Entity Details

Primary name GUC2C_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP25092
EntryNameGUC2C_HUMAN
FullNameHeat-stable enterotoxin receptor
TaxID9606
Evidenceevidence at protein level
Length1073
SequenceStatuscomplete
DateCreated1992-05-01
DateModified2021-06-02

Ontological Relatives

GenesGUCY2C

GO terms

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GOName
GO:0001653 peptide receptor activity
GO:0004383 guanylate cyclase activity
GO:0004672 protein kinase activity
GO:0005524 ATP binding
GO:0005525 GTP binding
GO:0005789 endoplasmic reticulum membrane
GO:0005886 plasma membrane
GO:0006182 cGMP biosynthetic process
GO:0007165 signal transduction
GO:0007168 receptor guanylyl cyclase signaling pathway
GO:0007586 digestion
GO:0009636 response to toxic substance
GO:0015643 toxic substance binding
GO:0016021 integral component of membrane
GO:0016941 natriuretic peptide receptor activity
GO:0017046 peptide hormone binding
GO:0035556 intracellular signal transduction
GO:0042127 regulation of cell population proliferation

Subcellular Location

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Subcellular Location
Cell membrane
Endoplasmic reticulum membrane

Domains

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DomainNameCategoryType
IPR000719 Protein kinase domainDomainDomain
IPR001054 Adenylyl cyclase class-3/4/guanylyl cyclaseDomainDomain
IPR001245 Serine-threonine/tyrosine-protein kinase, catalytic domainDomainDomain
IPR011009 Protein kinase-like domain superfamilyFamilyHomologous superfamily
IPR018297 Adenylyl cyclase class-4/guanylyl cyclase, conserved siteSiteConserved site
IPR028082 Periplasmic binding protein-like IFamilyHomologous superfamily
IPR029787 Nucleotide cyclaseFamilyHomologous superfamily
IPR042822 Membrane Guanylate Cyclase receptor GC-C, pseudokinase domainDomainDomain

Diseases

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Disease IDSourceNameDescription
614616 OMIMDiarrhea 6 (DIAR6)A relatively mild, early-onset chronic diarrhea that may be associated with increased susceptibility to inflammatory bowel disease, small bowel obstruction, and esophagitis. The disease is caused by variants affecting the gene represented in this entry.
614665 OMIMMeconium ileus (MECIL)A condition characterized by intestinal obstruction due to inspissated meconium in the distal ileum and cecum, which develops in utero and presents shortly after birth as a failure to pass meconium. Meconium ileus is a known clinical manifestation of cystic fibrosis. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB08890 LinaclotideDrugbanksmall molecule

Interactions

4 interactions