Familial Benign Pemphigus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0085106
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Genes

34 genes associated with the disease Familial Benign Pemphigus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ADRA1A adrenoceptor alpha 1A
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
ATP2C1 ATPase, Ca++ transporting, type 2C, member 1
CASP3 caspase 3, apoptosis-related cysteine peptidase
CKAP4 cytoskeleton-associated protein 4
COL11A2 collagen, type XI, alpha 2
CXCL8 chemokine (C-X-C motif) ligand 8
DNAH8 dynein, axonemal, heavy chain 8
DSP desmoplakin
ERBB2 erb-b2 receptor tyrosine kinase 2
GABPA GA binding protein transcription factor, alpha subunit 60kDa
GDE1 glycerophosphodiester phosphodiesterase 1
HLA-B major histocompatibility complex, class I, B
IRF6 interferon regulatory factor 6
IVL involucrin
LRP1 low density lipoprotein receptor-related protein 1
MFAP4 microfibrillar-associated protein 4
NFE2L2 nuclear factor, erythroid 2-like 2
NOTCH1 notch 1
ORAI1 ORAI calcium release-activated calcium modulator 1
PARP1 poly (ADP-ribose) polymerase 1
PMAIP1 phorbol-12-myristate-13-acetate-induced protein 1
PPARA peroxisome proliferator-activated receptor alpha
PXDNL peroxidasin-like
RPE65 retinal pigment epithelium-specific protein 65kDa
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
SLURP1 secreted LY6/PLAUR domain containing 1
SP1 Sp1 transcription factor
TP63 tumor protein p63
TPO thyroid peroxidase
UVRAG UV radiation resistance associated
YY1 YY1 transcription factor