Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14321 to 14330 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14321
TRNA-yW synthesizing protein 3 homolog
C1orf171
Alzheimer disease, Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Dementia, Major depressive disorder, Neurotic disorder, Obstructive sleep apnea syndrome, Orofacial cleft, Scoliosis, Substance abuse

14322
TRNA-yW synthesizing protein 5
C2orf60, hTYW5
Schizophrenia

14323
U2 small nuclear RNA auxiliary factor 1
FP793, RN, RNU2AF1, U2AF35, U2AFBP
Iron metabolism disorder, Metabolic syndrome, Myelodysplastic syndrome, Osteoporosis, Prostatic neoplasms

14324
U2 small nuclear RNA auxiliary factor 2
DEVDFB, U2AF65
Developmental delay with dysmorphic facies and brain anomalies, Insomnia, Leukodystrophy, Neurodevelopmental disorder

14325
U2 snRNP associated SURP domain containing
SR140, fSAPa
Gout, Liver cirrhosis, Metabolic syndrome, Diabetes mellitus type 2

14326
Uveal autoantigen with coiled-coil domains and ankyrin repeats
NUCLING
Breast cancer

14327
UDP-N-acetylglucosamine pyrophosphorylase 1
AGX, AGX1, AGX2, SPAG2
Coronary artery disease, Gout, Rheumatoid arthritis

14328
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

14329
Ubiquitin like modifier activating enzyme 2
ACCES, ARX, HRIHFB2115, SAE2
Acces syndrome, Aplasia cutis congenita, Chromosome 19q13.11 deletion syndrome, Colorectal cancer, Ectrodactyly

14330
Ubiquitin like modifier activating enzyme 5
DEE44, EIEE44, SCAR24, THIFP1, UBE1DC1
Spinocerebellar ataxia, Cholelithiasis, Developmental and epileptic encephalopathy