Del(2)Pax6^13Neu
Spontaneous Allele Detail

Summary

• Symbol: Del(2)Pax6^13Neu
• Name: deletion, Chr 2, Neuherberg 13
• MGI ID: MGI:3845753
• Synonyms: Del(2)Pax6^13Neu3Neu
• Gene: Del(2)Pax6^13Neu Location: unknown Genetic Position: Chr2, Syntenic

Mutation origin

• Strain of Origin: (102 x C3H)F1

Mutation description

• Allele Type: Spontaneous
• Mutation: Intergenic deletion
• Del(2)Pax6^13Neu involves 8 genes/genome features (Gm35885, Pax6os1, Pax6 ...) View all
• Mutation details: This is a 237,725 bp deletion in chromosome 2 starting at position 105.488 and extending to 105.726 (Ensembl build 51). The deletion starts in intron 6 of Pax6 and includes the entire Elp4 gene. The deletion ends in intron 2 of Immp1l. (J:151902)

Expression

In Structures Affected by this Mutation:

2 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 Del(2)Pax6 13Neu Mutation: 0 strains or lines available

References

• Original: J:151902 Favor J, et al., Analysis of Pax6 Contiguous Gene Deletions in the Mouse, Mus musculus, Identifies Regions Distinct from Pax6 Responsible for Extreme Small-Eye and Belly-Spotting Phenotypes. Genetics. 2009 Aug;182(4):1077-88
• All: 1 reference(s)