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

Symbol:	Smc1bm1Ham
Name:	structural maintenance of chromosomes 1B; mutation 1, Hamamatsu University School of Medicine
MGI ID:	MGI:4836167
Synonyms:	Smc1bm1-Ham
Gene:	Smc1b  Location: Chr15:84948890-85016158 bp, - strand  Genetic Position: Chr15, 40.25 cM, cytoband E3
Alliance:	Smc1bm1Ham page

Strain of Origin:

ICR

Allele Type:    Spontaneous Mutation:    Intragenic deletion     A 16 bp deletion in exon 5 results in a frame-shift that generates a stop codon (TAA) at codon 247. (J:164958) Inheritance:    Recessive

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

In Structures Affected by this Mutation:

3 anatomical structure(s)

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 Smc1b Mutation:	69 strains or lines available

Original:	J:164958 Takabayashi S, et al., A spontaneous smc1b mutation causes cohesin protein dysfunction and sterility in mice. Exp Biol Med (Maywood). 2009 Aug;234(8):994-1001
All:	1 reference(s)