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Nptx1tm1Mspn
Targeted Allele Detail
Summary
Symbol: Nptx1tm1Mspn
Name: neuronal pentraxin 1; targeted mutation 1, Mark S Perin
MGI ID: MGI:3628746
Synonyms: NARP-, NP1-
Gene: Nptx1  Location: Chr11:119429545-119438579 bp, - strand  Genetic Position: Chr11, 83.95 cM, cytoband E1-E2
Alliance: Nptx1tm1Mspn page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:62756
Parent Cell Line:  AB2.1 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1b-m2
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 1 and the signal peptide were replaced with a PGK-hprt cassette. Western blot failed to detect protein in mutants. (J:62756)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Nptx1 Mutation:  24 strains or lines available
References
Original:  J:62756 Kirkpatrick LL, et al., Biochemical interactions of the neuronal pentraxins. Neuronal pentraxin (NP) receptor binds to taipoxin and taipoxin-associated calcium-binding protein 49 via NP1 and NP2. J Biol Chem. 2000 Jun 9;275(23):17786-92
All:  7 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