Ichthyosiform Erythroderma, Congenital Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0079583
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Genes

31 genes associated with the disease Ichthyosiform Erythroderma, Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ALDH3A2 aldehyde dehydrogenase 3 family, member A2
ALOX12B arachidonate 12-lipoxygenase, 12R type
ALOXE3 arachidonate lipoxygenase 3
CAPN12 calpain 12
CERS3 ceramide synthase 3
CST6 cystatin E/M
CYB5A cytochrome b5 type A (microsomal)
CYP4F22 cytochrome P450, family 4, subfamily F, polypeptide 22
DMKN dermokine
EBP emopamil binding protein (sterol isomerase)
ELOVL4 ELOVL fatty acid elongase 4
FLG filaggrin
GATA3 GATA binding protein 3
GBA glucosidase, beta, acid
IL17A interleukin 17A
IL22 interleukin 22
IL2RB interleukin 2 receptor, beta
LIPN lipase, family member N
LOR loricrin
LOX lysyl oxidase
NIPAL4 NIPA-like domain containing 4
NSDHL NAD(P) dependent steroid dehydrogenase-like
PNPLA1 patatin-like phospholipase domain containing 1
SDR9C7 short chain dehydrogenase/reductase family 9C, member 7
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4
SPINK5 serine peptidase inhibitor, Kazal type 5
ST14 suppression of tumorigenicity 14 (colon carcinoma)
STS steroid sulfatase (microsomal), isozyme S
SULT2B1 sulfotransferase family, cytosolic, 2B, member 1
TGM1 transglutaminase 1