|
1101
|
|
|
Sialic acid binding Ig like lectin 5 |
CD170, CD33L2, OB-BP2, OBBP2, SIGLEC-5 |
|
|
1102
|
|
|
Succinate-CoA ligase GDP-forming subunit beta |
G-SCS, GBETA, GTPSCS |
|
|
1103
|
|
|
Succinate-CoA ligase GDP/ADP-forming subunit alpha |
GALPHA, MTDPS9, SUCLA1 |
Cerebral atrophy, Developmental delay, Epileptic encephalopathy, Gastric cancer, Hypoglycemia, Mental retardation, Leigh syndrome, Mitochondrial dna depletion syndrome, Necrotizing encephalomyelopathy, Respiratory failure, Stomach neoplasms |
|
1104
|
|
|
Succinate-CoA ligase ADP-forming subunit beta |
A-BETA, A-SCS, LINC00444, MTDPS5, SCS-betaA |
Cerebral atrophy, Developmental delay, Dwarfism, Hearing loss, Leigh syndrome, Microcephaly, Necrotizing encephalomyelopathy, Nervous system diseases, Obesity, Ptosis, Strabismus |
|
1105
|
|
|
Synaptic Ras GTPase activating protein 1 |
MRD5, RASA1, RASA5, SYNGAP |
Angelman syndrome, Attention deficit hyperactivity disorder, Autism, Camptodactyly of fingers, Cerebral atrophy, Development disorder, Developmental and epileptic encephalopathy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Dysmorphic features, Epilepsy, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Mental retardation, Language disorders, Macrotia, Melanocytic nevus, Microcephaly, Motor delay, Movement disorders, Multiple congenital anomalies, Myopia, Neurodevelopmental disorders, Non-specifi epileptic encephalopathy, Non-syndromic intellectual disability, Nystagmus, Optic atrophy, Posteriorly rotated ear, Ptosis, Rheumatoid arthritis, Schizophrenia, Status epilepticus, Syndactyly of the toesView all (21 more) |
|
1106
|
|
|
Suppressor of cytokine signaling 2 |
CIS2, Cish2, SOCS-2, SSI-2, SSI2, STATI2 |
|
|
1107
|
|
|
Synaptojanin 1 |
DEE53, EIEE53, INPP5G, PARK20 |
Akinesia, Alzheimer disease, Anarthria speech disorder, Attention deficit hyperactivity disorder, Autism, Brain atrophy, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Hypoplasia of corpus callosum, Mental retardation, Microcephaly, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy, Parkinson disease, Parkinsonian disease, Ptosis, Scoliosis, Spastic quadriplegia, Status epilepticusView all (13 more) |
|
1108
|
|
|
ST3 beta-galactoside alpha-2,3-sialyltransferase 5 |
SATI, SIAT9, SIATGM3S, SPDRS, ST3Gal V, ST3GalV |
Central visual impairment, Cerebral cortical atrophy, Cerebral palsy, Choreoathetosis, Developmental delay, Developmental regression, Dyskinetic syndrome, Gm3 synthase deficiency, Hearing loss, Mental retardation, Microcephaly, Nystagmus, Optic atrophy, Paroxysmal nonkinesigenic dyskinesia, Salt and pepper developmental regression syndrome, Seizure, Status epilepticus, Stereotyped behaviorView all (3 more) |
|
1109
|
|
|
Synaptojanin 2 |
INPP5H |
|
|
1110
|
|
|
Sphingosine kinase 1 |
SPHK |
|
