Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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13061 to 13070 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

13061
SUV39H2 histone lysine methyltransferase
KMT1B
Migraine

13062
SUZ12 polycomb repressive complex 2 subunit
CHET9, IMMAS, JJAZ1
Alzheimer disease, Developmental disability, Endometrial neoplasms, Endometrial stromal sarcoma, Glioblastoma, Glioma, Non-immune hydrops fetalis, Melanoma, Neurodevelopmental disorder, Weaver syndrome

13063
Synaptic vesicle glycoprotein 2A
DEE113, SLC22B1, SV2
Developmental and epileptic encephalopathy, Epilepsy, Schizophrenia, Diabetes mellitus type 2

13064
Synaptic vesicle glycoprotein 2B
HsT19680, SLC22B2
Brain aneurysm, Gout, Kidney disease, Oligodendroglioma, Diabetes mellitus type 2

13065
Synaptic vesicle glycoprotein 2C
SLC22B3
Migraine, Mood disorder, Parkinson disease, Venous thromboembolism

13066
Small vasohibin binding protein
CCDC23, NEDAHM, SPG94
Intellectual developmental disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

13067
Sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1
C9orf13, CCP22, POLYDOM, SEL-OB, SELOB
Bipolar disorder, Cardiovascular disease, Coronary artery disease, Hypertension, Open angle glaucoma, Diabetes mellitus type 2

13068
Supervillin
MFM10
Alzheimer disease, Bone fracture, Obstructive pulmonary disease, Liver cirrhosis, Diverticulitis, Myeloid leukemia, Major depressive disorder, Migraine, Multiple sclerosis, Myofibrillar myopathy, Nonalcoholic fatty liver disease, Orofacial cleft, Upper aerodigestive tract neoplasm

13069
Small VCP interacting protein
-
Kidney disease, Hearing loss, Lung cancer

13070
SV2 related protein
SLC22B4
Alzheimer disease, Uterine fibroid