FAM120C

Family with sequence similarity 120C is a protein in humans that is encoded by the FAM120C gene. [5]

FAM120C
Identifiers
Aliases	FAM120C, CXorf17, ORF34, family with sequence similarity 120C
External IDs	OMIM: 300741 MGI: 2387687 HomoloGene: 9876 GeneCards: FAM120C
Gene location (Human) Chr. X chromosome (human)[1] Band Xp11.22 Start 54,068,324 bp[1] End 54,183,281 bp[1]
Gene location (Mouse) Chr. X chromosome (mouse)[2] Band X|X F3 Start 150,127,171 bp[2] End 150,254,838 bp[2]
RNA expression pattern Bgee Top expressed in ovary globus pallidus brain amygdala inferior ganglion of vagus nerve corpus callosum medulla oblongata substantia nigra More reference expression data BioGPS n/a
Orthologs
Species	Human	Mouse
Entrez	54954	207375
Ensembl	ENSG00000184083	ENSMUSG00000025262
UniProt	Q9NX05	Q8C3F2
RefSeq (mRNA)	NM_001300788 NM_017848 NM_198456	NM_198105
RefSeq (protein)	NP_001287717 NP_060318 NP_940858	NP_932773
Location (UCSC)	Chr X: 54.07 – 54.18 Mb	Chr X: 150.13 – 150.25 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

This gene encodes a potential transmembrane protein and lies in a region where mutations and deletions have been associated with intellectual disability and autism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011].