| SCARB2 | 
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| Identifiers | 
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| Aliases | SCARB2, AMRF, CD36L2, EPM4, HLGP85, LGP85, LIMP-2, LIMPII, SR-BII, scavenger receptor class B member 2 | 
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| External IDs | OMIM: 602257; MGI: 1196458; HomoloGene: 48353; GeneCards: SCARB2; OMA:SCARB2 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 5 (mouse) | 
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 |  |  | Band | 5|5 E2 | Start | 92,589,173 bp | 
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 | End | 92,654,692 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | inferior ganglion of vagus nerve
 subthalamic nucleus
 germinal epithelium
 superior vestibular nucleus
 external globus pallidus
 Pons
 pars reticulata
 pars compacta
 lactiferous duct
 trigeminal ganglion
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 | | Top expressed in |  | transitional epithelium of urinary bladder
 iris
 carotid body
 ciliary body
 median eminence
 right lung
 arcuate nucleus
 ventral tegmental area
 deep cerebellar nuclei
 dorsal tegmental nucleus
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Lysosomal integral membrane protein 2 (LIMP-2) is a protein that in humans is encoded by the SCARB2 gene. LIMP-2 is expressed in brain, heart, liver, lung and kidney, mainly in the membrane of lysosome organelles; however, in cardiac muscle, LIMP-2 is also expressed at intercalated discs. LIMP-2 in a membrane protein in lysosomes that functions to regulate lysosomal/endosomal transport. Mutations in LIMP-2 have been shown to cause Gaucher disease, myoclonic epilepsy, and action myoclonus–renal failure syndrome. Abnormal levels of LIMP-2 have also been found in patients with hypertrophic cardiomyopathy.