Results for "AMMECR1, N-terminal": 4 genes

Name

AMMECR1-IT1 Gene

AMMECR1 intronic transcript 1

AMMECR1 Gene

Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1

The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010]

AMMECR1L Gene

AMMECR1-like

Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025]

AMMECR1LP1 Gene

AMMECR1-like pseudogene 1