-
while aldolases A and C
prefer FBP. In humans,
aldolase B is
encoded by the
ALDOB gene
located on
chromosome 9. The gene is 14,500 base
pairs long and contains...
- diagnosis. HFI is an
autosomal recessive condition caused by
mutations in the
ALDOB gene,
located at 9q31.1. HFI is
typically suspected based on
dietary history...
-
Hepatic and
renal dysfunction. NLM/GHR:ALDOB OMIM:
ALDOB NLM/GHR:
ALDOB D OMIM:
ALDOB D GARD:
ALDOB D ORPHA:
ALDOB D
Glycolysis step 4
Aldolase C ALDOC:
Brain Unclear...
- HGNC:28114 Q8IZ83 559 ALDH18A1 HGNC:9722 P54886 560
ALDOA HGNC:414 P04075 561
ALDOB HGNC:417 P05062 562
ALDOC HGNC:418 P09972 563 ALG1 HGNC:18294 Q9BT22 564...
-
ryanodine receptor, Cytohesin-2, and V-ATPase (vacuolar-type H+-ATPase).
ALDOB ALDOC Fructose-bisphosphate
aldolase GRCh38:
Ensembl release 89: ENSG00000149925...
-
highly similar to
those of the
other isozymes,
sharing a 68%
identity with
ALDOB and 78%
identity with ALDOA. In particular, the
residues Asp33, Arg42, Lys107...
- degeneration, TARDBP-related; 612069;
TARDBP Fructose intolerance; 229600;
ALDOB Fructose-1,6-bisphosphatase deficiency; 229700; FBP1 Fucosidosis; 230000;...
- be
under the
control of Nfe2l1. Insulin-regulated
glycolytic genes—Gck,
Aldob, Pgk1, and Pklr,
hepatic glucose transporter gene — SLC2A2, and gluconeogenic...
