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Bhlha9tm1Nba
Targeted Allele Detail
Summary
Symbol: Bhlha9tm1Nba
Name: basic helix-loop-helix family, member a9; targeted mutation 1, Nissim Ben-Arie
MGI ID: MGI:5604430
Synonyms: Fingerin null
Gene: Bhlha9  Location: Chr11:76563296-76564502 bp, + strand  Genetic Position: Chr11, 45.97 cM
Alliance: Bhlha9tm1Nba page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:214852
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe targeting vector eliminates the coding sequence and replaces it by a promoterless nuclear lacZ reporter gene and a Neomycin resistance gene. X-gal staining is seen in the limb bud as early as E9.5. (J:214852)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 45 assay results
In Structures Affected by this Mutation: 3 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 Bhlha9 Mutation:  10 strains or lines available
References
Original:  J:214852 Schatz O, et al., Gene dosage of the transcription factor Fingerin (bHLHA9) affects digit development and links syndactyly to ectrodactyly. Hum Mol Genet. 2014 Oct 15;23(20):5394-401
All:  2 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
03/19/2024
MGI 6.23
The Jackson Laboratory