acanthosis nigricans Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_3138)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000956
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Genes

25 genes associated with the acanthosis nigricans phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AIP aryl hydrocarbon receptor interacting protein
AKT2 v-akt murine thymoma viral oncogene homolog 2
ALMS1 Alstrom syndrome protein 1
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CAV1 caveolin 1, caveolae protein, 22kDa
CIDEC cell death-inducing DFFA-like effector c
CLDN1 claudin 1
CUL4B cullin 4B
ERF Ets2 repressor factor
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FOS FBJ murine osteosarcoma viral oncogene homolog
HRAS Harvey rat sarcoma viral oncogene homolog
HSD11B1 hydroxysteroid (11-beta) dehydrogenase 1
INSR insulin receptor
JUP junction plakoglobin
LMNA lamin A/C
PLIN1 perilipin 1
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
PTEN phosphatase and tensin homolog
PTRF polymerase I and transcript release factor
SPINK5 serine peptidase inhibitor, Kazal type 5
WNT10A wingless-type MMTV integration site family, member 10A