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
9341 to 9350 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9341
Prolyl 4-hydroxylase subunit alpha 1
P4HA
Atrial fibrillation, Bone fragility with contractures, arterial rupture, and deafness, Larsen syndrome, Osteoporosis-pseudoglioma syndrome

9342
Prolyl 4-hydroxylase subunit alpha 2
MYP25, lncRNA-PE
Asthma, Eczema, Basal cell carcinoma, Cardiovascular disease, Coronary artery disease, Crohn disease, Giant cell arteritis, Gout, Inflammatory bowel disease, Myopia, Retinitis pigmentosa, Ulcerative colitis, Vasculitis

9343
Prolyl 4-hydroxylase subunit alpha 3
-
Alzheimer disease

9344
Prolyl 4-hydroxylase subunit beta
CLCRP1, DSI, ERBA2L, GIT, P4Hbeta, PDI, PDIA1, PHDB, PO4DB, PO4HB, PROHB
Bone fragility with contractures, arterial rupture, and deafness, Cole-carpenter syndrome, Desbuquois syndrome, Heart disease, Myocardial ischemia, Osteogenesis imperfecta, Osteoporosis, Osteoporosis-pseudoglioma syndrome, Prostatic neoplasms, Spinocerebellar ataxia

9345
Prolyl 4-hydroxylase, transmembrane
EGLN4, HIDEA, HIFPH4, P4H-TM, PH-4, PH4, PHD4
Intellectual developmental disorder, Intellectual disability

9346
Proliferation-associated 2G4
EBP1, HG4-1, ITAF45, p38-2G4
Alzheimer disease, Eczema, Stomach neoplasms

9347
PABIR family member 2
FAM122B, SPACIA2
Gout

9348
Poly(A) binding protein cytoplasmic 1
PAB1, PABP, PABP1, PABPC2, PABPL1
Breast neoplasms, Transitional cell carcinoma, Congenital pulmonary artery atresia, Intellectual developmental disorder, Urinary bladder neoplasms

9349
Poly(A) binding protein cytoplasmic 1 like
C20orf119, EPAB, OZEMA22, PABPC1L1, dJ1069P2.3
Oocyte maturation defect

9350
Poly(A) binding protein cytoplasmic 3
PABP3, PABPL3, tPABP
Brain aneurysm