Entity Details

Primary name CCD47_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ96A33
EntryNameCCD47_HUMAN
FullNamePAT complex subunit CCDC47
TaxID9606
Evidenceevidence at protein level
Length483
SequenceStatuscomplete
DateCreated2006-05-16
DateModified2021-06-02

Ontological Relatives

GenesCCDC47

GO terms

Show/Hide Table
GOName
GO:0001649 osteoblast differentiation
GO:0003723 RNA binding
GO:0005509 calcium ion binding
GO:0005783 endoplasmic reticulum
GO:0006983 ER overload response
GO:0009791 post-embryonic development
GO:0016020 membrane
GO:0030176 integral component of endoplasmic reticulum membrane
GO:0030433 ubiquitin-dependent ERAD pathway
GO:0030867 rough endoplasmic reticulum membrane
GO:0032469 endoplasmic reticulum calcium ion homeostasis
GO:0036503 ERAD pathway
GO:0043022 ribosome binding
GO:0044183 protein folding chaperone
GO:0045048 protein insertion into ER membrane

Subcellular Location

Show/Hide Table
Subcellular Location
Endoplasmic reticulum membrane
Rough endoplasmic reticulum membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR012879 PAT complex subunit CCDC47FamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
618268 OMIMTrichohepatoneurodevelopmental syndrome (THNS)An autosomal recessive complex multisystem disorder characterized by woolly or coarse hair, liver dysfunction, pruritus, dysmorphic features, hypotonia, and global developmental delay. The disease is caused by variants affecting the gene represented in this entry.