Human (GRCh38.p14)
Description

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

Location

Chromosome X: 37,008,366-37,011,664 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 1 transcript (splice variant), 117 orthologues, 18 paralogues and is associated with 54 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000358047.5FAM47C-20132991035aaENSP00000367913.3
 
Protein coding
CCDS35227Q5HY64 NM_001013736.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:NA