Entity Details
Primary name |
CLMP_HUMAN |
Entity type |
UniProt |
Source |
Source Link |
Details
Accession | Q9H6B4 |
EntryName | CLMP_HUMAN |
FullName | CXADR-like membrane protein |
TaxID | 9606 |
Evidence | evidence at protein level |
Length | 373 |
SequenceStatus | complete |
DateCreated | 2007-06-26 |
DateModified | 2021-06-02 |
Subcellular Location
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Subcellular Location |
Cell junction |
Cell membrane |
Domains
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Domain | Name | Category | Type |
IPR003598 | Immunoglobulin subtype 2 | Domain | Domain |
IPR003599 | Immunoglobulin subtype | Domain | Domain |
IPR007110 | Immunoglobulin-like domain | Domain | Domain |
IPR013106 | Immunoglobulin V-set domain | Domain | Domain |
IPR013783 | Immunoglobulin-like fold | Family | Homologous superfamily |
IPR036179 | Immunoglobulin-like domain superfamily | Family | Homologous superfamily |
IPR042454 | CXADR-like membrane protein | Family | Family |
Diseases
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Disease ID | Source | Name | Description |
615237 | OMIM | Congenital 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