S100A10

S100 Calcium Binding Protein A10 (p11)

Gene Information Card

Symbol S100A10
Full Name S100 calcium binding protein A10
Gene Type protein-coding
Chromosomal Location 1q21.3
NCBI Gene ID 6281 ncbi.nlm.nih.gov/gene/6281
Ensembl ID ENSG00000197771
UniProt ID P60903
OMIM ID 114085
HGNC ID 10494
Aliases p11, ANX2LG, CAL1L, CLP11, GP11, 42C

Description

S100A10 (p11) is a member of the S100 family of calcium-binding proteins. Unlike most S100 proteins, S100A10 is not calcium-responsive due to mutations in its EF-hand motifs. It functions primarily as a ligand for annexin II, forming a heterotetrameric complex that regulates membrane trafficking, exocytosis, and fibrinolysis. S100A10 is involved in cell proliferation, migration, and invasion, and its dysregulation is linked to cancer and psychiatric disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (multiple types) Overexpression of S100A10 promotes tumor cell invasion and metastasis by enhancing plasmin generation via annexin II binding. ClinVar, COSMIC
Major Depressive Disorder Reduced S100A10 expression in brain regions alters serotonin receptor signaling and synaptic plasticity. OMIM, NCBI Gene
Anxiety Disorders S100A10 knockout mice exhibit increased anxiety-like behaviors, linked to altered 5-HT1B receptor function. OMIM, NCBI Gene

Expression Profile

Tissue Expression
Tissue nTPM level
Lung 28.5 High
Kidney 22.3 High
Liver 18.7 Medium
Brain 15.2 Medium
Heart 12.1 Medium
Skeletal Muscle 8.4 Low
Cell Line Expression
Cell Line nTPM Notes
A549 (lung carcinoma) 35.2 High expression
HEK293 (embryonic kidney) 25.6 Moderate expression
HepG2 (hepatocellular carcinoma) 20.1 Moderate expression
SH-SY5Y (neuroblastoma) 14.8 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.94G>A (p.Gly32Arg) Missense <0.1% Unknown functional effect; rare variant
c.205C>T (p.Arg69Cys) Missense <0.1% Reported in COSMIC; potential loss of function
c.310_311insA Frameshift <0.1% Predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense mutations are predicted to cause loss of function, though no confirmed pathogenic variants are documented.

Gain of Function (GOF)

No gain-of-function mutations have been reported.

Dominant Negative (DN)

No dominant-negative mutations have been described.

Gene Ontology (GO)

• calcium ion binding • protein heterodimerization activity
• annexin binding • phospholipase A2 inhibitor activity
• cell surface

Pathways

Annexin II-mediated plasmin generation
Fibrinolysis
Serotonin receptor signaling

Protein Summary

S100A10 (p11) is a 97-amino acid protein that forms a heterotetrameric complex with annexin II. It lacks calcium-binding activity due to critical mutations in its EF-hand domains. The protein is localized to the plasma membrane and endosomal compartments, where it regulates membrane trafficking, exocytosis, and cell surface proteolysis. S100A10 is overexpressed in many cancers and contributes to metastasis. In the brain, it modulates serotonin receptor function and is implicated in mood disorders.

Related Products

Product name Cat.No. Species Gene ID
S100A10 Knockout HEK293 Cell Line EDJ-KQ3811 Human 6281 Details Get a Quote
S100A10 Knockout A-549 Cell Line EDJ-KQ25938 Human 6281 Details Get a Quote
S100A10 Knockout HCT 116 Cell Line EDJ-KQ25939 Human 6281 Details Get a Quote
S100A10 Knockout HeLa Cell Line EDJ-KQ25940 Human 6281 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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