Genes | GeDiPNet - Gene Disease Pathway & Associations

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9731 to 9740 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
9731	5195	PEX14	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
9732	9409	PEX16	Peroxisomal biogenesis factor 16	PBD8A, PBD8B	Autosomal recessive ataxia, Insomnia, Methylmalonic acidemia, Peroxisome biogenesis disorder, Synovitis, acne, pustulosis, hyperostosis, and osteitis, Zellweger spectrum disorder
9733	5824	PEX19	Peroxisomal biogenesis factor 19	D1S2223E, HK33, PBD12A, PMP1, PMPI, PXF, PXMP1	Peroxisome biogenesis disorder, Zellweger spectrum disorder
9734	5828	PEX2	Peroxisomal biogenesis factor 2	PAF1, PBD5A, PBD5B, PMP3, PMP35, PXMP3, RNF72, ZWS3	Autosomal recessive ataxia, Hypogonadism, Peroxisome biogenesis disorder, Retinitis pigmentosa, Zellweger spectrum disorder
9735	55670	PEX26	Peroxisomal biogenesis factor 26	PBD7A, PBD7B, PEX26M1T, Pex26pM1T	Heimler syndrome, Optic atrophy, Peroxisome biogenesis disorder, Zellweger spectrum disorder
9736	8504	PEX3	Peroxisomal biogenesis factor 3	PBD10A, PBD10B, TRG18	Peroxisome biogenesis disorder, Zellweger spectrum disorder
9737	441150	PEX39	Peroxisomal biogenesis factor 39	C6orf226	Coronary artery disease, Ocular sarcoidosis
9738	5830	PEX5	Peroxisomal biogenesis factor 5	PBD2A, PBD2B, PTS1-BP, PTS1R, PXR1, RCDP5	Chondrodysplasia, Desbuquois syndrome, Peroxisome biogenesis disorder, Rhizomelic chondrodysplasia punctata, Zellweger spectrum disorder
9739	51555	PEX5L	Peroxisomal biogenesis factor 5 like	PEX5R, PEX5RP, PXR2, PXR2B, TRIP8b	Bipolar disorder, Major depressive disorder, Lung cancer, Scoliosis, Throat disease, Diabetes mellitus type 2
9740	5190	PEX6	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 View all (2 more)

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