hypertrophic cardiomyopathy Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. (Human Disease Ontology, DOID_11984)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:11984
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Genes

63 genes associated with the disease hypertrophic cardiomyopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
RYR1 ryanodine receptor 1 (skeletal) 1.42467
COL17A1 collagen, type XVII, alpha 1 1.39396
ESRRG estrogen-related receptor gamma 1.31635
LMNTD2 lamin tail domain containing 2 1.27419
RAF1 Raf-1 proto-oncogene, serine/threonine kinase 1.21996
FGF1 fibroblast growth factor 1 (acidic) 1.21019
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1 1.18117
WWOX WW domain containing oxidoreductase 1.16174
CNKSR3 CNKSR family member 3 1.15061
LDLRAD3 low density lipoprotein receptor class A domain containing 3 1.14104
EXT1 exostosin glycosyltransferase 1 1.11846
PAIP2B poly(A) binding protein interacting protein 2B 1.11614
ZNF204P zinc finger protein 204, pseudogene 1.09313
RBMS3 RNA binding motif, single stranded interacting protein 3 1.08934
FBXL18 F-box and leucine-rich repeat protein 18 1.07869
DYSF dysferlin 1.07024
PHF11 PHD finger protein 11 1.04846
SCN11A sodium channel, voltage gated, type XI alpha subunit 1.02272
MARCH1 membrane-associated ring finger (C3HC4) 1, E3 ubiquitin protein ligase 0.988199
AKAP6 A kinase (PRKA) anchor protein 6 0.988032
TDP2 tyrosyl-DNA phosphodiesterase 2 0.971169
DNAJC7 DnaJ (Hsp40) homolog, subfamily C, member 7 0.959568
SHISA9 shisa family member 9 0.952622
ARMC2 armadillo repeat containing 2 0.938237
NCAM2 neural cell adhesion molecule 2 0.923572
APCDD1L adenomatosis polyposis coli down-regulated 1-like 0.90636
CTNNA3 catenin (cadherin-associated protein), alpha 3 0.890776
NRP1 neuropilin 1 0.890183
KCNB2 potassium channel, voltage gated Shab related subfamily B, member 2 0.88034
CALCR calcitonin receptor 0.856323
SCARA3 scavenger receptor class A, member 3 0.821119
SOX5 SRY (sex determining region Y)-box 5 0.813813
DPYD dihydropyrimidine dehydrogenase 0.811614
EPB41L4A erythrocyte membrane protein band 4.1 like 4A 0.808405
SLC35F3 solute carrier family 35, member F3 0.785994
MCTP2 multiple C2 domains, transmembrane 2 0.783487
SEZ6L seizure related 6 homolog (mouse)-like 0.778649
LOC145845 uncharacterized LOC145845 0.777475
C16ORF45 chromosome 16 open reading frame 45 0.768478
NELL1 NEL-like 1 (chicken) 0.766699
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila) 0.763511
PPP6R1 protein phosphatase 6, regulatory subunit 1 0.761811
XDH xanthine dehydrogenase 0.759036
CHN2 chimerin 2 0.751629
PPARD peroxisome proliferator-activated receptor delta 0.749355
ERBB4 erb-b2 receptor tyrosine kinase 4 0.743993
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific) 0.737324
CDHR5 cadherin-related family member 5 0.720532
MPZL1 myelin protein zero-like 1 0.719058
C11ORF44 chromosome 11 open reading frame 44 0.715762
SPATA17 spermatogenesis associated 17 0.714151
LHFPL3 lipoma HMGIC fusion partner-like 3 0.705334
RASSF8 Ras association (RalGDS/AF-6) domain family (N-terminal) member 8 0.701191
CDH18 cadherin 18, type 2 0.696714
TMEM258 transmembrane protein 258 0.693072
GLRX3 glutaredoxin 3 0.687994
PSORS1C3 psoriasis susceptibility 1 candidate 3 (non-protein coding) 0.684944
DCDC2 doublecortin domain containing 2 0.676587
COL25A1 collagen, type XXV, alpha 1 0.674399
KCNIP4 Kv channel interacting protein 4 0.672126
FHIT fragile histidine triad 0.671467
LIN7A lin-7 homolog A (C. elegans) 0.670361
FADS2 fatty acid desaturase 2 0.669037