MBTPS1 Chromosome 16

Membrane bound transcription factor peptidase, site 1
19 variants 19 Health Risk

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What This Gene Does
This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to the cis/medial-Golgi where a second autocatalytic event takes place and the catalytic activity is acquired. It encodes a type 1 membrane bound protease which is ubiquitously expressed and regulates cholesterol or lipid homeostasis via cleavage of substrates at non-basic residues. Mutations in this gene may be associated with lysosomal dysfunction. [provided by RefSeq, Feb 2014]
Gene Info
Gene Group
Proprotein convertase subtilisin/kexin family
Locus Type
gene with protein product
Location
16q23.3-q24.1
Ensembl
ENSG00000140943
Associated Conditions (5)
Inborn genetic diseases
MBTPS1-related disorder
Spondyloepiphyseal dysplasia
kondo-fu type
See cases
Key Variants
All Variants (19)
RSID Category Clinical Significance Conditions
RS190540580 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS192093489 Health Risk Conflicting classifications of pathogenicity
RS192912251 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201667603 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS35417190 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MBTPS1-related disorder, Inborn genetic diseases
RS369928148 Health Risk Conflicting classifications of pathogenicity
RS553862782 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1223135985 Health Risk Likely pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, Spondyloepiphyseal dysplasia
RS2086110956 Health Risk Likely pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, Spondyloepiphyseal dysplasia
RS2507731785 Health Risk Likely pathogenic
RS774069326 Health Risk Likely pathogenic
RS967208601 Health Risk Likely pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, Spondyloepiphyseal dysplasia
RS1226321681 Health Risk Pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, Spondyloepiphyseal dysplasia
RS1273822522 Health Risk Pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, Spondyloepiphyseal dysplasia
RS2085516391 Health Risk Pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, See cases
RS2151136903 Health Risk Pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, Spondyloepiphyseal dysplasia
RS2151160106 Health Risk Pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, Spondyloepiphyseal dysplasia
RS771258750 Health Risk Pathogenic Spondyloepiphyseal dysplasia, kondo-fu type, Spondyloepiphyseal dysplasia
RS777614151 Health Risk Pathogenic
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