Congenital Nonbullous Ichthyosiform Erythroderma Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0079154
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Genes

36 genes associated with the disease Congenital Nonbullous Ichthyosiform Erythroderma 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
ABHD5 abhydrolase domain containing 5
ALDH3A2 aldehyde dehydrogenase 3 family, member A2
ALOX12B arachidonate 12-lipoxygenase, 12R type
ALOXE3 arachidonate lipoxygenase 3
BCL2 B-cell CLL/lymphoma 2
CAPN12 calpain 12
CERS3 ceramide synthase 3
COG7 component of oligomeric golgi complex 7
COL17A1 collagen, type XVII, alpha 1
CST6 cystatin E/M
CYB5A cytochrome b5 type A (microsomal)
CYP4F22 cytochrome P450, family 4, subfamily F, polypeptide 22
DMKN dermokine
ELF3 E74-like factor 3 (ets domain transcription factor, epithelial-specific )
ERCC2 excision repair cross-complementation group 2
ERCC3 excision repair cross-complementation group 3
FLG filaggrin
GATA3 GATA binding protein 3
GBA glucosidase, beta, acid
GTF2H5 general transcription factor IIH, polypeptide 5
IL1A interleukin 1, alpha
LIPN lipase, family member N
LOR loricrin
LOX lysyl oxidase
NIPAL4 NIPA-like domain containing 4
PNPLA1 patatin-like phospholipase domain containing 1
POMP proteasome maturation protein
SDR9C7 short chain dehydrogenase/reductase family 9C, member 7
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4
SPINK5 serine peptidase inhibitor, Kazal type 5
STS steroid sulfatase (microsomal), isozyme S
SULT2B1 sulfotransferase family, cytosolic, 2B, member 1
TARS threonyl-tRNA synthetase
TGM1 transglutaminase 1