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4930453N24Rikdin
Spontaneous Allele Detail
Nomenclature
Symbol: 4930453N24Rikdin
Name: RIKEN cDNA 4930453N24 gene; dense incisors
MGI ID: MGI:1856802
Gene: 4930453N24Rik  Location: Chr16:64762205-64772372 bp, - strand  Genetic Position: Chr16, 37.1 cM, cytoband C1.3
Mutation
origin
Strain of Origin:  C3H/HeJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA T-to-A point mutation at postition 729 of the cDNA (NM_026273) is predicted to result in premature truncation at position 243 of the encoded protein (p.C243X). (J:222308)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any 4930453N24Rik Mutation:  4 strains or lines available
References
Original:  J:32738 Sweet HO, et al., Dense incisors (din): a new mouse mutation on chromosome 16 affecting tooth eruption and body size. J Hered. 1996 Mar-Apr;87(2):162-7
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
01/14/2020
MGI 6.14
The Jackson Laboratory