2681
|
|
|
Biogenesis of lysosomal organelles complex 1 subunit 4 |
BCAS4L, BLOS4, CNO |
Curated: Alzheimer disease, Language development disorders
Unreviewed: Anxiety Disorder, Hermansky-Pudlak Syndrome, Melanoma
|
2682
|
|
|
Biogenesis of lysosomal organelles complex 1 subunit 5 |
BLOS5, HPS11, MU, MUTED |
Curated: Hermansky-pudlak syndrome, hermansky-pudlak syndrome 11
Unreviewed: Hermansky-Pudlak Syndrome, Schizophrenia
|
2683
|
|
|
BLOC1S5-TXNDC5 readthrough (NMD candidate) |
MUTED-TXNDC5 |
Curated: N/A
Unreviewed: N/A
|
2684
|
|
|
Biogenesis of lysosomal organelles complex 1 subunit 6 |
BLOS6, HPS9, PA, PALLID, PLDN |
Curated: Autoinflammatory syndrome, Hermansky-pudlak syndrome, hermansky-pudlak syndrome 9
Unreviewed: Albinism, Congenital nystagmus, Hermansky-Pudlak Syndrome, Hypopigmentation Disorder, Leukopenia, Ocular albinism, Platelet disorder, Platelet Storage Pool Deficiency, Schizophrenia
|
2685
|
|
|
BLOC1S6 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
2686
|
|
|
Bridge-like lipid transfer protein family member 1 |
ALKKUCS, FSA, KIAA1109, Tweek |
Curated: Alkuraya-kucinskas syndrome, Arthrogryposis multiplex congenita, Asthma, Eczema, Bipolar disorder, Celiac disease, Renal agenesis, Congenital clubfoot, Congenital hemivertebra, Crohn disease, Dandy-walker syndrome, Generalized anxiety disorder, Hydrocephalus, Inflammatory bowel disease, Inflammatory skin disease, Insomnia, Irritable bowel syndrome, Major depressive disorder, Micrognathism, Mood disorder, Pena-shokeir syndrome , Post-traumatic stress disorder, Psoriasis, Rheumatoid arthritis, Right aortic arch, Seasonal allergic rhinitis, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis
Unreviewed: Alkuraya-Kucinskas Syndrome, Ankylosing spondylitis, Autoimmune disease, Autoimmune Diseases, Behcet disease, Behcet Syndrome, Breast Cancer, Breast Carcinoma, Cardiovascular Diseases, Cataract, Cerebellar Hypoplasia, Clinodactyly, Congenital Camptodactyly, Congenital Clubfoot, Crohn Disease, Cystic hygroma, Dandy-Walker Syndrome, Dermatitis, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 1, Esophageal squamous cell carcinoma, Fragile X Syndrome, High palate, Hyperopia, Immune System Diseases, Inflammatory Bowel Disease, Lissencephaly, Macrocephaly, Mental Depression, Mental retardation, Mood Disorder, Multiple Sclerosis, Neck Webbing, Neural tube defect, Neuronal Heterotopia, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Penis Agenesis, Plagiocephaly, Pleural effusion, Posteriorly Rotated Ear, Prostatic neoplasm, Sclerosing Cholangitis, Strabismus, Uveitis
|
2687
|
|
|
Bridge-like lipid transfer protein family member 2 |
BCOX, BCOX1, CT101, FMP27, Hob, KIAA0100 |
Curated: Gout
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Ductal carcinoma, Malignant Neoplasm, Open angle glaucoma, Prostate cancer, Triple Negative Breast Neoplasms
|
2688
|
|
|
Bridge-like lipid transfer protein family member 3A |
C6orf107, ICBP90, SHIP164B, UHRF1BP1, dJ349A12.1 |
Curated: Alzheimer disease, Anorexia nervosa, Coronary artery disease, Eating disorder, Gastroesophageal reflux disease, Graves disease, Insomnia, Systemic lupus erythematosus, Myocardial infarction, Osteoarthritis, Prostate cancer, Urinary bladder cancer
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Colorectal neoplasm, Developmental disability, Liver carcinoma, Lung neoplasms, Lupus Erythematosus, Malignant Neoplasm, Neoplasms, Neurodevelopmental Disorders, Nonbacterial verrucal endocardiosis, Prostate Cancer, Hereditary, Rheumatoid arthritis, Sjogren syndrome
|
2689
|
|
|
Bridge-like lipid transfer protein family member 3B |
SHIP164, SHIP164A, UHRF1BP1L |
Curated: Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis
Unreviewed: Arthritis, Myopia, Polyarthritis, Rheumatoid Factor Positive, Seronegative polyarthritis, Still Disease
|
2690
|
|
|
BLTP3B divergent transcript |
UHRF1BP1L-DT |
Curated: N/A
Unreviewed: N/A
|