Atp7atm1.1Mjp
Targeted Allele Detail
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Symbol: |
Atp7atm1.1Mjp |
Name: |
ATPase, Cu++ transporting, alpha polypeptide; targeted mutation 1.1, Michael J Petris |
MGI ID: |
MGI:5447640 |
Synonyms: |
Atp7afl |
Gene: |
Atp7a Location: ChrX:105070882-105168532 bp, + strand Genetic Position: ChrX, 47.36 cM
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Alliance: |
Atp7atm1.1Mjp page
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Patches of hypopigmentation in coats of Atp7atm1.1Mjp/Atp7a+ Cldn6tm1(cre)Dkwu/Cldn6+ females
Show the 3 phenotype image(s) involving this allele.
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Germline Transmission: |
Earliest citation of germline transmission:
J:189931
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
Not Specified
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Allele Type: |
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Targeted (Conditional ready, No functional change) |
Mutation: |
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Insertion
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Mutation details: A loxP site was inserted upstream of exon 11. An FRT-flanked neo cassette with a 3' loxP site was inserted downstream of exon 11. Flp-mediated recombination removed the neo cassette and left exon 11 floxed.
(J:189931)
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Generation of the Atp7atm1.1Mjp allele |
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View phenotypes and curated references for all genotypes (concatenated display).
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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
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Carrying any Atp7a Mutation: |
69 strains or lines available
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Original: |
J:189931 Wang Y, et al., Conditional knockout of the Menkes disease copper transporter demonstrates its critical role in embryogenesis. PLoS One. 2012;7(8):e43039 |
All: |
6 reference(s) |
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