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SPG21 Identifiers Aliases SPG21 , ACP33, GL010, MAST, BM-019, spastic paraplegia 21 (autosomal recessive, Mast syndrome), maspardin, ABHD21, SPG21 abhydrolase domain containing, maspardinExternal IDs OMIM : 608181 ; MGI : 106403 ; HomoloGene : 9603 ; GeneCards : SPG21 ; OMA :SPG21 - orthologs Wikidata
Maspardin is a protein that in humans is encoded by the SPG21 gene .[5] [6] [7]
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Interactions
SPG21 has been shown to interact with CD4 .[5]
References
^ a b c GRCh38: Ensembl release 89: ENSG00000090487 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032388 – Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ a b Zeitlmann L, Sirim P, Kremmer E, Kolanus W (Mar 2001). "Cloning of ACP33 as a novel intracellular ligand of CD4". J Biol Chem . 276 (12): 9123–32. doi :10.1074/jbc.M009270200 . PMID 11113139 . {{cite journal }}
: CS1 maint: multiple names: authors list (link ) CS1 maint: unflagged free DOI (link )
^ Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH (Oct 2003). "Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia" . Am J Hum Genet . 73 (5): 1147–56. doi :10.1086/379522 . PMC 1180493 . PMID 14564668 . {{cite journal }}
: CS1 maint: multiple names: authors list (link )
^ Cite error: The named reference entrez
was invoked but never defined (see the help page ).
Further reading
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