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
9811 to 9820 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9811
PHD finger protein 24
GINIP
Ovarian epithelial cancer, Ovarian cancer

9812
PHD finger protein 3
-
Alzheimer disease, Astigmatism, Retinitis pigmentosa, Dyschromatopsia, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder, Schizophrenia, Tourette syndrome

9813
PHD finger protein 5A
INI, Rds3, SAP14b, SF3B7, SF3b14b, bK223H9.2
Asthma, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Respiratory system disease

9814
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

9815
PHD finger protein 7
HSPC045, HSPC226, NYD-SP6
Gout, Myocardial infarction

9816
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

9817
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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9818
Proline, histidine and glycine rich 1
-
Digestive system disease, Diverticular disease, Diabetes mellitus type 2

9819
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

9820
Phosphorylase kinase regulatory subunit alpha 1
PHKA
Glycogen phosphorylase kinase deficiency, Glycogen storage disease, Peripheral neuropathy