Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14261 to 14270 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14261
U2 small nuclear RNA auxiliary factor 2
DEVDFB, U2AF65
Developmental delay with dysmorphic facies and brain anomalies, Insomnia, Leukodystrophy, Neurodevelopmental disorder

14262
U2 snRNP associated SURP domain containing
SR140, fSAPa
Gout, Metabolic syndrome, Diabetes mellitus type 2

14263
Uveal autoantigen with coiled-coil domains and ankyrin repeats
NUCLING
Breast cancer

14264
UDP-N-acetylglucosamine pyrophosphorylase 1
AGX, AGX1, AGX2, SPAG2
Coronary artery disease, Gout, Rheumatoid arthritis

14265
Ubiquitin like modifier activating enzyme 1
A1S9, A1S9T, A1ST, AMCX1, CFAP124, GXP1, POC20, SMAX2, UBA1A, UBE1, UBE1X, VEXAS
Arthrogryposis multiplex congenita, Squamous cell carcinoma, Spinal muscular atrophy, Vexas syndrome

14266
Ubiquitin like modifier activating enzyme 2
ACCES, ARX, HRIHFB2115, SAE2
Acces syndrome, Aplasia cutis congenita, Chromosome 19q13.11 deletion syndrome, Colorectal cancer, Ectrodactyly

14267
Ubiquitin like modifier activating enzyme 5
DEE44, EIEE44, SCAR24, THIFP1, UBE1DC1
Spinocerebellar ataxia, Cholelithiasis, Developmental and epileptic encephalopathy

14268
Ubiquitin A-52 residue ribosomal protein fusion product 1
CEP52, HUBCEP52, L40, RPL40
Osteoarthritis

14269
Ubiquitin like modifier activating enzyme 6
E1-L2, MOP-4, UBE1L2
Intellectual developmental disorder

14270
Ubiquitin like modifier activating enzyme 7
D8, UBA1B, UBE1L, UBE2, UBE7
Attention deficit hyperactivity disorder, Autism, Squamous cell carcinoma, Inflammatory bowel disease, Insomnia, Intellectual developmental disorder, Major depressive disorder, Mood disorder, Substance abuse, Diabetes mellitus type 2