Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14481 to 14490 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14481
Unc-93B1 regulator of TLR signaling
IIAE1, UNC-93B, UNC93, UNC93B, Unc-93B1
Brain disease, Liver cirrhosis, Systemic lupus erythematosus

14482
UNC homeobox
UNCX4.1
Kidney disease, Color vision deficiency, Duchenne muscular dystrophy, Gout, Metabolic syndrome, Willis-ekbom disease, Scoliosis, Diabetes mellitus type 2

14483
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

14484
Unk zinc finger
UNKEMPT, ZC3H5, ZC3HDC5
Alzheimer disease, Asthma, Multiple sclerosis

14485
Unk like zinc finger
C16orf28, ZC3H5L, ZC3HDC5L
Tourette syndrome, Mucolipidosis, Orofacial cleft

14486
Beta-ureidopropionase 1
BUP1
Autism, Beta-ureidopropionase deficiency, Celiac disease, Cryptogenic west syndrome, Metabolic syndrome, Myocardial infarction, Infantile spasms, West syndrome

14487
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

14488
UPF2 regulator of nonsense mediated mRNA decay
HUPF2, RENT2, smg-3
Autism, Diverticular disease

14489
UPF3A regulator of nonsense mediated mRNA decay
HUPF3A, RENT3A, UPF3
Cardiovascular disease

14490
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