Entity Details

Primary name NUP37_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8NFH4
EntryNameNUP37_HUMAN
FullNameNucleoporin Nup37
TaxID9606
Evidenceevidence at protein level
Length326
SequenceStatuscomplete
DateCreated2003-01-27
DateModified2021-06-02

Ontological Relatives

GenesNUP37

GO terms

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GOName
GO:0005634 nucleus
GO:0005635 nuclear envelope
GO:0005654 nucleoplasm
GO:0005829 cytosol
GO:0006110 regulation of glycolytic process
GO:0006406 mRNA export from nucleus
GO:0006409 tRNA export from nucleus
GO:0007052 mitotic spindle organization
GO:0007059 chromosome segregation
GO:0007084 mitotic nuclear membrane reassembly
GO:0016032 viral process
GO:0016925 protein sumoylation
GO:0019058 viral life cycle
GO:0019083 viral transcription
GO:0031080 nuclear pore outer ring
GO:0043657 host cell
GO:0051301 cell division
GO:0060964 regulation of gene silencing by miRNA
GO:0075733 intracellular transport of virus
GO:1900034 regulation of cellular response to heat

Subcellular Location

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Subcellular Location
Chromosome
Nucleus

Domains

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DomainNameCategoryType
IPR001680 WD40 repeatRepeatRepeat
IPR015943 WD40/YVTN repeat-like-containing domain superfamilyFamilyHomologous superfamily
IPR019775 WD40 repeat, conserved siteSiteConserved site
IPR036322 WD40-repeat-containing domain superfamilyFamilyHomologous superfamily
IPR037626 Nucleoporin Nup37FamilyFamily

Diseases

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Disease IDSourceNameDescription
618179 OMIMMicrocephaly 24, primary, autosomal recessive (MCPH24)A form of microcephaly, a disease defined as a head circumference more than 3 standard deviations below the age, sex and ethnically matched mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. MCPH24 patients additionally manifest mildly impaired intellectual development, cerebellar vermis hypoplasia, and fifth finger clinodactyly. The disease may be caused by variants affecting the gene represented in this entry.