Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
9721 to 9730 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9721
Pescadillo ribosomal biogenesis factor 1
NOP7, PES
Cholangiocarcinoma, Dementia, Schizophrenia

9722
PET100 cytochrome c oxidase chaperone
C19orf79, MC4DN12
Congenital lactic acidosis, Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency

9723
PET117 cytochrome c oxidase chaperone
CSRP2BP, MC4DN19
Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency

9724
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

9725
Peroxisomal biogenesis factor 10
NALD, PBD6A, PBD6B, RNF69
Autosomal recessive ataxia, Glomerulonephritis, Pericarditis, Peroxisome biogenesis disorder, Spastic ataxia, Zellweger spectrum disorder

9726
Peroxisomal biogenesis factor 11 alpha
PEX11-ALPHA, PEX11alpha, PMP28, hsPEX11p
Dyslipidemias, Obesity, Peroxisome biogenesis disorder

9727
Peroxisomal biogenesis factor 11 beta
PEX11-BETA, PEX11beta, PEX14B
Congenital cataract, Peroxisome biogenesis disorder, Zellweger spectrum disorder

9728
Peroxisomal biogenesis factor 11 gamma
PEX11gamma
Peroxisome biogenesis disorder

9729
Peroxisomal biogenesis factor 12
PAF-3, PBD3A
Peroxisome biogenesis disorder, Zellweger spectrum disorder

9730
Peroxisomal biogenesis factor 13
NALD, PBD11A, PBD11B, ZWS
Erectile dysfunction, Peroxisome biogenesis disorder, Zellweger spectrum disorder