Entity Details

Primary name CLMP_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9H6B4
EntryNameCLMP_HUMAN
FullNameCXADR-like membrane protein
TaxID9606
Evidenceevidence at protein level
Length373
SequenceStatuscomplete
DateCreated2007-06-26
DateModified2021-06-02

Ontological Relatives

GenesCLMP

GO terms

Show/Hide Table
GOName
GO:0005881 cytoplasmic microtubule
GO:0005886 plasma membrane
GO:0005923 bicellular tight junction
GO:0009986 cell surface
GO:0016021 integral component of membrane
GO:0048565 digestive tract development

Subcellular Location

Show/Hide Table
Subcellular Location
Cell junction
Cell membrane

Domains

Show/Hide Table
DomainNameCategoryType
IPR003598 Immunoglobulin subtype 2DomainDomain
IPR003599 Immunoglobulin subtypeDomainDomain
IPR007110 Immunoglobulin-like domainDomainDomain
IPR013106 Immunoglobulin V-set domainDomainDomain
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR036179 Immunoglobulin-like domain superfamilyFamilyHomologous superfamily
IPR042454 CXADR-like membrane proteinFamilyFamily

Diseases

Show/Hide Table
Disease IDSourceNameDescription
615237 OMIMCongenital short bowel syndrome (CSBS)A disease characterized by a shortened small intestine, intestinal malrotation, and malabsorption. The mean length of the small intestine in CSBS patients is approximately 50 cm, compared with a normal length at birth of 190-280 cm. Patients with CSBS may develop severe malnutrition as a result of the hugely reduced absorptive surface of the small intestine. Infants require parenteral nutrition for survival. However, parenteral nutrition itself causes life-threatening complications such as sepsis and liver failure which are associated with a high rate of mortality early in life. The disease is caused by variants affecting the gene represented in this entry.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
CLMP_HUMANCLMP_HUMANBioGRID, IntAct21982860 details
CLMP_HUMANNGAL_HUMANBioGRID, IntAct32296183 details