Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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5961 to 5970 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5961
Hepsin
TMPRSS1
Atrial fibrillation, Lipidoses, Lipoidosis, Intellectual developmental disorder, Prostatic neoplasms

5962
Haptoglobin-related protein
A-259H10.2, HP
Cardiovascular disease, Coronary artery disease, Metabolic syndrome

5963
Hypoxanthine phosphoribosyltransferase 1
HGPRT, HPRT
Gout, Hyperuricemia, Hyperuricemia syndrome, Neurotic disorder, Partial hypoxanthine-guanine phosphoribosyltransferase deficiency

5964
HPS1 biogenesis of lysosomal organelles complex 3 subunit 1
BLOC3S1, HPS
Hermansky-pudlak syndrome, Oligodendroglioma

5965
HPS3 biogenesis of lysosomal organelles complex 2 subunit 1
BLOC2S1, SUTAL
Ferroxidase deficiency, Hermansky-pudlak syndrome, Thrombocytopenia

5966
HPS4 biogenesis of lysosomal organelles complex 3 subunit 2
BLOC3S2, LE
Epilepsy, Generalized epilepsy, Hermansky-pudlak syndrome, Interstitial lung disease, Schizophrenia, Stroke

5967
HPS5 biogenesis of lysosomal organelles complex 2 subunit 2
AIBP63, BLOC2S2
Attention deficit hyperactivity disorder, Hermansky-pudlak syndrome, Lewy body disease, Scoliosis, Substance abuse, Thrombocytopenia

5968
HPS6 biogenesis of lysosomal organelles complex 2 subunit 3
BLOC2S3
Atrial fibrillation, Hermansky-pudlak syndrome, Thrombocytopenia, Vascular dementia

5969
Heparanase
HPA, HPA1, HPR1, HPSE1, HSE1
Breast neoplasms, Color vision deficiency, Major depressive disorder, Iga nephropathy, Melanoma, Nephrotic syndrome, Depression

5970
Heparanase 2 (inactive)
HPA2, HPR2, UFS, UFS1
Asthma, Astrocytoma, Congenital anomalies of the kidney and urinary tract, Central nervous system cancer, Gestational diabetes, Glioma, Migraine, Multinodular goiter, Neurotic disorder, Obesity, Ochoa syndrome, Peripheral neuropathy, Diabetes mellitus type 1, Diabetes mellitus type 2, Urofacial syndrome