Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14461 to 14470 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14461
Unc-51 like kinase 4
FAM7C1, REC01035
Alzheimer disease, Androgenetic alopecia, Bipolar disorder, Lymphocytic leukemia, Hodgkin lymphoma, Hypertension, Major depressive disorder, Metabolic syndrome, Multiple myeloma, Prostate cancer, Schizophrenia, Stroke, Diabetes mellitus type 2

14462
UBAP1-MVB12-associated (UMA) domain containing 1
RPA3-AS1, RPA3OS
Alzheimer disease, Biliary atresia, Interstitial lung disease, Melanoma, Neurotic disorder, Obesity, Small cell lung carcinoma, Smooth surface dental caries, Stevens-johnson syndrome, Toxic epidermal necrolysis, Diabetes mellitus type 2

14463
Uromodulin
ADMCKD2, ADTKD1, FJHN, HNFJ, HNFJ1, MCKD2, THGP, THP
Anemia, Tubulointerstitial kidney disease, Kidney disease, Diabetic neuropathy, Hypertension, Juvenile hyperuricemic nephropathy, Gout, Hydronephrosis, Hypertensive heart disease, Hyperuricemia, Hyperuricemic nephropathy, Kidney failure, Nephrolithiasis, Rheumatoid arthritis, Diabetes mellitus type 1
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14464
Uromodulin like 1
-
Osteonecrosis of the femoral head, Male infertility, Obesity, Diabetes mellitus type 2

14465
Uridine monophosphate synthetase
ODC, OPRT
Hypoplastic anemia, Sickle cell anemia, Beta thalassemia, Breast neoplasms, Hepatocellular carcinoma, Squamous cell carcinoma, Cardiomyopathy, Carpal tunnel syndrome, Colonic neoplasms, Colorectal neoplasms, Congenital hypoplastic anemia, Aplastic anemia, Coronary artery disease, Mouth neoplasms, Open angle glaucoma
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14466
Unc-119 lipid binding chaperone
CORD24, HRG4, IMD13, POC7, POC7A
Cone-rod dystrophy, Immunodeficiency, Macular dystrophy, Retinitis pigmentosa

14467
Unc-119 lipid binding chaperone B
POC7B
Diabetes mellitus type 2

14468
Unc-13 homolog A
Munc13-1
Alzheimer disease, Amyotrophic lateral sclerosis, Autism, Benign prostatic hyperplasia, Cerebellar ataxia, Congenital nervous system disorder, Congenital neurologic anomalies, Developmental regression, Febrile convulsion, Frontotemporal dementia, Neurodevelopmental disorder, Obesity

14469
Unc-13 homolog B
MUNC13, UNC13, Unc13h2, munc13-2
Dry eye syndrome, Parkinson disease

14470
Unc-13 homolog C
-
Alzheimer disease, Asthma, Eczema, Attention deficit hyperactivity disorder, Breast cancer, Congenital clubfoot, Coronary artery disease, Cystic kidney disease, Estrogen-receptor negative breast cancer, Gestational diabetes, Inflammatory skin disease, Oropharyngeal cancer, Post-traumatic stress disorder, Psoriasis, Willis-ekbom disease
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