CSTB Chromosome 21

Cystatin B
27 variants 27 Health Risk

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What This Gene Does
The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and kininogens. This gene encodes a stefin that functions as an intracellular thiol protease inhibitor. The protein is able to form a dimer stabilized by noncovalent forces, inhibiting papain and cathepsins l, h and b. The protein is thought to play a role in protecting against the proteases leaking from lysosomes. Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1). One type of mutation responsible for EPM1 is the expansion in the promoter region of this gene of a CCCCGCCCCGCG repeat from 2-3 copies to 30-78 copies. [provided by RefSeq, Jul 2016]
Gene Info
Gene Group
Cystatins, type 1
Locus Type
gene with protein product
Location
21q22.3
Ensembl
ENSG00000160213
Associated Conditions (13)
Progressive myoclonic epilepsy
Unverricht-Lundborg syndrome
Inborn genetic diseases
CSTB-related disorder
Glioma susceptibility 1
Chorea
Dyskinesia
Encephalopathy
Microcephaly
Cerebral dysmyelination
Hepatocellular carcinoma
8 conditions
Self-limited epilepsy with centrotemporal spikes
Key Variants
RS1044894207
Conflicting classifications of pathogenicity
Progressive myoclonic epilepsy, Progressive myoclonic epilepsy
Health Risk
RS1057521317
Conflicting classifications of pathogenicity
Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy
Health Risk
RS143062585
Conflicting classifications of pathogenicity
Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
Health Risk
RS143153487
Conflicting classifications of pathogenicity
Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy, Inborn genetic diseases
Health Risk
RS1555888363
Conflicting classifications of pathogenicity
Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy
Health Risk
RS2084002305
Conflicting classifications of pathogenicity
Progressive myoclonic epilepsy, Progressive myoclonic epilepsy
Health Risk
RS555930471
Conflicting classifications of pathogenicity
Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome
Health Risk
RS570768038
Conflicting classifications of pathogenicity
Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy
Health Risk
RS757593576
Conflicting classifications of pathogenicity
Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome
Health Risk
RS776181852
Conflicting classifications of pathogenicity
Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
Health Risk
RS779920568
Conflicting classifications of pathogenicity
Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
Health Risk
RS11553836
Likely pathogenic
Health Risk
All Variants (27)
RSID Category Clinical Significance Conditions
RS1044894207 Health Risk Conflicting classifications of pathogenicity Progressive myoclonic epilepsy, Progressive myoclonic epilepsy
RS1057521317 Health Risk Conflicting classifications of pathogenicity Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy
RS143062585 Health Risk Conflicting classifications of pathogenicity Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
RS143153487 Health Risk Conflicting classifications of pathogenicity Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy, Inborn genetic diseases
RS1555888363 Health Risk Conflicting classifications of pathogenicity Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy
RS2084002305 Health Risk Conflicting classifications of pathogenicity Progressive myoclonic epilepsy, Progressive myoclonic epilepsy
RS555930471 Health Risk Conflicting classifications of pathogenicity Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome
RS570768038 Health Risk Conflicting classifications of pathogenicity Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy
RS757593576 Health Risk Conflicting classifications of pathogenicity Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome
RS776181852 Health Risk Conflicting classifications of pathogenicity Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
RS779920568 Health Risk Conflicting classifications of pathogenicity Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
RS11553836 Health Risk Likely pathogenic
RS386833439 Health Risk Likely pathogenic Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
RS386833440 Health Risk Likely pathogenic Unverricht-Lundborg syndrome, Glioma susceptibility 1, Unverricht-Lundborg syndrome
RS386833441 Health Risk Likely pathogenic Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
RS386833443 Health Risk Likely pathogenic Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
RS74315443 Health Risk Likely pathogenic Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
RS763450239 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS121909346 Health Risk Pathogenic Unverricht-Lundborg syndrome, Unverricht-Lundborg syndrome
RS1257171692 Health Risk Pathogenic Progressive myoclonic epilepsy, Progressive myoclonic epilepsy
RS147484110 Health Risk Pathogenic Unverricht-Lundborg syndrome, Inborn genetic diseases, Progressive myoclonic epilepsy
RS1601855887 Health Risk Pathogenic Progressive myoclonic epilepsy, Progressive myoclonic epilepsy
RS2517171405 Health Risk Pathogenic Progressive myoclonic epilepsy, Progressive myoclonic epilepsy
RS74315442 Health Risk Pathogenic Unverricht-Lundborg syndrome, 8 conditions, Self-limited epilepsy with centrotemporal spikes
RS1569006250 Health Risk Pathogenic/Likely pathogenic Progressive myoclonic epilepsy, Unverricht-Lundborg syndrome, Progressive myoclonic epilepsy
RS545986367 Health Risk Pathogenic/Likely pathogenic Unverricht-Lundborg syndrome, Inborn genetic diseases, Progressive myoclonic epilepsy
RS796943858 Health Risk Pathogenic/Likely pathogenic Unverricht-Lundborg syndrome, Inborn genetic diseases, Progressive myoclonic epilepsy
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