Entity Details

Primary name TENM3
Entity type gene
Source Source Link

Details

PrimaryID55714
RefseqGeneNG_042859
SymbolTENM3
Nameteneurin transmembrane protein 3
Chromosome4
Location4q34.3-q35.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-07-03
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTEN3_HUMAN

GO terms

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GOName
GO:0005887 integral component of plasma membrane
GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules
GO:0007157 heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules
GO:0007165 signal transduction
GO:0010976 positive regulation of neuron projection development
GO:0016020 membrane
GO:0030424 axon
GO:0042803 protein homodimerization activity
GO:0043005 neuron projection
GO:0046982 protein heterodimerization activity
GO:0048593 camera-type eye morphogenesis
GO:0048666 neuron development
GO:0050839 cell adhesion molecule binding
GO:1903385 regulation of homophilic cell adhesion

Diseases

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Disease IDSourceNameDescription
615145 OMIMMicrophthalmia, isolated, with coloboma, 9 (MCOPCB9)A disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Ocular abnormalities like opacities of the cornea and lens, scaring of the retina and choroid, and other abnormalities may also be present. Ocular colobomas are a set of malformations resulting from abnormal morphogenesis of the optic cup and stalk, and the fusion of the fetal fissure (optic fissure). The disease is caused by variants affecting the gene represented in this entry.
615145 OMIMMicrophthalmia, isolated, with coloboma, 9 (MCOPCB9)A disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Ocular abnormalities like opacities of the cornea and lens, scaring of the retina and choroid, and other abnormalities may also be present. Ocular colobomas are a set of malformations resulting from abnormal morphogenesis of the optic cup and stalk, and the fusion of the fetal fissure (optic fissure). The disease is caused by variants affecting the gene represented in this entry.