Gene: LOC107984989

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

Gene: DRC3

Alternate names for this Gene: CFAP134|LRRC48

Gene Summary:

Gene is located in Chromosome: 17

Location in Chromosome : 17p11.2|17p11.2

Description of this Gene: dynein regulatory complex subunit 3

Type of Gene: protein-coding

Gene: ATPAF2

Alternate names for this Gene: ATP12|ATP12p|LP3663|MC5DN1

Gene Summary: This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith-Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined.

Gene is located in Chromosome: 17

Location in Chromosome : 17p11.2

Description of this Gene: ATP synthase mitochondrial F1 complex assembly factor 2

Type of Gene: protein-coding

rs7219320 in LOC107984989;DRC3;ATPAF2 gene and Coronary Artery Disease PMID 23202125 2013 Large-scale association analysis identifies new risk loci for coronary artery disease.