abnormal body mass index Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaloy in the average of a measure of weight for height compared to the control (Mammalian Phenotype Ontology, MP_0020182)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0020182
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24 gene mutations causing the abnormal body mass index phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADORA2A adenosine A2a receptor
BBS2 Bardet-Biedl syndrome 2
BCAM basal cell adhesion molecule (Lutheran blood group)
CISD2 CDGSH iron sulfur domain 2
GAA glucosidase, alpha; acid
GATM glycine amidinotransferase (L-arginine:glycine amidinotransferase)
GCGR glucagon receptor
GNAS GNAS complex locus
GPD2 glycerol-3-phosphate dehydrogenase 2 (mitochondrial)
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
IL1R1 interleukin 1 receptor, type I
LPAR1 lysophosphatidic acid receptor 1
LTA lymphotoxin alpha
PNPLA2 patatin-like phospholipase domain containing 2
PPARG peroxisome proliferator-activated receptor gamma
PRCP prolylcarboxypeptidase (angiotensinase C)
PREP prolyl endopeptidase
PTP4A3 protein tyrosine phosphatase type IVA, member 3
RB1 retinoblastoma 1
SAMD4A sterile alpha motif domain containing 4A
SDC3 syndecan 3
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
TNF tumor necrosis factor
TWSG1 twisted gastrulation BMP signaling modulator 1