abnormal adipocyte glucose uptake Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability of adipocytes to take in glucose (Mammalian Phenotype Ontology, MP_0004185)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004185
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27 gene mutations causing the abnormal adipocyte glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACOT11 acyl-CoA thioesterase 11
AKT2 v-akt murine thymoma viral oncogene homolog 2
BBS12 Bardet-Biedl syndrome 12
BGLAP bone gamma-carboxyglutamate (gla) protein
CEBPA CCAAT/enhancer binding protein (C/EBP), alpha
COL5A3 collagen, type V, alpha 3
E2F1 E2F transcription factor 1
FABP5 fatty acid binding protein 5 (psoriasis-associated)
GATM glycine amidinotransferase (L-arginine:glycine amidinotransferase)
INS insulin
MARK2 MAP/microtubule affinity-regulating kinase 2
MARK3 MAP/microtubule affinity-regulating kinase 3
NPY1R neuropeptide Y receptor Y1
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PPARG peroxisome proliferator-activated receptor gamma
PRKCA protein kinase C, alpha
PRKCI protein kinase C, iota
PRKCQ protein kinase C, theta
SESN2 sestrin 2
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
SSFA2 sperm specific antigen 2
STEAP4 STEAP family member 4
STRA6 stimulated by retinoic acid 6
TBC1D4 TBC1 domain family, member 4
TLR2 toll-like receptor 2
TNKS2 tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2
TRIP10 thyroid hormone receptor interactor 10