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Bbs1tm2Vcs
Targeted Allele Detail
Nomenclature
Symbol: Bbs1tm2Vcs
Name: Bardet-Biedl syndrome 1 (human); targeted mutation 2, Val C Sheffield
MGI ID: MGI:5474481
Synonyms: Bbs1loxP
Gene: Bbs1  Location: Chr19:4936906-4956656 bp, - strand  Genetic Position: Chr19, 4.14 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:194096
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
    Exon 3 was floxed. (J:194096)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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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 Bbs1 Mutation:  56 strains or lines available
References
Original:  J:194096 Carter CS, et al., Abnormal development of NG2+PDGFR-alpha+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model. Nat Med. 2012 Dec;18(12):1797-804
All:  5 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
01/12/2022
MGI 6.17
The Jackson Laboratory