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| Nomenclature |
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Symbol:
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Ddr2slie
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Name:
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discoidin domain receptor family, member 2;
smallie
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MGI ID: |
MGI:3640081 |
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Gene:
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Ddr2
Location:
Chr1:169972307-170088944 bp, - strand
Genetic Position: Chr1,
76.84 cM, cytoband H1-H5
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Mutation
origin |
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Strain of Origin:
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BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpefat/LtJng
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Intragenic deletion |
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Mutation details: The mutation is a deletion of approximately 150kb encompassing most of the Ddr2 gene, of which genomic PCR analysis failed to amplify exons 1-17; exon 18 of this gene and the final exon of the proximal gene, Hsd17b7, both were amplified. (J:134371)
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Inheritance: | |
Recessive |
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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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| References |
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Original: |
J:134371
Kano K et al.,
"A novel dwarfism with gonadal dysfunction due to loss-of-function allele of the collagen receptor gene, Ddr2, in the mouse."
Mol Endocrinol 2008 Aug;22(8):1866-80
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All: |
3 reference(s)
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Analysis Tools
