carbohydrate metabolism disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An acquired metabolic disease that is characterized by abnormal carbohydrate metabolism. (Human Disease Ontology, DOID_0050013)
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Genes

69 genes involed in the disease carbohydrate metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
ADIPOQ adiponectin, C1Q and collagen domain containing
ADRB3 adrenoceptor beta 3
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AKT2 v-akt murine thymoma viral oncogene homolog 2
ALMS1 Alstrom syndrome protein 1
BLK BLK proto-oncogene, Src family tyrosine kinase
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CAPN10 calpain 10
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CD38 CD38 molecule
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1
CEL carboxyl ester lipase
CISD2 CDGSH iron sulfur domain 2
CLPS colipase, pancreatic
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DYRK1B dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FOXP3 forkhead box P3
GCGR glucagon receptor
GCK glucokinase (hexokinase 4)
GSK3A glycogen synthase kinase 3 alpha
GSK3B glycogen synthase kinase 3 beta
GYS1 glycogen synthase 1 (muscle)
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HNF1A HNF1 homeobox A
HNF1B HNF1 homeobox B
HNF4A hepatocyte nuclear factor 4, alpha
IER3IP1 immediate early response 3 interacting protein 1
IFIH1 interferon induced with helicase C domain 1
IL2RA interleukin 2 receptor, alpha
IL6 interleukin 6
INPPL1 inositol polyphosphate phosphatase-like 1
INS insulin
INSR insulin receptor
IRS1 insulin receptor substrate 1
ITPR3 inositol 1,4,5-trisphosphate receptor, type 3
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KLF11 Kruppel-like factor 11
LEP leptin
MAPK8IP1 mitogen-activated protein kinase 8 interacting protein 1
MCF2L2 MCF.2 cell line derived transforming sequence-like 2
NEUROD1 neuronal differentiation 1
OAS1 2'-5'-oligoadenylate synthetase 1, 40/46kDa
PAX4 paired box 4
PDX1 pancreatic and duodenal homeobox 1
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
PTF1A pancreas specific transcription factor, 1a
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
PTRF polymerase I and transcript release factor
RETN resistin
RFX6 regulatory factor X, 6
SH2B3 SH2B adaptor protein 3
SLC16A11 solute carrier family 16, member 11
SLC16A13 solute carrier family 16, member 13
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
SLC30A8 solute carrier family 30 (zinc transporter), member 8
SUMO4 small ubiquitin-like modifier 4
TCF7L2 transcription factor 7-like 2 (T-cell specific, HMG-box)
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
UCP3 uncoupling protein 3 (mitochondrial, proton carrier)
WFS1 Wolfram syndrome 1 (wolframin)
ZFP57 ZFP57 zinc finger protein