About   Help   FAQ
Gene Expression Literature Summary
Symbol
Name
ID
Ammecr1
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
MGI:1860206

1 matching records from 1 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.
Age A
Northern blot 1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available
Ammecr1  Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1   (Synonyms: 6230420G18Rik)
Results  Reference
1*J:62787 Vitelli F, Meloni I, Fineschi S, Favara F, Tiziana Storlazzi C, Rocchi M, Renieri A, Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3. Cytogenet Cell Genet. 2000;88(3-4):259-63

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
09/09/2014
MGI 5.19
The Jackson Laboratory