SGCE

Sarcoglycan, epsilon
Identifiers
Symbols	SGCE ; DYT11; ESG
External IDs	OMIM: 604149 MGI: 1329042 HomoloGene: 31205 GeneCards: SGCE Gene
Gene ontology Molecular function • calcium ion binding Cellular component • Golgi apparatus • cytoskeleton • plasma membrane • integral component of plasma membrane • dystrophin-associated glycoprotein complex • sarcoglycan complex • dendrite • dendrite membrane • sarcolemma Biological process • cell-matrix adhesion • muscle organ development Sources: Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	8910	20392
Ensembl	ENSG00000127990	ENSMUSG00000004631
UniProt	O43556	O70258
RefSeq (mRNA)	NM_001099400	NM_001130188
RefSeq (protein)	NP_001092870	NP_001123660
Location (UCSC)	Chr 7: 94.59 – 94.66 Mb	Chr 6: 4.67 – 4.75 Mb
PubMed search

Epsilon-sarcoglycan is a protein that in humans is encoded by the SGCE gene.^[1][2][3]

The SGCE gene encodes the epsilon member of the sarcoglycan family, transmembrane components of the dystrophin-glycoprotein complex, which links the cytoskeleton to the extracellular matrix.[supplied by OMIM]^[3]

See also

• Myoclonic dystonia

References

1. McNally EM, Ly CT, Kunkel LM (Mar 1998). "Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene". FEBS Lett 422 (1): 27–32. doi:10.1016/S0014-5793(97)01593-7. PMID 9475163.
2. Ettinger AJ, Feng G, Sanes JR (Jan 1998). "epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D". J Biol Chem 272 (51): 32534–8. doi:10.1074/jbc.272.51.32534. PMID 9405466.
3. "Entrez Gene: SGCE sarcoglycan, epsilon".

Further reading

• Nygaard TG, Raymond D, Chen C, et al. (1999). "Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.". Ann. Neurol. 46 (5): 794–8. doi:10.1002/1531-8249(199911)46:5<794::AID-ANA19>3.0.CO;2-2. PMID 10554001.
• Barresi R, Moore SA, Stolle CA, et al. (2001). "Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex.". J. Biol. Chem. 275 (49): 38554–60. doi:10.1074/jbc.M007799200. PMID 10993904.
• Zimprich A, Grabowski M, Asmus F, et al. (2001). "Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.". Nat. Genet. 29 (1): 66–9. doi:10.1038/ng709. PMID 11528394.
• Fanin M, Angelini C (2002). "Defective assembly of sarcoglycan complex in patients with beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubes.". Neuropathol. Appl. Neurobiol. 28 (3): 190–9. doi:10.1046/j.1365-2990.2002.00389.x. PMID 12060343.
• Asmus F, Zimprich A, Tezenas Du Montcel S, et al. (2002). "Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype.". Ann. Neurol. 52 (4): 489–92. doi:10.1002/ana.10325. PMID 12325078.
• Klein C, Liu L, Doheny D, et al. (2002). "Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutations.". Ann. Neurol. 52 (5): 675–9. doi:10.1002/ana.10358. PMID 12402271.
• Müller B, Hedrich K, Kock N, et al. (2003). "Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia.". Am. J. Hum. Genet. 71 (6): 1303–11. doi:10.1086/344531. PMC 378568. PMID 12444570.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Smallwood A, Papageorghiou A, Nicolaides K, et al. (2004). "Temporal regulation of the expression of syncytin (HERV-W), maternally imprinted PEG10, and SGCE in human placenta.". Biol. Reprod. 69 (1): 286–93. doi:10.1095/biolreprod.102.013078. PMID 12620933.
• Grabowski M, Zimprich A, Lorenz-Depiereux B, et al. (2003). "The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted.". Eur. J. Hum. Genet. 11 (2): 138–44. doi:10.1038/sj.ejhg.5200938. PMID 12634861.
• Maréchal L, Raux G, Dumanchin C, et al. (2004). "Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation.". Am. J. Med. Genet. B Neuropsychiatr. Genet. 119 (1): 114–7. doi:10.1002/ajmg.b.10062. PMID 12707948.
• Foncke EM, Klein C, Koelman JH, et al. (2004). "Hereditary myoclonus-dystonia associated with epilepsy.". Neurology 60 (12): 1988–90. doi:10.1212/01.wnl.0000066020.99191.76. PMID 12821748.
• Hillier LW, Fulton RS, Fulton LA, et al. (2003). "The DNA sequence of human chromosome 7.". Nature 424 (6945): 157–64. doi:10.1038/nature01782. PMID 12853948.
• Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
• Kock N, Kasten M, Schüle B, et al. (2004). "Clinical and genetic features of myoclonus-dystonia in 3 cases: a video presentation.". Mov. Disord. 19 (2): 231–4. doi:10.1002/mds.10635. PMID 14978685.
• Nishiyama A, Endo T, Takeda S, Imamura M (2004). "Identification and characterization of epsilon-sarcoglycans in the central nervous system.". Brain Res. Mol. Brain Res. 125 (1-2): 1–12. doi:10.1016/j.molbrainres.2004.01.012. PMID 15193417.
• Asmus F, Schoenian S, Lichtner P, et al. (2005). "Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome.". Neurogenetics 6 (1): 55–6. doi:10.1007/s10048-004-0206-z. PMID 15627203.
• Valente EM, Edwards MJ, Mir P, et al. (2005). "The epsilon-sarcoglycan gene in myoclonic syndromes.". Neurology 64 (4): 737–9. doi:10.1212/01.WNL.0000151979.68010.9B. PMID 15728306.

External links

• GeneReviews/NIH/NCBI/UW entry on Myoclonus-Dystonia
• LOVD mutation database: SGCE