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| Nomenclature |
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Symbol:
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Slc17a5tm1Lex
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Name:
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solute carrier family 17 (anion/sugar transporter), member 5;
targeted mutation 1, Lexicon Genetics
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MGI ID: |
MGI:3529082 |
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Synonyms: |
sialin- |
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Gene:
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Slc17a5
Location:
Chr9:78536488-78588041 bp, - strand
Genetic Position: Chr9,
43.65 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:103485
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129S5/SvEvBrd
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Mutation
description |
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Allele
Type: | |
Targeted (Reporter) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: The first 104 nucleotides of the coding region were replaced with an IRES and beta-geo cassette. The absence of transcript expression was confirmed by RT-PCR analysis on liver extracts. The absence of protein expression was confirmed by immunhistochemistry on granule cell layer and hilar neurons of the dentate gyrus samples. (J:103485, J:158444)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Notes |
Phenotypic Similarity to Human Syndrome: lysosomal storage disease (J:103485)
See also,
data
as provided by Lexicon Genetics, Inc.
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| References |
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Original: |
J:103485
Lexicon Genetics Inc,
"NIH initiative supporting placement of Lexicon Genetics, Inc. mice into public repositories"
MGI Direct Data Submission 2005;():
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All: |
2 reference(s)
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Analysis Tools
