Entity Details

Primary name TEN3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9P273
EntryNameTEN3_HUMAN
FullNameTeneurin-3
TaxID9606
Evidenceevidence at transcript level
Length2699
SequenceStatuscomplete
DateCreated2006-10-31
DateModified2021-06-02

Ontological Relatives

GenesTENM3

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

Subcellular Location

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Subcellular Location
Cell membrane
Cell projection

Domains

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DomainNameCategoryType
IPR000742 EGF-like domainDomainDomain
IPR006530 YD repeatRepeatRepeat
IPR008969 Carboxypeptidase-like, regulatory domain superfamilyFamilyHomologous superfamily
IPR009471 Teneurin intracellular, N-terminalDomainDomain
IPR011042 Six-bladed beta-propeller, TolB-likeFamilyHomologous superfamily
IPR022385 Rhs repeat-associated coreDomainDomain
IPR027691 Teneurin-3/4FamilyFamily
IPR028916 Tox-GHH domainDomainDomain
IPR036322 WD40-repeat-containing domain superfamilyFamilyHomologous superfamily

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.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
TEN3_HUMANSMAD4_HUMANBioGRID, HPRD, MINT15231748 details
TEN3_HUMANMTEF1_HUMANIntAct20195357 details
TEN3_HUMANGAN_HUMANBioGRID26460568 details