Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
731 to 740 of 1032 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

731
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, Liver cirrhosis, Major depressive disorder, Neurotic disorder, Proteasome associated autoinflammatory syndrome, Rheumatoid arthritis, Systemic lupus erythematosus, Diabetes mellitus, type 1

732
Poly(ADP-ribose) polymerase family member 6
ARTD17, PARP-6-B1, PARP-6-C, pART17
Neurodevelopmental disorders, Ulcerative colitis

733
Peptide YY
PYY-I, PYY1
Alzheimer disease, Anorexia, Major depressive disorder, Diarrhea, Diverticular disease, Dysentery, Hyperandrogenism, Depression, Neural tube defect, Obesity, Vomiting

734
PR/SET domain 8
EPM10, KMT8D, PFM5
Androgenetic alopecia, Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Cardioembolic stroke, Cardiovascular disease, Kidney disease, Coronary artery disease, Progressive myoclonic epilepsy with intracellular inclusions, Hypertension, Gout, Heart failure, Hypertensive heart disease, Kidney failure, Major depressive disorder
View all (4 more)

735
Proteasome 20S subunit beta 9
LMP2, PRAAS3, PRAAS6, PSMB6i, RING12, beta1i
Ankylosing spondylitis, Autism, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Interstitial cystitis, Hypothyroidism, Liver cirrhosis, Multiple sclerosis, Proteasome associated autoinflammatory syndrome, Psoriasis, Rheumatoid arthritis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus, type 1
View all (1 more)

736
PR/SET domain 10
BHD2, PFM7, TRIS
Birt-hogg-dube syndrome, Central nervous system cancer, Color vision deficiency, Dementia, Glioblastoma, Glioma

737
PR/SET domain 11
PFM8
Asthma, Atrial fibrillation, Central nervous system cancer, Obstructive pulmonary disease, Erectile dysfunction, Glioblastoma, Glioma, Hyperthyroidism, Hypothyroidism, Major depressive disorder, Meniere disease, Multinodular goiter, Neurotic disorder, Toxic nodular goiter

738
Protein O-glucosyltransferase 1
C3orf9, CLP46, KDELCL1, KTELC1, LGMD2Z, LGMDR21, MDS010, MDSRP, Rumi, hCLP46
Limb girdle muscular dystrophy, Biliary cirrhosis, Dowling degos disease, Limb-girdle muscular dystrophy, Biliary cholangitis

739
Proteasome 26S subunit, ATPase 3
DCIDP, RPT5, TBP1
Alzheimer disease, Anomalous pulmonary venous return, Neurodevelopmental disorder, Congenital cataract, Deafness with cataract, intellectual disability, and polyneuropathy, Glaucoma, Global developmental delay, Human immunodeficiency virus infection, Hypertension, Insomnia, Major depressive disorder, Neurodevelopmental disorders, Neurotic disorder, Non-specific syndromic intellectual disability, Patent ductus arteriosus
View all (2 more)

740
Proteasome 26S subunit, ATPase 5
RPT6, S8, SUG-1, SUG1, TBP10, TRIP1, p45, p45/SUG
Human immunodeficiency virus infection, Neurodevelopmental disorders, Stevens-johnson syndrome