ORF » Species Summary » Homo sapiens » KEGG » Vitamin digestion and absorption
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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 |
LRAT | lecithin retinol acyltransferase |
SLC5A6 | solute carrier family 5 member 6 |
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 |