtKB/Swiss-Prot
PharmGKB PA145148360 PharmGKB
UniProt A0A0S2Z5B5 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z5E8 ENTREZGENE, UniProtKB/TrEMBL
  D3DUX4 ENTREZGENE
  H0Y6X7_HUMAN UniProtKB/TrEMBL
  N62CL_HUMAN UniProtKB/Swiss-Prot
  Q5JSN5_HUMAN UniProtKB/TrEMBL
  Q8WVL6 ENTREZGENE
  Q9H1M0 ENTREZGENE
  Q9NXP2 ENTREZGENE
UniProt Secondary D3DUX4 UniProtKB/Swiss-Prot
  Q8WVL6 UniProtKB/Swiss-Prot
  Q9NXP2 UniProtKB/Swiss-Prot
1 to 30 of 30 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-07 NUP62CL  nucleoporin 62 C-terminal like    nucleoporin 62kDa C-terminal like  Symbol and/or name change 5135510 APPROVED
2011-09-13 NUP62CL  nucleoporin 62kDa C-terminal like  NUP62CL  nucleoporin 62kDa C-terminal like  Symbol and/or name change 5135510 APPROVED