691
|
|
|
Ninjurin 1 |
NIN1, NINJURIN, hNINJ1 |
Curated: Alzheimer disease, Allergic contact dermatitis, Gout, Obesity
Unreviewed: Alopecia, Aortic Valve Sclerosis, Bone Disease, Colorectal neoplasm, Dermatitis, Diabetes Mellitus, Diabetic neuropathy, Endometrioma, Endometriosis, Glioblastoma, Hereditary sensory and autonomic neuropathy, Interstitial cystitis, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Multiple Sclerosis, Native American Myopathy, Neoplasms, Prune belly syndrome, Pulmonary Fibrosis, Sensory Neuropathy, Hereditary, Stroke, Triple negative breast cancer
|
692
|
|
|
Ninjurin 2 |
- |
Curated: Color vision deficiency
Unreviewed: Alzheimer disease, Arteriosclerosis, Atherosclerosis, Borderline personality disorder, Colorectal Cancer, Coronary artery disease, Dementia, Diabetes mellitus, Glioma, Hypertension, Ischemic Stroke, Mouth disease, Multiple Sclerosis, Myocardial ischemia, Senile Dementia, Stroke
|
693
|
|
|
NINJ2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
694
|
|
|
Ninein like |
NLP |
Curated: Attention deficit hyperactivity disorder, Autism, Gout, Prostate cancer, Substance abuse
Unreviewed: Ankylosing Spondylitis, Brain atrophy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Carcinoma Of The Head And Neck, Cerebral Atrophy, Ciliopathies, Classical Hodgkin lymphoma, Hodgkin Disease, Hodgkin Lymphoma, Leber Congenital Amaurosis, Lung Cancer, Lung carcinoma, Lymphoma, Malignant Neoplasm, Neoplasms, Nystagmus, Pancreatitis, Usher Syndrome
|
695
|
|
|
Nucleolar pre-rRNA processing protein NIP7 |
CGI-37, HSPC031, KD93 |
Curated: N/A
Unreviewed: Breast Cancer, Liposarcoma
|
696
|
|
|
NIP7 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
697
|
|
|
NIP7 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
698
|
|
|
NIP7 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
699
|
|
|
NIPA magnesium transporter 1 |
FSP3, SLC57A1, SPG6 |
Curated: 15q11.2 microdeletion syndrome, Amyotrophic lateral sclerosis, Spastic paraplegia, Hereditary spastic paraplegia, Hypertension
Unreviewed: Amyotrophic Lateral Sclerosis, Angelman Syndrome, Anorexia, Anorexia nervosa, Atrophy, Autism, Cerebellar diseases, Cognition disorder, Congenital heart defect, Developmental disability, Diabetes mellitus, type 2, Epilepsy, Henoch-Schonlein Nephritis, Hydrocephalus, Impaired Cognition, Language development disorders, Leukemia, Microcephaly, Motor Neuron Disease, Nervous System Diseases, Neurodegenerative disorder, Neurodegenerative Disorders, Paraplegia, Peripheral Neuropathy, Prader-Willi Syndrome, Schizophrenia, Seizure, Spastic Paraplegia, Uveal melanoma
|
700
|
|
|
NIPA magnesium transporter 2 |
SLC57A2 |
Curated: 15q11.2 microdeletion syndrome
Unreviewed: N/A
|