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Slc26a5mpc234H
Chemically induced Allele Detail
Nomenclature
Symbol: Slc26a5mpc234H
Name: solute carrier family 26, member 5; muta-ped-c3pde 234, Harwell
MGI ID: MGI:5792083
Gene: Slc26a5  Location: Chr5:21810655-21865604 bp, - strand  Genetic Position: Chr5, 9.97 cM, cytoband A3
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Harwell ENU Mutagenesis
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a G to T point mutation that results in the amino acid substitution of valine for glycine at position 379 (G379V). (J:234901)
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Slc26a5 Mutation:  34 strains or lines available
References
Original:  J:234901 Potter PK, et al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nat Commun. 2016;7:12444
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
06/30/2020
MGI 6.15
The Jackson Laboratory