increased body temperature Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the level of heat natural to a living being (Mammalian Phenotype Ontology, MP_0005533)
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32 gene mutations causing the increased body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCG1 ATP-binding cassette, sub-family G (WHITE), member 1
AGRP agouti related neuropeptide
BCAT2 branched chain amino-acid transaminase 2, mitochondrial
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CAMKK2 calcium/calmodulin-dependent protein kinase kinase 2, beta
CBL Cbl proto-oncogene, E3 ubiquitin protein ligase
CCDC7 coiled-coil domain containing 7
CIDEC cell death-inducing DFFA-like effector c
CRTC3 CREB regulated transcription coactivator 3
GPD2 glycerol-3-phosphate dehydrogenase 2 (mitochondrial)
HADH hydroxyacyl-CoA dehydrogenase
IL6 interleukin 6
LGMN legumain
MCHR1 melanin-concentrating hormone receptor 1
MGLL monoglyceride lipase
MOGAT2 monoacylglycerol O-acyltransferase 2
NTSR1 neurotensin receptor 1 (high affinity)
PITX3 paired-like homeodomain 3
PPARG peroxisome proliferator-activated receptor gamma
PRKAR2B protein kinase, cAMP-dependent, regulatory, type II, beta
PTPN1 protein tyrosine phosphatase, non-receptor type 1
RYR1 ryanodine receptor 1 (skeletal)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SERTAD2 SERTA domain containing 2
SIK3 SIK family kinase 3
SLC27A5 solute carrier family 27 (fatty acid transporter), member 5
TAAR1 trace amine associated receptor 1
TGFB1 transforming growth factor, beta 1
THRA thyroid hormone receptor, alpha
TNKS tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase
TPH2 tryptophan hydroxylase 2
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)