KOMP Knock Out Knockout Mouse Mice
Ammecr1 Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 Synonyms: 6230420G18Rik Gene nomenclature, locus information, and GO, OMIM, and PMID associations
are updated daily from MGI
MGI: MGI:1860206 ( Current, 63.74cM, Gene) Ensembl: ENSMUSG42225 ( Ammecr1) NCBI: 18861, 56068 Vega: OTTMUSG18861 ( Ammecr1, "Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human)") CCDS: 30452, 30452.1 OMIM:
, AMME COMPLEX
ALPORT SYNDROME, MENTAL RETARDATION, MIDFACE HYPOPLASIA, AND ELLIPTOCYTOSIS Gene Ontology: Ammecr1
Mouse Phenome DB: Ammecr1
UCSC: Chr.X:142,853,474-142,966,728(-) IMPC: Ammecr1
Non-KOMP projects associated with this gene exist at: EUCOMM, NORCOMM, TIGM. You can view the status of all IKMC projects for Ammecr1. Researchers interested in Ammecr1 are also interested* in
* Based on co-mentions in published literature. For more gene-gene associations visit genecloud.org.
The KOMP Repository Collection is located at the MMRRC at the University of California, Davis and Children’s Hospital Oakland Research Institute. Question? Comments? For Mice, Cells, and germplasm please contact us at email@example.com, US 1-888-KOMP-MICE or International +1-530-752-KOMP, or for vectors firstname.lastname@example.org or +1-510-450-7917.