Entity Details

Primary name MSR1
Entity type gene
Source Source Link

Details

PrimaryID4481
RefseqGeneNG_012102
SymbolMSR1
Namemacrophage scavenger receptor 1
Chromosome8
Location8p22
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1993-03-16
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsMSRE_HUMAN

GO terms

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GOName
GO:0001540 amyloid-beta binding
GO:0005044 scavenger receptor activity
GO:0005581 collagen trimer
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0006898 receptor-mediated endocytosis
GO:0006911 phagocytosis, engulfment
GO:0009897 external side of plasma membrane
GO:0010629 negative regulation of gene expression
GO:0010744 positive regulation of macrophage derived foam cell differentiation
GO:0010886 positive regulation of cholesterol storage
GO:0016021 integral component of membrane
GO:0030169 low-density lipoprotein particle binding
GO:0030301 cholesterol transport
GO:0030666 endocytic vesicle membrane
GO:0034362 low-density lipoprotein particle
GO:0034381 plasma lipoprotein particle clearance
GO:0038024 cargo receptor activity
GO:0097242 amyloid-beta clearance

Diseases

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Disease IDSourceNameDescription
176807 OMIMProstate cancer (PC)A malignancy originating in tissues of the prostate. Most prostate cancers are adenocarcinomas that develop in the acini of the prostatic ducts. Other rare histopathologic types of prostate cancer that occur in approximately 5% of patients include small cell carcinoma, mucinous carcinoma, prostatic ductal carcinoma, transitional cell carcinoma, squamous cell carcinoma, basal cell carcinoma, adenoid cystic carcinoma (basaloid), signet-ring cell carcinoma and neuroendocrine carcinoma. The disease may be caused by variants affecting the gene represented in this entry. MSR1 variants may play a role in susceptibility to prostate cancer. MSR1 variants have been found in individuals with prostate cancer and co-segregate with the disease in some families.
614266 OMIMBarrett esophagus (BE)A condition characterized by a metaplastic change in which normal esophageal squamous epithelium is replaced by a columnar and intestinal-type epithelium. Patients with Barrett esophagus have an increased risk of esophageal adenocarcinoma. The main cause of Barrett esophagus is gastroesophageal reflux. The retrograde movement of acid and bile salts from the stomach into the esophagus causes prolonged injury to the esophageal epithelium and induces chronic esophagitis, which in turn is believed to trigger the pathologic changes. The disease may be caused by variants affecting the gene represented in this entry. Genetic variants in MSR1 have been found in individuals with Barrett esophagus and are thought to contribute to disease susceptibility.

Interactions

16 interactions