FAM47B gene homepage

General information
Gene symbol FAM47B
Gene name family with sequence similarity 47, member B
Chromosome X
Chromosomal band p21.1
Imprinted Unknown
Genomic reference NG_021372.1
Transcript reference NM_152631.2
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 74
Unique public DNA variants reported 74
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 26659
Entrez Gene 170062
PubMed articles FAM47B

Active transcripts




NCBI ID     

NCBI Protein ID     

00005626 X family with sequence similarity 47, member B NM_152631.2 NP_689844.2 74