Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
5681 to 5690 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5681
Hyaluronan synthase 3
-
Atrial fibrillation, Attention deficit hyperactivity disorder, Fatty liver, Fatty liver, alcoholic

5682
Histone H3 associated protein kinase
GSG2
Parkinson disease

5683
Histone acetyltransferase 1
KAT1
Schizophrenia, Diabetes mellitus type 2

5684
HAUS augmin like complex subunit 1
CCDC5, HEI-C, HEIC, HsT1461
Migraine

5685
HAUS augmin like complex subunit 6
Dgt6, FAM29A
Basal cell carcinoma, Coronary artery disease, Keratinocyte carcinoma, Ovarian neoplasms, Prostate cancer, Diabetes mellitus type 2

5686
HAUS augmin like complex subunit 7
UCHL5IP, UIP1
Androgenetic alopecia

5687
HAUS augmin like complex subunit 8
DGT4, HICE1, NY-SAR-48
Asthma, Hypertension, Hypothyroidism, Selective iga deficiency disease

5688
Hepatitis A virus cellular receptor 1
CD365, HAVCR, HAVCR-1, KIM-1, KIM1, TIM, TIM-1, TIM1, TIMD-1, TIMD1
Dementia, Atopic dermatitis, Hyperlipidemia, Focal glomerulosclerosis, Hypertriglyceridemia, Kidney disease, Kidney failure, Metabolic syndrome, Necrosis, Oligodendroglioma, Proteinuria

5689
Hepatitis A virus cellular receptor 2
CD366, HAVcr-2, KIM-3, SPTCL, TIM3, TIMD-3, TIMD3, Tim-3
Alzheimer disease, Lewy body disease, Hemophagocytic lymphohistiocytosis, Oligodendroglioma

5690
HCLS1 associated protein X-1
HCLSBP1, HS1BP1, SCN3
Bipolar disorder, Severe congenital neutropenia, Schizophrenia, Congenital neutropenia