Sphingomyelin phosphodiesterase 1

SMPD1
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 5JG8
Identifiers
Aliases	SMPD1, ASM, ASMASE, NPD, Sphingomyelin phosphodiesterase 1
External IDs	MGI: 98325 HomoloGene: 457 GeneCards: SMPD1
Gene ontology Molecular function • sphingomyelin phosphodiesterase activity • hydrolase activity, acting on glycosyl bonds • protein binding • hydrolase activity • metal ion binding • zinc ion binding • acid sphingomyelin phosphodiesterase activity Cellular component • endosome • plasma membrane • lamellar body • extracellular fluid • lysosomal lumen • lysosome • extracellular exosome • extracellular region Biological process • termination of signal transduction • glycosphingolipid metabolic process • positive regulation of protein dephosphorylation • ceramide biosynthetic process • nervous system development • sphingomyelin catabolic process • negative regulation of MAP kinase activity • positive regulation of apoptotic process • metabolic process • response to drug • signal transduction • sphingomyelin metabolic process • response to cocaine Sources:Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	6609	20597
Ensembl	ENSG00000166311	ENSMUSG00000037049
UniProt	P17405	Q04519
RefSeq (mRNA)	NM_000543 NM_001007593 NM_001318087 NM_001318088	NM_011421
RefSeq (protein)	NP_000534.3 NP_001007594.2 NP_001305016.1 NP_001305017.1	NP_035551.1
Location (UCSC)	Chr 11: 6.39 – 6.39 Mb	Chr 7: 105.55 – 105.56 Mb
PubMed search	[1]	[2]
Wikidata

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Sphingomyelin phosphodiesterase 1 (SMPD1), also known as acid sphingomyelinase (ASM), is an enzyme that in humans is encoded by the SMPD1 gene.

Sphingomyelin phosphodiesterase 1 belongs to the sphingomyelin phosphodiesterase family.^[3]

Clinical significance

Defects in SMPD1 gene cause Niemann-Pick disease, SMPD1-associated.^[3]

A L302P mutation in the SMPD1 gene as a risk factor for Parkinson disease.^[4]

References

1. "Human PubMed Reference:".
2. "Mouse PubMed Reference:".
3. "Entrez Gene: SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal (acid sphingomyelinase)".
4. Gan-Or Z, Ozelius LJ, Bar-Shira A, Saunders-Pullman R, Mirelman A, Kornreich R, Gana-Weisz M, Raymond D, Rozenkrantz L, Deik A, Gurevich T, Gross SJ, Schreiber-Agus N, Giladi N, Bressman SB, Orr-Urtreger A (April 2013). "The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease". Neurology. 80 (17): 1606–10. doi:10.1212/WNL.0b013e31828f180e. PMC 3662322. PMID 23535491.

Further reading

• Stoffel W (November 1999). "Functional analysis of acid and neutral sphingomyelinases in vitro and in vivo". Chemistry and Physics of Lipids. 102 (1-2): 107–21. doi:10.1016/S0009-3084(99)00079-1. PMID 11001565.
• Newrzella D, Stoffel W (December 1992). "Molecular cloning of the acid sphingomyelinase of the mouse and the organization and complete nucleotide sequence of the gene". Biological Chemistry Hoppe-Seyler. 373 (12): 1233–8. doi:10.1515/bchm3.1992.373.2.1233. PMID 1292508.
• Takahashi T, Desnick RJ, Takada G, Schuchman EH (1993). "Identification of a missense mutation (S436R) in the acid sphingomyelinase gene from a Japanese patient with type B Niemann-Pick disease". Human Mutation. 1 (1): 70–1. doi:10.1002/humu.1380010111. PMID 1301192.
• Levran O, Desnick RJ, Schuchman EH (October 1992). "Identification and expression of a common missense mutation (L302P) in the acid sphingomyelinase gene of Ashkenazi Jewish type A Niemann-Pick disease patients". Blood. 80 (8): 2081–7. PMID 1391960.
• Takahashi T, Suchi M, Desnick RJ, Takada G, Schuchman EH (June 1992). "Identification and expression of five mutations in the human acid sphingomyelinase gene causing types A and B Niemann-Pick disease. Molecular evidence for genetic heterogeneity in the neuronopathic and non-neuronopathic forms". The Journal of Biological Chemistry. 267 (18): 12552–8. PMID 1618760.
• Schuchman EH, Levran O, Suchi M, Desnick RJ (June 1991). "An MspI polymorphism in the human acid sphingomyelinase gene (SMPD1)". Nucleic Acids Research. 19 (11): 3160. doi:10.1093/nar/19.11.3160. PMC 328296. PMID 1711683.
• Ferlinz K, Hurwitz R, Sandhoff K (September 1991). "Molecular basis of acid sphingomyelinase deficiency in a patient with Niemann-Pick disease type A". Biochemical and Biophysical Research Communications. 179 (3): 1187–91. doi:10.1016/0006-291X(91)91697-B. PMID 1718266.
• Schuchman EH, Levran O, Pereira LV, Desnick RJ (February 1992). "Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SMPD1)". Genomics. 12 (2): 197–205. doi:10.1016/0888-7543(92)90366-Z. PMID 1740330.
• Schuchman EH, Suchi M, Takahashi T, Sandhoff K, Desnick RJ (May 1991). "Human acid sphingomyelinase. Isolation, nucleotide sequence and expression of the full-length and alternatively spliced cDNAs". The Journal of Biological Chemistry. 266 (13): 8531–9. PMID 1840600.
• Levran O, Desnick RJ, Schuchman EH (September 1991). "Niemann-Pick type B disease. Identification of a single codon deletion in the acid sphingomyelinase gene and genotype/phenotype correlations in type A and B patients". The Journal of Clinical Investigation. 88 (3): 806–10. doi:10.1172/JCI115380. PMC 295465. PMID 1885770.
• da Veiga Pereira L, Desnick RJ, Adler DA, Disteche CM, Schuchman EH (February 1991). "Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1----p15.4". Genomics. 9 (2): 229–34. doi:10.1016/0888-7543(91)90246-B. PMID 2004772.
• Levran O, Desnick RJ, Schuchman EH (May 1991). "Niemann-Pick disease: a frequent missense mutation in the acid sphingomyelinase gene of Ashkenazi Jewish type A and B patients". Proceedings of the National Academy of Sciences of the United States of America. 88 (9): 3748–52. doi:10.1073/pnas.88.9.3748. PMC 51530. PMID 2023926.
• Quintern LE, Schuchman EH, Levran O, Suchi M, Ferlinz K, Reinke H, Sandhoff K, Desnick RJ (September 1989). "Isolation of cDNA clones encoding human acid sphingomyelinase: occurrence of alternatively processed transcripts". The EMBO Journal. 8 (9): 2469–73. PMC 401234. PMID 2555181.
• Horinouchi K, Erlich S, Perl DP, Ferlinz K, Bisgaier CL, Sandhoff K, Desnick RJ, Stewart CL, Schuchman EH (July 1995). "Acid sphingomyelinase deficient mice: a model of types A and B Niemann-Pick disease". Nature Genetics. 10 (3): 288–93. doi:10.1038/ng0795-288. PMID 7670466.
• Sperl W, Bart G, Vanier MT, Christomanou H, Baldissera I, Steichen-Gersdorf E, Paschke E (1994). "A family with visceral course of Niemann-Pick disease, macular halo syndrome and low sphingomyelin degradation rate". Journal of Inherited Metabolic Disease. 17 (1): 93–103. doi:10.1007/BF00735404. PMID 8051942.
• Ida H, Rennert OM, Eto Y, Chan WY (July 1993). "Cloning of a human acid sphingomyelinase cDNA with a new mutation that renders the enzyme inactive". Journal of Biochemistry. 114 (1): 15–20. PMID 8407868.
• Ida H, Rennert OM, Maekawa K, Eto Y (1996). "Identification of three novel mutations in the acid sphinogomyelinase gene of Japanese patients with Niemann-Pick disease type A and B". Human Mutation. 7 (1): 65–7. doi:10.1002/(SICI)1098-1004(1996)7:1<65::AID-HUMU10>3.0.CO;2-Q. PMID 8664904.
• Schuchman EH (1996). "Two new mutations in the acid sphingomyelinase gene causing type a Niemann-pick disease: N389T and R441X". Human Mutation. 6 (4): 352–4. doi:10.1002/humu.1380060412. PMID 8680412.
• Takahashi T, Suchi M, Sato W, Ten SB, Sakuragawa N, Desnick RJ, Schuchman EH, Takada G (October 1995). "Identification and expression of a missense mutation (Y446C) in the acid sphingomyelinase gene from a Japanese patient with type A Niemann-Pick disease". The Tohoku Journal of Experimental Medicine. 177 (2): 117–23. doi:10.1620/tjem.177.117. PMID 8693491.
• Ferlinz K, Hurwitz R, Moczall H, Lansmann S, Schuchman EH, Sandhoff K (January 1997). "Functional characterization of the N-glycosylation sites of human acid sphingomyelinase by site-directed mutagenesis". European Journal of Biochemistry / FEBS. 243 (1-2): 511–7. doi:10.1111/j.1432-1033.1997.511_1a.x. PMID 9030779.

External links

• GeneReviews/NCBI/NIH/UW entry on Acid Sphingomyelinase Deficiency Includes: Niemann-Pick Disease Type A, Niemann-Pick Disease Type B
• OMIM entries on Acid Sphingomyelinase Deficiency