|
431
|
|
|
- |
- |
|
|
432
|
|
|
SH2 domain containing 4B |
- |
|
|
433
|
|
|
Solute carrier family 16 member 12 |
CJMG, CRT2, CTRCT47, MCT12 |
|
|
434
|
|
|
Solute carrier family 22 member 10 (gene/pseudogene) |
OAT5, hOAT5 |
|
|
435
|
|
|
SH3 domain binding kinase 1 |
SBK |
Ankylosing spondylitis, Asthma, Attention deficit hyperactivity disorder, Autism, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Common variable immunodeficiency, Coronary artery disease, Crohn disease, Inflammatory bowel disease, Juvenile idiopathic arthritis, Metabolic syndrome, Psoriasis, Systemic lupus erythematosus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Ulcerative colitisView all (3 more) |
|
436
|
|
|
SLP adaptor and CSK interacting membrane protein |
C17orf87, UNQ5783 |
|
|
437
|
|
|
Shisa family member 6 |
- |
Alzheimer disease, Conotruncal cardiac defect, Developmental dysplasia of the hip, Eye disease, Gastroesophageal reflux disease, Hyperopia, Insomnia, Irritable bowel syndrome, Obesity, Schizophrenia, Squamous cell carcinoma, Stroke |
|
438
|
|
|
Solute carrier family 6 member 17 |
MRT48, NTT4 |
|
|
439
|
|
|
Small nucleolar RNA host gene 17 |
- |
|
|
440
|
|
|
Solute carrier family 9 member A4 |
NHE4 |
Ankylosing spondylitis, Imperforate anus, Asthma, Eczema, Atypical femoral fracture, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Common variable immunodeficiency, Crohn disease, Inflammatory bowel disease, Juvenile idiopathic arthritis, Leprosy, Nasal polyp, Psoriasis, Respiratory system disease, Skin disease, Systemic lupus erythematosus, Diabetes mellitus, type 1, Ulcerative colitisView all (5 more) |