The FAM20C gene homepage

General information
Gene symbol FAM20C
Gene name family with sequence similarity 20, member C
Chromosome 7
Chromosomal band p22.3
Imprinted Unknown
Genomic reference NC_000007.13
Transcript reference NM_020223.3
Associated with diseases ID, Raine syndrome
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 1
Hidden variants 23
Date created October 29, 2013
Date last updated September 20, 2016
Version FAM20C:160920

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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:22140
Entrez Gene 56975
PubMed articles FAM20C
OMIM - Gene 611061
OMIM - Diseases Raine syndrome
HGMD FAM20C
GeneCards FAM20C
GeneTests FAM20C


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00002818 7 family with sequence similarity 20, member C NM_020223.3 NP_064608.2 1


Copyright & disclaimer
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