FAM120C

FAM120C
Identifiers
Aliases	FAM120C, CXorf17, ORF34, family with sequence similarity 120C
External IDs	OMIM: 300741; MGI: 2387687; HomoloGene: 9876; GeneCards: FAM120C; OMA:FAM120C - orthologs
Gene location (Human)
Chr.	X chromosome (human)
End	54,183,281 bp
Gene location (Mouse)
Chr.	X chromosome (mouse)
End	150,254,838 bp
RNA expression pattern
	Top expressed in
	inferior ganglion of vagus nerve; ; ventral tegmental area; ; internal globus pallidus; ; subthalamic nucleus; ; superior vestibular nucleus; ; pars reticulata; ; cerebellar vermis; ; mucosa of paranasal sinus; ; trigeminal ganglion; ; gonad;
	Top expressed in
	arcuate nucleus; ; paraventricular nucleus of hypothalamus; ; suprachiasmatic nucleus; ; dorsomedial hypothalamic nucleus; ; interventricular septum; ; median eminence; ; ventral tegmental area; ; central gray substance of midbrain; ; habenula; ; olfactory tubercle;
	More reference expression data
	n/a
Orthologs
	54954
	207375
	ENSG00000184083
	ENSMUSG00000025262
	Q9NX05
	Q8C3F2
	NM_001300788; NM_017848; NM_198456
	NM_198105
	NP_001287717; NP_060318; NP_940858
	NP_932773
	Wikidata
View/Edit Human	View/Edit Mouse

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

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].

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000184083 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000025262 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: Family with sequence similarity 120C". Retrieved 2012-10-30.

References

Further reading