loose skin Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	A skin disease characterized by skin that is loose, hanging, wrinkled and lacking in elasticity; it can also affect connective tissue in other parts of the body, including the heart, blood vessels, joints, intestines and lungs. (Human Disease Ontology, DOID_3144)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005421
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Genes

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

Symbol	Name
ATOX1	antioxidant 1 copper chaperone
CACNA1S	calcium channel, voltage-dependent, L type, alpha 1S subunit
DCN	decorin
DPT	dermatopontin
EFEMP1	EGF containing fibulin-like extracellular matrix protein 1
FBLN5	fibulin 5
HAP1	huntingtin-associated protein 1
HR	hair growth associated
LOXL1	lysyl oxidase-like 1
LUM	lumican
MMP14	matrix metallopeptidase 14 (membrane-inserted)
PPIB	peptidylprolyl isomerase B (cyclophilin B)
PSEN1	presenilin 1
TCF15	transcription factor 15 (basic helix-loop-helix)