Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
371 to 380 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

371
Peroxisomal biogenesis factor 19
D1S2223E, HK33, PBD12A, PMP1, PMPI, PXF, PXMP1
Peroxisome biogenesis disorder, Zellweger spectrum disorder

372
Peroxisomal biogenesis factor 2
PAF1, PBD5A, PBD5B, PMP3, PMP35, PXMP3, RNF72, ZWS3
Autosomal recessive ataxia, Hypogonadism, Peroxisome biogenesis disorder, Retinitis pigmentosa, Zellweger spectrum disorder

373
Peroxisomal biogenesis factor 26
PBD7A, PBD7B, PEX26M1T, Pex26pM1T
Heimler syndrome, Optic atrophy, Peroxisome biogenesis disorder, Zellweger spectrum disorder

374
Peroxisomal biogenesis factor 3
PBD10A, PBD10B, TRG18
Peroxisome biogenesis disorder, Zellweger spectrum disorder

375
Peroxisomal biogenesis factor 39
C6orf226
Coronary artery disease, Ocular sarcoidosis

376
Peroxisomal biogenesis factor 5
PBD2A, PBD2B, PTS1-BP, PTS1R, PXR1, RCDP5
Chondrodysplasia, Desbuquois syndrome, Peroxisome biogenesis disorder, Rhizomelic chondrodysplasia punctata, Zellweger spectrum disorder

377
Peroxisomal biogenesis factor 5 like
PEX5R, PEX5RP, PXR2, PXR2B, TRIP8b
Bipolar disorder, Major depressive disorder, Lung cancer, Scoliosis, Throat disease, Diabetes mellitus, type 2

378
Peroxisomal biogenesis factor 6
HMLR2, PAF-2, PAF2, PBD4A, PDB4B, PXAAA1
Alzheimer disease, Cerebellar ataxia, Spinocerebellar ataxia blindness deafness syndrome, Central nervous system demyelinating disease, Deafness enamel hypoplasia nail defects, Deafness-enamel hypoplasia-nail defects syndrome, Desbuquois syndrome, Global developmental delay, Heimler syndrome, Intellectual developmental disorder, Leukodystrophy, Peripheral neuropathy, Peroxisome biogenesis disorder, Retinitis pigmentosa, Hearing loss
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379
Peroxisomal biogenesis factor 7
PBD9B, PTS2R, RCDP1, RD
Refsum disease, Chondrodysplasia, Connective tissue disease, Desbuquois syndrome, Intellectual developmental disorder, Peroxisome biogenesis disorder, Retinitis pigmentosa, Rhizomelic chondrodysplasia punctata

380
PF4
Platelet factor 4
CXCL4, PF-4, SCYB4
Ankylosing spondylitis, Autoimmune disease, Glaucoma, Hypersensitivity, Thrombocytopenia, Thrombosis