abnormal fasted circulating glucose level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the amount of glucose in the blood at some defined time point after eating compared to controls (Mammalian Phenotype Ontology, MP_0013277)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013277
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22 gene mutations causing the abnormal fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADORA2B adenosine A2b receptor
ATN1 atrophin 1
BBS5 Bardet-Biedl syndrome 5
CABP1 calcium binding protein 1
CD33 CD33 molecule
CINP cyclin-dependent kinase 2 interacting protein
CNOT3 CCR4-NOT transcription complex, subunit 3
DNAJC5G DnaJ (Hsp40) homolog, subfamily C, member 5 gamma
ELMO1 engulfment and cell motility 1
F10 coagulation factor X
JAM3 junctional adhesion molecule 3
MACROD2 MACRO domain containing 2
MAP3K1 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
MIR184 microRNA 184
NAGK N-acetylglucosamine kinase
NCOA5 nuclear receptor coactivator 5
NRCAM neuronal cell adhesion molecule
P2RX6 purinergic receptor P2X, ligand gated ion channel, 6
RNF183 ring finger protein 183
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
SLC25A4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
TBKBP1 TBK1 binding protein 1