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C7orf10 encodes a protein that is similar to members of the CaiB/baiF CoA-transferase protein family. Additionally we are shipping and and many more products for this protein.
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Chromosome microarray analysis showed a 125kb homozygous pathogenic deletion, which includes genes MPLKIP and SUGCT, not described before. This is the first case described in Peru of a novel contiguous gene deletion of Trichothiodystrophy type 4 and Glutaric aciduria type 3 performed by chromosome microarray analysis.
C7orf10 encodes succinate-hydroxymethylglutarate CoA-transferase, which is the enzyme that converts glutarate to glutaryl-CoA
Identified as a candidate disease gene for OXPHOS disorders by next-generation sequencing
Geneic mapping of GA3 to chromosome 7 and identification of mutations in c7orf10 are reported.
This gene encodes a protein that is similar to members of the CaiB/baiF CoA-transferase protein family. Mutations in this gene are associated with glutaric aciduria type III. Alternate splicing results in multiple transcript variants.
Russel-Silver syndrome candidate
, caiB/baiF CoA-transferase family protein C7orf10
, dermal papilla-derived protein 13
, succinylCoA:glutarate-CoA transferase
, uncharacterized protein LOC734617