abnormal inguinal fat pad morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the encapsulated adipose tissue found in the groin (Mammalian Phenotype Ontology, MP_0005336)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005336
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Genes

41 gene mutations causing the abnormal inguinal fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASIP agouti signaling protein
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CEBPA CCAAT/enhancer binding protein (C/EBP), alpha
CIDEC cell death-inducing DFFA-like effector c
DOK1 docking protein 1, 62kDa (downstream of tyrosine kinase 1)
DRD2 dopamine receptor D2
EIF4EBP1 eukaryotic translation initiation factor 4E binding protein 1
EIF4H eukaryotic translation initiation factor 4H
ESR1 estrogen receptor 1
ESRRA estrogen-related receptor alpha
G0S2 G0/G1 switch 2
GDF15 growth differentiation factor 15
GHR growth hormone receptor
GNG3 guanine nucleotide binding protein (G protein), gamma 3
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
IL1R1 interleukin 1 receptor, type I
LEP leptin
LGALS12 lectin, galactoside-binding, soluble, 12
LIPA lipase A, lysosomal acid, cholesterol esterase
LPIN1 lipin 1
MSTN myostatin
NOS3 nitric oxide synthase 3 (endothelial cell)
NPY6R neuropeptide Y receptor Y6 (pseudogene)
PCSK1 proprotein convertase subtilisin/kexin type 1
PITPNA phosphatidylinositol transfer protein, alpha
PLIN1 perilipin 1
PNPLA2 patatin-like phospholipase domain containing 2
PNRC2 proline-rich nuclear receptor coactivator 2
POMC proopiomelanocortin
PPARG peroxisome proliferator-activated receptor gamma
PTPN1 protein tyrosine phosphatase, non-receptor type 1
RBL1 retinoblastoma-like 1
SAMD4A sterile alpha motif domain containing 4A
SELM selenoprotein M
SIRT1 sirtuin 1
SLC30A5 solute carrier family 30 (zinc transporter), member 5
WRN Werner syndrome, RecQ helicase-like
ZEB1 zinc finger E-box binding homeobox 1