CCL18

Name
CCL18
HGNC ID
HGNC:10616
Cytogenetic Location
17q12
External Resources
View external resources
ClinVar Variants
View ClinVar Variants
GeneReviews®
View GeneReviews
External Resources

MedGen: Genetics Summary

Organizes information related to human medical genetics, such as attributes of conditions with a genetic contribution.

Genetic Practice Guidelines: Gene

As guidelines are identified that relate to a disorder, gene, or variation, staff at NCBI connect them to the appropriate records. This page provides an alphabetical list of the professional practice guidelines, position statements, and recommendations that have been identified.

GTR: Gene Tests

A voluntary registry of genetic tests and laboratories, with detailed information about the tests such as what is measured and analytic and clinical validity. GTR also is a nexus for information about genetic conditions and provides context-specific links to a variety of resources, including practice guidelines, published literature, and genetic data/information. The scope of GTR includes single gene tests for Mendelian disorders, somatic/cancer tests and pharmacogenetic tests including complex arrays, panels.

CPIC Pharmacogenomics Prescribing Guidelines

The Clinical Pharmacogenetics Implementation Consortium (CPIC) was formed as a shared project between PharmGKB and the Pharmacogenomics Research Network (PGRN).

PharmGKB: Gene

PharmGKB is a comprehensive resource that curates knowledge about the impact of genetic variation on drug response for clinicians and researchers.

OMIM: Gene

An Online Catalog of Human Genes and Genetic Disorders.

Genetics Home Reference

Genetics Home Reference provides consumer-friendly information about the effects of genetic variation on human health.

Gene Reviews

An international point-of-care resource for busy clinicians, provides clinically relevant and medically actionable information for inherited conditions in a standardized journal-style format, covering diagnosis, management, and genetic counseling for patients and their families.

ClinVar - Gene

ClinGen and ClinVar are close partners and have established a collaborative working relationship. ClinVar is a critical resource for ClinGen. ClinVar aggregates information about genomic variation and its relationship to human health.

1000 Genomes

An interactive graphical viewer that allows users to explore variant calls, genotype calls and supporting evidence (such as aligned sequence reads) that have been produced by the 1000 Genomes Project. View Information

NCBI Browser

The 1000 Genomes Browser allows users to explore variant calls, genotype calls and supporting sequence read alignments that have been produced by the 1000 Genomes project.
Additional Genomic Resources & Websites
1000 Genomes
An interactive graphical viewer that allows users to explore variant calls, genotype calls and supporting evidence (such as aligned sequence reads) that have been produced by the 1000 Genomes Project.
American Society of Human Genetics - Patient Information
Enhance genetics education by preparing future professionals and informing the public.
Cancer Genetics Overview (PDQ®)
Provides a number of resources for patients and consumers about cancer and genetics.
CDC Public Health Genomics
The CDC Office of Public Health Genomics provides timely and credible information for the effective and responsible translation of genomics research into population health benefits.
Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines
The Clinical Pharmacogenetics Implementation Consortium (CPIC) was formed in late 2009, as a shared project between PharmGKB and the Pharmacogenomics Research Network. CPIC guidelines are peer-reviewed and published in a leading journal (in partnership with Clinical Pharmacology and Therapeutics) with simultaneous posting to PharmGKB with supplemental information/data and updates.
dbGaP Registration Required
An archive and distribution center for the description and results of studies which investigate the interaction of genotype and phenotype. These studies include genome-wide association (GWAS), medical resequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.
Exome Aggregation Consortium
The Exome Aggregation Consortium (ExAC) is a coalition of investigators seeking to aggregate and harmonize exome sequencing data from a wide variety of large-scale sequencing projects, and to make summary data available for the wider scientific community.
Exome Variant Server
The goal of the NHLBI GO Exome Sequencing Project (ESP) is to discover novel genes and mechanisms contributing to heart, lung and blood disorders by pioneering the application of next-generation sequencing of the protein coding regions of the human genome across diverse, richly-phenotyped populations and to share these datasets and findings with the scientific community to extend and enrich the diagnosis, management and treatment of heart, lung and blood disorders.
GARD - Get Involved In Research
Learn more about how to find and participate in a research study, clinical trial, or patient registry.
GeneReviews
GeneReviews are expert-authored, peer-reviewed disease descriptions presented in a standardized format and focused on clinically relevant, medically actionable information on the diagnosis, management and genetic counseling of patients and families with specific inherited conditions.
GeneTests
A medical genetics information resource. GeneTests has grown to reflect the advances in genetic testing capabilities and to address the needs of our ever widening user community.
Genetic Alliance
A dynamic network that serves as an open space for sharing valuable information and interventions for disease resources, creative tools, and innovative programs
Genetic/Genomic Competency Center (g-2-c-2)
A searchable repository of peer-reviewed genetic and genomic resources.
Genetic Practice Guidelines
As guidelines are identified that relate to a disorder, gene, or variation, staff at NCBI connect them to the appropriate records. This page provides an alphabetical list of the professional practice guidelines, position statements, and recommendations that have been identified.
Genetic Testing Registry
A voluntary registry of genetic tests and laboratories, with detailed information about the tests such as what is measured and analytic and clinical validity.  GTR also is a nexus for information about genetic conditions and provides context-specific links to a variety of resources, including practice guidelines, published literature, and genetic data/information. The scope of GTR includes single gene tests for Mendelian disorders, somatic/cancer tests and pharmacogenetic tests including complex arrays, panels.
Genetics Home Reference
Genetics Home Reference provides consumer-friendly information about the effects of genetic variations on human health.
Human Genetic Mutation Database Registration Required Fee
HGMD®  is a resource for comprehensive data on published human inherited disease mutations.
Human Phenotype Ontology
The Human Phenotype Ontology (HPO) aims to provide a standardized vocabulary of phenotypic abnormalities encountered in human disease. The HPO is currently being developed using the medical literature, Orphanet, DECIPHER, and OMIM. HPO currently contains approximately 11,000 terms and over 115,000 annotations to hereditary diseases.
IGNITE
IGNITE is an NIH-funded network dedicated to supporting the implementation of genomics in healthcare.
Matchmaker Exchange
Matchmaker Exchange provides a robust approach to rare disease gene discovery through the creation of a federated network connecting databases of genotypes and rare phenotypes.
National Human Genome Research Institute (NHGRI)
The National Human Genome Research Institute (NHGRI) is working towards a future when health care providers will use information about our individual genomes to better diagnose and treat disease.
National Human Genome Research Institute (NHGRI) - HealthProfessionals
The National Human Genome Research Institute (NHGRI) is working towards a future when health care providers will use information about our individual genomes to better diagnose and treat disease.
National Organization for Rare Disorders
The National Organization for Rare Disorders (NORD), a 501(c)(3) organization, is the leading voice of the rare disease community.  We are a unique federation of voluntary health organizations dedicated to helping people with rare "orphan" diseases and assisting the organizations that serve them. For more than 30 years, we have been committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and service.
Online Medelian Inheritance in Man (OMIM)
An Online Catalog of Human Genes and Genetic Disorders
OrphaNet
Orphanet is the reference portal for information on rare diseases and orphan drugs, for all audiences. Orphanet’s aim is to help improve the diagnosis, care and treatment of patients with rare diseases.
PharmGKB
The PharmGKB is a pharmacogenomics knowledge resource that encompasses clinical information including dosing guidelines and drug labels, potentially clinically actionable gene-drug associations and genotype-phenotype relationships.
UCSC Genome Browser
The UCSC Genome Browser is a visualization tool for the human genome providing a view of its genes and chromosomal features.  Results from GWAS studies, conservation between other species, and results from many genomic and epigenomic studies are also provided.  The Browser also has similar genomic information for a large number of animal species.
Undiagnosed Diseases Network
The Undiagnosed Diseases Network (UDN) is an NIH-funded research study with the goal of providing answers for individuals with mysterious conditions that have long eluded diagnosis.  
Unique
Proving information to inform, support and alleviate the isolation of anyone affected by a rare chromosome disorder and to raise public awareness.