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Wnt9atm1.1Chha
Targeted Allele Detail
Nomenclature
Symbol: Wnt9atm1.1Chha
Name: wingless-type MMTV integration site family, member 9A; targeted mutation 1.1, Christine Hartmann
MGI ID: MGI:3701349
Synonyms: Wnt9adelta
Gene: Wnt9a  Location: Chr11:59306928-59333552 bp, + strand  Genetic Position: Chr11, 37.55 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:119030
Parent Cell Line:  C1 (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
    Exon 2 was removed by cre recombination resulting in a truncated transcript confirmed by RT-PCR. (J:119030)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Wnt9a Mutation:  10 strains or lines available
References
Original:  J:119030 Spater D, et al., Wnt9a signaling is required for joint integrity and regulation of Ihh during chondrogenesis. Development. 2006 Aug;133(15):3039-49
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/20/2017
MGI 6.10
The Jackson Laboratory