Slc26a5<mpc234H> Chemically induced Allele Detail MGI Mouse (MGI:5792083)

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Slc26a5^mpc234H
Chemically induced Allele Detail

Summary | Mutation origin | Mutation description | Phenotypes | Find Mice (IMSR) | References

Summary

Symbol:	Slc26a5^mpc234H
Name:	solute carrier family 26, member 5; muta-ped-c3pde 234, Harwell
MGI ID:	MGI:5792083
Gene:	Slc26a5 Location: Chr5:22015653-22070602 bp, - strand Genetic Position: Chr5, 9.97 cM, cytoband A3
Alliance:	Slc26a5^mpc234H page

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 details: ENU 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

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:	58 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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