thin epidermis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the superficial epithelial portion of the skin (Mammalian Phenotype Ontology, MP_0001218)
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26 gene mutations causing the thin epidermis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ATR ATR serine/threonine kinase
BCL11B B-cell CLL/lymphoma 11B (zinc finger protein)
CD44 CD44 molecule (Indian blood group)
DGAT2 diacylglycerol O-acyltransferase 2
EGFR epidermal growth factor receptor
ESR2 estrogen receptor 2 (ER beta)
FERMT1 fermitin family member 1
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
GAB1 GRB2-associated binding protein 1
IGF1R insulin-like growth factor 1 receptor
JUP junction plakoglobin
KL klotho
MAP3K11 mitogen-activated protein kinase kinase kinase 11
MAPK8 mitogen-activated protein kinase 8
MIR205 microRNA 205
MPV17 MpV17 mitochondrial inner membrane protein
NR1H2 nuclear receptor subfamily 1, group H, member 2
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PORCN porcupine homolog (Drosophila)
PTGES3 prostaglandin E synthase 3 (cytosolic)
PTHLH parathyroid hormone-like hormone
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RUNX2 runt-related transcription factor 2
SFN stratifin