Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
861 to 870 of 1032 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

861
Peroxiredoxin 2
HEL-S-2a, NKEF-B, NKEFB, PRP, PRX2, PRXII, PTX1, TDPX1, TPX1, TSA
Asbestosis, Carcinoma, Hepatocellular carcinoma, Down syndrome, Esophageal neoplasm, Myeloid leukemia, Melanoma, Osteosarcoma, Prostatic neoplasm

862
Pleckstrin homology like domain family A member 2
BRW1C, BWR1C, HLDA2, IPL, TSSC3
Non-small-cell lung carcinoma, Gout, Osteosarcoma

863
PDYN antisense RNA 1
-

864
Peptidylprolyl isomerase E like (pseudogene)
PPIEP1

865
Profilin 1 pseudogene 1
-

866
Photoreceptor disc component
RP36
Diabetic neuropathy, Retinitis pigmentosa, Squamous cell carcinoma, Diabetes mellitus, type 2

867
Polycomb group ring finger 2
MEL-18, RNF110, TPFS, ZNF144
Global developmental delay, Intellectual developmental disorder, Turnpenny-fry syndrome, Wolfram syndrome

868
PR/SET domain 2
HUMHOXY1, KMT8, KMT8A, MTB-ZF, RIZ, RIZ1, RIZ2
Amphetamine or related acting sympathomimetic abuse, Brain aneurysm, Osteoarthritis, Schizophrenia, Thyroid cancer, Urinary bladder cancer

869
Peroxidasin
ASGD7, COPOA, D2S448, D2S448E, MG50, PRG2, PXN, VPO, hsPxd01
Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Congenital cataract microcornea with corneal opacity, Glaucoma, Myeloid leukemia, Liver cirrhosis, Retinitis pigmentosa, Systemic sclerosis, Diabetes mellitus, type 2, Visual disorder

870
Paired box 8
PAX-8
Congenital hypothyroidism , Breast cancer, Cancer, Cervical cancer, Cervical intraepithelial neoplasia, Colorectal cancer, Colorectal neoplasm, Thyroid agenesis, Congenital thyroid atrophy, Differentiated thyroid carcinoma, Estrogen-receptor negative breast cancer, Gout, Insomnia, Lung cancer, Ovarian cancer
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