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Rab38m1Btlr
Chemically induced Allele Detail
Summary
Symbol: Rab38m1Btlr
Name: RAB38, member RAS oncogene family; mutation 1, Bruce Beutler
MGI ID: MGI:5497994
Synonyms: fenrir
Gene: Rab38  Location: Chr7:88079481-88140780 bp, + strand  Genetic Position: Chr7, 49.19 cM
Alliance: Rab38m1Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsCapillary sequencing of the mutated genes identified the causative mutation as a T to A transversion at base pair 88450541 (v38) on Chromosome 7 in the GenBank genomic region NC_000073 encoding Rab38. The mutation corresponds to residue 263 in the mRNA sequence within exon 2 of 3 total exons. The mutation results in a Isoleucine (I) to Asparagine (N) at position 88 (I88N). (J:198554)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Rab38 Mutation:  15 strains or lines available
Notes
Whole genome HiSeq sequencing of the G1 grandsire identified 61 mutations.
References
Original:  J:198554 Beutler B, Direct data submission for a Rab38 allele. MGI Direct Data Submission. 2013;
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