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Phenotypic Alleles
Query Results -- Summary
 Symbol
Name
ID
Mmadhc
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
MGI:1923786

4 matching Alleles (1 Gene/Marker represented)
                                                                      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) Mmadhctm1e(KOMP)Wtsi
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria; targeted mutation 1e, Wellcome Trust Sanger Institute 2 Targeted (Reporter)
(Cell Line) Mmadhctm2e(KOMP)Wtsi
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria; targeted mutation 2e, Wellcome Trust Sanger Institute 2 Targeted (Reporter)
(Cell Line)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory