The following gene names and symbols are associated with antigen Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 across different species:

Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (ammecr1), Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (Ammecr1)

Other aliases include:

AMMERC1, ammerc1, MGC84095, AMMECR1, Ammecr1

On the protein level the following designations are being used for antigen Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1:

AMMECR1 protein – Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 – Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1 – AMME syndrome candidate gene 1 protein homolog

Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 fulfills a number of functions:

molecular_function

Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 is relevant to the following processes:

biological_process

Locations for Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1:

cellular_component

Source: NCBI Entrez Gene, Gene Ontology