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"
361 to 370 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
Peroxisomal biogenesis factor 1
HMLR1, PBD1A, PBD1B, ZWS, ZWS1
Deafness enamel hypoplasia nail defects, Deafness-enamel hypoplasia-nail defects syndrome, Global developmental delay, Heimler syndrome, Optic atrophy, Penile hypospadia, Peroxisomal disorder, Peroxisome biogenesis disorder, Polymicrogyria, Respiratory system disease, Retinitis pigmentosa, Zellweger spectrum disorder

362
Peroxisomal biogenesis factor 10
NALD, PBD6A, PBD6B, RNF69
Autosomal recessive ataxia, Glomerulonephritis, Pericarditis, Peroxisome biogenesis disorder, Spastic ataxia, Zellweger spectrum disorder

363
Peroxisomal biogenesis factor 11 alpha
PEX11-ALPHA, PEX11alpha, PMP28, hsPEX11p
Dyslipidemias, Obesity, Peroxisome biogenesis disorder

364
Peroxisomal biogenesis factor 11 beta
PEX11-BETA, PEX11beta, PEX14B
Congenital cataract, Peroxisome biogenesis disorder, Zellweger spectrum disorder

365
Peroxisomal biogenesis factor 11 gamma
PEX11gamma
Peroxisome biogenesis disorder

366
Peroxisomal biogenesis factor 12
PAF-3, PBD3A
Peroxisome biogenesis disorder, Zellweger spectrum disorder

367
Peroxisomal biogenesis factor 13
NALD, PBD11A, PBD11B, ZWS
Erectile dysfunction, Peroxisome biogenesis disorder, Zellweger spectrum disorder

368
Peroxisomal biogenesis factor 14
NAPP2, PBD13A, Pex14p, dJ734G22.2
Alzheimer disease, Androgenetic alopecia, Asthma, Breast cancer, Diverticular disease, Estrogen-receptor negative breast cancer, Ovarian cysts, Peroxisome biogenesis disorder, Prostate cancer, Respiratory system disease, Zellweger spectrum disorder

369
Peroxisomal biogenesis factor 16
PBD8A, PBD8B
Autosomal recessive ataxia, Insomnia, Methylmalonic acidemia, Peroxisome biogenesis disorder, Synovitis, acne, pustulosis, hyperostosis, and osteitis, Zellweger spectrum disorder

370
Peroxisomal biogenesis factor 19
D1S2223E, HK33, PBD12A, PMP1, PMPI, PXF, PXMP1
Peroxisome biogenesis disorder, Zellweger spectrum disorder