GPC4
Glypican-4
Also known as: GPC4_HUMAN, K-glypican
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75487
- Gene
- GPC4
- Ensembl
- ENSG00000076716
- Chromosome
- X
- Canonical length
- 556 aa
- Protein class
- Disease related genes, Human disease related genes, Plasma proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Plasma membrane
- Secretome location
- Intracellular and membrane
OverviewNCBI 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 protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The GPC4 gene is adjacent to the 3' end of GPC3 and may also play a role in Simpson-Golabi-Behmel syndrome. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
556 residues, UniProt reviewed canonical sequence.
>O75487|GPC4
1 MARFGLPALL CTLAVLSAAL LAAELKSKSC SEVRRLYVSK GFNKNDAPLH EINGDHLKIC
61 PQGSTCCSQE MEEKYSLQSK DDFKSVVSEQ CNHLQAVFAS RYKKFDEFFK ELLENAEKSL
121 NDMFVKTYGH LYMQNSELFK DLFVELKRYY VVGNVNLEEM LNDFWARLLE RMFRLVNSQY
181 HFTDEYLECV SKYTEQLKPF GDVPRKLKLQ VTRAFVAART FAQGLAVAGD VVSKVSVVNP
241 TAQCTHALLK MIYCSHCRGL VTVKPCYNYC SNIMRGCLAN QGDLDFEWNN FIDAMLMVAE
301 RLEGPFNIES VMDPIDVKIS DAIMNMQDNS VQVSQKVFQG CGPPKPLPAG RISRSISESA
361 FSARFRPHHP EERPTTAAGT SLDRLVTDVK EKLKQAKKFW SSLPSNVCND ERMAAGNGNE
421 DDCWNGKGKS RYLFAVTGNG LANQGNNPEV QVDTSKPDIL ILRQIMALRV MTSKMKNAYN
481 GNDVDFFDIS DESSGEGSGS GCEYQQCPSE FDYNATDHAG KSANEKADSA GVRPGAQAYL
541 LTVFCILFLV MQREWRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against GPC4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.34
- Highest tissue expression
- 27 nTPM
Expression across tissuesHPA
Tissue
- placenta: 27 nTPM
- blood vessel: 27 nTPM
- skeletal muscle: 23 nTPM
- colon: 21 nTPM
- kidney: 19 nTPM
- tongue: 19 nTPM
Single-cell type
- gonadotrophs: 349 nCPM
- proximal tubule cells: 156 nCPM
- pituitary stem cells: 137 nCPM
- ependymal cells: 103 nCPM
- alveolar cells type 2: 90 nCPM
- loop of henle epithelial cells: 84 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 15 nTPM
- hypothalamus: 13 nTPM
- medulla oblongata: 13 nTPM
- midbrain: 12 nTPM
- spinal cord: 11 nTPM
- basal ganglia: 11 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about GPC4.
Disease | AllUniProt
Conditions GPC4 is implicated in, by any mechanism.
- Keipert syndrome (KPTS) MIM:301026
Disease | GeneticClinVar
16 pathogenic / likely-pathogenic of 241 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Keipert syndrome
- Distal shortening of limbs
- Craniosynostosis syndrome
- GPC4-related disorder
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.37
- gnomAD pLI
- 0.93
- gnomAD missense Z
- 1.66
- DepMap mean gene effect
- 0.19
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell migration
- regulation of neurotransmitter receptor localization to postsynaptic specialization membrane
- regulation of presynapse assembly
- regulation of signal transduction
- synaptic membrane adhesion
- Wnt signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of GPC4 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads GPC4 as an antibody target. Whether an autoantibody or antibody against GPC4 could matter depends on whether native GPC4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
GPC4 is annotated at the cell surface, where native GPC4 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label GPC4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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