thin skin Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Reduction in thickness of the skin, generally associated with a loss of suppleness and elasticity of the skin. (Human Phenotype Ontology, HP_0000963)
External Link
Similar Terms
Downloads & Tools


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

Symbol Name
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
ALX4 ALX homeobox 4
ARRDC3 arrestin domain containing 3
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1
CRH corticotropin releasing hormone
DCN decorin
EDA ectodysplasin A
EDARADD EDAR-associated death domain
ELOVL4 ELOVL fatty acid elongase 4
ERCC1 excision repair cross-complementation group 1
FGF10 fibroblast growth factor 10
FGF23 fibroblast growth factor 23
FGFR2 fibroblast growth factor receptor 2
FOXN1 forkhead box N1
GFRA1 GDNF family receptor alpha 1
GFRA2 GDNF family receptor alpha 2
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
HR hair growth associated
KRT71 keratin 71, type II
LEF1 lymphoid enhancer-binding factor 1
MIR205 microRNA 205
MORF4L1 mortality factor 4 like 1
MPV17 MpV17 mitochondrial inner membrane protein
ORAI1 ORAI calcium release-activated calcium modulator 1
PDX1 pancreatic and duodenal homeobox 1
PPARD peroxisome proliferator-activated receptor delta
RAD23B RAD23 homolog B (S. cerevisiae)
SCG5 secretogranin V
SFN stratifin
SLC9A1 solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
SPINK1 serine peptidase inhibitor, Kazal type 1
STAG1 stromal antigen 1
TWIST2 twist family bHLH transcription factor 2