1201
|
|
|
NSA2 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1202
|
|
|
NSA2 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
1203
|
|
|
NSA2 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
1204
|
|
|
NSA2 pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
1205
|
|
|
NSA2 pseudogene 5 |
- |
Curated: N/A
Unreviewed: N/A
|
1206
|
|
|
NSA2 pseudogene 6 |
- |
Curated: N/A
Unreviewed: N/A
|
1207
|
|
|
NSA2 pseudogene 7 |
- |
Curated: N/A
Unreviewed: N/A
|
1208
|
|
|
Nuclear receptor binding SET domain protein 1 |
ARA267, KMT3B, SOTOS, SOTOS1, STO |
Curated: Asthma, Autism, Beckwith-wiedemann syndrome, Adenoid cystic carcinoma, Cholecystolithiasis, Deletion 5q35 syndrome, Desbuquois syndrome, Global developmental delay, Gout, Gross motor development delay, Holoprosencephaly, Non-immune hydrops fetalis, Intellectual developmental disorder, Microcephaly, Migraine, Neurodevelopmental disorder, Osteoarthritis, Osteopenia, Prostate cancer, Scoliosis, Sotos syndrome, Spastic paraplegia, Tetralogy of fallot, Diabetes mellitus type 2, Weaver syndrome
Unreviewed: 5q35 microduplication syndrome, Accessory Kidney, Acute Myeloid Leukemia, Adenocarcinoma, alpha Thalassemia, Arnold-Chiari malformation, Atrial Septal Defect, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, B-cell Lymphoma, Basal cell carcinoma, Beckwith-Wiedemann Syndrome, Bohring syndrome, Breast Cancer, Breast Carcinoma, Breast neoplasm, Brugada syndrome, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Cardiovascular abnormalities, Chronobiology disorder, Congenital Clubfoot, Congenital heart defect, Congenital hyperinsulinism, Congenital Hypoplasia Of Penis, Congenital Pectus Carinatum, Craniosynostosis, Cryptorchidism, Deletion 5q36, Developmental Delay, Developmental disability, Developmental dysplasia of the hip, Diabetes Mellitus, Diffuse Lymphoma, Dolichocephaly, Dwarfism, Dysmorphic Features, Endometrial neoplasm, Epilepsy, Facial dysmorphism syndrome, Frontal bossing, Ganglioglioma, Glioma, Glycogen storage disease, Growth disorder, Head and neck neoplasm, Hearing Loss, Heart disease, Heart Septal Defects, High palate, Hyperinsulinemic hypoglycemia, Hyperopia, Hypodontia, Hypoglycemia, Hypoplasia Of Corpus Callosum, Hypospadias, Hypotonia, Impaired Cognition, Laryngeal neoplasm, Learning disorders, Leukemia, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung Diseases, Lymphoma, Macrocephaly, Macrotia, Malignant Neoplasm, Malocclusion, Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome, Mental Depression, Mental retardation, Micrognathism, Microvascular Angina, Monocytic Leukemia, Monosomy 5q35, Multiple Congenital Anomalies, Multiple renal cysts, Myeloblastic Leukemia, Myelodysplastic syndrome, Myeloid Leukemia, Myelomonocytic Leukemia, Myopia, Neoplasms, Nephroblastoma, Nervous System Neoplasms, Neuroblastoma, Nevo Syndrome, Non-Alcoholic Fatty Liver Disease, Nystagmus, Obesity, Osteoporosis, Otitis media, Ovarian neoplasm, Pancreatic adenocarcinoma, Pancreatic ductal carcinoma, Partial Agenesis Of Corpus Callosum, Patent ductus arteriosus, Patent foramen ovale, Precocious puberty, Prostatic neoplasm, Renal cell carcinoma, Russell-Silver Syndrome, Sacrococcygeal teratoma, Sotos` Syndrome, Specific Learning Disorder, Spondyloocular Syndrome, Squamous cell carcinoma, Stomach neoplasms, Strabismus, Stroke, Syndactyly of fingers, Syndromic Mental Retardation, X-linked, Talipes Transversoplanus, Talipes valgus, Tatton Brown Rahman Syndrome, Trichohepatoenteric Syndrome, Triple negative breast cancer, Uranostaphyloschisis, Uterine neoplasm, Ventricular septal defect, Vesicoureteral Reflux, Weaver Syndrome, Williams Syndrome
|
1209
|
|
|
Nuclear receptor binding SET domain protein 2 |
KMT3F, KMT3G, MMSET, RAUST, REIIBP, TRX5, WHS, WHSC1 |
Curated: Anemia, Breast neoplasms, Congenital clubfoot, Congenital retrognathism, Desbuquois syndrome, Global developmental delay, Hypertrophic cardiomyopathy, Hypoglycemia, Neurodevelopmental disorder, Thrombocytopenia, Ventricular septal defect, Wolf-hirschhorn syndrome, syndromic intellectual disability
Unreviewed: Absence Of Septum Pellucidum, Adenocarcinoma, Agenesis Of Corpus Callosum, Aplasia Cutis Congenita, Arachnodactyly, Atrial Septal Defect, Axenfeld anomaly, Basal cell carcinoma, Bone disease, Bone neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Cardiovascular Diseases, Cervical Cancer, Cervical Intraepithelial Neoplasia, Cervical Tumor, Cervix carcinoma, Chondroblastoma, Colonic neoplasm, Colorectal Cancer, Colorectal neoplasm, Congenital anomaly of eye, Congenital Chromosomal Disease, Congenital Clubfoot, Congenital Coloboma Of Iris, Congenital diaphragmatic hernia, Congenital Epicanthus, Congenital Gallbladder Anomaly, Congenital heart defect, Congenital Keratoglobus, Congestive Heart Failure, Constipation, Crohn disease, Cryptorchidism, Developmental Delay, Developmental disability, Diabetes, Diabetes Mellitus, Dolichocephaly, Dry Eye Syndromes, Dwarfism, Dysmorphic Features, Emery dreifuss muscular dystrophy, Endometrial Cancer, Endometrial carcinoma, Endometriosis, Fatty Liver, Fatty liver, alcoholic, Frontal bossing, Gastroesophageal Reflux Disease, Glioblastoma, Growth disorder, Heart Failure, Hemangioma, Hepatocellular carcinoma, Hypertension, Hypodontia, Hypoplasia Of Thumb, Hypospadias, Hypoxia, Immunologic Deficiency Syndromes, Infertility, Intellectual developmental disorder, Intrahepatic Cholangiocarcinoma, Kidney Cancer, Kidney neoplasm, Language development disorders, Laryngeal neoplasm, Learning disorders, Leukemia, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Lymphatic metastasis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Mammary Neoplasms, Mantle Cell Lymphoma, Marfan Syndrome, Mental Depression, Mental retardation, Metastatic Prostate Carcinoma, Microcephaly, Micrognathism, Microtia, Miscarriage, Monoclonal Gammapathies, Movement Disorders, Multicystic renal dysplasia, Multiple myeloma, Myeloid leukemia, Neoplasms, Nystagmus, Optic Atrophy, Orofacial cleft, Osteoporosis, Osteosarcoma, Otitis media, Otofaciocervical syndrome, Ovarian cancer, Ovarian Carcinoma, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pachyonychia Congenita, Pitt-Rogers-Danks Syndrome, Polydactyly, Precocious puberty, Primary Tethered cord syndrome, Proptosis, Prostate cancer, Prostatic hyperplasia, Prostatic intraepithelial neoplasia, Prostatic neoplasm, Ptosis, Pulmonary arterial hypertension, Radioulnar Synostosis, Renal Carcinoma, Renal cell carcinoma, Retinal Diseases, Rib fusion, Rieger syndrome, Sclerocornea, Scoliosis, Situs Inversus, Skin carcinoma, Speech Delay, Squamous cell carcinoma, Stenosis Of External Auditory Canal, Stereotyped Behavior, Stomach Carcinoma, Stomach Neoplasms, Strabismus, Testicular germ cell tumor, Trichohepatoenteric Syndrome, Triple Negative Breast Neoplasms, Ventricular hypertrophy, Wilms tumor, Wolf-Hirschhorn Syndrome, Wolfram Syndrome
|
1210
|
|
|
Nuclear receptor binding SET domain protein 3 |
KMT3F, KMT3G, WHISTLE, WHSC1L1, pp14328 |
Curated: Attention deficit hyperactivity disorder, Obesity, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome
Unreviewed: Adenocarcinoma, Bladder carcinoma, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Carcinoma Of The Head And Neck, Colorectal Cancer, Head and neck cancer, Head And Neck Carcinoma, Head and neck neoplasm, Hematologic Neoplasms, Invasive Duct and Lobular Carcinoma, Leukemia, Liver Cancer, Lung Cancer, Lung carcinoma, Lung Neoplasms, Malignant Neoplasm, Mammary Neoplasms, Multiple myeloma, Myelodysplastic Syndrome, Myeloid leukemia, Neoplasms, Nephrosis, Nephrotic Syndrome, Osteosarcoma, Pancreatic adenocarcinoma, Pancreatic ductal carcinoma, Pancreatic neoplasm, Prostatic neoplasm, Squamous cell carcinoma, Thyroid cancer, Urinary bladder neoplasms
|