Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "U"
201 to 210 of 268 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
USH1 protein network component sans
ANKS4A, SANS
Colorectal cancer, Deafness, Hearing impairment, Hearing loss, Idiopathic pulmonary fibrosis, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa-deafness syndrome, Usher syndrome

202
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, Congenital ear anomaly, Congenital sensorineural hearing loss, Deafness, Aplasia of the vermis, Hearing impairment
View all (11 more)

203
USH1 protein network component harmonin binding protein 1
AIEBP, MCC2
Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Ovarian epithelial cancer, Non-hodgkins lymphoma, Ovarian cancer, Ovarian serous carcinoma
View all (3 more)

204
USO1 vesicle transport factor
P115, TAP, VDP
Dermatologic disorder, Prostatic neoplasms, Skin disease

205
Ubiquitin specific peptidase 1
UBP
Crohn disease, Tourette syndrome, Inflammatory bowel disease, Metabolic syndrome, Nonalcoholic fatty liver disease, Peritonitis, Diabetes mellitus type 2

206
Ubiquitin specific peptidase 10
UBPO
Asthma, Diverticular disease, Alzheimer disease, Ocular sarcoidosis

207
Ubiquitin specific peptidase 11
UHX1
Bronchiectasis

208
Ubiquitin specific peptidase 12
UBH1, USP12L1
Alzheimer disease

209
Ubiquitin specific peptidase 13
ISOT3, IsoT-3
Color vision deficiency, Dermatologic disorder, Skin disease

210
Ubiquitin specific peptidase 14
TGT, Ubp6
Neurodevelopmental disorder, Metabolic syndrome, Non-specific syndromic intellectual disability, Diabetes mellitus type 2