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
14421 to 14430 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14421
Unk zinc finger
UNKEMPT, ZC3H5, ZC3HDC5
Alzheimer disease, Asthma, Multiple sclerosis

14422
Unk like zinc finger
C16orf28, ZC3H5L, ZC3HDC5L
Tourette syndrome, Mucolipidosis, Orofacial cleft

14423
Beta-ureidopropionase 1
BUP1
Autism, Beta-ureidopropionase deficiency, Celiac disease, Cryptogenic west syndrome, Metabolic syndrome, Myocardial infarction, Infantile spasms, West syndrome

14424
UPF1 RNA helicase and ATPase
HUPF1, NORF1, RENT1, UTF, pNORF1, smg-2
Attention deficit hyperactivity disorder, Autism, Congenital heart disease, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Right atrial isomerism, Schizophrenia, Strabismus, Transposition of the great arteries

14425
UPF2 regulator of nonsense mediated mRNA decay
HUPF2, RENT2, smg-3
Autism, Diverticular disease

14426
UPF3A regulator of nonsense mediated mRNA decay
HUPF3A, RENT3A, UPF3
Cardiovascular disease

14427
UPF3B regulator of nonsense mediated mRNA decay
HUPF3B, MRX62, MRX82, MRXS14, RENT3B, UPF3BP1, UPF3BP2, UPF3BP3, UPF3X, Upf3p-X
Cataract, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Ovarian epithelial cancer, Neurodevelopmental disorder, X-linked intellectual disability, Ovarian cancer, X-linked complex neurodevelopmental disorder

14428
Uroplakin 1B
TSPAN20, UPIB, UPK1
Breast neoplasms, Neutropenia

14429
Uroplakin 2
UP2, UPII
Hematuria

14430
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