Thiamine Deficiency Gene Set
Genes
17 genes associated with the disease Thiamine Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
APP
|
amyloid beta (A4) precursor protein
|
|
BECN1
|
beclin 1, autophagy related
|
|
BNIP3
|
BCL2/adenovirus E1B 19kDa interacting protein 3
|
|
CHAT
|
choline O-acetyltransferase
|
|
HIF1A
|
hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
|
|
HNF1A
|
HNF1 homeobox A
|
|
JAK2
|
Janus kinase 2
|
|
MAOB
|
monoamine oxidase B
|
|
PDP1
|
pyruvate dehyrogenase phosphatase catalytic subunit 1
|
|
PSEN1
|
presenilin 1
|
|
SERPINA1
|
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
|
|
SLC19A2
|
solute carrier family 19 (thiamine transporter), member 2
|
|
SLC19A3
|
solute carrier family 19 (thiamine transporter), member 3
|
|
SLC22A1
|
solute carrier family 22 (organic cation transporter), member 1
|
|
SLC35F3
|
solute carrier family 35, member F3
|
|
TKT
|
transketolase
|
|
WFS1
|
Wolfram syndrome 1 (wolframin)
|
