Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14411 to 14420 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14411
Unc-50 inner nuclear membrane RNA binding protein
GMH1, HSD23, PDLs22, UNCL, URP
Arthrogryposis multiplex congenita, Diverticular disease, Pena-shokeir syndrome

14412
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

14413
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
View all (3 more)

14414
Unc-5 family C-terminal like
MUXA, ZUD
Alzheimer disease, Colorectal cancer, Esophageal cancer, Gastric cancer, Gout, Insomnia, Oligodendroglioma, Schizophrenia, Diabetes mellitus type 2

14415
Unc-5 netrin receptor D
PRO34692, Unc5h4
Diabetic foot, Dyslexia, Insomnia, Major depressive disorder, Neuropathy, Neurotic disorder, Obesity, Psoriasis, Scoliosis

14416
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

14417
Unc-80 subunit of NALCN channel complex
C2orf21, UNC-80
Autism, Global developmental delay, Intellectual developmental disorder

14418
Unc-93B1 regulator of TLR signaling
IIAE1, UNC-93B, UNC93, UNC93B, Unc-93B1
Brain disease, Liver cirrhosis, Systemic lupus erythematosus

14419
UNC homeobox
UNCX4.1
Kidney disease, Color vision deficiency, Duchenne muscular dystrophy, Gout, Metabolic syndrome, Willis-ekbom disease, Scoliosis, Diabetes mellitus type 2

14420
Uracil DNA glycosylase
DGU, HIGM4, HIGM5, UDG, UNG1, UNG15, UNG2
Bloom syndrome, Color vision deficiency, Colorectal neoplasms, Dysfibrinogenemia, Hyper-igm immunodeficiency syndrome, Hyper-immunoglobulin m syndrome