hailey-hailey disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050429)
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Genes

36 genes co-occuring with the disease hailey-hailey disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ATP2C1 ATPase, Ca++ transporting, type 2C, member 1 3.21065
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 1.9164
DNAH8 dynein, axonemal, heavy chain 8 1.68226
ATP2C2 ATPase, Ca++ transporting, type 2C, member 2 1.68
JUP junction plakoglobin 1.27519
ASTE1 asteroid homolog 1 (Drosophila) 1.24776
DSP desmoplakin 1.17679
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2 0.754934
IVL involucrin 0.718443
PKP1 plakophilin 1 0.692697
AATF apoptosis antagonizing transcription factor 0.687091
DSG3 desmoglein 3 0.652484
DSG1 desmoglein 1 0.651694
ATP2A1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1 0.650903
PLG plasminogen 0.606543
DDX21 DEAD (Asp-Glu-Ala-Asp) box helicase 21 0.592116
DSC2 desmocollin 2 0.563335
ITPR3 inositol 1,4,5-trisphosphate receptor, type 3 0.529608
KRT9 keratin 9, type I 0.497703
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1 0.467684
OCLN occludin 0.445805
TJP1 tight junction protein 1 0.444676
CDH1 cadherin 1, type 1, E-cadherin (epithelial) 0.440914
P2RY2 purinergic receptor P2Y, G-protein coupled, 2 0.436026
IFT122 intraflagellar transport 122 0.43227
KRT10 keratin 10, type I 0.395608
CLDN4 claudin 4 0.340906
YY1 YY1 transcription factor 0.333218
P2RX7 purinergic receptor P2X, ligand gated ion channel, 7 0.264431
CLDN1 claudin 1 0.212608
VCL vinculin 0.206248
CLDN7 claudin 7 0.200656
SCN10A sodium channel, voltage gated, type X alpha subunit 0.178126
BRWD1 bromodomain and WD repeat domain containing 1 0.170544
RYR1 ryanodine receptor 1 (skeletal) 0.161139
NOTCH1 notch 1 0.160761