Mus musculus Protein: Ammecr1
Summary
InnateDB Protein IDBP-176605.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Ammecr1
Protein Name Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human)
Synonyms 6230420G18Rik;
Species Mus musculus
Ensembl Protein ENSMUSP00000036085
InnateDB Gene IDBG-176603 (Ammecr1)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0005515 protein binding
Biological Process
GO:0008150 biological_process
Cellular Component
GO:0005575 cellular_component
Protein Structure and Domains
PDB ID MGI:1860206
InterPro IPR002733 AMMECR1 domain
IPR023473 AMMECR1
PFAM PF01871
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9JHT5
PhosphoSite PhosphoSite-Q9JHT5
TrEMBL
UniProt Splice Variant
Entrez Gene 56068
UniGene Mm.409950
RefSeq NP_062369
MGI ID
MGI Symbol Ammecr1
OMIM
CCDS CCDS30452
HPRD
IMGT
EMBL AJ243485 AK051736
GenPept BAC34745 CAB95767