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| Nomenclature |
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Symbol:
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bpck
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Name:
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bilateral polycystic kidney deletion region;
bilateral polycystic kidneys
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MGI ID: |
MGI:3688712 |
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Synonyms: |
Tmem67bpck |
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Gene:
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bpck
Location:
unknown
Genetic Position: Chr4,
Syntenic
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Mutation
origin |
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Strain of Origin:
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B6C3Fe a/a-tip/J
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Intergenic deletion |
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Mutation details: This spontaneous deletion spans approximately 0.6 cM between D4Mit261 and D4Mit19, including the coding region of 6 genes, but the bilateral polycystic kidney phenotype was traced specifically to the absence of Tmem67 via BAC rescue with various length BACs. (J:144929)
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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:144929
Cook SA et al.,
"A Mouse Model for Meckel Syndrome Type 3."
J Am Soc Nephrol 2009 Apr;20(4):753-64
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All: |
2 reference(s)
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Analysis Tools
