731
|
|
|
PERP pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
732
|
|
|
Pescadillo ribosomal biogenesis factor 1 |
NOP7, PES |
Curated: Cholangiocarcinoma, Dementia, Schizophrenia
Unreviewed: Aggressive Periodontitis, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Diabetes, Diabetes Mellitus, Diabetic Nephropathy, Epithelial ovarian carcinoma, Esophagus Neoplasm, Hepatocellular carcinoma, Hereditary breast and ovarian cancer syndrome, Hyperglycemia, Liver Cancer, Liver carcinoma, Lymphatic metastasis, Malignant Neoplasm, Mammary Neoplasms, Neoplasms, Neuroblastoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Papillary thyroid cancer, Papillary thyroid carcinoma, Periodontal Diseases, Sepsis, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms
|
733
|
|
|
PES1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
734
|
|
|
Pescadillo ribosomal biogenesis factor 1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
735
|
|
|
Pescadillo ribosomal biogenesis factor 1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
736
|
|
|
PET100 cytochrome c oxidase chaperone |
C19orf79, MC4DN12 |
Curated: Congenital lactic acidosis, Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, mitochondrial disease
Unreviewed: Anemia, Cerebellar Ataxia, Cytochrome-C Oxidase Deficiency, Developmental Delay, Dysarthria, Fanconi syndrome, Hearing Loss, High palate, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Lactic acidosis, Leigh Syndrome, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Leukoencephalopathy, Mental retardation, Mood swings, Motor delay, Necrotizing encephalomyelopathy, Nervous System Diseases, Nystagmus, Optic Atrophy, Phosphate Diabetes, Ptosis, Renal Tubular Disorder, Retinitis Pigmentosa, Strabismus, Ventricular septal defect
|
737
|
|
|
PET100 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
738
|
|
|
PET117 cytochrome c oxidase chaperone |
CSRP2BP, MC4DN19 |
Curated: Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, mitochondrial disease
Unreviewed: CORNEAL ENDOTHELIAL DYSTROPHY, Cytochrome-C Oxidase Deficiency, Diabetes mellitus, Isolated Cytochrome C Oxidase Deficiency, Leigh Syndrome, Mitochondrial disease, Mitochondrial Diseases, Mouth disease, Necrotizing encephalomyelopathy, Polymorphous corneal dystrophy, Uterine neoplasm
|
739
|
|
|
PET117 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
740
|
|
|
Peroxisomal biogenesis factor 1 |
HMLR1, PBD1A, PBD1B, ZWS, ZWS1 |
Curated: 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, peroxisome biogenesis disorder due to PEX1 defect
Unreviewed: N/A
|