Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "U"
41 to 50 of 184 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

41
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

42
Unc-13 homolog A
Munc13-1
Alzheimer disease, Amyotrophic lateral sclerosis, Autism, Cerebellar ataxia, Congenital neurologic anomalies , Developmental regression, Febrile convulsion, Frontotemporal dementia, Neurodevelopmental disorders, Obesity

43
UBX domain protein 4
UBXD2, UBXDC1, erasin
Keratoconus, Lung cancer, Non-small cell lung carcinoma

44
Ubiquitin protein ligase E3 component n-recognin 4
RBAF600, ZUBR1, p600
Crohn disease, Developmental disability, Episodic ataxia, Inflammatory bowel disease, Long qt syndrome, Neurodevelopmental disorders, Psychiatric disorders, Ulcerative colitis

45
Ubiquitin specific peptidase 24
-
Myocardial infarction

46
Ubiquitin B pseudogene 4
-

47
Ubiquitin specific peptidase 49
-
Central nervous system cancer, Glioblastoma, Glioma, Insomnia, Oligodendroglioma, Psoriasis, Diabetes mellitus, type 2

48
Unc-50 inner nuclear membrane RNA binding protein
GMH1, HSD23, PDLs22, UNCL, URP
Arthrogryposis multiplex congenita, Diverticular disease, Pena-shokeir syndrome type i

49
UTP25 small subunit processome component
C1orf107, DEF, DIEXF, DJ434O14.5
Androgenetic alopecia, Hirschsprung disease, Hypertension, Orofacial cleft, Scoliosis

50
Ubiquinol-cytochrome c reductase complex III subunit VII
MC3DN4, QCR8, QP-C, QPC, UQCR7
Leigh syndrome, Mitochondrial complex deficiency