131
|
|
|
Family with sequence similarity 138 member D |
F379 |
Curated: N/A
Unreviewed: N/A
|
132
|
|
|
Family with sequence similarity 138 member E |
F379 |
Curated: N/A
Unreviewed: N/A
|
133
|
|
|
Family with sequence similarity 138 member F |
F379 |
Curated: N/A
Unreviewed: N/A
|
134
|
|
|
Family with sequence similarity 13 member A |
ARHGAP48, FAM13A1 |
Curated: Attention deficit hyperactivity disorder, Bronchitis, Obstructive airway disease, Obstructive pulmonary disease, Gastroesophageal reflux disease, Gout, Hypertension, Idiopathic pulmonary fibrosis, Inflammatory bowel disease, Interstitial lung disease, Metabolic syndrome, Open angle glaucoma, Osteoarthritis, Chronic obstructive pulmonary disease, Pulmonary fibrosis, Substance abuse, Diabetes mellitus type 2
Unreviewed: Alveolitis, Aplastic anemia, Asthma, Breast Cancer, Breast Carcinoma, Bronchiectasis, Chronic Obstructive Pulmonary Disease, Cognition disorder, Connective tissue disease, Cystic Fibrosis, Diabetes mellitus, type 2, Diffuse interstitial pulmonary fibrosis, Emphysema, Gastric Cancer, Gastroesophageal Reflux Disease, Gestational diabetes, Hamman-Rich syndrome, Honeycomb lung, Hyperlipidemia, Hypoxia, Leiomyoma, Liver Cirrhosis, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lung Diseases, Lung Neoplasms, Mental Depression, Mouth neoplasm, Multiple sclerosis, Neoplasms, Neuroblastoma, Obesity, Pulmonary Cystic Fibrosis, Pulmonary Emphysema, Pulmonary Fibrosis, Respiratory system infectious disease, Rheumatoid arthritis, Thyroid cancer, Tremor
|
135
|
|
|
FAM13A antisense RNA 1 |
FAM13A1OS, FAM13AOS, NCRNA00039 |
Curated: N/A
Unreviewed: N/A
|
136
|
|
|
Family with sequence similarity 13 member B |
ARHGAP49, C5orf5, FAM13B1, KHCHP, N61 |
Curated: Androgenetic alopecia, Atrial fibrillation, Atrial flutter, Breast cancer, Cardiac arrhythmia, Cardioembolic stroke, Myocardial infarction
Unreviewed: N/A
|
137
|
|
|
FAM13B antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
138
|
|
|
Family with sequence similarity 13 member C |
FAM13C1 |
Curated: Scoliosis
Unreviewed: Malignant Neoplasm, Prostate cancer
|
139
|
|
|
Family with sequence similarity 149 member A |
MST119, MSTP119 |
Curated: N/A
Unreviewed: Ablepharon macrostomia syndrome, Leukemia
|
140
|
|
|
Family with sequence similarity 149 member B1 |
JBTS36, KIAA0974 |
Curated: Congenital brain malformation, Congenital hypoplasia of part of brain, Aplasia of the vermis, Hydranencephaly, Joubert syndrome, Lissencephaly, Macrogyria, Microgyria, Orofaciodigital syndrome, joubert syndrome 36
Unreviewed: Ataxia, Brachydactyly, Cerebellar vermis agenesis, Ciliopathies, Ciliopathy, Clinodactyly, Congenital Epicanthus, Congenital heart defects, Cryptorchidism, Developmental Delay, Duane retraction syndrome, Dwarfism, Esotropia, Frontal bossing, Hearing Loss, High palate, Hypothalamic Hamartomas, Malformation of cortical development, Mental retardation, Micrognathism, Nystagmus, Osteofibrous dysplasia, Peritonitis, Polydactyly, Polydactyly Of Toes, Progressive external ophthalmoplegia, Radial Polydactyly, Renal agenesis, Situs inversus, Syndactyly
|