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B9d1tm1d(EUCOMM)Wtsi
Targeted Allele Detail
Summary
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
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:178421
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6N
Project Collection: EUCOMM
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsCre-mediated recombination of B9d1tm1c(EUCOMM)Wtsi removed exon 3. (J:178421)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 34 assay results
In Structures Affected by this Mutation: 8 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 B9d1 Mutation:  14 strains or lines available
References
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)

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
07/05/2024
MGI 6.24
The Jackson Laboratory