steatorrhea Gene Set
Genes
16 genes associated with the steatorrhea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AKR1D1
|
aldo-keto reductase family 1, member D1
|
|
BAAT
|
bile acid CoA:amino acid N-acyltransferase
|
|
COX4I2
|
cytochrome c oxidase subunit IV isoform 2 (lung)
|
|
CYP7B1
|
cytochrome P450, family 7, subfamily B, polypeptide 1
|
|
EPHX1
|
epoxide hydrolase 1, microsomal (xenobiotic)
|
|
HSD3B7
|
hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
|
|
LBR
|
lamin B receptor
|
|
LIPA
|
lipase A, lysosomal acid, cholesterol esterase
|
|
PEX12
|
peroxisomal biogenesis factor 12
|
|
PNLIP
|
pancreatic lipase
|
|
PRSS1
|
protease, serine, 1 (trypsin 1)
|
|
SAR1B
|
secretion associated, Ras related GTPase 1B
|
|
SBDS
|
Shwachman-Bodian-Diamond syndrome
|
|
SLC10A2
|
solute carrier family 10 (sodium/bile acid cotransporter), member 2
|
|
SPINK1
|
serine peptidase inhibitor, Kazal type 1
|
|
TJP2
|
tight junction protein 2
|
