abnormal skin turgor Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability of the skin to resist deformation; influential factors include dehydration and age (Mammalian Phenotype Ontology, MP_0003652)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003652
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6 gene mutations causing the abnormal skin turgor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FBN1 fibrillin 1
GBA glucosidase, beta, acid
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KIFAP3 kinesin-associated protein 3
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1