abnormal keratinocyte apoptosis Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	aberrant programmed cell death or anomaly in the number of the cells of the epidermis that produce keratin in the process of differentiating into the dead and fully keratinized cells of the stratum corneum (Mammalian Phenotype Ontology, MP_0001224)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001224
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Genes

14 gene mutations causing the abnormal keratinocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
CASP3	caspase 3, apoptosis-related cysteine peptidase
CEBPB	CCAAT/enhancer binding protein (C/EBP), beta
ESR2	estrogen receptor 2 (ER beta)
IKBKG	inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
KLF10	Kruppel-like factor 10
KRT14	keratin 14, type I
MAP3K6	mitogen-activated protein kinase kinase kinase 6
MC1R	melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
PKP3	plakophilin 3
PPARD	peroxisome proliferator-activated receptor delta
RELB	v-rel avian reticuloendotheliosis viral oncogene homolog B
SHARPIN	SHANK-associated RH domain interactor
TREX2	three prime repair exonuclease 2
TYR	tyrosinase