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Kdrorv
Chemically induced Allele Detail
Summary
Symbol: Kdrorv
Name: kinase insert domain protein receptor; orvieto
MGI ID: MGI:5004965
Synonyms: Flk-1-
Gene: Kdr  Location: Chr5:76093487-76139118 bp, - strand  Genetic Position: Chr5, 40.23 cM
Alliance: Kdrorv page
Absence of blood cells and vasculature in E9.5-10.5 Kdrorv/Kdrorv embryos

Show the 5 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  129S1/Sv or C57BL/6
Mutation
description
Allele Type:    Chemically induced (ENU) (Null/knockout)
Mutation:    Single point mutation
 
Mutation detailsThis phenotypic mutant was generated in an ENU mutagenesis screen for early craniofacial development phenotypes. The molecular mutation is a C-to-A mutation at bp 1311 of the coding sequence, which results in translation change of TYR to STOP. (J:243205)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 27 assay results
In Structures Affected by this Mutation: 6 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 Kdr Mutation:  71 strains or lines available
References
Original:  J:171522 Sandell LL, et al., A phenotype-driven ENU mutagenesis screen identifies novel alleles with functional roles in early mouse craniofacial development. Genesis. 2011 Apr;49(4):342-59
All:  2 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
04/16/2024
MGI 6.23
The Jackson Laboratory