1221
|
|
|
NSMCE1 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
1222
|
|
|
NSE2 SUMO ligase component of SMC5/6 complex |
C8orf36, MMS21, NSE2, ZMIZ7 |
Curated: Alzheimer disease, Behcet disease, Central nervous system cancer, Obstructive pulmonary disease, Desbuquois syndrome, Glioblastoma, Glioma, Global developmental delay, Metabolic syndrome, Oligodendroglioma, Psoriasis, Seckel syndrome, Diabetes mellitus type 2, seckel syndrome 10
Unreviewed: Acanthosis Nigricans, Aortic Aneurysm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cap myopathy, Colorectal neoplasm, Congenital blindness, Congestive Heart Failure, Diabetes Mellitus, Dwarfism, Fatty Liver, Hypertension, Insulin-resistant diabetes mellitus, Leukemia, Malignant Neoplasm, Microcephalic Primordial Dwarfism-Insulin Resistance Syndrome, Microcephaly, Micrognathism, Myeloid leukemia, Oral Ulcer, Pancreatitis, Pituitary dwarfism, Prostatic neoplasm, Retinal Detachment, Schizophrenia, Seckel Syndrome, Short-Limb Dwarfism, Thyroid cancer, Urinary bladder neoplasms, Ventricular hypertrophy
|
1223
|
|
|
NSE3 component of SMC5/6 complex |
HCA4, LICS, MAGEG1, MAGEL3, NDNL2, NSE3 |
Curated: Lung disease, lung disease, immunodeficiency, and chromosome breakage syndrome;
Unreviewed: Autism, Bronchiolitis Obliterans, Eczema, Glaucoma, Lung Disease, Immunodeficiency, And Chromosome Breakage Syndrome, Neoplasms, Prader-Willi Syndrome, Respiratory Distress Syndrome, Retinitis Pigmentosa
|
1224
|
|
|
NSE4A component of SMC5/6 complex |
C10orf86, NS4EA, NSE4A |
Curated: N/A
Unreviewed: N/A
|
1225
|
|
|
NMDA receptor synaptonuclear signaling and neuronal migration factor |
HH9, NELF |
Curated: Carcinoma, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Male infertility single gene azoospermia, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Pituitary stalk interruption syndrome, Sheehan syndrome
Unreviewed: Anaplastic Carcinoma, Anxiety Disorder, Breast hypoplasia, Breast neoplasm, Clinodactyly, Congenital Camptodactyly, Congenital Sensorineural Hearing Loss, Cryptorchidism, Dysarthria, Erectile Dysfunction, Female Hypogonadism Syndrome, Gynecomastia, Hearing Loss, Hypogonadism, Hypogonadotropic Hypogonadism, Hypogonadotropic Hypogonadism With Or Without Anosmia, Hypoplasia of the ovary, Ichthyosis, Kallmann Syndrome, Mental Depression, Mirror Movements, Non-obstructive azoospermia, Normosmic Congenital Hypogonadotropic Hypogonadism, Nystagmus, Obesity, Osteochondrodysplasia, Osteopenia, Osteoporosis, Paraplegia, Penis Agenesis, Physiologic Amenorrhea, Ptosis, Renal agenesis, Secondary Physiologic Amenorrhea, Skeletal Dysplasia, Testicular Hypogonadism
|
1226
|
|
|
Nuclear speckle splicing regulatory protein 1 |
CCDC55, HSPC095, NEDSSBA, NSrp70 |
Curated: Obstructive pulmonary disease, Neurodevelopmental disorder, neurodevelopmental disorder with spasticity, seizures, and brain abnormalities
Unreviewed: Breast neoplasm, Cerebral palsy, Developmental disability, Epilepsy, Leukemia, Microcephaly
|
1227
|
|
|
Nuclear speckle splicing regulatory protein 1 pseudogene 1 |
CCDC55P1 |
Curated: N/A
Unreviewed: N/A
|
1228
|
|
|
NOP2/Sun RNA methyltransferase 2 |
MISU, MRT5, SAKI, TRM4 |
Curated: Autism, Nonsyndromic intellectual disability, Dubowitz syndrome, Intellectual developmental disorder, Hypertension, syndromic intellectual disability
Unreviewed: Absence Of Septum Pellucidum, Alzheimer disease, Anemia, Aortic aneurysm, Asthma, Ataxia telangiectasia, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Blepharophimosis, Brachydactyly, Breast Cancer, Breast Carcinoma, Breast neoplasm, Camptodactyly of fingers, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Cataract, Central Visual Impairment, Cerebral Atrophy, Colorectal Cancer, Congenital Epicanthus, Congenital Pectus Excavatum, Corneal disease, Cortical Dysplasia, Craniosynostosis, Cryptorchidism, Cutis marmorata, Developmental Delay, Developmental disability, Dubowitz Syndrome, Dwarfism, Dysarthria, Dyskinetic Syndrome, Dyssomnia, Eczema, Endometrial neoplasm, Esophagus Neoplasm, Facial dysmorphism, Facial dysmorphism syndrome, Gallbladder cancer, Glycogen Storage Disease, Growth disorder, Hereditary Hemochromatosis, High palate, Hydrocephalus, Hydronephrosis, Hyperhomocysteinemia, Hypoparathyroidism, Hypophosphatemic Vitamin D Refractory Rickets, X-Linked, Hypoplasia Of Corpus Callosum, Hypospadias, Leukemia, Lymphoblastic Leukemia, Lymphoma, Macrostomia, Malabsorption Syndrome, Malignant Neoplasm, Mental Depression, Mental retardation, Microcephaly, Micrognathism, Motor delay, Myopia, Neoplasms, Neurodevelopmental Disorders, Non-Syndromic Intellectual Disability, Nystagmus, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pfaundler-Hurler Syndrome, Polymicrogyria, Prostatic neoplasm, Ptosis, Rectal Prolapse, Retinoblastoma, Salaam Seizures, Scoliosis, Seizure, Sleep Disorders, Spina bifida occulta, Squamous cell carcinoma, Stereotyped Behavior, Stomach neoplasms, Strabismus, Submucosal cleft palate, Syndactyly Of The Toes, Synophrys, Thyroid cancer, Uterine neoplasm, Uveal melanoma
|
1229
|
|
|
NOP2/Sun RNA methyltransferase 3 |
COXPD48, MST077, MSTP077 |
Curated: Anorexia nervosa, Asthma, Attention deficit hyperactivity disorder, Combined oxidative phosphorylation deficiency, Gastric cancer, Gout, Hyperuricemia, Kidney cancer, Major depressive disorder, Metabolic syndrome, Substance abuse, Diabetes mellitus type 2
Unreviewed: Hepatocellular carcinoma, Lung adenocarcinoma, Mitochondrial disease, Mitochondrial encephalomyopathy, Optic atrophy, Seizures
|
1230
|
|
|
NOP2/Sun RNA methyltransferase 4 |
SHTAP |
Curated: Alzheimer disease, Bipolar disorder, Major depressive disorder, Prostate cancer, Schizophrenia
Unreviewed: Breast neoplasm, Hepatocellular carcinoma, Leber hereditary optic neuropathy, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Prostatic neoplasm, Thyroid cancer
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