Entity Details

Primary name KNL1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8NG31
EntryNameKNL1_HUMAN
FullNameKinetochore scaffold 1
TaxID9606
Evidenceevidence at protein level
Length2342
SequenceStatuscomplete
DateCreated2005-05-24
DateModified2021-06-02

Ontological Relatives

GenesKNL1

GO terms

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GOName
GO:0001669 acrosomal vesicle
GO:0001675 acrosome assembly
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005829 cytosol
GO:0007052 mitotic spindle organization
GO:0008608 attachment of spindle microtubules to kinetochore
GO:0010923 negative regulation of phosphatase activity
GO:0016604 nuclear body
GO:0034080 CENP-A containing nucleosome assembly
GO:0034501 protein localization to kinetochore
GO:0051301 cell division

Subcellular Location

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Subcellular Location
Chromosome
Nucleus

Domains

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DomainNameCategoryType
IPR037388 Kinetochore scaffold 1FamilyFamily
IPR040850 Knl1, RWD C-terminal domainDomainDomain
IPR043651 KNL1 MELT repeatRepeatRepeat

Diseases

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Disease IDSourceNameDescription
604321 OMIMMicrocephaly 4, primary, autosomal recessive (MCPH4)A disease defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Affected individuals are mentally retarded. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits due to degenerative brain disorder. The disease is caused by variants affecting the gene represented in this entry.