Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
391 to 400 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

391
Phosphofructokinase, platelet
ATP-PFK, PFK-C, PFK-P, PFKF
Connective tissue disease, Liver cirrhosis, Mixed connective tissue disease

392
Profilin 1
ALS18
Amyotrophic lateral sclerosis, Esophageal squamous cell carcinoma, Liver cirrhosis

393
Profilin 2
D3S1319E, PFL
Ocular hypotension

394
Pepsinogen A3
-
Breast benign neoplasm

395
Pepsinogen A5
Pg5
Esotropia

396
Phosphoglycerate mutase 1
HEL-S-35, PGAM-B, PGAMA
Bipolar disorder, Carcinoma, Non-small-cell lung carcinoma, Squamous cell carcinoma, Mouth neoplasm, Stomach neoplasms, Vascular brain injury

397
Phosphoglycerate mutase 2
GSD10, PGAM-M, PGAMM
Dimauro disease, Glycogen storage disease, Prostatic neoplasm

398
Post-GPI attachment to proteins inositol deacylase 1
Bst1, ISPD3024, MRT42, NEDDSBA, SPG67
Nonsyndromic intellectual disability, Spastic paraplegia, Intellectual developmental disorder, Neurodevelopmental disorder, Myopia, Hereditary spastic paraplegia, Thyroid cancer

399
Post-GPI attachment to proteins 2
CWH43-N, FRAG1, HPMRS3, MRT17, MRT21
Congenital omphalocele, Hyperphosphatasia with intellectual disability syndrome, Micrognathism

400
Post-GPI attachment to proteins phospholipase 3
AGLA546, CAB2, PERLD1, PP1498, hCOS16
Asthma, Bipolar disorder, Cardiovascular disease, Congestive heart failure, Crohn disease, Hyperphosphatasia with intellectual disability syndrome, Inflammatory bowel disease, Diabetes mellitus, type 1, Diabetes mellitus, type 2