Bhlhe22^tm1Gan
Targeted Allele Detail

Summary

• Symbol: Bhlhe22^tm1Gan
• Name: basic helix-loop-helix family, member e22; targeted mutation 1, Lin Gan
• MGI ID: MGI:3707409
• Synonyms: Bhlhb5^lacZ
• Gene: Bhlhe22 Location: Chr3:18108489-18111678 bp, + strand Genetic Position: Chr3, 4.98 cM, cytoband A2
• Alliance: Bhlhe22^tm1Gan page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:119663
• Parent Cell Line: AB1 (ES Cell)
• Strain of Origin: 129S7/SvEvBrd-Hprt1⁺

Mutation description

• Allele Type: Targeted (Null/knockout, Reporter)
• Mutations: Insertion, Intragenic deletion
• The entire coding sequence is replaced by a lacZ/neo cassette. (J:119663)

Expression

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 Bhlhe22 Mutation: 12 strains or lines available

References

• Original: J:119663 Feng L, et al., Requirement for Bhlhb5 in the specification of amacrine and cone bipolar subtypes in mouse retina. Development. 2006 Dec;133(24):4815-25
• All: 5 reference(s)