SLC35F1
Solute carrier family 35, member F1 is a protein that in humans is encoded by the SLC35F1 gene.[1] The gene is also known as C6orf169 or dJ230I3.1.[1]
References
- "Solute carrier family 35, member F1". Retrieved 2011-12-04.
Further reading
- Sotoodehnia, N.; Isaacs, A.; De Bakker, P. I. W.; Dörr, M.; Newton-Cheh, C.; Nolte, I. M.; Van Der Harst, P.; Müller, M.; Eijgelsheim, M.; Alonso, A.; Hicks, A. A.; Padmanabhan, S.; Hayward, C.; Smith, A. V.; Polasek, O.; Giovannone, S.; Fu, J.; Magnani, J. W.; Marciante, K. D.; Pfeufer, A.; Gharib, S. A.; Teumer, A.; Li, M.; Bis, J. C.; Rivadeneira, F.; Aspelund, T.; Köttgen, A.; Johnson, T.; Rice, K.; et al. (2010). "Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction". Nature Genetics. 42 (12): 1068–1076. doi:10.1038/ng.716. PMC 3338195. PMID 21076409.
- Eijgelsheim, M.; Newton-Cheh, C.; Sotoodehnia, N.; De Bakker, P. I. W.; Müller, M.; Morrison, A. C.; Smith, A. V.; Isaacs, A.; Sanna, S.; Dörr, M.; Navarro, P.; Fuchsberger, C.; Nolte, I. M.; De Geus, E. J. C.; Estrada, K.; Hwang, S. -J.; Bis, J. C.; Rückert, I. -M.; Alonso, A.; Launer, L. J.; Hottenga, J. J.; Rivadeneira, F.; Noseworthy, P. A.; Rice, K. M.; Perz, S.; Arking, D. E.; Spector, T. D.; Kors, J. A.; Aulchenko, Y. S.; Tarasov, K. V. (2010). "Genome-wide association analysis identifies multiple loci related to resting heart rate". Human Molecular Genetics. 19 (19): 3885–3894. doi:10.1093/hmg/ddq303. PMC 3657480. PMID 20639392.
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