CCL27
- Aliases
-
- ALP
- C-C motif chemokine 27
- CC chemokine ILC
- CCL27
- CTACK
- CTAK
- Cutaneous T-cell-attracting chemokine
- ESKINE
- ESkine
- IL-11 R-alpha-locus chemokine
- IL-11 Ralpha-locus chemokine
- ILC
- PESKY
- SCYA27
- Skinkine
- Small-inducible cytokine A27
- chemokine (C-C motif) ligand 27
- cutaneous T-cell attracting chemokine
- cutaneous T-cell-attracting chemokine
- skinkine
- small inducible cytokine subfamily A (Cys-Cys), member 27
- small-inducible cytokine A27
- Description
- CCL27 is a member of the CC cytokine family, and is involved in immunoregulatory and inflammatory processes. CC cytokines are characterized by two adjacent cysteines. CCL27 functions as a chemotactic factor that attracts skin-associated memory T-lymphocytes. CCL27 may also play a role in mediating homing of lymphocytes to cutaneous sites. CCL27 binds specifically to chemokine receptor 10 (CCR10).
Attributes
- QA State
- Curated
- Type
- Protein
- HGNC Name
- CCL27
- Certifications
-
- None
- QA State for Breast
- Under Review
Non-Public Biomarker
Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.
Non-Public Biomarker
Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.
- Development and validation of sandwich ELISA microarrays with minimal assay interference.
- Discovery and preliminary confirmation of novel early detection biomarkers for triple-negative breast cancer using preclinical plasma samples from the Women's Health Initiative observational study.
- Plasma biomarker profiles differ depending on breast cancer subtype but RANTES is consistently increased.
Non-Public Biomarker
Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.