Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2262
Gene name Gene Name - the full gene name approved by the HGNC.
Glypican 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GPC5
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q31.3
Summary Summary of gene provided in NCBI Entrez Gene.
Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protei
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT438314 hsa-miR-217 Luciferase reporter assay, Northern blot, qRT-PCR, Western blot 26098560
MIRT438314 hsa-miR-217 Luciferase reporter assay, Northern blot, qRT-PCR, Western blot 26098560
MIRT438314 hsa-miR-217 Luciferase reporter assay, Northern blot, qRT-PCR, Western blot 26098560
MIRT438314 hsa-miR-217 Luciferase reporter assay, Northern blot, qRT-PCR, Western blot 26098560
MIRT657706 hsa-miR-548ac HITS-CLIP 23824327
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 32814053
GO:0005576 Component Extracellular region TAS
GO:0005615 Component Extracellular space IEA
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
602446 4453 ENSG00000179399
Protein
UniProt ID P78333
Protein name Glypican-5 [Cleaved into: Secreted glypican-5]
Protein function Cell surface proteoglycan that bears heparan sulfate.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01153 Glypican 12 570 Glypican Family
Tissue specificity TISSUE SPECIFICITY: In adult, primarily expressed in the brain. Also detected in fetal brain, lung and liver. {ECO:0000269|PubMed:9070915, ECO:0000269|PubMed:9331333}.
Sequence
Sequence length 572
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Rheumatoid arthritis Rheumatoid arthritis GWAS
Multiple Sclerosis Multiple Sclerosis GWAS
Tetralogy of Fallot Tetralogy of Fallot GWAS
Endometriosis Endometriosis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 27554041
Amyloidosis Hereditary Transthyretin Related Associate 30414409
Arthritis Rheumatoid Associate 30423114
Carcinogenesis Inhibit 32970968
Carcinoma Endometrioid Associate 26399219
Carcinoma Hepatocellular Associate 25818666
Carcinoma Ovarian Epithelial Associate 26399219
Carcinoma Pancreatic Ductal Associate 33302876
Colorectal Neoplasms Associate 20085586
Death Associate 36165234