abnormal skin development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation of the membranous protective covering of the body (Mammalian Phenotype Ontology, MP_0003941)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003941
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14 gene mutations causing the abnormal skin development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ABHD5 abhydrolase domain containing 5
CERS3 ceramide synthase 3
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
FH fumarate hydratase
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
IRF6 interferon regulatory factor 6
MIR205 microRNA 205
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
TCF15 transcription factor 15 (basic helix-loop-helix)
TGM3 transglutaminase 3
TP63 tumor protein p63
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor