Entity Details

Primary name CAD11_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP55287
EntryNameCAD11_HUMAN
FullNameCadherin-11
TaxID9606
Evidenceevidence at transcript level
Length796
SequenceStatuscomplete
DateCreated1996-10-01
DateModified2021-06-02

Ontological Relatives

GenesCDH11

GO terms

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GOName
GO:0000902 cell morphogenesis
GO:0001501 skeletal system development
GO:0001503 ossification
GO:0005509 calcium ion binding
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0005912 adherens junction
GO:0007043 cell-cell junction assembly
GO:0007155 cell adhesion
GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules
GO:0007275 multicellular organism development
GO:0016021 integral component of membrane
GO:0016339 calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules
GO:0016342 catenin complex
GO:0021957 corticospinal tract morphogenesis
GO:0034332 adherens junction organization
GO:0045296 cadherin binding
GO:0050804 modulation of chemical synaptic transmission
GO:0070062 extracellular exosome
GO:0098685 Schaffer collateral - CA1 synapse
GO:0098742 cell-cell adhesion via plasma-membrane adhesion molecules
GO:0098978 glutamatergic synapse

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR000233 Cadherin, cytoplasmic domainDomainDomain
IPR002126 Cadherin-likeDomainDomain
IPR015919 Cadherin-like superfamilyFamilyHomologous superfamily
IPR020894 Cadherin conserved siteSiteConserved site
IPR027397 Catenin binding domain superfamilyFamilyHomologous superfamily
IPR039808 CadherinFamilyFamily

Diseases

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Disease IDSourceNameDescription
211380 OMIMElsahy-Waters syndrome (ESWS)An autosomal recessive syndrome characterized by moderate mental retardation, hypospadias and characteristic craniofacial morphology, which includes brachycephaly, facial asymmetry, exotropia, hypertelorism, telechantus, broad nose, concave nasal ridge, underdeveloped mid-face, prognathism, and radicular dentin dysplasia. The disease is caused by variants affecting the gene represented in this entry.