NDP (gene)

From Wikipedia, the free encyclopedia

Norrie disease (pseudoglioma)

Identifiers

NDP; EVR2; FEVR; ND

External IDs

OMIM: 310600 MGI: 102570 HomoloGene: 225

Gene ontology
Molecular Function:	• growth factor activity
Cellular Component:	• extracellular space
Biological Process:	• placenta development • vacuole organization and biogenesis • signal transduction • cell-cell signaling • nervous system development • visual perception • sensory perception of sound • cell proliferation • response to stimulus

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_000266 (mRNA)
NP_000257 (protein)

NM_010883 (mRNA)
NP_035013 (protein)

Location

Chr X: 43.69 - 43.72 Mb

Chr X: 16.04 - 16.07 Mb

Pubmed search

[1]

[2]

Norrie disease (pseudoglioma), also known as NDP, is a human gene^[1] associated with the Norrie disease.

NDP is the genetic locus identified as harboring mutations that result in Norrie disease. Norrie disease is a rare genetic disorder characterized by bilateral congenital blindness that is caused by a vascularized mass behind each lens due to a maldeveloped retina (pseudoglioma).^[1]

[edit] References

^ ^a ^b Entrez Gene: NDP Norrie disease (pseudoglioma).

[edit] Further reading

Berger W, van de Pol D, Warburg M, et al. (1993). "Mutations in the candidate gene for Norrie disease.". Hum. Mol. Genet. 1 (7): 461-5. PMID 1307245.
Black G, Redmond RM (1995). "The molecular biology of Norrie's disease.". Eye (London, England) 8 ( Pt 5): 491-6. PMID 7835440.
Masckauchán TN, Kitajewski J (2007). "Wnt/Frizzled signaling in the vasculature: new angiogenic factors in sight.". Physiology (Bethesda, Md.) 21: 181-8. doi:10.1152/physiol.00058.2005. PMID 16714476.
Berger W, Meindl A, van de Pol TJ, et al. (1993). "Isolation of a candidate gene for Norrie disease by positional cloning.". Nat. Genet. 1 (3): 199-203. doi:10.1038/ng0692-199. PMID 1303235.
Chen ZY, Hendriks RW, Jobling MA, et al. (1993). "Isolation and characterization of a candidate gene for Norrie disease.". Nat. Genet. 1 (3): 204-8. doi:10.1038/ng0692-204. PMID 1303236.
Berger W, Meindl A, van de Pol TJ, et al. (1993). "Isolation of a candidate gene for Norrie disease by positional cloning.". Nat. Genet. 2 (1): 84. doi:10.1038/ng0992-84. PMID 1303256.
Meindl A, Berger W, Meitinger T, et al. (1993). "Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.". Nat. Genet. 2 (2): 139-43. doi:10.1038/ng1092-139. PMID 1303264.
Shastry BS, Hejtmancik JF, Plager DA, et al. (1995). "Linkage and candidate gene analysis of X-linked familial exudative vitreoretinopathy.". Genomics 27 (2): 341-4. doi:10.1006/geno.1995.1052. PMID 7558002.
Schuback DE, Chen ZY, Craig IW, et al. (1995). "Mutations in the Norrie disease gene.". Hum. Mutat. 5 (4): 285-92. doi:10.1002/humu.1380050403. PMID 7627181.
Meindl A, Lorenz B, Achatz H, et al. (1995). "Missense mutations in the NDP gene in patients with a less severe course of Norrie disease.". Hum. Mol. Genet. 4 (3): 489-90. PMID 7795608.
Joos KM, Kimura AE, Vandenburgh K, et al. (1995). "Ocular findings associated with a Cys39Arg mutation in the Norrie disease gene.". Arch. Ophthalmol. 112 (12): 1574-9. PMID 7993212.
Fuchs S, Xu SY, Caballero M, et al. (1994). "A missense point mutation (Leu13Arg) of the Norrie disease gene in a large Cuban kindred with Norrie disease.". Hum. Mol. Genet. 3 (4): 655-6. PMID 8069314.
Wong F, Goldberg MF, Hao Y (1993). "Identification of a nonsense mutation at codon 128 of the Norrie's disease gene in a male infant.". Arch. Ophthalmol. 111 (11): 1553-7. PMID 8240113.
Chen ZY, Battinelli EM, Fielder A, et al. (1994). "A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy.". Nat. Genet. 5 (2): 180-3. doi:10.1038/ng1093-180. PMID 8252044.
Chen ZY, Battinelli EM, Woodruff G, et al. (1994). "Characterization of a mutation within the NDP gene in a family with a manifesting female carrier.". Hum. Mol. Genet. 2 (10): 1727-9. PMID 8268931.
Meitinger T, Meindl A, Bork P, et al. (1994). "Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure.". Nat. Genet. 5 (4): 376-80. doi:10.1038/ng1293-376. PMID 8298646.
Strasberg P, Liede HA, Stein T, et al. (1996). "A novel mutation in the Norrie disease gene predicted to disrupt the cystine knot growth factor motif.". Hum. Mol. Genet. 4 (11): 2179-80. PMID 8589700.
Johnson K, Mintz-Hittner HA, Conley YP, Ferrell RE (1997). "X-linked exudative vitreoretinopathy caused by an arginine to leucine substitution (R121L) in the Norrie disease protein.". Clin. Genet. 50 (3): 113-5. PMID 8946107.