Entity Details

Primary name K1C25_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ7Z3Z0
EntryNameK1C25_HUMAN
FullNameKeratin, type I cytoskeletal 25
TaxID9606
Evidenceevidence at protein level
Length450
SequenceStatuscomplete
DateCreated2007-12-04
DateModified2021-06-02

Ontological Relatives

GenesKRT25

GO terms

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GOName
GO:0005198 structural molecule activity
GO:0005829 cytosol
GO:0005882 intermediate filament
GO:0007010 cytoskeleton organization
GO:0007568 aging
GO:0031069 hair follicle morphogenesis
GO:0031424 keratinization
GO:0042633 hair cycle
GO:0045109 intermediate filament organization
GO:0046982 protein heterodimerization activity
GO:0070062 extracellular exosome
GO:0070268 cornification

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR002957 Keratin, type IFamilyFamily
IPR039008 Intermediate filament, rod domainDomainDomain

Diseases

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Disease IDSourceNameDescription
616760 OMIMWoolly hair autosomal recessive 3 (ARWH3)A hair shaft disorder characterized by fine and tightly curled hair. Compared to normal curly hair that is observed in some populations, woolly hair grows slowly and stops growing after a few inches. Under light microscopy, woolly hair shows some structural anomalies, including trichorrhexis nodosa and tapered ends. Some individuals may present with hypotrichosis. The disease is caused by variants affecting the gene represented in this entry.