Symbol Name ID

Ammecr1 Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 MGI:1860206

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2 matching Alleles (1 Gene/Marker represented)

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                                                                                 Allele Symbol
Name                                                                                   Chr  Synonyms              Category              Phenotypic Classes  Human Diseases

Ammecr1tm1a(EUCOMM)Hmgu
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1; targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH   X              Targeted (Floxed/Frt)
(Cell Line)                                    

Ammecr1tm1(NCOM)Mfgc
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1; targeted mutation 1, Mammalian Functional Genomics Centre  X              Targeted (knock-out)
(Cell Line)