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"
451 to 460 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

451
PHD finger protein 6
BFLS, BORJ, CENP-31
Borjeson-forssman-lehmann syndrome, Congenital fusion of ribs, Congenital hypoplasia of penis, Congestive heart failure, Developmental disability, Global developmental delay, Heart failure, Intellectual developmental disorder, Cortical development malformation, Neurotic disorder, Pulmonary arterial hypertension, Spastic paraplegia

452
PHD finger protein 7
HSPC045, HSPC226, NYD-SP6
Gout, Myocardial infarction

453
PHD finger protein 8
JHDM1F, KDM7B, MRXSSD, ZNF422
Bipolar disorder, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Major depressive disorder, Schizophrenia, X-linked intellectual disability

454
Phosphoglycerate dehydrogenase
3-PGDH, 3PGDH, HEL-S-113, NLS, NLS1, PDG, PGAD, PGD, PGDH, PHGDHD, SERA
Amino acid metabolism disorder, Breast cancer, Breast neoplasms, Non-small-cell lung carcinoma, Desbuquois syndrome, Developmental and epileptic encephalopathy, Gout, Liver neoplasms, Macular telangiectasia, Melanoma, Multiple sclerosis, Neuropathy, Osteoarthritis, Osteomyelitis, Peripheral neuropathy
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455
Proline, histidine and glycine rich 1
-
Digestive system disease, Diverticular disease, Diabetes mellitus type 2

456
PHIP subunit of CUL4-Ring ligase complex
BRWD2, CHUJANS, DCAF14, DIDOD, RepID, WDR11, ndrp
Chung-jansen syndrome, Developmental delay with intellectual disability and obesity, Gout, Heart failure, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, Schizophrenia, Sjogren syndrome

457
Phosphorylase kinase regulatory subunit alpha 1
PHKA
Glycogen phosphorylase kinase deficiency, Glycogen storage disease, Peripheral neuropathy

458
Phosphorylase kinase regulatory subunit alpha 2
GSD9A, PHK, PYK, PYKL, XLG, XLG2
Glycogen phosphorylase kinase deficiency, Glycogen storage disease, Ocular albinism

459
Phosphorylase kinase regulatory subunit beta
-
Glycogen phosphorylase kinase deficiency, Glycogen storage disease

460
Phosphorylase kinase catalytic subunit gamma 1
PHKG
Glycogen storage disease, Multiple sclerosis