| 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.