9681
|
|
|
PET100 cytochrome c oxidase chaperone |
C19orf79, MC4DN12 |
|
9682
|
|
|
PET117 cytochrome c oxidase chaperone |
CSRP2BP, MC4DN19 |
|
9683
|
|
|
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 |
9684
|
|
|
Peroxisomal biogenesis factor 10 |
NALD, PBD6A, PBD6B, RNF69 |
|
9685
|
|
|
Peroxisomal biogenesis factor 11 alpha |
PEX11-ALPHA, PEX11alpha, PMP28, hsPEX11p |
|
9686
|
|
|
Peroxisomal biogenesis factor 11 beta |
PEX11-BETA, PEX11beta, PEX14B |
|
9687
|
|
|
Peroxisomal biogenesis factor 11 gamma |
PEX11gamma |
|
9688
|
|
|
Peroxisomal biogenesis factor 12 |
PAF-3, PBD3A |
|
9689
|
|
|
Peroxisomal biogenesis factor 13 |
NALD, PBD11A, PBD11B, ZWS |
|
9690
|
|
|
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 |