Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "H"
401 to 410 of 426 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

401
Histone deacetylase 3
HD3, KDAC3, RPD3, RPD3-2
Atrial fibrillation, Neurodevelopmental disorder, Heart disease, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Schizophrenia, Stomach neoplasms

402
Hydroxycarboxylic acid receptor 3
GPR109B, HCA3, HM74, PUMAG, Puma-g
Bipolar disorder, Squamous cell carcinoma, Hypertension, Metabolic syndrome, Obsessive-compulsive disorder, Schizophrenia, Skin neoplasm, Diabetes mellitus, type 2

403
HECT and RLD domain containing E3 ubiquitin protein ligase 3
-
Cystic kidney disease, Gout, Liver neoplasm

404
HECT and RLD domain containing E3 ubiquitin protein ligase 2
D15F37S1, MRT38, SHEP1, jdf2, p528
Alzheimer disease, Asthma, Eczema, Atrophy, Basal cell carcinoma, Cataract, Ulcerative colitis, Colorectal cancer, Corneal astigmatism, Melanoma, Macular and posterior pole degeneration, Developmental delay with autism spectrum disorder, Eye disease, Glaucoma, Global developmental delay
View all (23 more)

405
HECT and RLD domain containing E3 ubiquitin protein ligase family member 1
MDFPMR, p532, p619
Atrial fibrillation, Attention deficit hyperactivity disorder, Obstructive pulmonary disease, Dental caries, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Neurodevelopmental disorders, Neurotic disorder, Substance abuse, Diabetes mellitus, type 2

406
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2
BLOC3S2, LE
Epilepsy, Generalized epilepsy, Hermansky-pudlak syndrome, Interstitial lung disease, Schizophrenia, Stroke

407
Heat shock protein family B (small) member 3
DHMN2C, HMN2C, HMND4, HSPL27
Charcot-marie-tooth disease, Major depressive disorder, Distal hereditary motor neuropathy, Distal spinal muscular atrophy, Hypertrophic cardiomyopathy, Neuronopathy, distal hereditary motor, Spinal muscular atrophy

408
Heparan sulfate 6-O-sulfotransferase 2
MRXSPM
Human immunodeficiency virus infection, Neurotic disorder, Periodontitis

409
Huntingtin interacting protein 1 related
HIP12, HIP3, ILWEQ
Alzheimer disease, Atrial fibrillation, Bipolar disorder, Heart failure, Insomnia, Parkinson disease, Schizophrenia

410
Hepatocyte growth factor-regulated tyrosine kinase substrate
HRS