Entity Details

Primary name CHAP1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96JM3
EntryNameCHAP1_HUMAN
FullNameChromosome alignment-maintaining phosphoprotein 1
TaxID9606
Evidenceevidence at protein level
Length812
SequenceStatuscomplete
DateCreated2006-09-05
DateModified2021-06-02

Ontological Relatives

GenesCHAMP1

GO terms

Show/Hide Table
GOName
GO:0000793 condensed chromosome
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0005819 spindle
GO:0016604 nuclear body
GO:0031134 sister chromatid biorientation
GO:0034501 protein localization to kinetochore
GO:0035372 protein localization to microtubule
GO:0046872 metal ion binding
GO:0051315 attachment of mitotic spindle microtubules to kinetochore
GO:0090543 Flemming body

Subcellular Location

Show/Hide Table
Subcellular Location
Chromosome
Cytoplasm
Nucleus

Domains

Show/Hide Table
DomainNameCategoryType
IPR013087 Zinc finger C2H2-typeDomainDomain
IPR036236 Zinc finger C2H2 superfamilyFamilyHomologous superfamily
IPR039330 Chromosome alignment-maintaining phosphoprotein 1FamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
616579 OMIMMental retardation, autosomal dominant 40 (MRD40)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease is caused by variants affecting the gene represented in this entry.