Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
14501 to 14510 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14501
Ubiquitin specific peptidase 49
-
Central nervous system cancer, Glioblastoma, Glioma, Insomnia, Oligodendroglioma, Psoriasis, Diabetes mellitus type 2

14502
Ubiquitin specific peptidase 50
-
Alzheimer disease, Osteoarthritis, Parkinson disease, Hereditary spastic paraplegia

14503
Ubiquitin specific peptidase 51
-
Androgenetic alopecia

14504
Ubiquitin specific peptidase 53
PFIC7
Cholelithiasis, Corneal astigmatism, Progressive intrahepatic cholestasis

14505
Ubiquitin specific peptidase 54
C10orf29, bA137L10.3, bA137L10.4
Venous thromboembolism

14506
USP6 N-terminal like
RNTRE, TRE2NL, USP6NL-IT1
Melanoma

14507
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

14508
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

14509
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

14510
Ubiquitin specific peptidase 9 Y-linked
DFFRY, FAF-Y, SPGFY2
Chromosome y microdeletion syndrome, Male infertility y chromosome microdeletion, Spermatogenic failure, y-linked