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. 2020 Feb 11;21(4):1194. doi: 10.3390/ijms21041194
ABCA12 ATP-binding cassette transporter A12
ABHD5 α/β hydrolase domain containing protein 5
ARS Syndrome arthrogryposis, renal dysfunction and cholestasis
LD Linear dichroism
ASPRV1 Aspartic peptidase, retroviral-like 1
CaR Calcium-sensing receptor
CE Cornified envelope
CGI58 Comparative gene identification-58
CHILD syndrome Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
CLSP Calmodulin-like skin protein
Cystatin A Cysteine protease inhibitor A
Cx26 Connexin 26
ELOVL Fatty acid elongases
FATP4 Fatty acid transport protein 4
GJB2/GJB6 Gap junction protein beta 2/gap junction protein beta 6
KID Keratitis-ichthyosis-deafness
KLK Kallikrein-related peptidase
LEKTI Lymphoepithelial-Kazal-type 5 inhibitor
LXR Liver X receptor
NIPAL4 NIPA like domain containing 4
NSDHL NADP dependent steroid dehydrogenase-like
Orai1 ORAI calcium release-activated calcium modulator 1
PNPLA1 Patatin-like phospholipase domain-containing lipase 1
PPAR Peroxisome proliferating activated receptor
SAM Syndrome severe skin dermatitis, multiple allergies, and metabolic wasting
SASPase Skin aspartic protease
SC Stratum corneum
SDR9C7 Short-chain dehydrogenase/reductase family 9C member 7
SGMS Sphingomyelin synthase
SOCE Store-operated calcium entry
SPINK5 Serine-specific inhibitor Kazal type 5
SPRR Small proline-rich protein
STIM1 Stromal interaction molecule1
TGases Transglutaminases
TSLP Thymic stromal lymphoprotein
TRP Transient receptor potential
TRPV TRP vanilloid type
UGCG UDP-glucose:ceramide glucosyltransferase