Human (GRCh37.p13)
Description

family with sequence similarity 47, member C [Source:HGNC Symbol;Acc:25301]

Location

Chromosome X: 37,026,432-37,029,739 forward strand.

GRCh37:CM000685.1

View alleles of this gene on alternative sequences

About this gene

This gene has 1 transcript (splice variant), 1 gene allele, 4 paralogues and is associated with 72 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000358047.3FAM47C-00133081035aaENSP00000367913.2
 
Protein coding
CCDS35227Q5HY64 NM_001013736.2GENCODE basic