ORF » Species Summary » Homo sapiens » KEGG » Vitamin digestion and absorption

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Homo sapiens (human) Vitamin digestion and absorption (provided by KEGG)

Browse by Letter Index, Genomic Locus

24 gene

The longest variant of each gene is displayed. Click the see gene variants link to see all gene variants.


Gene Symbol Full Name
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
APOB apolipoprotein B
APOA1 apolipoprotein A1
AWAT2 acyl-CoA wax alcohol acyltransferase 2
GIF gastric intrinsic factor
SLC19A2 solute carrier family 19 member 2
SLC19A1 solute carrier family 19 member 1
PLB1 phospholipase B1
LMBRD1 LMBR1 domain containing 1
SLC52A3 solute carrier family 52 member 3
ABCC1 ATP binding cassette subfamily C member 1
SLC19A3 solute carrier family 19 member 3
SLC5A6 solute carrier family 5 member 6
LRAT lecithin retinol acyltransferase
TCN2 transcobalamin 2
APOA4 apolipoprotein A4
PNLIP pancreatic lipase
SCARB1 scavenger receptor class B member 1
BTD biotinidase
RBP2 retinol binding protein 2
SLC23A1 solute carrier family 23 member 1
SLC46A1 solute carrier family 46 member 1
CUBN cubilin
FOLH1 folate hydrolase 1
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