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

Symbol:	B9d1tm1d(EUCOMM)Wtsi
Name:	B9 protein domain 1; targeted mutation 1d, Wellcome Trust Sanger Institute
MGI ID:	MGI:5301332
Gene:	B9d1  Location: Chr11:61395970-61403757 bp, + strand  Genetic Position: Chr11, 37.96 cM
Alliance:	B9d1tm1d(EUCOMM)Wtsi page
IMPC:	B9d1 gene page

Germline Transmission:	Earliest citation of germline transmission: J:178421
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	C57BL/6N
Project Collection:	EUCOMM

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: Cre-mediated recombination of B9d1tm1c(EUCOMM)Wtsi removed exon 3. (J:178421)

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

In Mice Carrying this Mutation:	34 assay results
In Structures Affected by this Mutation:	8 anatomical structure(s)

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 B9d1 Mutation:	14 strains or lines available

Original:	J:178421 Dowdle WE, et al., Disruption of a ciliary B9 protein complex causes Meckel syndrome. Am J Hum Genet. 2011 Jul 15;89(1):94-110
All:	3 reference(s)