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Del(2)Pax611Neu
Spontaneous Allele Detail
Summary
Symbol: Del(2)Pax611Neu
Name: deletion, Chr 2, Neuherberg 11
MGI ID: MGI:3845668
Synonyms: Del(2)Pax611Neu, Pax611Neu
Gene: Del(2)Pax611Neu  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)Pax611Neu involves 9 genes/genome features (Gm35885, Rcn1, 4930527A07Rik ...) View all
 
Mutation detailsThis 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)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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)Pax611Neu 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)

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