SZT2 Chromosome 1

SZT2 subunit of KICSTOR complex
223 variants 223 Health Risk

Upload your DNA to see your personal genotypes for variants in SZT2.

What This Gene Does
The protein encoded by this gene is expressed in the brain, predominantly in the parietal and frontal cortex as well as in dorsal root ganglia. It is localized to the peroxisome, and is implicated in resistance to oxidative stress. It likely functions by increasing superoxide dismutase (SOD) activity, but itself has no direct SOD activity. Studies in mice show that this gene confers low seizure threshold, and may also enhance epileptogenesis. [provided by RefSeq, Jun 2011]
Gene Info
Gene Group
"KICSTOR complex|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
1p34.2
Ensembl
ENSG00000198198
Associated Conditions (15)
Inborn genetic diseases
SZT2-related disorder
Colon adenocarcinoma
Thyroid cancer
nonmedullary
1
Developmental and epileptic encephalopathy
18
Intellectual disability
Severe hydrocephalus
Encephalocele
Seizure
See cases
Self-limited epilepsy with centrotemporal spikes
Cervical cancer
Key Variants
RS112994383
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS138028425
Conflicting classifications of pathogenicity
Inborn genetic diseases, SZT2-related disorder, Colon adenocarcinoma
Health Risk
RS138401303
Conflicting classifications of pathogenicity
Health Risk
RS138585463
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 18, Inborn genetic diseases
Health Risk
RS138762270
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 18, Inborn genetic diseases
Health Risk
RS139147641
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS139803823
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
Health Risk
RS140004653
Conflicting classifications of pathogenicity
Developmental and epileptic encephalopathy, 18, Inborn genetic diseases
Health Risk
RS1404132920
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS140427193
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS142611359
Conflicting classifications of pathogenicity
Inborn genetic diseases, Developmental and epileptic encephalopathy, 18
Health Risk
RS143185010
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
All Variants (223)
RSID Category Clinical Significance Conditions
RS2545826394 Health Risk Likely pathogenic
RS2545827197 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS2545841470 Health Risk Likely pathogenic
RS2545841958 Health Risk Likely pathogenic
RS2545842119 Health Risk Likely pathogenic
RS2545852780 Health Risk Likely pathogenic
RS2545857117 Health Risk Likely pathogenic
RS2545876835 Health Risk Likely pathogenic
RS374964399 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS552956642 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS756625074 Health Risk Likely pathogenic
RS756942804 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS765848129 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS766399416 Health Risk Likely pathogenic
RS989588546 Health Risk Likely pathogenic
RS1168668932 Health Risk Pathogenic
RS1180634449 Health Risk Pathogenic
RS1187853717 Health Risk Pathogenic
RS1215221860 Health Risk Pathogenic
RS1276523236 Health Risk Pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS1293522591 Health Risk Pathogenic
RS1295389410 Health Risk Pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS1302034044 Health Risk Pathogenic See cases, Developmental and epileptic encephalopathy, 18
RS1306918506 Health Risk Pathogenic Self-limited epilepsy with centrotemporal spikes, Self-limited epilepsy with centrotemporal spikes
RS1325815399 Health Risk Pathogenic
RS1367454316 Health Risk Pathogenic SZT2-related disorder, SZT2-related disorder
RS1391105203 Health Risk Pathogenic
RS1394131270 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1438773569 Health Risk Pathogenic Cervical cancer, Cervical cancer
RS1448210053 Health Risk Pathogenic
RS1553138299 Health Risk Pathogenic Self-limited epilepsy with centrotemporal spikes, Self-limited epilepsy with centrotemporal spikes
RS1557589101 Health Risk Pathogenic
RS1570733929 Health Risk Pathogenic
RS1570741194 Health Risk Pathogenic SZT2-related disorder, SZT2-related disorder
RS1650058382 Health Risk Pathogenic
RS1651557199 Health Risk Pathogenic
RS1651685926 Health Risk Pathogenic
RS1652116565 Health Risk Pathogenic
RS1652887200 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1653192107 Health Risk Pathogenic
RS1653321651 Health Risk Pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS1653397925 Health Risk Pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS1653847504 Health Risk Pathogenic
RS1653916498 Health Risk Pathogenic
RS1653925536 Health Risk Pathogenic
RS1654007685 Health Risk Pathogenic
RS1654084368 Health Risk Pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
RS1654576202 Health Risk Pathogenic
RS1654858951 Health Risk Pathogenic
RS1655170724 Health Risk Pathogenic Developmental and epileptic encephalopathy, 18, Developmental and epileptic encephalopathy
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