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"
241 to 250 of 268 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

241
Ubiquitin specific peptidase 48
DFNA85, RAP1GA1, USP31
Amphetamine or sympathomimetic abuse, Isolated sensorineural deafness, Coronary artery disease, Cushing syndrome, Deafness, Diabetes mellitus type 2, Hearing loss, Cushing's disease, Schizophrenia

242
Ubiquitin specific peptidase 49
-
Central nervous system cancer, Glioblastoma, Glioma, Insomnia, Oligodendroglioma, Psoriasis, Diabetes mellitus type 2

243
Ubiquitin specific peptidase 50
-
Alzheimer disease, Osteoarthritis, Parkinson disease, Hereditary spastic paraplegia

244
Ubiquitin specific peptidase 51
-
Androgenetic alopecia

245
Ubiquitin specific peptidase 53
PFIC7
Cholelithiasis, Corneal astigmatism, Progressive intrahepatic cholestasis

246
Ubiquitin specific peptidase 54
C10orf29, bA137L10.3, bA137L10.4
Venous thromboembolism

247
USP6 N-terminal like
RNTRE, TRE2NL, USP6NL-IT1
Melanoma

248
Ubiquitin specific peptidase 7
C16DELp13.2, DEL16P13.2, HAFOUS, HAUSP, TEF1
16p13.2 microdeletion syndrome, Androgenetic alopecia, Diabetic maculopathy, Insomnia, Intellectual developmental disorder, Neurodevelopmental disorder, Ovarian cancer, Ovarian serous carcinoma, Prostatic neoplasms, Scoliosis, Urinary bladder neoplasms

249
Ubiquitin specific peptidase 8
HumORF8, PITA4, SPG59, UBPY
Alzheimer disease, Ankylosing spondylitis, Spastic paraplegia, Neurodevelopmental disorder, Cushing syndrome, Developmental and epileptic encephalopathy, Esophageal squamous cell carcinoma, Hypertension, Non-specific syndromic intellectual disability, Osteoarthritis, Parkinson disease, Cushing's disease, Hereditary spastic paraplegia

250
Ubiquitin specific peptidase 9 X-linked
DFFRX, FAF, FAF-X, FAM, MRX99, MRXS99F, XLID99, hFAM
Developmental delay, Developmental disability, Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability, Partington syndrome, X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability