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Symbol Name ID |
Mmadhc methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria MGI:1923786 |
Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases
MmadhcGt(EUCE0066d05)Hmgu
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria; gene trap EUCE0066d05, Helmholtz Zentrum Muenchen GmbH 2 Gene trapped
(Cell Line)
MmadhcGt(EUCE0071f09)Hmgu
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria; gene trap EUCE0071f09, Helmholtz Zentrum Muenchen GmbH 2 Gene trapped
(Cell Line)
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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