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NischV33A
Chemically induced Allele Detail
Summary
Symbol: NischV33A
Name: nischarin; V33A
MGI ID: MGI:6100940
Gene: Nisch  Location: Chr14:30892885-30928783 bp, - strand  Genetic Position: Chr14, 19.09 cM, cytoband B
Alliance: NischV33A page
Mutation
origin
Strain of Origin:  BALB/c
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to C mutation that results in the substitution of alanine for valine at position 33 (V33A). (J:244907)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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 Nisch Mutation:  72 strains or lines available
References
Original:  J:244907 Crompton M, et al., A mutation in Nischarin causes otitis media via LIMK1 and NF-kappaB pathways. PLoS Genet. 2017 Aug;13(8):e1006969
All:  2 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