Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14331 to 14340 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14331
Ubiquitin A-52 residue ribosomal protein fusion product 1
CEP52, HUBCEP52, L40, RPL40
Osteoarthritis

14332
Ubiquitin like modifier activating enzyme 6
E1-L2, MOP-4, UBE1L2
Intellectual developmental disorder

14333
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

14334
UBA domain containing 1
GBDR1, KPC2, UBADC1
Colorectal cancer, Lung cancer

14335
UBA domain containing 2
PHGDHL1
Ankylosing spondylitis, Asthma, Eczema, Basal cell carcinoma, Behcet disease, Obstructive pulmonary disease, Crohn disease, Hypothyroidism, Inflammatory bowel disease, Keratinocyte carcinoma, Non-small cell lung carcinoma, Peripheral arterial disease, Psoriasis, Respiratory system disease, Sclerosing cholangitis
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14336
UBA like domain containing 2
FAM100B
Scoliosis

14337
Ubiquitin associated protein 1
NAG20, SPG80, UAP, UBAP, UBAP-1
Spastic paraplegia, Breast cancer, Colorectal cancer, Tourette syndrome

14338
Ubiquitin associated protein 1 like
UBAP-1L
Cone-rod dystrophy, Retinal degeneration

14339
Ubiquitin associated protein 2
UBAP-2
Alzheimer disease, Atrial fibrillation, Bipolar disorder, Colorectal cancer, Metabolic syndrome, Osteoporosis, Parkinson disease, Prostate cancer, Schizophrenia, Diabetes mellitus type 2

14340
Ubiquitin associated protein 2 like
NEDLBF, NICE-4, NICE4
Attention deficit hyperactivity disorder, Global developmental delay, Insomnia, Neurodevelopmental disorder, Substance abuse