Gene: ETFDH

Alternate names for this Gene: ETFQO|MADD

Gene Summary: This gene encodes a component of the electron-transfer system in mitochondria and is essential for electron transfer from a number of mitochondrial flavin-containing dehydrogenases to the main respiratory chain. Mutations in this gene are associated with glutaric acidemia. Alternatively spliced transcript variants that encode distinct isoforms have been observed.

Gene is located in Chromosome: 4

Location in Chromosome : 4q32.1

Description of this Gene: electron transfer flavoprotein dehydrogenase

Type of Gene: protein-coding

Gene: PPID

Alternate names for this Gene: CYP-40|CYPD

Gene Summary: The protein encoded by this gene is a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family. PPIases catalyze the cis-trans isomerization of proline imidic peptide bonds in oligopeptides and accelerate the folding of proteins. This protein has been shown to possess PPIase activity and, similar to other family members, can bind to the immunosuppressant cyclosporin A.

Gene is located in Chromosome: 4

Location in Chromosome : 4q32.1

Description of this Gene: peptidylprolyl isomerase D

Type of Gene: protein-coding

rs8396 in ETFDH;PPID gene and Acylcarnitines measurement PMID 26068415 2015 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.

rs8396 in ETFDH;PPID gene and Glucose measurement PMID 21886157 2011 Human metabolic individuality in biomedical and pharmaceutical research.

rs8396 in ETFDH;PPID gene and Serum albumin measurement PMID 20037589 2010 A genome-wide perspective of genetic variation in human metabolism.

rs8396 in ETFDH;PPID gene and elevated blood glucose level PMID 21886157 2011 Human metabolic individuality in biomedical and pharmaceutical research.