Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14471 to 14480 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14471
Unc-13 homolog D
FHL3, HLH3, HPLH3, Munc13-4
Asthma, Autoinflammatory syndrome, Cardiovascular disease, Coronary artery disease, Hemophagocytic lymphohistiocytosis, Hereditary hemophagocytic lymphohistiocytosis, Hyperlipidemia, Major depressive disorder, Metabolic syndrome, Prostatic neoplasms

14472
Unc-45 myosin chaperone A
GC-UNC45, GCUNC-45, GCUNC45, IRO039700, OOHE, SMAP-1, SMAP1, UNC-45A
Cholestasis, Colorectal cancer, Hearing impairment, Osteootohepatoenteric syndrome

14473
Unc-45 myosin chaperone B
CMYA4, CTRCT43, MFM11, SMUNC45, UNC-45B, UNC45
Cardiomyopathy, Cataract, Color vision deficiency, Congenital cataract, Craniofacial abnormalities, Nuclear cataract, Posterior subcapsular cataract, Heart disease, Myofibrillar myopathy, Myopathy, Paralysis, Systemic sclerosis

14474
Unc-50 inner nuclear membrane RNA binding protein
GMH1, HSD23, PDLs22, UNCL, URP
Arthrogryposis multiplex congenita, Diverticular disease, Pena-shokeir syndrome

14475
Unc-5 netrin receptor B
UNC5H2, p53RDL1
Eczema, Attention deficit hyperactivity disorder, Coronary aneurysm, Multiple myeloma, Obesity, Oligodendroglioma, Willis-ekbom disease, Scoliosis, Seborrheic dermatitis, Substance abuse, Uveal melanoma

14476
Unc-5 netrin receptor C
UNC5H3
Alzheimer disease, Astrocytoma, Renal cell carcinoma, Cardiovascular disease, Central nervous system cancer, Color vision deficiency, Coronary artery disease, Glioma, Hypertension, Major depressive disorder, Metabolic syndrome, Myocardial infarction, Obesity, Osteoarthritis, Polycystic ovary syndrome
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14477
Unc-5 family C-terminal like
MUXA, ZUD
Alzheimer disease, Colorectal cancer, Esophageal cancer, Gastric cancer, Gout, Insomnia, Liver cirrhosis, Oligodendroglioma, Schizophrenia, Diabetes mellitus type 2

14478
Unc-5 netrin receptor D
PRO34692, Unc5h4
Diabetic foot, Dyslexia, Insomnia, Major depressive disorder, Neuropathy, Neurotic disorder, Obesity, Psoriasis, Scoliosis

14479
Unc-79 subunit of NALCN channel complex
KIAA1409
Asthma, Attention deficit hyperactivity disorder, Autism, Neurodevelopmental disorder, Hypertension, Gastroesophageal reflux disease, Heart disease, Insomnia, Irritable bowel syndrome, Metabolic syndrome, Non-specific syndromic intellectual disability, Substance abuse, Diabetes mellitus type 2

14480
Unc-80 subunit of NALCN channel complex
C2orf21, UNC-80
Autism, Global developmental delay, Intellectual developmental disorder