LRSAM1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

E3 ubiquitin-protein ligase LRSAM1, previously known as Tsg101-associated ligase (Tal), is an enzyme that in humans is encoded by the LRSAM1 gene.[5][6]

AliasesLRSAM1, CMT2P, RIFLE, TAL, leucine rich repeat and sterile alpha motif containing 1
End127,503,499 bp[1]
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LRSAM1
Identifiers
AliasesLRSAM1, CMT2P, RIFLE, TAL, leucine rich repeat and sterile alpha motif containing 1
External IDsOMIM: 610933; MGI: 2684789; HomoloGene: 44526; GeneCards: LRSAM1; OMA:LRSAM1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)
RefSeq (protein)
Location (UCSC)Chr 9: 127.45 – 127.5 MbChr 2: 32.82 – 32.85 Mb
PubMed search[3][4]
Wikidata
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Clinical significance

Mutations in LRSAM1 have been reported in the peripheral neuropathy Charcot-Marie-Tooth type 2P (OMIM 614436),[7][8][9] while disruption of the mouse Lrsam1 gene has been shown to sensitize peripheral axons to acrylamide-induced degeneration.[10]

Interactions

LRSAM1 has been shown to interact with TSG101.[11][12]

References

Further reading

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