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Phe
Spontaneous Allele Detail
Summary
Symbol: Phe
Name: patch deletion region; patch extended
MGI ID: MGI:1889551
Gene: Ph  Location: Chr5:75315348-75330641 bp  Genetic Position: Chr5, Syntenic
Alliance: Phe page
Mutation
origin
Strain of Origin:  STOCK Ph
Mutation
description
Allele Type:    Spontaneous
Mutation:    Deletion
  Phe involves 1 genes/genome features (Pdgfra) View all
 
Mutation detailsThis allele comprises a deletion including the Pdgfra gene. Precise breakpoints have not been mapped, but does not extend into the coding sequences of the adjacent Kit gene. However, expression of a functional KIT protein is altered in these mutants. (J:52810)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Ph Mutation:  1 strain or line available
Notes
Double heterozygotes of Phe with the closely linked genes KitW-v and Rw were different in color from those with Ph. In particular, Phe +/+ KitW-v mice resembled KitW-v homozygotes, and were sterile (J:5811).
References
Original:  J:5811 Truslove GM, A new allele at the patch locus in the mouse. Genet Res. 1977 Apr;29(2):183-6
All:  3 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
12/10/2024
MGI 6.24
The Jackson Laboratory