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Ndptm1.1Nat
Targeted Allele Detail
Summary
Symbol: Ndptm1.1Nat
Name: Norrie disease (pseudoglioma) (human); targeted mutation 1.1, Jeremy Nathans
MGI ID: MGI:4412060
Synonyms: NdpAP
Gene: Ndp  Location: ChrX:16751760-16778013 bp, - strand  Genetic Position: ChrX, 12.07 cM
Alliance: Ndptm1.1Nat page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:154020
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsAn alkaline phosphatase sequence was inserted in exon2 along with an frt flanked PGK-neomycin cassette. Excision of the PGK-neo cassette was accomplished by crossing mice to Tg(ACTFLPe)9205Dym. (J:154020)
Expression
In Mice Carrying this Mutation: 61 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Ndp Mutation:  7 strains or lines available
References
Original:  J:154020 Ye X, et al., Norrin, frizzled-4, and Lrp5 signaling in endothelial cells controls a genetic program for retinal vascularization. Cell. 2009 Oct 16;139(2):285-98
All:  4 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory