|
181
|
|
|
Solute carrier family 25 member 10 |
DIC, MTDPS19 |
|
|
182
|
|
|
SIX homeobox 5 |
BOR2, DMAHP |
Bor syndrome, Branchioma, Branchiooculofacial syndrome, Branchiootorenal syndrome, Facial paralysis, Hemifacial hypoplasia, Hydronephrosis, Melnick-fraser syndrome, Microtia, Multicystic renal dysplasia, Renal dysplasia, Renal insufficiency, Stenosis of external auditory canal, Vesicoureteral reflux |
|
183
|
|
|
Solute carrier family 35 member F3 |
- |
|
|
184
|
|
|
Solute carrier family 30 member 7 |
ZHS, ZNT7, ZnT-7, ZnTL2 |
|
|
185
|
|
|
Steroid receptor associated and regulated protein |
C1orf64, ERRF |
|
|
186
|
|
|
Salt inducible kinase 1 |
DEE30, MSK, SIK, SIK-1, SIK1B, SNF1LK |
Arthritis, Autism, Cardiomyopathy, Cerebellar atrophy, Choreoathetosis, Clonic seizures, Congenital exomphalos, Developmental delay, Developmental regression, Dyskinetic syndrome, Dysphagia, Dyssomnia, Eczema, Epileptic encephalopathy, Episodic ataxia, Eyelid myoclonias, Febrile seizures, Focal seizures, Focal tonic seizures, Glioblastoma, Hypoplasia of corpus callosum, Hypotonic seizures, Juvenile arthritis, Mental retardation, Metastatic melanoma, Microcephaly, Myoclonic encephalopathy, Myoclonic seizures, Pachygyria, Penis agenesis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Precocious puberty, Renal dysplasia, Seizure, Sleep disorders, Spasms syndrome, Spasms x-linked, Stereotyped behavior, Still disease, Strabismus, Ureterocele, Ventricular septal defect, West syndromeView all (29 more) |
|
187
|
|
|
Solute carrier family 9 member B1 |
NHA1, NHEDC1 |
|
|
188
|
|
|
Shugoshin 2 |
SGOL2, TRIPIN |
|
|
189
|
|
|
Solute carrier family 23 member 3 |
E2BP3, SVCT3, Yspl1 |
|
|
190
|
|
|
Shugoshin 1 |
CAID, NY-BR-85, SGO, SGOL1 |
|
