1741
|
|
|
SMC5 divergent transcript |
MAMDC2-AS2, SMC5-AS1 |
Curated: N/A
Unreviewed: N/A
|
1742
|
|
|
Structural maintenance of chromosomes 6 |
SMC-6, SMC6L1, hSMC6 |
Curated: Benign prostatic hyperplasia, Hypothyroidism
Unreviewed: Anemia, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiovascular abnormalities, Hepatocellular carcinoma, Lung disease, Sarcoma
|
1743
|
|
|
Structural maintenance of chromosomes flexible hinge domain containing 1 |
BAMS, FSHD2 |
Curated: Arhinia-choanal atresia-microphthalmia syndrome, Atrial fibrillation, Bosma arhinia microphthalmia syndrome, Chediak-higashi syndrome, Conotruncal cardiac defect, Crohn disease, Cryptorchidism, Facial nerve disorder, Facioscapulohumeral muscular dystrophy, Inflammatory bowel disease, Male infertility single gene azoospermia, Muscular dystrophy, Myopathy, Diabetes mellitus type 2, Ulcerative colitis
Unreviewed: Arrhinia, Arrhinia with choanal atresia and microphthalmia syndrome, Bone disease, Bundle branch block, Cataract, Choanal Atresia, Combined pituitary hormone deficiency, Congenital Coloboma Of Iris, Congenital Hypoplasia Of Penis, Congenital ocular coloboma, Craniofacial abnormalities, Development Disorder, Developmental disability, Dysmorphic Features, Facioscapulohumeral Dystrophy, Facioscapulohumeral Muscular Dystrophy, Gynecomastia, Hearing Loss, Hematopoietic Neoplasms, Hemochromatosis, High palate, Hypogonadism, Hypoplasia of the olfactory bulb, Hyposmia-Nasal And Ocular Hypoplasia-Hypogonadotropic Hypogonadism Syndrome, Immunologic Deficiency Syndromes, Kallmann syndrome, Leukemia, Lymphoma, Microphthalmos, Neoplasms, Neuroblastoma, Neuromuscular disease, Penis Agenesis, Physiologic Amenorrhea, Porokeratosis, Skin Erosion, Submucosal cleft palate, Syndromic microphthalmia, Turner syndrome, Urinary bladder neoplasms
|
1744
|
|
|
Single-pass membrane protein with coiled-coil domains 1 |
C3orf43 |
Curated: Colorectal cancer
Unreviewed: Colorectal neoplasm
|
1745
|
|
|
Single-pass membrane protein with coiled-coil domains 2 |
C12orf70 |
Curated: Hyperopia, Lung cancer, Obstructive sleep apnea syndrome
Unreviewed: Sleep Apnea
|
1746
|
|
|
Single-pass membrane protein with coiled-coil domains 3 |
C12orf69 |
Curated: N/A
Unreviewed: N/A
|
1747
|
|
|
Single-pass membrane protein with coiled-coil domains 4 |
C11orf75, FN5 |
Curated: Metabolic syndrome, Diabetes mellitus type 2
Unreviewed: N/A
|
1748
|
|
|
Single-pass membrane protein with coiled-coil domains 4 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1749
|
|
|
Sperm mitochondria associated cysteine rich protein |
HSMCSGEN1, MCS, MCSP |
Curated: Eczema, Scoliosis
Unreviewed: Anemia, Anxiety Disorder, Aortic Valve Insufficiency, Arteriosclerosis, Arthritis, Atherosclerosis, Cardiomyopathy, Chronic Obstructive Pulmonary Disease, Congestive Heart Failure, Dementia, Diabetes, Diabetes Mellitus, Fatty Liver, Freeman-Sheldon Syndrome, Giant Cell Arteritis, Heart Failure, Idiopathic pulmonary fibrosis, Kidney Disease, Kidney Failure, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Manic Disorder, Melanoma, Mental Depression, Migraine, Mixed Anxiety And Depressive Disorder, Non-alcoholic Fatty Liver Disease, Osteosarcoma, Prolactinoma, Psoriasis, Restless Legs Syndrome, Senile Dementia, Sleep Disorders, Stress Disorder, Stroke, Subarachnoid hemorrhage, Submucosal cleft palate, Ullrich Congenital Muscular Dystrophy
|
1750
|
|
|
Smith-Magenis syndrome chromosome region, candidate 2 |
TCONS_00025215 |
Curated: N/A
Unreviewed: N/A
|