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| Nomenclature |
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Symbol:
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Slc2a10G128E
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Name:
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solute carrier family 2 (facilitated glucose transporter), member 10;
Gly128Glu
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MGI ID: |
MGI:3814338 |
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Gene:
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Slc2a10
Location:
Chr2:165503787-165519917 bp, + strand
Genetic Position: Chr2,
85.66 cM
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Mutation
origin |
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Strain of Origin:
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C3HeB/FeJ
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Mutation
description |
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Allele
Type: | |
Chemically induced (ENU) |
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Mutation: | |
Single point mutation |
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Mutation details: ENU induced a point mutation of G>A at position 383 that results in the amino acid substitution of glutamic acid for glycine at position 128 (G128E). (J:140316)
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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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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Slc2a10 Mutation:
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1 strain or line available |
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| References |
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Original: |
J:140316
Callewaert BL et al.,
"Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutions."
Genesis 2008 Aug;46(8):385-9
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All: |
3 reference(s)
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Analysis Tools
