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
14541 to 14550 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14541
Ubiquitin specific peptidase 24
-
Myocardial infarction

14542
Ubiquitin specific peptidase 25
EIG19, USP21
Epilepsy, Idiopathic generalized epilepsy, Panic disorder

14543
Ubiquitin specific peptidase 26
SPGFX6
Congenital impairment of spermatozoa motility, Male infertility, Neurotic disorder, Scoliosis, Spermatogenic failure, x-linked, Teratozoospermia

14544
Ubiquitin specific peptidase 27 X-linked
MRX105, USP22L, USP27, XLID105
Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability

14545
Ubiquitin specific peptidase 28
-
Atrial fibrillation, Attention deficit hyperactivity disorder, Breast cancer, Prostate cancer, Prostatic neoplasms, Substance abuse

14546
Ubiquitin specific peptidase 29
HOM-TES-84/86
Alzheimer disease, Colorectal cancer, Diabetes mellitus type 2

14547
Ubiquitin specific peptidase 3
SIH003, UBP
Alzheimer disease, Atrial fibrillation, Obstructive pulmonary disease, Heart failure, Major depressive disorder, Diabetes mellitus type 2, Uterine fibroid

14548
Ubiquitin specific peptidase 31
-
Breast cancer, Color vision deficiency, Major depressive disorder, Multiple sclerosis, Multiple system atrophy, Hearing loss, Diabetes mellitus type 1

14549
Ubiquitin specific peptidase 32
NY-REN-60, USP10
Alzheimer disease, Epithelial ovarian carcinoma

14550
Ubiquitin specific peptidase 34
-
Appendicitis, Atrial fibrillation, Brugada syndrome, Cardioembolic stroke, Cardiovascular disease, Chromosome 2p16.1-p15 deletion syndrome, Congenital heart disease, Crohn disease, Gastroesophageal reflux disease, Gout, Hypothyroidism, Inflammatory bowel disease, Metabolic syndrome, Psoriasis, Diabetes mellitus type 2