FAM120C
FAM120C | |||||||
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Identifiers | |||||||
Aliases | FAM120C, CXorf17, ORF34, family with sequence similarity 120C | ||||||
External IDs | MGI: 2387687 HomoloGene: 9876 GeneCards: FAM120C | ||||||
Orthologs | |||||||
Species | Human | Mouse | |||||
Entrez | |||||||
Ensembl | |||||||
UniProt | |||||||
RefSeq (mRNA) | |||||||
RefSeq (protein) | |||||||
Location (UCSC) | Chr X: 54.07 – 54.18 Mb | Chr X: 151.34 – 151.47 Mb | |||||
PubMed search | [1] | [2] | |||||
Wikidata | |||||||
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Family with sequence similarity 120C is a protein in humans that is encoded by the FAM120C gene. [3]
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
- ↑ "Human PubMed Reference:".
- ↑ "Mouse PubMed Reference:".
- ↑ "Entrez Gene: Family with sequence similarity 120C". Retrieved 2012-10-30.
Further reading
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