Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "U"
61 to 70 of 184 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

61
UBE2Q2 pseudogene 1
UBE2QP1
Coronary artery disease, Coronary heart disease, Schizophrenia

62
Ubiquitin specific peptidase 27 X-linked
MRX105, USP22L, USP27, XLID105
Attention deficit hyperactivity disorder, Autism, Developmental delay, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Non-syndromic intellectual disability, x-linked, Obesity, Seizure, Syndactyly of the toes

63
Ubiquitin associated protein 1 like
UBAP-1L
Retinitis pigmentosa

64
Urate oxidase (pseudogene)
UOXP, URICASE
Corpus luteum cyst, Kidney failure, Ovarian cysts, Acute kidney insufficiency, Tumor lysis syndrome

65
Unc-13 homolog C
-
Parkinson disease

66
UBX domain protein 1
2B28, SAKS1, UBXD10
Gastric cancer, Stomach neoplasms

67
Ubiquitin associated protein 1
NAG20, SPG80, UAP, UBAP, UBAP-1
Spastic paraplegia

68
Ubiquitin protein ligase E3 component n-recognin 5
DD5, EDD, EDD1, HYD
Benign neoplasm of stomach, Colorectal cancer, Impaired cognition, Malignant lymphoma, lymphocytic, intermediate differentiation, Stomach neoplasms, Stomach carcinoma

69
Ubiquitin-fold modifier conjugating enzyme 1
HSPC155, NEDSG
Dwarfism, Mental retardation, Microcephaly, Neurodevelopmental disorder with spasticity and poor growth, Oculomotor apraxia, Oculovestibuloauditory syndrome

70
Ubiquitin fold modifier 1
BM-002, C13orf20, HLD14
Cerebellar atrophy, Cerebral atrophy, Hypomyelinating leukodystrophy, Hypomyelination with atrophy of basal ganglia and cerebellum, Mental retardation, Microcephaly