thin dermal layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the dermis (Mammalian Phenotype Ontology, MP_0001244)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001244
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Genes

17 gene mutations causing the thin dermal layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BGN biglycan
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CBS cystathionine-beta-synthase
COL5A2 collagen, type V, alpha 2
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1
DCN decorin
DPT dermatopontin
EDARADD EDAR-associated death domain
FGFR2 fibroblast growth factor receptor 2
LMNA lamin A/C
PNN pinin, desmosome associated protein
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RGN regucalcin
SCG5 secretogranin V
TP53 tumor protein p53
TWIST2 twist family bHLH transcription factor 2
ZDHHC13 zinc finger, DHHC-type containing 13