FAM120C | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | FAM120C, CXorf17, ORF34, family with sequence similarity 120C | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 300741; MGI: 2387687; HomoloGene: 9876; GeneCards: FAM120C; OMA:FAM120C - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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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
[edit]- ^ 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.
Further reading
[edit]