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Tulp1rd18
Spontaneous Allele Detail
Summary
Symbol: Tulp1rd18
Name: TUB like protein 1; retinal degeneration 18
MGI ID: MGI:6842317
Gene: Tulp1  Location: Chr17:28570489-28584190 bp, - strand  Genetic Position: Chr17, 14.66 cM
Alliance: Tulp1rd18 page
Mutation
origin
Strain of Origin:  NOD.B6-Tg(IghelMD4)4Ccg/DvsJ
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Not Specified
 
Mutation detailsAlthough no sequence defect was found in the coding sequence, this mutation mapped to the area of Chromosome 17 around Tulp1 and failed to complement Tulp1tm1Pjn in an allele test.
Inheritance:    Recessive
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 Tulp1 Mutation:  40 strains or lines available
References
Original:  J:316780 Chang B, et al., New mouse model of retinal degeneration (RD18)B. ISER Annual Meeting. 2010;:P352A
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
04/23/2024
MGI 6.23
The Jackson Laboratory