821
|
|
|
Phosphoglycerate mutase family member 4 |
PGAM-B, PGAM1, PGAM3, dJ1000K24.1 |
Curated: N/A
Unreviewed: Adenocarcinoma, Alzheimer disease, Anaplastic Carcinoma, Anemia, Arthritis, Astrocytoma, Bipolar Disorder, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cholangiocarcinoma, Colorectal Cancer, Colorectal neoplasm, Gastric Cancer, Glaucoma, Glioblastoma, Glioma, Hepatocellular carcinoma, Hypothyroidism, Hypoxia, Leiomyoma, Leukemia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lymphatic Metastasis, Male infertility, Malignant Neoplasm, Malignant neoplasm of mouth, Mouth Neoplasms, Neoplasms, Neuroblastoma, Non-obstructive azoospermia, Oligospermia, Open angle glaucoma, Osteosarcoma, Ovarian neoplasm, Pancreatic adenocarcinoma, Pancreatic ductal carcinoma, Prostate cancer, Renal cell carcinoma, Sepsis, Squamous cell carcinoma, Stomach Neoplasms, Syndromic microphthalmia, Systemic lupus erythematosus, Triple negative breast cancer, Urinary bladder cancer, Uterine Fibroids
|
822
|
|
|
Phosphoglycerate mutase family member 4 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
823
|
|
|
Phosphoglycerate mutase family member 4 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
824
|
|
|
PGAM family member 5, mitochondrial serine/threonine protein phosphatase |
BXLBV68 |
Curated: N/A
Unreviewed: Autoimmune Diseases, Autoimmune hepatitis, Bronchiolitis, Chronic Obstructive Pulmonary Disease, Colorectal Cancer, Hepatocellular carcinoma, Ischemic stroke, Liver carcinoma, Lung carcinoma, Male infertility, Malignant Neoplasm, Mesothelioma, Mitochondrial disease, Neoplasms, Obesity, Optic Atrophy, Osteoglophonic dwarfism, Prolactinoma, Pulmonary Fibrosis, Renal Insufficiency, Uterine neoplasm
|
825
|
|
|
PGAM family member 5, mitochondrial serine/threonine protein phosphatase pseudogene 1 |
- |
Curated: N/A
Unreviewed: Alzheimer disease
|
826
|
|
|
Post-GPI attachment to proteins inositol deacylase 1 |
Bst1, ISPD3024, MRT42, NEDDSBA, SPG67 |
Curated: Nonsyndromic intellectual disability, Spastic paraplegia, Intellectual developmental disorder, Neurodevelopmental disorder, Myopia, Hereditary spastic paraplegia, Thyroid cancer
Unreviewed: Absence Of Septum Pellucidum, Agenesis Of Corpus Callosum, Amyotrophy, Asthma, Attention deficit hyperactivity disorder, Autism, Autism spectrum disorder, Brain atrophy, Brain disease, Central Visual Impairment, Cerebral Atrophy, Cerebral cortical atrophy, Cognition disorder, Congenital disorder of glycosylation, Cortical Dysplasia, Developmental Delay, Dwarfism, Dyskinetic Syndrome, Dyssomnia, Epileptic encephalopathy, Epithelial ovarian carcinoma, Facial dysmorphism, Factor XII Deficiency, Gout, Heart disease, Hemoglobinuria paroxysmal, Hypertension, Hypoplasia Of Corpus Callosum, Hypotonia, Ischemic stroke, Leukemia, Lung Cancer, Lung carcinoma, Lung Diseases, Lymphoblastic Leukemia, Lymphocytic Leukemia, Macrostomia, Macrotia, Malignant Mesothelioma, Malignant Neoplasm, Mental Depression, Mental retardation, Mesothelioma, Microcephaly, Monocytic Leukemia, Motor delay, Myeloid leukemia, Nasopharyngeal carcinoma, Neoplasms, Non-Syndromic Intellectual Disability, Osteoarthritis, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Parkinson disease, Paroxysmal nocturnal hemoglobinuria, Pleural effusion, Polymicrogyria, Prostate cancer, Prostatic neoplasm, Retinal Dystrophy, Rheumatoid arthritis, Salaam Seizures, Seizure, Sleep Disorders, Spastic Paraplegia, Stereotyped Behavior, Stroke, Visual disorder
|
827
|
|
|
Post-GPI attachment to proteins 2 |
CWH43-N, FRAG1, HPMRS3, MRT17, MRT21 |
Curated: Congenital omphalocele, Hyperphosphatasia with intellectual disability syndrome, Micrognathism
Unreviewed: Accessory Nipple, Anencephaly, Autism, Beckwith-Wiedemann Syndrome, Brachycephaly, Brain atrophy, Clinodactyly, Congenital Epicanthus, Congenital Pectus Excavatum, Developmental Delay, Developmental disability, Esotropia, High palate, Hirschsprung Disease, Hydronephrosis, Hyperopia, Hyperphosphatasia With Mental Retardation, Hyperphosphatemia, Hypotonia, Intellectual developmental disorder, Learning disorders, Malignant Neoplasm, Malocclusion, Mental retardation, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Osteosarcoma, Plagiocephaly, Scoliosis, Seizure
|
828
|
|
|
Post-GPI attachment to proteins phospholipase 3 |
AGLA546, CAB2, PERLD1, PP1498, hCOS16 |
Curated: Asthma, Bipolar disorder, Cardiovascular disease, Congestive heart failure, Crohn disease, Hyperphosphatasia with intellectual disability syndrome, Inflammatory bowel disease, Diabetes mellitus type 1, Diabetes mellitus type 2, hyperphosphatasia with intellectual disability syndrome 4
Unreviewed: Accessory Nipple, Autism, Bipolar Disorder, Brachycephaly, Breast Cancer, Breast Carcinoma, Carcinogenesis, Clinodactyly, Congenital abnormalities, Congenital diaphragmatic hernia, Congenital disorder of glycosylation, Congenital Epicanthus, Congenital Pectus Excavatum, Corpus callosum agenesis with facial anomalies and robin sequence, Crohn Disease, Developmental Delay, Developmental disability, Drachtman Weinblatt Sitarz syndrome, Dysmorphic Features, Esotropia, High palate, Hirschsprung Disease, Hydronephrosis, Hyperopia, Hyperphosphatasia With Mental Retardation, Inflammatory Bowel Disease, Intellectual developmental disorder, Malocclusion, Mental retardation, Micrognathism, Movement Disorders, Multiple sclerosis, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Pancreatic neoplasm, Plagiocephaly, Scoliosis, Seizure, Stomach Carcinoma, Stomach Neoplasms, Toriello-Carey syndrome, Uranostaphyloschisis
|
829
|
|
|
Post-GPI attachment to proteins GalNAc transferase 4 |
C9orf125, TMEM246 |
Curated: Thyroiditis
Unreviewed: N/A
|
830
|
|
|
Post-GPI attachment to proteins 6 |
GPI-PLA2, M83, TMEM6, TMEM8, TMEM8A |
Curated: Anemia
Unreviewed: Non-Alcoholic Fatty Liver Disease
|