About   Help   FAQ
Phenotypic Alleles
Query Results -- Summary
 Symbol
Name
ID
Ammecr1
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
MGI:1860206

2 matching Alleles (1 Gene/Marker represented)
                                                                                 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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/15/2014
MGI 5.17
The Jackson Laboratory