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| Nomenclature |
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Symbol:
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Pdcd10tm1Wami
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Name:
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programmed cell death 10;
targeted mutation 1, Wang Min
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MGI ID: |
MGI:5002630 |
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Synonyms: |
CCM3loxP, Pdcd10tm1Wmin |
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Gene:
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Pdcd10
Location:
Chr3:75516490-75556856 bp, - strand
Genetic Position: Chr3,
33.76 cM, cytoband E3
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:171969
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129 and C57BL/6
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Mutation
description |
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Allele
Type: | |
Targeted (Floxed/Frt) |
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Mutation: | |
Insertion |
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Mutation details: A loxP site was inserted upstream of exon 4. A floxed neo cassette was inserted downstream of exon 5. (J:171969)
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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 Pdcd10 Mutation:
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7 strains or lines available |
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| References |
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Original: |
J:171969
He Y et al.,
"Stabilization of VEGFR2 signaling by cerebral cavernous malformation 3 is critical for vascular development."
Sci Signal 2010;3(116):ra26
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All: |
2 reference(s)
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Analysis Tools
