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FAM120C

From Wikipedia, the free encyclopedia
FAM120C
Identifiers
AliasesFAM120C, CXorf17, ORF34, family with sequence similarity 120C
External IDsOMIM: 300741; MGI: 2387687; HomoloGene: 9876; GeneCards: FAM120C; OMA:FAM120C - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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 MbChr X: 150.13 – 150.25 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/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

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000184083Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025262Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Family with sequence similarity 120C". Retrieved 2012-10-30.

Further reading

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