Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "U"
131 to 140 of 184 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

131
Uroplakin 3A
UP3A, UPIII, UPIIIA, UPK3
Congenital anomalies of the kidney and urinary tract, Congenital anomalies of kidney and urinary tract, Melanoma, Osteoarthritis, Prostate cancer, Psoriatic arthritis

132
Ubiquinol-cytochrome c reductase binding protein
MC3DN3, QCR7, QP-C, QPC, UQBC, UQBP, UQCR6, UQPC
Diverticular disease, Mitochondrial complex deficiency, Diabetes mellitus, type 2

133
Ubiquinol-cytochrome c reductase core protein 2
MC3DN5, QCR2, UQCR2
Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Venous thromboembolism

134
Ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1
MC3DN10, RIP1, RIS1, RISP, UQCR5
Alzheimer disease, Cardiomyopathy, Dementia, Mitochondrial complex deficiency, Myocardial ischemia

135
Uroporphyrinogen decarboxylase
PCT, UPD
Head and neck neoplasm, Hepatoerythropoietic porphyria, Porphyria cutanea tarda

136
Uroporphyrinogen III synthase
Mgu, UROIIIS
Cutaneous porphyria, Porphyria

137
Upstream transcription factor 1
FCHL, FCHL1, HYPLIP1, MLTF, MLTFI, UEF, bHLHb11
Cardiovascular disease, Diabetes mellitus type 2, Hyperlipidemia

138
-
-

139
Usherin
RP39, US2, USH2, dJ1111A8.1
Alzheimer disease, Amblyopia, Attention deficit hyperactivity disorder, Autism, Retinitis pigmentosa, Bardet-biedl syndrome, Blindness, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Color vision deficiency, Cone-rod dystrophy, Deafness, Aplasia of the vermis, Hearing impairment, Leber congenital amaurosis, Macular dystrophy
View all (12 more)

140
Utrophin
DMDL, DRP, DRP1
Attention deficit hyperactivity disorder, Color vision deficiency, Dementia, Eye disease, Peripheral arterial disease, Proliferative diabetic retinopathy, Willis-ekbom disease, Schizophrenia, Scoliosis, Substance abuse