|
341
|
|
|
Solute carrier family 17 member 5 |
AST, ISSD, NSD, SD, SIALIN, SIASD, SLD, VEAT |
Cerebral atrophy, Congenital epicanthus, Congestive heart failure, Conjugated hyperbilirubinemia, Developmental delay, Dysarthria, Exotropia, Free sialic acid storage disease, High palate, Hydrocephalus, Hydrops fetalis, Hypopigmentation disorder, Leukodystrophy, Melanoma, Mental retardation, Nephrotic syndrome, Nystagmus, Osteopenia, Ptosis, Salla disease, Sialic acid storage disease, SialuriaView all (7 more) |
|
342
|
|
|
SRSF protein kinase 3 |
MSSK-1, MSSK1, STK23, XLID114 |
|
|
343
|
|
|
Small nucleolar RNA, C/D box 50A |
RNU50, U50 |
|
|
344
|
|
|
Sialic acid binding Ig like lectin 7 |
AIRM-1, AIRM1, CD328, CDw328, D-siglec, QA79, SIGLEC-7, SIGLEC19P, SIGLECP2, p75, p75/AIRM1 |
|
|
345
|
|
|
Staphylococcal nuclease and tudor domain containing 1 |
TDRD11, TSN, Tudor-SN, p100 |
|
|
346
|
|
|
Staufen double-stranded RNA binding protein 2 |
39K2, 39K3 |
|
|
347
|
|
|
Syndecan binding protein 2 |
SITAC, SITAC18, ST-2, ST2 |
|
|
348
|
|
|
Structural maintenance of chromosomes 1B |
SMC1BETA, SMC1L2 |
|
|
349
|
|
|
Sorting nexin 5 |
- |
|
|
350
|
|
|
Serine/threonine kinase 36 |
CILD46, FU |
Amyotrophic lateral sclerosis, Asthenozoospermia, Asthma, Bronchiectasis, Ciliary dyskinesia, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Bronchitis, Gastrointestinal stromal tumor, Hearing loss, Hydrocephalus, Kartagener syndrome, Lung diseases, Nasal polyposis, Otitis media, Ovarian serous adenocarcinoma, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (6 more) |
