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
14571 to 14580 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14571
Ubiquitin specific peptidase 8
HumORF8, PITA4, SPG59, UBPY
Alzheimer disease, Ankylosing spondylitis, Spastic paraplegia, Neurodevelopmental disorder, Cushing syndrome, Developmental and epileptic encephalopathy, Esophageal squamous cell carcinoma, Hypertension, Non-specific syndromic intellectual disability, Osteoarthritis, Parkinson disease, Cushing's disease, Hereditary spastic paraplegia

14572
Ubiquitin specific peptidase 9 X-linked
DFFRX, FAF, FAF-X, FAM, MRX99, MRXS99F, XLID99, hFAM
Developmental delay, Developmental disability, Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability, Partington syndrome, X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability

14573
Ubiquitin specific peptidase 9 Y-linked
DFFRY, FAF-Y, SPGFY2
Chromosome y microdeletion syndrome, Male infertility y chromosome microdeletion, Spermatogenic failure, y-linked

14574
Uronyl 2-sulfotransferase
2OST, CS-2OST
Atrial fibrillation, Attention deficit hyperactivity disorder, Basal cell carcinoma, Diabetic retinopathy, Diverticulitis, Dupuytren contracture, Endometriosis, Glaucoma, Occupational disease, Polycystic ovary syndrome, Post-traumatic stress disorder

14575
UTP14A small subunit processome component
NYCO16, SDCCAG16, Utp14, dJ537K23.3
Periodontitis

14576
UTP14C small subunit processome component
2700066J21Rik, KIAA0266, UTP14B
Congenital disorder of glycosylation

14577
UTP15 small subunit processome component
NET21
Hearing loss

14578
UTP20 small subunit processome component
1A6/DRIM, DRIM
Infective arthritis

14579
UTP23 small subunit processome component
C8orf53
Colorectal cancer, Colonic neoplasms, Colorectal adenoma, Digestive system disease, Schizoaffective disorder

14580
UTP25 small subunit processome component
C1orf107, DEF, DIEXF, DJ434O14.5
Androgenetic alopecia, Hirschsprung disease, Hypertension, Orofacial cleft, Scoliosis