abnormal keratinocyte proliferation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability of keratinocytes to undergo expansion by cell division (Mammalian Phenotype Ontology, MP_0009582)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009582
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27 gene mutations causing the abnormal keratinocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD151 CD151 molecule (Raph blood group)
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CHUK conserved helix-loop-helix ubiquitous kinase
CST6 cystatin E/M
CTSV cathepsin V
CYLD cylindromatosis (turban tumor syndrome)
FERMT1 fermitin family member 1
GRHL3 grainyhead-like 3 (Drosophila)
IL17C interleukin 17C
IRF6 interferon regulatory factor 6
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KDF1 keratinocyte differentiation factor 1
KLF10 Kruppel-like factor 10
KRT9 keratin 9, type I
LRIG1 leucine-rich repeats and immunoglobulin-like domains 1
PAQR3 progestin and adipoQ receptor family member III
PKP3 plakophilin 3
PPARD peroxisome proliferator-activated receptor delta
PPP1R13L protein phosphatase 1, regulatory subunit 13 like
RASSF9 Ras association (RalGDS/AF-6) domain family (N-terminal) member 9
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
SGPP1 sphingosine-1-phosphate phosphatase 1
SHARPIN SHANK-associated RH domain interactor
SHH sonic hedgehog
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4
TNF tumor necrosis factor
TP63 tumor protein p63