Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "U"
101 to 110 of 184 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

101
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

102
Ubiquitin conjugating enzyme E2 A
HHR6A, MRXS30, MRXSN, RAD6A, UBC2
Intellectual developmental disorder, x-linked, X-linked intellectual disability

103
Ubiquitin conjugating enzyme E2 E1
UBCH6
Juvenile arthritis, Attention deficit hyperactivity disorder, Dermatologic disorder, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis, Skin disease, Substance abuse

104
Ubiquitin conjugating enzyme E2 E2
UBCH8
Asthma, Hepatocellular carcinoma, Diabetes mellitus, Diabetes mellitus type 2, Diabetic retinopathy, Metabolic syndrome, Prostate cancer, Respiratory system disease, Severe acute respiratory syndrome, Diabetes mellitus, type 2, Vitiligo

105
Ubiquitin conjugating enzyme E2 H
E2-20K, GID3, UBC8, UBCH, UBCH2
Astrocytoma, Autism, Polycystic ovary syndrome

106
Ubiquitin conjugating enzyme E2 I
C358B7.1, P18, UBC9
Carcinoma

107
Ubiquitin conjugating enzyme E2 L3
E2-F1, L-UBC, UBCH7, UbcM4
Alzheimer disease, Ankylosing spondylitis, Atrial fibrillation, Autoimmune disease, Celiac disease, Crohn disease, Hepatitis b, Inflammatory bowel disease, Juvenile idiopathic arthritis, Systemic lupus erythematosus, Metabolic syndrome, Myositis, Oligoarticular juvenile idiopathic arthritis, Polyarticular juvenile idiopathic arthritis, Psoriasis
View all (6 more)

108
Ubiquitin protein ligase E3A
ANCR, AS, E6-AP, EPVE6AP, HPVE6A, PIX1
15q11q13 microduplication syndrome, Angelman syndrome, Autism, Craniofacial abnormalities, Developmental delay, Developmental disability, Epilepsy, Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder, Neurodevelopmental disorders, Obesity, Prostate cancer

109
Upstream binding transcription factor
CONDBA, NOR-90, UBF, UBF-1, UBF1, UBF2
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder, Neurodevelopmental disorder, Neurodevelopmental disorders, Parkinson disease

110
Ubiquitin C-terminal hydrolase L1
HEL-117, HEL-S-53, NDGOA, PARK5, PGP 9.5, PGP9.5, PGP95, SPG79, SPG79A, UCHL-1, Uch-L1
Alzheimer disease, Breast benign neoplasm, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Esophageal neoplasm, Gallbladder neoplasm, Glomerulonephritis, Non-neoplastic peripheral nervous system disease, Parkinson disease, Peripheral nervous system disease, Peripheral neuropathy, Spastic paraplegia, Young-onset parkinson disease