Vitamin digestion and absorption Gene Set

Dataset KEGG Pathways 2026
Category structural or functional annotations
Type pathway
Description Vitamins are a diverse and chemically unrelated group of organic substances that share a common feature of being essential for normal health and well-being. They catalyze numerous biochemical reactions. Because humans and other mammals cannot synthesize these compounds (except for some synthesis of niacin), they must obtain them from exogenous sources via intestinal absorption. Vitamins are classified based on their solubility in water or fat. Most of the water-soluble vitamins are transported across the small intestinal membrane by carrier-mediated mechanisms, but vitamin B12, cobalamin, is transported by a receptor-mediated mechanism. Intestinal absorption of fat-soluble vitamins requires all of the processes needed for fat absorption. After digestion, these vitamins and the products of pancreatic hydrolysis of triglycerides (TG) are emulsified by bile salts to form mixed micelles which are taken up by intestinal enterocytes and incorporated into chylomicrons (CM). CM are then secreted into the lymphatic system, and finally moves into the plasma. (Kyoto Encyclopedia of Genes and Genomes, hsa04977)
External Link https://www.kegg.jp/entry/hsa04977
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Genes

26 proteins participating in the Vitamin digestion and absorption pathway from the KEGG Pathways 2026 dataset.

Symbol Name
ABCC1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
AMN amnion associated transmembrane protein
APOA1 apolipoprotein A-I
APOA4 apolipoprotein A-IV
APOB apolipoprotein B
AWAT2 acyl-CoA wax alcohol acyltransferase 2
CBLIF cobalamin binding intrinsic factor
CUBN cubilin (intrinsic factor-cobalamin receptor)
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
LMBRD1 LMBR1 domain containing 1
LRAT lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
PLB1 phospholipase B1
PNLIP pancreatic lipase
RIMBP2 RIMS binding protein 2
SCARB1 scavenger receptor class B, member 1
SLC19A1 solute carrier family 19 (folate transporter), member 1
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC23A1 solute carrier family 23 (ascorbic acid transporter), member 1
SLC46A1 solute carrier family 46 (folate transporter), member 1
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
SLC5A6 solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6
SP8 Sp8 transcription factor
TCN2 transcobalamin II