Entity Details

Primary name CNDD3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP42695
EntryNameCNDD3_HUMAN
FullNameCondensin-2 complex subunit D3
TaxID9606
Evidenceevidence at protein level
Length1498
SequenceStatuscomplete
DateCreated1995-11-01
DateModified2021-06-02

Ontological Relatives

GenesNCAPD3

GO terms

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GOName
GO:0000779 condensed chromosome, centromeric region
GO:0000796 condensin complex
GO:0003682 chromatin binding
GO:0005654 nucleoplasm
GO:0005721 pericentric heterochromatin
GO:0007076 mitotic chromosome condensation
GO:0010032 meiotic chromosome condensation
GO:0016020 membrane
GO:0035064 methylated histone binding
GO:0042393 histone binding
GO:0051301 cell division

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR012371 Condensin-2 complex subunit D3FamilyFamily
IPR016024 Armadillo-type foldFamilyHomologous superfamily
IPR026971 Condensin subunit 1/Condensin-2 complex subunit D3FamilyFamily
IPR032682 Condensin complex subunit 1, C-terminalDomainDomain

Diseases

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Disease IDSourceNameDescription
617984 OMIMMicrocephaly 22, primary, autosomal recessive (MCPH22)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.
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.