mixed cellular infiltration to dermis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description gradual accumulation of mixed cell types in the dermis that are not normally found there (Mammalian Phenotype Ontology, MP_0001246)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001246
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15 gene mutations causing the mixed cellular infiltration to dermis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BRD4 bromodomain containing 4
CDSN corneodesmosin
CST6 cystatin E/M
CTSE cathepsin E
DSG4 desmoglein 4
HPGDS hematopoietic prostaglandin D synthase
IL22 interleukin 22
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
RAG1 recombination activating gene 1
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
SHARPIN SHANK-associated RH domain interactor
TTC7A tetratricopeptide repeat domain 7A
UROS uroporphyrinogen III synthase
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
ZAP70 zeta-chain (TCR) associated protein kinase 70kDa