FAM47C gene homepage

General information
Gene symbol FAM47C
Gene name family with sequence similarity 47, member C
Chromosome X
Chromosomal band p21.1
Imprinted Unknown
Genomic reference NG_021373.1
Transcript reference NM_001013736.2
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 112
Unique public DNA variants reported 112
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 25301
Entrez Gene 442444
PubMed articles FAM47C

Active transcripts




NCBI ID     

NCBI Protein ID     

00005627 X family with sequence similarity 47, member C NM_001013736.2 NP_001013758.1 112