-
ACADSB is a
human gene that
encodes short/branched
chain specific acyl-CoA
dehydrogenase (SBCAD), an
enzyme in the acyl CoA
dehydrogenase family. It can...
- 2-methylbutyryl-CoA dehydrogenase. The
disorder is
caused by a
mutation in the
ACADSB gene,
located on the long arm of
human chromosome 10 (10q25-q26). It is...
-
ACADL HGNC:88 P28330 126
ACADM HGNC:89 P11310 127
ACADS HGNC:90 P16219 128
ACADSB HGNC:91 P45954 129
ACADVL HGNC:92 P49748 130 ACAN HGNC:319 P16112 131 ACAP1...
-
members of the ACAD family,
including ACADVL, ACADS, ACADM, ACADL, IVD, GCD,
ACADSB, and ACD8. The
calculated molecular weight of the ACAD9 is 68.8 kDa. The...
-
dehydrogenase X deficiency; 300438; HSD17B10 2-methylbutyrylglycinuria; 610006;
ACADSB 3-hydroxyacyl-coa
dehydrogenase deficiency; 231530;
HADHSC 3-hydroxyisobutryl-CoA...
