RSRC2
Arginine/serine-rich coiled-coil protein 2
Also known as: FLJ11021, RSRC2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7L4I2
- Gene
- RSRC2
- Ensembl
- ENSG00000111011
- Chromosome
- 12
- Canonical length
- 434 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli fibrillar center,Nuclear speckles,Cytosol
OverviewNCBI Gene
Enables RNA binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
434 residues, UniProt reviewed canonical sequence.
>Q7L4I2|RSRC2
1 MAASDTERDG LAPEKTSPDR DKKKEQSEVS VSPRASKHHY SRSRSRSRER KRKSDNEGRK
61 HRSRSRSKEG RRHESKDKSS KKHKSEEHND KEHSSDKGRE RLNSSENGED RHKRKERKSS
121 RGRSHSRSRS RERRHRSRSR ERKKSRSRSR ERKKSRSRSR ERKKSRSRSR ERKRRIRSRS
181 RSRSRHRHRT RSRSRTRSRS RDRKKRIEKP RRFSRSLSRT PSPPPFRGRN TAMDAQEALA
241 RRLERAKKLQ EQREKEMVEK QKQQEIAAAA ATGGSVLNVA ALLASGTQVT PQIAMAAQMA
301 ALQAKALAET GIAVPSYYNP AAVNPMKFAE QEKKRKMLWQ GKKEGDKSQS AEIWEKLNFG
361 NKDQNVKFRK LMGIKSEDEA GCSSVDEESY KTLKQQEEVF RNLDAQYEMA RSQTHTQRGM
421 GLGFTSSMRG MDAVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RSRC2 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.63
- Highest tissue expression
- 62 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 62 nTPM
- skeletal muscle: 26 nTPM
- cerebellum: 20 nTPM
- esophagus: 16 nTPM
- blood vessel: 16 nTPM
- ovary: 16 nTPM
Single-cell type
- esophageal apical cells: 450 nCPM
- syncytiotrophoblasts: 399 nCPM
- late primary spermatocytes: 310 nCPM
- epididymal efferent duct absorptive cells: 291 nCPM
- early spermatids: 290 nCPM
- extravillous trophoblasts: 288 nCPM
Immune cell
- naive B-cell: 34 nTPM
- memory B-cell: 29 nTPM
- basophil: 27 nTPM
- eosinophil: 26 nTPM
- non-classical monocyte: 23 nTPM
- T-reg: 22 nTPM
Brain region
- cerebellum: 36 nTPM
- cerebral cortex: 33 nTPM
- hypothalamus: 31 nTPM
- midbrain: 28 nTPM
- white matter: 27 nTPM
- medulla oblongata: 25 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about RSRC2.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 59 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.22
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.99
- DepMap mean gene effect
- -0.43
- DepMap dependency class
- selective
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
Molecular functions
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RSRC2 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 RSRC2 as an antibody target. Whether an autoantibody or antibody against RSRC2 could matter depends on whether native RSRC2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RSRC2 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 RSRC2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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