Property Summary

NCBI Gene PubMed Count 31
PubMed Score 19.98
PubTator Score 14.02

Knowledge Summary


No data available


  Differential Expression (13)

Disease log2 FC p
osteosarcoma 3.005 2.3e-05
group 3 medulloblastoma 2.700 6.7e-06
cystic fibrosis 3.562 6.1e-08
atypical teratoid / rhabdoid tumor 1.800 3.5e-04
glioblastoma 1.400 6.7e-04
medulloblastoma, large-cell 2.500 2.5e-03
primitive neuroectodermal tumor 1.400 5.8e-03
pancreatic ductal adenocarcinoma liver m... -1.369 1.5e-02
intraductal papillary-mucinous neoplasm ... -2.300 2.3e-02
adult high grade glioma 1.300 5.5e-04
invasive ductal carcinoma -1.800 3.5e-02
psoriasis -1.600 6.0e-08
pituitary cancer 1.200 1.4e-02

Gene RIF (9)

26448945 Thus, GPC6 and TMEM132D may serve as predictors of CD8+ T-lymphocyte infiltration and as favorable prognostic markers in early stage ovarian cancer with important consequences for diagnosis.
24804215 Extracellular matrix proteins expression profiling in chemoresistant variants of the A2780 ovarian cancer cell line.
21871017 GPC6 promotes invasive migration by inhibition of canonical beta-catenin and Wnt signalling, and up-regulation of non-canonical Wnt5A signalling leading to the activation of JNK and p38 MAPK.
20692050 Observational study of gene-disease association. (HuGE Navigator)
20634892 Observational study and genome-wide association study of gene-disease association. (HuGE Navigator)
20379614 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
19834535 Observational study of gene-disease association. (HuGE Navigator)
19726429 a reduction in GPC6 mRNA in retinoblastoma is associated with the non-random allelic loss at 13q31 that could contribute to RB development.
19481194 Mutations in the heparan-sulfate proteoglycan glypican 6 impair endochondral ossification and cause recessive omodysplasia

AA Sequence


Text Mined References (32)

PMID Year Title
26448945 2015 Overexpression of GPC6 and TMEM132D in Early Stage Ovarian Cancer Correlates with CD8+ T-Lymphocyte Infiltration and Increased Patient Survival.
25189868 2015 Gene-smoking interactions identify several novel blood pressure loci in the Framingham Heart Study.
24804215 2014 Extracellular matrix proteins expression profiling in chemoresistant variants of the A2780 ovarian cancer cell line.
24554482 2014 Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384.
24431302 2014 Wnt signaling in midbrain dopaminergic neuron development and regenerative medicine for Parkinson's disease.
24159190 2014 Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
23535033 2014 Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
22993228 2013 Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.
22747683 2012 Genetic variants associated with breast size also influence breast cancer risk.
22589738 2012 Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.
22044751 2011 Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.
21871017 2011 NFAT promotes carcinoma invasive migration through glypican-6.
21630459 2011 Proteomic characterization of the human sperm nucleus.
20889312 2010 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
20692050 2010 Association to the Glypican-5 gene in multiple sclerosis.
20634892 2010 A genome-wide association study of neuroticism in a population-based sample.
20379614 Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
19834535 2009 Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging.
19726429 2010 Allelic imbalance at 13q31 is associated with reduced GPC6 in Chinese with sporadic retinoblastoma.
19481194 2009 Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasia.
18839057 2008 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.
17903302 2007 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.
16344560 2006 Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.
15489334 2004 The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
15057823 2004 The DNA sequence and analysis of human chromosome 13.
14702039 2004 Complete sequencing and characterization of 21,243 full-length human cDNAs.
12975309 2003 The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
10480909 1999 Glypican-6, a new member of the glypican family of cell surface heparan sulfate proteoglycans.
10329016 1999 GPC6, a novel member of the glypican gene family, encodes a product structurally related to GPC4 and is colocalized with GPC5 on human chromosome 13.
7657705 1995 K-glypican: a novel GPI-anchored heparan sulfate proteoglycan that is highly expressed in developing brain and kidney.