Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10082
Gene name Gene Name - the full gene name approved by the HGNC.
Glypican 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPC6
Synonyms (NCBI Gene) Gene synonyms aliases
OMIMD1
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q31.3-q32.1
Summary Summary of gene provided in NCBI Entrez Gene.
The glypicans comprise a family of glycosylphosphatidylinositol-anchored heparan sulfate proteoglycans, and they have been implicated in the control of cell growth and cell division. The glypican encoded by this gene is a putative cell surface coreceptor
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs863223282 C>- Pathogenic Genic upstream transcript variant, coding sequence variant, frameshift variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT044098 hsa-miR-361-5p CLASH 23622248
MIRT537100 hsa-miR-548u PAR-CLIP 22012620
MIRT537099 hsa-miR-7161-5p PAR-CLIP 22012620
MIRT537098 hsa-miR-32-3p PAR-CLIP 22012620
MIRT537097 hsa-miR-483-5p PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001523 Process Retinoid metabolic process TAS
GO:0005515 Function Protein binding IPI 29162697
GO:0005615 Component Extracellular space IEA
GO:0005634 Component Nucleus HDA 21630459
GO:0005796 Component Golgi lumen TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604404 4454 ENSG00000183098
Protein
UniProt ID Q9Y625
Protein name Glypican-6 [Cleaved into: Secreted glypican-6]
Protein function Cell surface proteoglycan that bears heparan sulfate. Putative cell surface coreceptor for growth factors, extracellular matrix proteins, proteases and anti-proteases (By similarity). Enhances migration and invasion of cancer cells through WNT5A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01153 Glypican 13 554 Glypican Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed. High expression in fetal kidney and lung and lower expressions in fetal liver and brain. In adult tissues, very abundant in ovary, high levels also observed in liver, kidney, small intestine and colon. Not detected in
Sequence
Sequence length 555
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Schizophrenia Schizophrenia GWAS
Pelvic Organ Prolapse Pelvic Organ Prolapse GWAS
Attention Deficit Hyperactivity Disorder Attention Deficit Hyperactivity Disorder GWAS
Neuroticism Neuroticism GWAS
Associations from Text Mining
Disease Name Relationship Type References
13q deletion syndrome Associate 28393221
Abnormalities Drug Induced Associate 32019583
Bone Diseases Developmental Associate 30982611
Breast Neoplasms Associate 21871017, 24357546, 35265226
Carcinoma Endometrioid Associate 26399219
Carcinoma Ovarian Epithelial Associate 26399219
Cardiovascular Diseases Associate 28393221
Diabetes Mellitus Type 2 Associate 36182916
Epidermolysis Bullosa Dystrophica Associate 16185268
Heart Defects Congenital Associate 28393221