661
|
|
|
ALF transcription elongation factor 2 |
FMR2, FMR2P, FRAXE, MRX2, OX19, XLID109 |
Curated: Colonic neoplasms, Colorectal cancer, Congenital microcephaly, Aplastic anemia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Kidney disease, Myopia, Neurotic disorder, X-linked intellectual disability, Premature ovarian failure, Scoliosis, non-syndromic X-linked intellectual disability
Unreviewed: Amyotrophic Lateral Sclerosis, Autism, Autism spectrum disorder, Bulbospinal Atrophy, X-Linked, Camptodactyly of fingers, Central nervous system neoplasm, CHARGE Syndrome, Coffin-Lowry Syndrome, Cognitive disorder, Colorectal neoplasm, Congenital Chromosomal Disease, Congenital Epicanthus, Dentatorubral Pallidoluysian Atrophy, Development Disorder, Developmental Delay, Developmental disability, Dwarfism, Endometriosis, Epilepsy, Eye neoplasms, Fragile X Syndrome, Frontotemporal dementia, Glioblastoma, Hand Flapping, Head and neck neoplasm, Hemophilia b, Huntington Disease, Impaired Cognition, Jacobsen Syndrome, Learning Disorders, Leukemia, Lymphoblastic Leukemia, Lymphocytic Leukemia, Macrocephaly, Mental Depression, Mental retardation, Mental Retardation, X-Linked, Mucopolysaccharidosis, Multiple myeloma, Myotonic dystrophy, Nervous System Disorder, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Neurodevelopmental Disorders, Obsessive-Compulsive Disorder, Oligodendroglioma, Ovarian Failure, Parkinson disease, Premature Menopause, Rheumatoid arthritis, Sarcoma, Specific Learning Disorder, Speech Delay, Speech Disorders, Spinocerebellar Ataxia, Squamous cell carcinoma, Stereotypy, Thoracic neoplasm, Uterine neoplasm
|
662
|
|
|
AFF2 intronic transcript 1 |
- |
Curated: N/A
Unreviewed: N/A
|
663
|
|
|
ALF transcription elongation factor 3 |
KINS, LAF4, MLLT2-like |
Curated: Alzheimer disease, Androgenetic alopecia, Rheumatoid arthritis, Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Autoimmune disease, Celiac disease, Kidney disease, Obstructive pulmonary disease, Desbuquois syndrome, Diabetic neuropathy, Endometriosis, Gastroesophageal reflux disease, Iga nephropathy, Inflammatory bowel disease, Insomnia, Intellectual developmental disorder, Juvenile idiopathic arthritis, Metabolic syndrome, Post-traumatic stress disorder, Schizophrenia, Scoliosis, Squamous cell carcinoma, Substance abuse, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2, Uterine polyp
Unreviewed: Arthritis, Autoimmune Diseases, Breast Cancer, Breast Carcinoma, Congenital deformity of foot, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetic Retinopathy, Gastroesophageal Reflux Disease, Glioblastoma, Glioma, Immune System Diseases, Juvenile arthritis, Kidney Disease, Kidney Failure, Leukemia, Lupus Erythematosus, Lymphatic metastasis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Malignant Neoplasm, Mammary Neoplasms, Mental retardation, Multiple Sclerosis, Neoplasms, Neurodevelopmental Disorders, Pancreatitis, Psoriasis vulgaris, Psoriatic Arthritis, Stomach neoplasms, Triple negative breast cancer, Uterine neoplasm, Xeroderma pigmentosum
|
664
|
|
|
ALF transcription elongation factor 4 |
AF5Q31, CHOPS, MCEF |
Curated: Bone disease, Dilated cardiomyopathy, Chops syndrome, Cognition disorder, Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome, Congenital heart defects, Cornelia de lange syndrome, Delirium, dementia, and cognitive disorders, Growth disorder, Lung disease, Obesity
Unreviewed: Bladder carcinoma, Bladder Neoplasm, Bone Disease, Brachydactyly, Breast neoplasm, Carcinogenesis, Carcinoma Of The Head And Neck, CHOPS Syndrome, Cognitive disorder, Congenital heart defect, Cornelia De Lange Syndrome, Cryptorchidism, De lange syndrome, Developmental and epileptic encephalopathy, Developmental Delay, Dwarfism, Gastroesophageal Reflux Disease, Heart Septal Defects, Impaired Cognition, Laryngomalacia, Leukemia, Lung adenocarcinoma, Lung Diseases, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoid leukemia, Malignant Neoplasm, Mental retardation, Multiple Congenital Anomalies, Myeloid leukemia, Neuroblastoma, Osteochondrodysplasia, Ovarian neoplasm, Pancreatic ductal carcinoma, Pancreatitis, Patent ductus arteriosus, Proptosis, Skeletal Dysplasia, Squamous cell carcinoma, Tracheal Stenosis, Urinary bladder cancer, Vesicoureteral Reflux
|
665
|
|
|
AFF4 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
666
|
|
|
AFF4 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
667
|
|
|
AFG1 like ATPase |
AFG1, LACE1, c222389 |
Curated: Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Dyskinesia, Obesity
Unreviewed: Bipolar Disorder, Hepatitis b
|
668
|
|
|
AAA ATPase AFG2A |
AFG2, EHLMRS, NEDHSB, SPAF, SPATA5 |
Curated: Central nervous system cancer, Concussion, Glioblastoma, Glioma, Irritable bowel syndrome, Microcephaly, Neurodevelopmental disorder, Schizophrenia, syndromic complex neurodevelopmental disorder
Unreviewed: Alopecia, Alopecia Areata, Astigmatism, Brachycephaly, Brain disease, Cerebral Atrophy, Charcot-Marie-Tooth disease, Congenital Sensorineural Hearing Loss, Developmental and epileptic encephalopathy, Developmental Delay, Developmental disability, Developmental regression, Dyskinetic Syndrome, Epilepsy, Hearing Loss, And Mental Retardation Syndrome, Epileptic encephalopathy, Gastroparesis, Hearing Loss, High palate, Hydrocephalus, Idiopathic pulmonary fibrosis, Immunoglobulin A deficiency, Infantile Spasms, Infertility, Intellectual developmental disorder, Irritable Bowel Syndrome, Mental retardation, Microcephaly-Intellectual Disability-Sensorineural Hearing Loss-Epilepsy-Abnormal Muscle Tone Syndrome, Mitochondrial Diseases, Neurodegenerative Disorders, Prostate cancer, Seizures, Stereotypy, Syndactyly Of The Toes, Visual disorder
|
669
|
|
|
AAA ATPase AFG2B |
DFNB119, NEDHLS, SPATA5L1 |
Curated: Isolated sensorineural deafness, Kidney disease, Deafness, Global developmental delay, Hearing loss, Neurodevelopmental disorder, Nonsyndromic hearing loss, Sensorineural hearing loss-spastic quadriplegia–intellectual disability, hearing loss, autosomal recessive 119
Unreviewed: Developmental disability, Kidney Disease, Kidney Failure, Microcephaly
|
670
|
|
|
AFG3 like matrix AAA peptidase subunit 1, pseudogene |
AFG3, AFG3L1 |
Curated: N/A
Unreviewed: Melanoma, Nasopharyngeal Carcinoma
|