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Gene Information
Gene ID:6387
Symbol:CXCL12
Full Name:chemokine (C-X-C motif) ligand 12 (stromal cell-derived factor 1)
Alias:PBSF|SCYB12|SDF-1a|SDF-1b|SDF1|SDF1A|SDF1B|TLSF-a|TLSF-b|TPAR1
Organism:Homo sapiens (Human)
Chromosome:10
Genetic Location:10q11.1
Physical Location:44185610-44200547 on NC_000010.9, complement
Gene Type:protein-coding
Orthologs:This gene has no orthologs in other dataset(s).
Gene in Ethanol Study Datasets
Gene Information
Original ID1:W02528
Fold Change:0.7
P Value:2.00E-04
Tissue:Prefrontal cortex
Dataset Information
Name:15816859
Method:Microarray
Tissue:Prefrontal cortex and nucleus accumbens
Phenotype:Alcohol dependence (AD)/Alcohol abuse/Alcoholism
Publication:Flatscher-Bader et al. J Neurochem.(2005) Alcohol-responsive genes in the frontal cortex and nucleus accumbens of human alcoholics. PubMed
Summary:Genes with a mean fold change > 1.5 or < 0.7 were selected and annotated. Values are taken from microarray analysis and represent mean ratios of alcoholic cases compared with matched control cases(n = 6). P values were from t-test.
Gene Information
Original IDNo. of PublicationsPhenotype
CXCL121Alcohol-Induced Disorders
CXCL121Alcohol-Related Disorders
HuGE Navigator Dataset
Name:HuGE Navigator
Method:Literature data mining
Publication:Wei Yu, Melinda Clyne, Anja Wulf, Ajay Yesupriya, Marta Gwinn and Muin J. Khoury. Phenopedia. HuGE Navigator. Available at: http://www.hugenavigator.net/HuGENavigator/startPagePhenoPedia.do. Accessed [Jun. 10, 2008].
Summary:HuGE Navigator Phenopedia provides a disease-centered view of genetic association studies summarized in the online Human Genome Epidemiology (HuGE) encyclopedia. We extracted genes associated to 9 Alcohol-related diseases (Alcohol Amnestic Disorder; Alcohol Withdrawal Delirium; Alcohol Withdrawal Seizures; Alcohol-Induced Disorders; Alcohol-Induced Disorders, Nervous System; Alcohol-Related Disorders; Alcoholic Intoxication; Alcoholic Neuropathy; Alcoholism) from HuGE Navigator Phenopedia.
Gene Refseq Sequence Annotation
mRNAProteinReference assembly Genomic
NM_000609.4NP_000600.1NC_000010.9 range: 44185610..44200547, complement
NM_001033886.1NP_001029058.1NC_000010.9 range: 44185610..44200547, complement
NM_199168.2NP_954637.1NC_000010.9 range: 44185610..44200547, complement
Gene Ontology (GO) Annotation
GO IDGO TermCategoryEvidence (PubMed)
GO:0005576extracellular regionCellular ComponentIEA
GO:0005615extracellular spaceCellular ComponentIEA
GO:0004871signal transducer activityMolecular FunctionTAS (10491003|10802710)
GO:0008083growth factor activityMolecular FunctionIEA
GO:0008009chemokine activityMolecular FunctionIEA
GO:0008009chemokine activityMolecular FunctionTAS (10772939)
GO:0007267cell-cell signalingBiological ProcessNR
GO:0008015blood circulationBiological ProcessTAS (10772939)
GO:0008064regulation of actin polymerization and/or depolymerizationBiological ProcessTAS (10570282)
GO:0007186G-protein coupled receptor protein signaling pathwayBiological ProcessTAS (8752280)
GO:0007165signal transductionBiological ProcessTAS (10491003)
GO:0007155cell adhesionBiological ProcessTAS (10198043)
GO:0006955immune responseBiological ProcessTAS (10802710)
GO:0006955immune responseBiological ProcessIEA
GO:0006954inflammatory responseBiological ProcessNR
GO:0006935chemotaxisBiological ProcessTAS (10620615)
GO:0006874cellular calcium ion homeostasisBiological ProcessTAS (10772939)
GO:0009615response to virusBiological ProcessTAS (10772939)
Other Database Cross Links
NCBI Entrez Gene:6387
HGNC:10672
Ensembl:ENSG00000107562
MIM:600835
HPRD:02904
HuGE Navigator:6387
dbSNP:CXCL12
GeneCard:CXCL12
AceView:CXCL12