Gene:
C7
complement component 7

PharmGKB contains no dosing guidelines for this . To report known genotype-based dosing guidelines, or if you are interested in developing guidelines, click here.

PharmGKB contains no drug labels with pharmacogenomic information for this . To report a drug label with PGx, click here.

Disclaimer: The PharmGKB's clinical annotations reflect expert consensus based on clinical evidence and peer-reviewed literature available at the time they are written and are intended only to assist clinicians in decision-making and to identify questions for further research. New evidence may have emerged since the time an annotation was submitted to the PharmGKB. The annotations are limited in scope and are not applicable to interventions or diseases that are not specifically identified.

The annotations do not account for individual variations among patients, and cannot be considered inclusive of all proper methods of care or exclusive of other treatments. It remains the responsibility of the health-care provider to determine the best course of treatment for a patient. Adherence to any guideline is voluntary, with the ultimate determination regarding its application to be made solely by the clinician and the patient. PharmGKB assumes no responsibility for any injury or damage to persons or property arising out of or related to any use of the PharmGKB clinical annotations, or for any errors or omissions.

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This is a non-comprehensive list of genetic tests with pharmacogenetics relevance, typically submitted by the manufacturer and manually curated by PharmGKB. The information listed is provided for educational purposes only and does not constitute an endorsement of any listed test or manufacturer.

A more complete listing of genetic tests is found at the Genetic Testing Registry (GTR).

PGx Test Variants Assayed Related Drugs?

Overview

Alternate Names:  None
Alternate Symbols:  None
PharmGKB Accession Id: PA25941

Details

Cytogenetic Location: chr5 : p13.1 - p13.1
GP mRNA Boundary: chr5 : 40909599 - 40983041
GP Gene Boundary: chr5 : 40899599 - 40986041
Strand: plus
The mRNA boundaries are calculated using the gene's default feature set from NCBI, mapped onto the UCSC Golden Path. PharmGKB sets gene boundaries by expanding the mRNA boundaries by no less than 10,000 bases upstream (5') and 3,000 bases downstream (3') to allow for potential regulatory regions.

PharmGKB Curated Pathways

Pathways created internally by PharmGKB based primarily on literature evidence.

PharmGKB contains no curated pathways for this gene. If you would like to volunteer to work on a pathway, please let us know.

External Pathways

Links to non-PharmGKB pathways.

  1. alternative complement pathway - (BioCarta via Pathway Interaction Database)
  2. classical complement pathway - (BioCarta via Pathway Interaction Database)
  3. lectin induced complement pathway - (BioCarta via Pathway Interaction Database)
  4. Terminal pathway of complement - (Reactome via Pathway Interaction Database)

LinkOuts

Entrez Gene:
730
OMIM:
217070
610102
UCSC Genome Browser:
NM_000587
RefSeq RNA:
NM_000587
RefSeq Protein:
NP_000578
RefSeq DNA:
AC_000048
AC_000137
NC_000005
NG_011692
NT_006576
NW_001838933
NW_922596
UniProtKB:
CO7_HUMAN (P10643)
Q05CI3_HUMAN (Q05CI3)
Ensembl:
ENSG00000112936
GenAtlas:
C7
GeneCard:
C7
MutDB:
C7
ALFRED:
LO000371L
HuGE:
C7
Comparative Toxicogenomics Database:
730
ModBase:
P10643
HumanCyc Gene:
HS03631
HGNC:
1346

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