shiny skin Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description skin with a glossy or glistening appearance (Mammalian Phenotype Ontology, MP_0001196)
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21 gene mutations causing the shiny skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ALOX12B arachidonate 12-lipoxygenase, 12R type
CASP14 caspase 14, apoptosis-related cysteine peptidase
CHUK conserved helix-loop-helix ubiquitous kinase
CTSV cathepsin V
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1
DGAT2 diacylglycerol O-acyltransferase 2
ELOVL1 ELOVL fatty acid elongase 1
ELOVL4 ELOVL fatty acid elongase 4
FLG filaggrin
FST follistatin
HR hair growth associated
HSD3B7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
IRF6 interferon regulatory factor 6
OED Oregon eye disease
PTGES3 prostaglandin E synthase 3 (cytosolic)
RARG retinoic acid receptor, gamma
SFN stratifin
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4
ST14 suppression of tumorigenicity 14 (colon carcinoma)
TP63 tumor protein p63