Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "U"
151 to 160 of 268 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

151
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

152
Unc-50 inner nuclear membrane RNA binding protein
GMH1, HSD23, PDLs22, UNCL, URP
Arthrogryposis multiplex congenita, Diverticular disease, Pena-shokeir syndrome

153
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

154
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)

155
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

156
Unc-5 netrin receptor D
PRO34692, Unc5h4
Diabetic foot, Dyslexia, Insomnia, Major depressive disorder, Neuropathy, Neurotic disorder, Obesity, Psoriasis, Scoliosis

157
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

158
Unc-80 subunit of NALCN channel complex
C2orf21, UNC-80
Autism, Global developmental delay, Intellectual developmental disorder

159
Unc-93B1 regulator of TLR signaling
IIAE1, UNC-93B, UNC93, UNC93B, Unc-93B1
Brain disease, Liver cirrhosis, Systemic lupus erythematosus

160
UNC homeobox
UNCX4.1
Kidney disease, Color vision deficiency, Duchenne muscular dystrophy, Gout, Metabolic syndrome, Willis-ekbom disease, Scoliosis, Diabetes mellitus type 2