Entity Details

Primary name NDP
Entity type gene
Source Source Link

Details

PrimaryID4693
RefseqGeneNG_009832
SymbolNDP
Namenorrin cystine knot growth factor NDP
ChromosomeX
LocationXp11.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsNDP_HUMAN

GO terms

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GOName
GO:0001890 placenta development
GO:0005109 frizzled binding
GO:0005125 cytokine activity
GO:0005615 extracellular space
GO:0007033 vacuole organization
GO:0007399 nervous system development
GO:0007601 visual perception
GO:0009986 cell surface
GO:0016055 Wnt signaling pathway
GO:0031012 extracellular matrix
GO:0035426 extracellular matrix-cell signaling
GO:0042803 protein homodimerization activity
GO:0045893 positive regulation of transcription, DNA-templated
GO:0051091 positive regulation of DNA-binding transcription factor activity
GO:0061299 retina vasculature morphogenesis in camera-type eye
GO:0062023 collagen-containing extracellular matrix
GO:0110135 Norrin signaling pathway

Diseases

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Disease IDSourceNameDescription
310600 OMIMNorrie disease (ND)Recessive disorder characterized by very early childhood blindness due to degenerative and proliferative changes of the neuroretina. Approximately 50% of patients show some form of progressive mental disorder, often with psychotic features, and about one-third of patients develop sensorineural deafness in the second decade. In addition, some patients have more complex phenotypes, including growth failure and seizure. The disease is caused by variants affecting the gene represented in this entry.
305390 OMIMVitreoretinopathy, exudative 2 (EVR2)A disorder of the retinal vasculature characterized by an abrupt cessation of growth of peripheral capillaries, leading to an avascular peripheral retina. This may lead to compensatory retinal neovascularization, which is thought to be induced by hypoxia from the initial avascular insult. New vessels are prone to leakage and rupture causing exudates and bleeding, followed by scarring, retinal detachment and blindness. Clinical features can be highly variable, even within the same family. Patients with mild forms of the disease are asymptomatic, and their only disease related abnormality is an arc of avascular retina in the extreme temporal periphery. The disease is caused by variants affecting the gene represented in this entry.

Interactions

9 interactions

InteractorPartnerSourcesPublicationsLink
NDPNDPBioGRID, HPRD, IntAct17955262 19837033 9407136 details
NDPPPP1CABioGRID, IntAct22321011 details
NDPAPPBioGRID21832049 details
NDPFZD4bhf-ucl, BioGRID, IntAct15035989 17955262 19837033 details
NDPLGALS8BioGRID22246324 details
NDPTSPAN12IntAct19837033 details
NDPLRP5IntAct19837033 details
NDPBAG3BioGRID23824909 details
NDPDDX58BioGRID32513696 details