221
|
|
|
Solute carrier family 26 member 2 |
D5S1708, DTD, DTDST, EDM4, MST153, MSTP157 |
Achondrogenesis, Acquired kyphoscoliosis, Arthritis, Atelosteogenesis, Bone disease, Brachydactyly, Camptodactyly of fingers, Congenital camptodactyly, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Short femur, Pulmonary hypoplasia, Congenital kyphoscoliosis, Cryptorchidism, Cystic lesions of the pinnae, De la chapelle dysplasia, Diastrophic dwarfism, Diastrophic dysplasia, Dwarfism, Ear diseases, Elbow flexion contracture, Epiphyseal dysplasia, Facial midline hemangioma, Frontal bossing, Glabellar hemangioma, Hernia, femoral, Hip contracture, Hydrops fetalis, Laryngostenosis, Cystic hygroma, Macrocephaly, Micrognathism, Micromelia, Movement disorders, Multiple epiphyseal dysplasia, Osteochondrodysplasia, Osteosclerosis, Plagiocephaly, Scoliosis, Spinal cord compression, Thoracic hypoplasia, Tracheobronchomalacia, Visceral angiomatosisView all (29 more) |
222
|
|
|
Sphingosine-1-phosphate receptor 1 |
CD363, CHEDG1, D1S3362, ECGF1, EDG-1, EDG1, S1P1 |
|
223
|
|
|
Secretory carrier membrane protein 5 |
- |
|
224
|
|
|
Sperm associated antigen 17 |
CT143, PF6, SPGF55 |
|
225
|
|
|
Sprouty related EVH1 domain containing 2 |
NS14, Spred-2 |
|
226
|
|
|
Solute carrier family 51 member A |
OSTA, OSTalpha, PFIC6, SLC51A1 |
|
227
|
|
|
Solute carrier family 16 member 13 |
MCT13 |
|
228
|
|
|
Solute carrier family 39 member 11 |
C17orf26, ZIP-11, ZIP11 |
|
229
|
|
|
SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative) |
SLC62A3, SLC63A3 |
|
230
|
|
|
STT3 oligosaccharyltransferase complex catalytic subunit B |
CDG1X, SIMP, STT3-B |
|