Seroatlas · Human Serome Atlas

MSR1

Macrophage scavenger receptor types I and II

Also known as: CD204, MSRE_HUMAN, SCARA1, SR-A, SR-AI, SR-AII, SR-AIII

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P21757
Gene
MSR1
Ensembl
ENSG00000038945
Chromosome
8
Canonical length
451 aa
Protein class
Cancer-related genes, CD markers, Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
Quaternary structure
Homotrimer

OverviewNCBI Gene

This gene encodes the class A macrophage scavenger receptors, which include three different types (1, 2, 3) generated by alternative splicing of this gene. These receptors or isoforms are macrophage-specific trimeric integral membrane glycoproteins and have been implicated in many macrophage-associated physiological and pathological processes including atherosclerosis, Alzheimer's disease, and host defense. The isoforms type 1 and type 2 are functional receptors and are able to mediate the endocytosis of modified low density lipoproteins (LDLs). The isoform type 3 does not internalize modified LDL (acetyl-LDL) despite having the domain shown to mediate this function in the types 1 and 2 isoforms. It has an altered intracellular processing and is trapped within the endoplasmic reticulum, making it unable to perform endocytosis. The isoform type 3 can inhibit the function of isoforms type 1 and type 2 when co-expressed, indicating a dominant negative effect and suggesting a mechanism for regulation of scavenger receptor activity in macrophages. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

451 residues, UniProt reviewed canonical sequence.

>P21757|MSR1
     1  MEQWDHFHNQ QEDTDSCSES VKFDARSMTA LLPPNPKNSP SLQEKLKSFK AALIALYLLV
    61  FAVLIPLIGI VAAQLLKWET KNCSVSSTNA NDITQSLTGK GNDSEEEMRF QEVFMEHMSN
   121  MEKRIQHILD MEANLMDTEH FQNFSMTTDQ RFNDILLQLS TLFSSVQGHG NAIDEISKSL
   181  ISLNTTLLDL QLNIENLNGK IQENTFKQQE EISKLEERVY NVSAEIMAMK EEQVHLEQEI
   241  KGEVKVLNNI TNDLRLKDWE HSQTLRNITL IQGPPGPPGE KGDRGPTGES GPRGFPGPIG
   301  PPGLKGDRGA IGFPGSRGLP GYAGRPGNSG PKGQKGEKGS GNTLTPFTKV RLVGGSGPHE
   361  GRVEILHSGQ WGTICDDRWE VRVGQVVCRS LGYPGVQAVH KAAHFGQGTG PIWLNEVFCF
   421  GRESSIEECK IRQWGTRACS HSEDAGVTCT L

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against MSR1 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
1
Mean surface accessibility (rSASA)
0.51
Highest tissue expression
113 nTPM

Expression across tissuesHPA

Tissue

  • lung: 113 nTPM
  • gallbladder: 28 nTPM
  • placenta: 26 nTPM
  • adipose tissue: 24 nTPM
  • liver: 23 nTPM
  • blood vessel: 19 nTPM

Single-cell type

  • kupffer cells: 1,199 nCPM
  • cone photoreceptor cells: 706 nCPM
  • macrophages: 671 nCPM
  • monocytes: 292 nCPM
  • renal connecting tubule cells: 285 nCPM
  • cdc: 188 nCPM

Immune cell

  • intermediate monocyte: 17 nTPM
  • non-classical monocyte: 8.7 nTPM
  • classical monocyte: 3.3 nTPM
  • neutrophil: 3.2 nTPM
  • basophil: 1.6 nTPM
  • naive B-cell: 1.5 nTPM

Brain region

  • white matter: 59 nTPM
  • thalamus: 49 nTPM
  • medulla oblongata: 43 nTPM
  • choroid plexus: 40 nTPM
  • pons: 29 nTPM
  • spinal cord: 26 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about MSR1.

Disease | AllUniProt

Conditions MSR1 is implicated in, by any mechanism.

Disease | GeneticClinVar

8 pathogenic / likely-pathogenic of 138 ClinVar records.

Conditions with pathogenic or likely-pathogenic variants.

Disease | ImmuneIEDB

Conditions an epitope on MSR1 was assayed in.

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)
1.7
gnomAD pLI
0
gnomAD missense Z
-2.07
DepMap mean gene effect
0.13
DepMap dependency class
none

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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of MSR1 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 MSR1 as an antibody target. Whether an autoantibody or antibody against MSR1 could matter depends on whether native MSR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

MSR1 is annotated at the cell surface, where native MSR1 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 MSR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/MSR1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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