View FAM126A gene homepage

General information
Gene symbol FAM126A
Gene name family with sequence similarity 126, member A
Chromosome 7
Chromosomal band p15.3
Imprinted Unknown
Genomic reference NG_008392.1
Transcript reference NM_032581.3
Associated with diseases Hypomyelination and Congenital Cataract
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 6
Unique public DNA variants reported 6
Individuals with public variants 6
Hidden variants 0
Date created May 03, 2013
Date last updated April 02, 2015
Version FAM126A:150402

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 24587
Entrez Gene 84668
PubMed articles FAM126A
OMIM - Gene 610531
OMIM - Diseases Hypomyelination and Congenital Cataract

Active transcripts




NCBI ID     

NCBI Protein ID     

00007563 7 family with sequence similarity 126, member A NM_032581.3 NP_115970.2 6