abnormality of subcutaneous fat tissue Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001001
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Genes

25 genes associated with the abnormality of subcutaneous fat tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CAV1 caveolin 1, caveolae protein, 22kDa
ERCC2 excision repair cross-complementation group 2
ERCC3 excision repair cross-complementation group 3
ERCC4 excision repair cross-complementation group 4
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
FBN1 fibrillin 1
FH fumarate hydratase
GTF2H5 general transcription factor IIH, polypeptide 5
INSR insulin receptor
LMNA lamin A/C
MEN1 multiple endocrine neoplasia I
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
PHGDH phosphoglycerate dehydrogenase
PMM2 phosphomannomutase 2
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
PTEN phosphatase and tensin homolog
PTF1A pancreas specific transcription factor, 1a
RBM28 RNA binding motif protein 28
SKI SKI proto-oncogene
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
TGFB1 transforming growth factor, beta 1
ZMPSTE24 zinc metallopeptidase STE24