FAM13C

VALUE_ERROR (nil)
Identifiers
Aliases
External IDs	GeneCards: [1]
Orthologs
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a
Wikidata
View/Edit Human

Family with sequence similarity 13, member C is a protein that in humans is encoded by the FAM13C gene.

Further reading

• Wu, J. H.; Lemaitre, R. N.; Manichaikul, A; Guan, W; Tanaka, T; Foy, M; Kabagambe, E. K.; Djousse, L; Siscovick, D; Fretts, A. M.; Johnson, C; King, I. B.; Psaty, B. M.; McKnight, B; Rich, S. S.; Chen, Y. D.; Nettleton, J. A.; Tang, W; Bandinelli, S; Jacobs Jr, D. R.; Browning, B. L.; Laurie, C. C.; Gu, X; Tsai, M. Y.; Steffen, L. M.; Ferrucci, L; Fornage, M; Mozaffarian, D (2013). "Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: Results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium". Circulation: Cardiovascular Genetics. 6 (2): 171–83. doi:10.1161/CIRCGENETICS.112.964619. PMC 3891054. PMID 23362303.
• Karasik, D; Hsu, Y. H.; Zhou, Y; Cupples, L. A.; Kiel, D. P.; Demissie, S (2010). "Genome-wide pleiotropy of osteoporosis-related phenotypes: The Framingham Study". Journal of Bone and Mineral Research. 25 (7): 1555–63. doi:10.1002/jbmr.38. PMC 3153998. PMID 20200953.