Summary | Mutation origin | Mutation description | Expression | Phenotypes | Disease models | Find Mice (IMSR) | References

Symbol:	Alms1bbb
Name:	ALMS1, centrosome and basal body associated; blobby
MGI ID:	MGI:3611799
Gene:	Alms1  Location: Chr6:85564513-85679735 bp, + strand  Genetic Position: Chr6, 37.48 cM
Alliance:	Alms1bbb page

Strain of Origin:	C57BL/6JSfdAnu
Project Collection:	APF ENU Mutagenesis

Allele Type:    Chemically induced (ENU) (Not Specified) Mutation:    Single point mutation   Mutation details: ENU mutagenesis induced an T to A point mutation that results in the amino acid substitution of a STOp codon for leucine at position 2130 (L2130X). Inheritance:    Recessive

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

4 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Alms1 Mutation:	149 strains or lines available

Original:	J:104190 The Australian Phenomics Facility at The Australian National University, Heritable mouse mutants from the ENU mutagenesis program at the Australian Phenomics Facility at The Australian National University. MGI Direct Data Submission. 2006-2014;
All:	3 reference(s)