increased brown adipose tissue amount Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased amount of the thermogenic form of adipose tissue that is composed of brown adipocytes (Mammalian Phenotype Ontology, MP_0000005)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000005
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Genes

37 gene mutations causing the increased brown adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACOT11 acyl-CoA thioesterase 11
ADIPOR1 adiponectin receptor 1
ANKRD26 ankyrin repeat domain 26
ASIP agouti signaling protein
BBS1 Bardet-Biedl syndrome 1
BRS3 bombesin-like receptor 3
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
C3 complement component 3
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CAMKK2 calcium/calmodulin-dependent protein kinase kinase 2, beta
CAV1 caveolin 1, caveolae protein, 22kDa
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CEBPA CCAAT/enhancer binding protein (C/EBP), alpha
CSHL1 chorionic somatomammotropin hormone-like 1
FGF21 fibroblast growth factor 21
FOXC2 forkhead box C2
GNAS GNAS complex locus
GPR68 G protein-coupled receptor 68
GRM1 glutamate receptor, metabotropic 1
HDC histidine decarboxylase
HRH1 histamine receptor H1
KDM3A lysine (K)-specific demethylase 3A
KL klotho
LEP leptin
LEPR leptin receptor
LIPE lipase, hormone-sensitive
MRAP2 melanocortin 2 receptor accessory protein 2
MYOG myogenin (myogenic factor 4)
NOS3 nitric oxide synthase 3 (endothelial cell)
NPY6R neuropeptide Y receptor Y6 (pseudogene)
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
PNPLA2 patatin-like phospholipase domain containing 2
PRLH prolactin releasing hormone
RYR1 ryanodine receptor 1 (skeletal)
SIM1 single-minded family bHLH transcription factor 1
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)