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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 Ammecr1Gt(XK571)Byg
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1; gene trap XK571, BayGenomics
images X Gene trapped
(Chimeric) no abnormal phenotype observed Ammecr1Gt(IST11924D7)Tigm
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1; gene trap IST11924D7, Texas A&M Institute for Genomic Medicine X Gene trapped
(Cell Line)

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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