Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "U"
91 to 100 of 184 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

91
Ubiquitin specific peptidase 28
-
Breast carcinoma, Prostatic neoplasms, Prostate cancer

92
UV stimulated scaffold protein A
KIAA1530, UVSS3
Diabetes mellitus, Uv-sensitive syndrome

93
Ubiquitin specific peptidase 46
-
Bipolar disorder, Mental depression

94
UPF3B regulator of nonsense mediated mRNA decay
HUPF3B, MRX62, MRX82, MRXS14, RENT3B, UPF3BP1, UPF3BP2, UPF3BP3, UPF3X, Upf3p-X
Arachnodactyly, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Brachycephaly, Brachydactyly, Congenital epicanthus, Congenital pectus carinatum, Congenital pectus excavatum, Developmental delay, Facial paralysis, Fg syndrome phenotypic spectrum, Frontal bossing, Hallucinations, Neurosensory hearing impairment
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95
UPF3A regulator of nonsense mediated mRNA decay
HUPF3A, RENT3A, UPF3
Cardiovascular diseases, Classical hodgkin lymphoma

96
Ubiquitin conjugating enzyme E2 Z
HOYS7, USE1
Coronary heart disease, Diabetes mellitus, Stroke

97
UBAP1-MVB12-associated (UMA) domain containing 1
RPA3-AS1, RPA3OS
Stevens-johnson syndrome

98
U2 small nuclear RNA auxiliary factor 1
FP793, RN, RNU2AF1, U2AF35, U2AFBP
Carcinoma of the head and neck, Uterine cervix neoplasm, Endometrial cancer, Lymphocytic leukemia, Leukemia, Lung adenocarcinoma, Malignant uterine corpus neoplasm, Myelodysplastic syndrome, Osteoporosis, Pancreatic adenocarcinoma, Prostatic neoplasms, Prostate cancer, Bladder carcinoma

99
Ubiquitin B
HEL-S-50
Cleft soft palate, Cleft uvula, Hearing loss, Hypoplasia of the maxilla, Oropharyngeal dysphagia, Otitis media, Receptive language delay, Submucosal cleft palate, Submucous cleft of soft and hard palate, Velopharyngeal insufficiency

100
Ubiquitin like modifier activating enzyme 1
A1S9, A1S9T, A1ST, AMCX1, CFAP124, GXP1, POC20, SMAX2, UBA1A, UBE1, UBE1X, VEXAS
Arthrogryposis multiplex congenita, Carcinoma, Congenital hypoplasia of penis, Cryptorchidism, Dolichocephaly, Facial paralysis, Hypospadias, Impaired cognition, Macrotia, Micrognathism, Myopathy, Penis agenesis, Ptosis, Scoliosis, Spinal muscular atrophy
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