AMMECR1 gene homepage

General information
Gene symbol AMMECR1
Gene name Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Chromosome X
Chromosomal band q22.3
Imprinted Unknown
Genomic reference NG_016469.1
Transcript reference NM_001025580.1
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 35
Unique public DNA variants reported 35
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 467
Entrez Gene 9949
PubMed articles AMMECR1
OMIM - Gene 300195


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000625 X transcript variant 2 NM_001025580.1 NP_001020751.1 35