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 "P"
1191 to 1200 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1191
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

1192
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

1193
Proteasome 26S subunit, ATPase 1
NEDGTH, P26S4, RPT2, S4, p56
Bipolar disorder, Birk-aharoni syndrome, Dementia, Major depressive disorder, Neurodevelopmental disorder

1194
Proteasome 26S subunit, ATPase 2
MSS1, Nbla10058, RPT1, S7
Hearing loss, Diabetes mellitus type 2

1195
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
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1196
PSMC3 interacting protein
GT198, HOP2, HUMGT198A, ODG3, TBPIP
46,xy gonadal dysgenesis, Gonadal dysgenesis, Ovarian dysgenesis, Prostatic neoplasms, Diabetes mellitus type 2

1197
Proteasome 26S subunit, ATPase 5
RPT6, S8, SUG-1, SUG1, TBP10, TRIP1, p45, p45/SUG
Neurodevelopmental disorder, Stevens-johnson syndrome

1198
Proteasome 26S subunit, ATPase 6
RPT5, SUG2, p42
Alzheimer disease

1199
Proteasome 26S subunit, non-ATPase 1
P112, Rpn2, S1
Bardet-biedl syndrome, Systemic lupus erythematosus

1200
Proteasome 26S subunit, non-ATPase 11
Rpn6, S9, p44.5
Attention deficit hyperactivity disorder, Neurodevelopmental disorder, Liver failure, Non-specific syndromic intellectual disability, Schizophrenia, Substance abuse