Del(2)Pax6^11Neu
Spontaneous Allele Detail

Summary

• Symbol: Del(2)Pax6^11Neu
• Name: deletion, Chr 2, Neuherberg 11
• MGI ID: MGI:3845668
• Synonyms: Del(2)Pax6^11Neu, Pax6^11Neu
• Gene: Del(2)Pax6^11Neu Location: unknown Genetic Position: Chr2, Syntenic

Mutation origin

• Strain of Origin: Oak Ridge Test-Stock x (102 x C3H)F1

Mutation description

• Allele Type: Spontaneous
• Mutation: Deletion
• Del(2)Pax6^11Neu involves 9 genes/genome features (Gm35885, Rcn1, 4930527A07Rik ...) View all
• Mutation details: This deletion in chromosome 2 is 540,470 bp long starting at position 105.001 and ending at 105.541 (Ensembl build 51). It extends from a point proximal to the Rcn1 gene and ends in intron 9 of the Elp4 gene. All of Rcn1 and Pax6 are thus deleted. Elp4 is truncated at its 3' end losing part of intron 9 and all of exon 10. (J:151902)

Expression

In Structures Affected by this Mutation:

10 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 11Neu 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)