Entity Details

Primary name CC174_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ6PII3
EntryNameCC174_HUMAN
FullNameCoiled-coil domain-containing protein 174
TaxID9606
Evidenceevidence at protein level
Length467
SequenceStatuscomplete
DateCreated2006-10-03
DateModified2021-06-02

Ontological Relatives

GenesCCDC174

GO terms

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GOName
GO:0005634 nucleus
GO:0005654 nucleoplasm

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR025066 Coiled-coil domain-containing protein 174-likeFamilyFamily

Diseases

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Disease IDSourceNameDescription
616816 OMIMHypotonia, infantile, with psychomotor retardation (IHPMR)An autosomal recessive disorder characterized by congenital axial hypotonia, weakness of the abducens nerve, psychomotor developmental delay with brain ventriculomegaly, variable thinning of corpus callosum and cardiac septal defects. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
CC174_HUMANIF4A3_HUMANBioGRID, HPRD, IntAct16189514 29395067 32296183 details
CC174_HUMANLOX5_HUMANBioGRID, IntAct32296183 details
CC174_HUMANNAA10_HUMANBioGRID, IntAct32296183 details
CC174_HUMANGSK3A_HUMANBioGRID, UniProt30824926 details