Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
14491 to 14500 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14491
Uroplakin 1B
TSPAN20, UPIB, UPK1
Breast neoplasms, Neutropenia

14492
Uroplakin 2
UP2, UPII
Hematuria

14493
Uroplakin 3A
UP3A, UPIII, UPIIIA, UPK3
Congenital anomalies of the kidney and urinary tract, Congenital anomalies of kidney and urinary tract, Melanoma, Osteoarthritis, Prostate cancer, Psoriatic arthritis

14494
Uridine phosphorylase 1
UDRPASE, UP, UPASE, UPP
Allergic contact dermatitis, Juvenile idiopathic arthritis

14495
Uridine phosphorylase 2
UDRPASE2, UP2, UPASE2
Autism, Congenital left-sided heart lesions, Psychiatric disorders, Diabetes mellitus type 2

14496
Ubiquinol-cytochrome c reductase complex assembly factor 1
BFZB, C20orf44, CBP3, UQCC
Central nervous system cancer, Developmental dysplasia of the hip, Diffuse idiopathic skeletal hyperostosis, Glioblastoma, Glioma, Hypertension, Melanoma, Non-melanoma skin carcinoma, Osteoarthritis, Prostate cancer, Venous thromboembolism

14497
Ubiquinol-cytochrome c reductase complex assembly factor 2
C6orf125, C6orf126, Cbp6, M19, MC3DN7, MNF1, bA6B20.2
Hodgkin lymphoma, Insomnia, Metabolic syndrome, Mitochondrial complex deficiency, Diabetes mellitus type 2

14498
Ubiquinol-cytochrome c reductase complex assembly factor 3
C11orf83, CCDS41658.1, MC3DN9, UNQ655
Mitochondrial complex deficiency

14499
Ubiquinol-cytochrome c reductase complex assembly factor 5
C3orf78, SMIM4
Mood disorder, Osteoarthritis

14500
Ubiquinol-cytochrome c reductase complex assembly factor 6
BR, BRAWNIN, C12orf73
Schizophrenia