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
10511 to 10520 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

10511
Proteasome 20S subunit beta 6
DELTA, LMPY
Systemic lupus erythematosus

10512
Proteasome 20S subunit beta 7
-
Atrial fibrillation, Hypothyroidism, Respiratory system disease

10513
Proteasome 20S subunit beta 8
ALDD, D6S216, D6S216E, JMP, LMP7, NKJO, PRAAS1, PSMB5i, RING10
Autoinflammatory syndrome, Candle syndrome, Dental caries, Hyperthyroidism, Hypothyroidism, Iga nephropathy, Kidney disease, Major depressive disorder, Neurotic disorder, Proteasome associated autoinflammatory syndrome, Rheumatoid arthritis, Systemic lupus erythematosus, Diabetes mellitus type 1

10514
Proteasome 20S subunit beta 9
LMP2, PRAAS3, PRAAS6, PSMB6i, RING12, beta1i
Ankylosing spondylitis, Autism, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Interstitial cystitis, Hypothyroidism, Multiple sclerosis, Proteasome associated autoinflammatory syndrome, Psoriasis, Rheumatoid arthritis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 1, Vitiligo

10515
Proteasome 26S subunit, ATPase 1
NEDGTH, P26S4, RPT2, S4, p56
Bipolar disorder, Birk-aharoni syndrome, Dementia, Major depressive disorder, Neurodevelopmental disorder

10516
Proteasome 26S subunit, ATPase 2
MSS1, Nbla10058, RPT1, S7
Hearing loss, Diabetes mellitus type 2

10517
Proteasome 26S subunit, ATPase 3
DCIDP, RPT5, TBP1
Alzheimer disease, Anomalous pulmonary venous , Neurodevelopmental disorder, Congenital cataract, Congenital hip dysplasia, Deafness with cataract, intellectual disability, and polyneuropathy, Glaucoma, Global developmental delay, Hypertension, Insomnia, Major depressive disorder, Neurotic disorder, Non-specific syndromic intellectual disability, Patent ductus arteriosus, Polymicrogyria
View all (1 more)

10518
PSMC3 interacting protein
GT198, HOP2, HUMGT198A, ODG3, TBPIP
46,xy gonadal dysgenesis, Gonadal dysgenesis, Ovarian dysgenesis, Prostatic neoplasms, Diabetes mellitus type 2

10519
Proteasome 26S subunit, ATPase 5
RPT6, S8, SUG-1, SUG1, TBP10, TRIP1, p45, p45/SUG
Neurodevelopmental disorder, Stevens-johnson syndrome

10520
Proteasome 26S subunit, ATPase 6
RPT5, SUG2, p42
Alzheimer disease