|
601
|
|
|
- |
- |
|
|
602
|
|
|
SPC25 component of NDC80 kinetochore complex |
AD024, SPBC25, hSpc25 |
|
|
603
|
|
|
SCY1 like pseudokinase 1 |
GKLP, HT019, NKTL, NTKL, P105, SCAR21, TAPK, TEIF, TRAP |
Spinocerebellar ataxia, Cerebellar ataxia, Cerebellar atrophy, Congenital clubfoot, Developmental delay, Limb muscle atrophy, Liver failure, Liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome, Liver fibrosis, Mental retardation, Metastatic melanoma, Motor delay, Optic atrophy, Sensorimotor neuropathy |
|
604
|
|
|
Solute carrier family 24 member 3 |
NCKX3 |
|
|
605
|
|
|
Solute carrier family 12 member 5 |
DEE34, EIEE34, EIG14, KCC2, hKCC2 |
Bilateral convulsive seizures, Cerebral atrophy, Clonic seizures, Colorectal cancer, Developmental delay, Developmental regression, Epilepsy, Epileptic encephalopathy, Febrile seizures, Grand mal status epilepticus, Hypotonic seizures, Jacksonian seizure, Malignant migrating partial seizures of infancy, Mental depression, Mental retardation, Mood disorder, Myoclonic seizures, Nonconvulsive status epilepticus, Petit mal status, Schizophrenia, Seizure, Status epilepticusView all (7 more) |
|
606
|
|
|
Shroom family member 4 |
MRXSSDS, SHAP, shrm4 |
Breast cancer, Cataract, Congenital clubfoot, Congenital hip dislocation, Congenital epicanthus, Developmental delay, Dwarfism, Gastroesophageal reflux disease, Mental retardation, Mental retardation, x-linked, Microcephaly, Scoliosis, Stocco dos santos syndrome, Strabismus |
|
607
|
|
|
StAR related lipid transfer domain containing 9 |
KIF16A |
|
|
608
|
|
|
SLIT-ROBO Rho GTPase activating protein 1 |
ARHGAP13, NMTC2 |
|
|
609
|
|
|
Sortilin related VPS10 domain containing receptor 2 |
- |
|
|
610
|
|
|
Semaphorin 6A |
HT018, SEMA, SEMA6A1, SEMAQ, VIA |
|
