Entity Details

Primary name NECTIN4
Entity type gene
Source Source Link

Details

PrimaryID81607
RefseqGeneNG_028109
SymbolNECTIN4
Namenectin cell adhesion molecule 4
Chromosome1
Location1q23.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-04-04
ModificationDate2021-06-20

Ontological Relatives

UniProt IDsNECT4_HUMAN

GO terms

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GOName
GO:0001618 virus receptor activity
GO:0005886 plasma membrane
GO:0005912 adherens junction
GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules
GO:0007157 heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules
GO:0016021 integral component of membrane
GO:0034332 adherens junction organization
GO:0042802 identical protein binding
GO:0070062 extracellular exosome

Diseases

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Disease IDSourceNameDescription
613573 OMIMEctodermal dysplasia-syndactyly syndrome 1 (EDSS1)A form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. EDSS1 is characterized by the association of hair and teeth abnormalities with cutaneous syndactyly of the hands and/or feet. Hair morphologic abnormalities include twists at irregular intervals (pilli torti) and swelling along the shafts, particularly associated with areas of breakage. Dental findings consist of abnormally widely spaced teeth, with peg-shaped and conical crowns. Patients have normal sweating. The disease is caused by variants affecting the gene represented in this entry.