Entity Details

Primary name NET1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO95631
EntryNameNET1_HUMAN
FullNameNetrin-1
TaxID9606
Evidenceevidence at protein level
Length604
SequenceStatuscomplete
DateCreated2002-11-15
DateModified2021-06-02

Ontological Relatives

GenesNTN1

GO terms

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GOName
GO:0001764 neuron migration
GO:0005576 extracellular region
GO:0005604 basement membrane
GO:0005737 cytoplasm
GO:0006915 apoptotic process
GO:0006930 substrate-dependent cell migration, cell extension
GO:0007097 nuclear migration
GO:0007265 Ras protein signal transduction
GO:0008045 motor neuron axon guidance
GO:0008284 positive regulation of cell population proliferation
GO:0009887 animal organ morphogenesis
GO:0009888 tissue development
GO:0016358 dendrite development
GO:0030334 regulation of cell migration
GO:0030517 negative regulation of axon extension
GO:0032488 Cdc42 protein signal transduction
GO:0033564 anterior/posterior axon guidance
GO:0042472 inner ear morphogenesis
GO:0045773 positive regulation of axon extension
GO:0051963 regulation of synapse assembly
GO:0060603 mammary gland duct morphogenesis
GO:0061643 chemorepulsion of axon
GO:0098609 cell-cell adhesion
GO:1902842 negative regulation of netrin-activated signaling pathway
GO:2000147 positive regulation of cell motility

Subcellular Location

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Subcellular Location
Cytoplasm
Secreted

Domains

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DomainNameCategoryType
IPR001134 Netrin domainDomainDomain
IPR002049 Laminin EGF domainDomainDomain
IPR008211 Laminin, N-terminalDomainDomain
IPR008979 Galactose-binding-like domain superfamilyFamilyHomologous superfamily
IPR008993 Tissue inhibitor of metalloproteinases-like, OB-foldFamilyHomologous superfamily
IPR018933 Netrin module, non-TIMP typeDomainDomain

Diseases

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Disease IDSourceNameDescription
618264 OMIMMirror movements 4 (MRMV4)A disorder characterized by contralateral involuntary movements that mirror voluntary ones. While mirror movements are occasionally found in young children, persistence beyond the age of 10 is abnormal. Mirror movements occur more commonly in the upper extremities. MRMV4 inheritance is autosomal dominant. The disease is caused by variants affecting the gene represented in this entry.