Entity Details

Primary name CP135_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ66GS9
EntryNameCP135_HUMAN
FullNameCentrosomal protein of 135 kDa
TaxID9606
Evidenceevidence at protein level
Length1140
SequenceStatuscomplete
DateCreated2005-02-01
DateModified2021-06-02

Ontological Relatives

GenesCEP135

GO terms

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GOName
GO:0000086 G2/M transition of mitotic cell cycle
GO:0005813 centrosome
GO:0005814 centriole
GO:0005829 cytosol
GO:0007099 centriole replication
GO:0008022 protein C-terminus binding
GO:0010389 regulation of G2/M transition of mitotic cell cycle
GO:0010457 centriole-centriole cohesion
GO:0097711 ciliary basal body-plasma membrane docking
GO:1902857 positive regulation of non-motile cilium assembly
GO:1904951 positive regulation of establishment of protein localization

Subcellular Location

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Subcellular Location
Cytoplasm

Domains

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DomainNameCategoryType
IPR026732 Centrosomal protein of 135kDaFamilyFamily

Diseases

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Disease IDSourceNameDescription
614673 OMIMMicrocephaly 8, primary, autosomal recessive (MCPH8)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.