Entity Details

Primary name CND2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ15003
EntryNameCND2_HUMAN
FullNameCondensin complex subunit 2
TaxID9606
Evidenceevidence at protein level
Length741
SequenceStatuscomplete
DateCreated2003-04-23
DateModified2021-06-02

Ontological Relatives

GenesNCAPH

GO terms

Show/Hide Table
GOName
GO:0000796 condensin complex
GO:0003682 chromatin binding
GO:0005654 nucleoplasm
GO:0005829 cytosol
GO:0007076 mitotic chromosome condensation
GO:0016020 membrane
GO:0044547 DNA topoisomerase binding
GO:0051301 cell division
GO:0072587 DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activator activity

Subcellular Location

Show/Hide Table
Subcellular Location
Chromosome
Cytoplasm
Nucleus

Domains

Show/Hide Table
DomainNameCategoryType
IPR022816 Condensin complex subunit 2/barrenFamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
617985 OMIMMicrocephaly 23, primary, autosomal recessive (MCPH23)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. The disease is caused by variants affecting the gene represented in this entry.