malabsorption Gene Set
Genes
12 genes co-occuring with the biological term malabsorption in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
| Symbol |
Name |
|
AMN
|
amnion associated transmembrane protein
|
|
CEL
|
carboxyl ester lipase
|
|
CFTR
|
cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
|
|
COX4I2
|
cytochrome c oxidase subunit IV isoform 2 (lung)
|
|
CUBN
|
cubilin (intrinsic factor-cobalamin receptor)
|
|
CYP7A1
|
cytochrome P450, family 7, subfamily A, polypeptide 1
|
|
GIF
|
gastric intrinsic factor (vitamin B synthesis)
|
|
PDK4
|
pyruvate dehydrogenase kinase, isozyme 4
|
|
SAR1B
|
secretion associated, Ras related GTPase 1B
|
|
SLC19A1
|
solute carrier family 19 (folate transporter), member 1
|
|
SLC46A1
|
solute carrier family 46 (folate transporter), member 1
|
|
SLC5A1
|
solute carrier family 5 (sodium/glucose cotransporter), member 1
|
