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Alms1L2131X
Chemically induced Allele Detail
Nomenclature
Symbol: Alms1L2131X
Name: ALMS1, centrosome and basal body associated; L2131
MGI ID: MGI:3699224
Gene: Alms1  Location: Chr6:85587531-85702753 bp, + strand  Genetic Position: Chr6, 37.48 cM
Kidney abnormalities of Alms1L2131X/Alms1L2131X mice at 6 months of age

Show the 3 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Nucleotide substitutions
 
Mutation detailsThis mutation causes premature truncation in exon 10, resulting in the coding of the N-terminal 2131 amino acids of the protein. (J:118221)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 11 anatomical structures
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 Alms1 Mutation:  89 strains or lines available
References
Original:  J:118221 Li G, et al., A Role for Alstrom Syndrome Protein, Alms1, in Kidney Ciliogenesis and Cellular Quiescence. PLoS Genet. 2007 Jan 5;3(1):e8
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/15/2018
MGI 6.12
The Jackson Laboratory