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Slc23a1tm1Mlev
Targeted Allele Detail
Summary
Symbol: Slc23a1tm1Mlev
Name: solute carrier family 23 (nucleobase transporters), member 1; targeted mutation 1, Mark Levine
MGI ID: MGI:4457389
Gene: Slc23a1  Location: Chr18:35747657-35760297 bp, - strand  Genetic Position: Chr18, 19.17 cM
Alliance: Slc23a1tm1Mlev page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:159697
Parent Cell Line:  Other (see notes) (ES Cell)
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExons 1 through 12 were replaced with a neo cassette. The absence of transcript expression was confirmed by RT-PCR on liver, kidney, and small intestine extracts. (J:159697)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Slc23a1 Mutation:  27 strains or lines available
Notes
ES cell line = HGTC-8 (C57BL/6J)
References
Original:  J:159697 Corpe CP, et al., Vitamin C transporter Slc23a1 links renal reabsorption, vitamin C tissue accumulation, and perinatal survival in mice. J Clin Invest. 2010 Apr;120(4):1069-83
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
03/19/2024
MGI 6.23
The Jackson Laboratory