Cathepsin K

Alternative Names

  • CTSK

Associated Diseases

Pycnodysostosis
Back to search Result
OMIM Number

601105

NCBI Gene ID

1513

Uniprot ID

P43235

Length

12,053 bases

No. of Exons

8

No. of isoforms

1

Protein Name

Cathepsin K

Molecular Mass

36966 Da

Amino Acid Count

329

Genomic Location

chr1:150,796,207-150,808,259

Gene Map Locus
1q21.3

Description

The protein encoded by this gene is a lysosomal cysteine proteinase involved in bone remodeling and resorption. This protein, which is a member of the peptidase C1 protein family, is predominantly expressed in osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers, where it could contribute to tumor invasiveness. Mutations in this gene are the cause of pycnodysostosis, an autosomal recessive disease characterized by osteosclerosis and short stature. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_000396.3:c.338delUnited Arab EmiratesNC_000001.11:g.150805923delLikely PathogenicPycnodysostosisNG_011848.1:g.7415del; NM_000396.3:c.338del; NP_000387.1:p.Gly113ValfsTer48
NM_000396.4:c.244-29A>GSaudi ArabiaNC_000001.11:g.150806045T>CLikely PathogenicLikely PathogenicPycnodysostosisNG_011848.1:g.7292A>G; NM_000396.4:c.244-29A>G1654085401982106
© CAGS 2024. All rights reserved.