skin fibrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description invasion of fibrous connective tissue into the skin, often resulting from inflammation or injury (Mammalian Phenotype Ontology, MP_0009932)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009932
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Genes

7 gene mutations causing the skin fibrosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD19 CD19 molecule
FBN1 fibrillin 1
IRF2 interferon regulatory factor 2
MMP14 matrix metallopeptidase 14 (membrane-inserted)
PBK PDZ binding kinase
RELA v-rel avian reticuloendotheliosis viral oncogene homolog A
SYT7 synaptotagmin VII