Gene: CTSK (cathepsin K)  Homo sapiens

Symbol: CTSK
Name: cathepsin K
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. [provided by RefSeq, Apr 2013]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: cathepsin K; cathepsin O; cathepsin O1; cathepsin O2; cathepsin X; CTS02; CTSO; CTSO1; CTSO2; MGC23107; OTTHUMP00000032938; PKND; PYCD
Orthologs: Mus musculus : Ctsk (cathepsin K)  MGI
Rattus norvegicus : Ctsk (cathepsin K)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11157,270,298 - 157,282,531-NCBI
Human Genome Assembly HuRef1122,146,309 - 122,158,545-NCBI
Human Genome Assembly GRCh371150,768,684 - 150,780,917-NCBI
Human Genome Assembly Build 361149,035,311 - 149,047,436-NCBI
Human Cytogenetic Map1q21 NCBI
Human Genome Assembly1147,581,759 - 147,593,885 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on CTSK
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 734172
Created: 2004-01-12
Species: Homo sapiens
Last Modified: 2013-04-30
Status: ACTIVE