Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9691 to 9700 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9691
Peroxisomal biogenesis factor 16
PBD8A, PBD8B
Autosomal recessive ataxia, Insomnia, Methylmalonic acidemia, Peroxisome biogenesis disorder, Synovitis, acne, pustulosis, hyperostosis, and osteitis, Zellweger spectrum disorder

9692
Peroxisomal biogenesis factor 19
D1S2223E, HK33, PBD12A, PMP1, PMPI, PXF, PXMP1
Peroxisome biogenesis disorder, Zellweger spectrum disorder

9693
Peroxisomal biogenesis factor 2
PAF1, PBD5A, PBD5B, PMP3, PMP35, PXMP3, RNF72, ZWS3
Autosomal recessive ataxia, Hypogonadism, Peroxisome biogenesis disorder, Retinitis pigmentosa, Zellweger spectrum disorder

9694
Peroxisomal biogenesis factor 26
PBD7A, PBD7B, PEX26M1T, Pex26pM1T
Heimler syndrome, Optic atrophy, Peroxisome biogenesis disorder, Zellweger spectrum disorder

9695
Peroxisomal biogenesis factor 3
PBD10A, PBD10B, TRG18
Peroxisome biogenesis disorder, Zellweger spectrum disorder

9696
Peroxisomal biogenesis factor 39
C6orf226
Coronary artery disease, Ocular sarcoidosis

9697
Peroxisomal biogenesis factor 5
PBD2A, PBD2B, PTS1-BP, PTS1R, PXR1, RCDP5
Chondrodysplasia, Desbuquois syndrome, Peroxisome biogenesis disorder, Rhizomelic chondrodysplasia punctata, Zellweger spectrum disorder

9698
Peroxisomal biogenesis factor 5 like
PEX5R, PEX5RP, PXR2, PXR2B, TRIP8b
Bipolar disorder, Major depressive disorder, Lung cancer, Scoliosis, Throat disease, Diabetes mellitus type 2

9699
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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9700
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