Entity Details

Primary name CLMP
Entity type gene
Source Source Link

Details

PrimaryID79827
RefseqGeneNG_042818
SymbolCLMP
NameCXADR like membrane protein
Chromosome11
Location11q24.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-03-12
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCLMP_HUMAN

GO terms

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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

Diseases

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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

9 interactions

InteractorPartnerSourcesPublicationsLink
CLMPCLMPBioGRID, IntAct21982860 details
CLMPLCN2BioGRID, IntAct32296183 details
CLMPKIDINS220BioGRID, IntAct28514442 details
CLMPMLST8BioGRID, IntAct28514442 details
CLMPIP6K1BioGRID, IntAct28514442 details
CLMPKIF14BioGRID, IntAct28514442 details
CLMPRRP1BioGRID, IntAct28514442 details
CLMPUTP20BioGRID, IntAct28514442 details
CLMPBRD1BioGRID31753913 details