CAPRIN1
Caprin-1
Also known as: CAPR1_HUMAN, caprin-1, GPIAP1, M11S1, RNG105
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14444
- Gene
- CAPRIN1
- Ensembl
- ENSG00000135387
- Chromosome
- 11
- Canonical length
- 709 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Cytosol
- Quaternary structure
- Homomultimer
OverviewNCBI Gene
Enables several functions, including ATP binding activity; molecular condensate scaffold activity; and signaling adaptor activity. Involved in membraneless organelle assembly; positive regulation of stress granule assembly; and regulation of gene expression. Located in cell leading edge and cytosol. Is active in intracellular membraneless organelle. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
709 residues, UniProt reviewed canonical sequence.
>Q14444|CAPRIN1
1 MPSATSHSGS GSKSSGPPPP SGSSGSEAAA GAGAAAPASQ HPATGTGAVQ TEAMKQILGV
61 IDKKLRNLEK KKGKLDDYQE RMNKGERLNQ DQLDAVSKYQ EVTNNLEFAK ELQRSFMALS
121 QDIQKTIKKT ARREQLMREE AEQKRLKTVL ELQYVLDKLG DDEVRTDLKQ GLNGVPILSE
181 EELSLLDEFY KLVDPERDMS LRLNEQYEHA SIHLWDLLEG KEKPVCGTTY KVLKEIVERV
241 FQSNYFDSTH NHQNGLCEEE EAASAPAVED QVPEAEPEPA EEYTEQSEVE STEYVNRQFM
301 AETQFTSGEK EQVDEWTVET VEVVNSLQQQ PQAASPSVPE PHSLTPVAQA DPLVRRQRVQ
361 DLMAQMQGPY NFIQDSMLDF ENQTLDPAIV SAQPMNPTQN MDMPQLVCPP VHSESRLAQP
421 NQVPVQPEAT QVPLVSSTSE GYTASQPLYQ PSHATEQRPQ KEPIDQIQAT ISLNTDQTTA
481 SSSLPAASQP QVFQAGTSKP LHSSGINVNA APFQSMQTVF NMNAPVPPVN EPETLKQQNQ
541 YQASYNQSFS SQPHQVEQTE LQQEQLQTVV GTYHGSPDQS HQVTGNHQQP PQQNTGFPRS
601 NQPYYNSRGV SRGGSRGARG LMNGYRGPAN GFRGGYDGYR PSFSNTPNSG YTQSQFSAPR
661 DYSGYQRDGY QQNFKRGSGQ SGPRGAPRGR GGPPRPNRGM PQMNTQQVNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CAPRIN1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.61
- Highest tissue expression
- 115 nTPM
Expression across tissuesHPA
Tissue
- testis: 115 nTPM
- thymus: 72 nTPM
- bone marrow: 66 nTPM
- smooth muscle: 62 nTPM
- tonsil: 59 nTPM
- fallopian tube: 58 nTPM
Single-cell type
- late primary spermatocytes: 511 nCPM
- early spermatids: 505 nCPM
- late spermatids: 367 nCPM
- megakaryocyte progenitors: 193 nCPM
- erythrocyte progenitors: 188 nCPM
- endometrial glandular cells: 181 nCPM
Immune cell
- non-classical monocyte: 44 nTPM
- intermediate monocyte: 40 nTPM
- myeloid DC: 39 nTPM
- classical monocyte: 33 nTPM
- total PBMC: 31 nTPM
- NK-cell: 31 nTPM
Brain region
- white matter: 126 nTPM
- spinal cord: 116 nTPM
- cerebral cortex: 108 nTPM
- hypothalamus: 108 nTPM
- hippocampal formation: 108 nTPM
- medulla oblongata: 108 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CAPRIN1.
Disease | AllUniProt
Conditions CAPRIN1 is implicated in, by any mechanism.
- Neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline (CONDCAC) MIM:620636
- Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder (NEDLAAD) MIM:620782
Disease | GeneticClinVar
30 pathogenic / likely-pathogenic of 186 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder
- Moyamoya angiopathy
- Focal-onset seizure
- CAPRIN1-related neurodevelopmental disorders
- Moderate global developmental delay
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)
- 0.31
- gnomAD pLI
- 0.97
- gnomAD missense Z
- 1.69
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- generation of neurons
- intracellular mRNA localization
- membraneless organelle assembly
- negative regulation of translation
- positive regulation of dendrite morphogenesis
- positive regulation of dendritic spine morphogenesis
- positive regulation of stress granule assembly
- synapse assembly
- regulation of deadenylation-dependent decapping of nuclear-transcribed mRNA
Molecular functions
- ATP binding
- molecular condensate scaffold activity
- molecular function activator activity
- mRNA binding
- RNA binding
- signaling adaptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CAPRIN1 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 CAPRIN1 as an antibody target. Whether an autoantibody or antibody against CAPRIN1 could matter depends on whether native CAPRIN1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CAPRIN1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CAPRIN1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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