decreased skin tensile strength Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the normal maximum tension the skin can withstand without tearing (Mammalian Phenotype Ontology, MP_0003089)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003089
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Genes

19 gene mutations causing the decreased skin tensile strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
COL14A1 collagen, type XIV, alpha 1
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
DCN decorin
DSE dermatan sulfate epimerase
DSG4 desmoglein 4
JUP junction plakoglobin
KRT10 keratin 10, type I
LAMC2 laminin, gamma 2
LOR loricrin
LOX lysyl oxidase
LUM lumican
MIA3 melanoma inhibitory activity family, member 3
OED Oregon eye disease
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SPINK5 serine peptidase inhibitor, Kazal type 5
THBS2 thrombospondin 2