MLC1
From Wikipedia, the free encyclopedia
Template:Cs1 config Template:Short description An Error has occurred retrieving Wikidata item for infobox Membrane protein MLC1 is a protein that in humans is encoded by the MLC1 gene.[1][2]
MLC1 (also called WKL1[3][4]) is the only human gene currently associated with megalencephalic leukoencephalopathy with subcortical cysts (MLC).[5] Evidence exists for at least one other gene for MLC, but it has not been mapped or identified.
Function
The function of this gene product is not known; however, homology to other proteins suggests that it may be an integral membrane transport protein.[3] Mutations in this gene have been associated with megalencephalic leukoencephalopathy with subcortical cysts, an autosomal recessive neurological disorder.[5]
The MLC1 protein contains six putative transmembrane domains (S1–S6) and a pore region (P) between S5 and S6. Furthermore, MLC1 has highest homology with the KCNA1 shaker-related voltage-gated potassium channel (Kv1.1). This analysis suggests that MLC1 may be a cation channel.[3]
References
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- ^ Page Module:Citation/CS1/styles.css has no content.Nomura N, Miyajima N, Sazuka T, Tanaka A, Kawarabayasi Y, Sato S, Nagase T, Seki N, Ishikawa K, Tabata S (1994). "Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1". DNA Res. 1 (1): 27–35. doi:10.1093/dnares/1.1.27. PMID 7584026.
- ^ Page Module:Citation/CS1/styles.css has no content.Leegwater PA, Yuan BQ, van der Steen J, Mulders J, Könst AA, Boor PK, Mejaski-Bosnjak V, van der Maarel SM, Frants RR, Oudejans CB, Schutgens RB, Pronk JC, van der Knaap MS (April 2001). "Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts". Am. J. Hum. Genet. 68 (4): 831–8. doi:10.1086/319519. PMC 1275636. PMID 11254442.
- ^ a b c Page Module:Citation/CS1/styles.css has no content.Meyer J, Huberth A, Ortega G, Syagailo YV, Jatzke S, Mössner R, Strom TM, Ulzheimer-Teuber I, Stöber G, Schmitt A, Lesch KP (May 2001). "A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree". Mol. Psychiatry. 6 (3): 302–6. doi:10.1038/sj.mp.4000869. PMID 11326298.
- ^ Page Module:Citation/CS1/styles.css has no content.McQuillin A, Kalsi G, Moorey H, Lamb G, Mayet S, Quested D, Baker P, Curtis D, Gurling HM (August 2002). "A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia". Eur. J. Hum. Genet. 10 (8): 491–4. doi:10.1038/sj.ejhg.5200837. PMID 12111645.
- ^ a b Page Module:Citation/CS1/styles.css has no content."Entrez Gene: MLC1 megalencephalic leukoencephalopathy with subcortical cysts 1".
Further reading
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- Page Module:Citation/CS1/styles.css has no content.Nakajima D, Okazaki N, Yamakawa H, et al. (2003). "Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones". DNA Res. 9 (3): 99–106. doi:10.1093/dnares/9.3.99. PMID 12168954.
- Page Module:Citation/CS1/styles.css has no content.Nomura N, Miyajima N, Sazuka T, et al. (1995). "Prediction of the coding sequences of unidentified human genes. I. The coding sequences of 40 new genes (KIAA0001-KIAA0040) deduced by analysis of randomly sampled cDNA clones from human immature myeloid cell line KG-1 (supplement)". DNA Res. 1 (1): 47–56. doi:10.1093/dnares/1.1.47. PMID 7584028.
- Page Module:Citation/CS1/styles.css has no content.Kawai T, Nomura F, Hoshino K, et al. (1999). "Death-associated protein kinase 2 is a new calcium/calmodulin-dependent protein kinase that signals apoptosis through its catalytic activity". Oncogene. 18 (23): 3471–80. doi:10.1038/sj.onc.1202701. PMID 10376525. S2CID 19035227.
- Page Module:Citation/CS1/styles.css has no content.Dunham I, Shimizu N, Roe BA, et al. (1999). "The DNA sequence of human chromosome 22". Nature. 402 (6761): 489–95. Bibcode:1999Natur.402..489D. doi:10.1038/990031. PMID 10591208.
- Page Module:Citation/CS1/styles.css has no content.Leegwater PA, Boor PK, Yuan BQ, et al. (2002). "Identification of novel mutations in MLC1 responsible for megalencephalic leukoencephalopathy with subcortical cysts". Hum. Genet. 110 (3): 279–83. doi:10.1007/s00439-002-0682-x. PMID 11935341. S2CID 52319912.
- Page Module:Citation/CS1/styles.css has no content.Zhang D, Li F, Weidner D, et al. (2002). "Physical and functional interaction between myeloid cell leukemia 1 protein (MCL1) and Fortilin. The potential role of MCL1 as a fortilin chaperone". J. Biol. Chem. 277 (40): 37430–8. doi:10.1074/jbc.M207413200. PMID 12149273.
- Page Module:Citation/CS1/styles.css has no content.Ben-Zeev B, Levy-Nissenbaum E, Lahat H, et al. (2002). "Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews". Hum. Genet. 111 (2): 214–8. doi:10.1007/s00439-002-0770-y. PMID 12189496. S2CID 25452424.
- Page Module:Citation/CS1/styles.css has no content.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. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Page Module:Citation/CS1/styles.css has no content.Rubie C, Lichtner P, Gärtner J, et al. (2003). "Sequence diversity of KIAA0027/MLC1: are megalencephalic leukoencephalopathy and schizophrenia allelic disorders?". Hum. Mutat. 21 (1): 45–52. doi:10.1002/humu.10145. PMID 12497630. S2CID 41349460.
- Page Module:Citation/CS1/styles.css has no content.Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nat. Biotechnol. 21 (5): 566–9. doi:10.1038/nbt810. PMID 12665801. S2CID 23783563.
- Page Module:Citation/CS1/styles.css has no content.Saijo H, Nakayama H, Ezoe T, et al. (2003). "A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease): molecular genetic study". Brain Dev. 25 (5): 362–6. doi:10.1016/S0387-7604(03)00006-8. PMID 12850517. S2CID 20304086.
- Page Module:Citation/CS1/styles.css has no content.Patrono C, Di Giacinto G, Eymard-Pierre E, et al. (2004). "Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cysts". Neurology. 61 (4): 534–7. doi:10.1212/01.wnl.0000076184.21183.ca. PMID 12939431. S2CID 43645063.
- Page Module:Citation/CS1/styles.css has no content.Tsujino S, Kanazawa N, Yoneyama H, et al. (2004). "A common mutation and a novel mutation in Japanese patients with van der Knaap disease". J. Hum. Genet. 48 (12): 605–8. doi:10.1007/s10038-003-0085-4. PMID 14615938.
- Page Module:Citation/CS1/styles.css has no content.Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Page Module:Citation/CS1/styles.css has no content.Gorospe JR, Singhal BS, Kainu T, et al. (2004). "Indian Agarwal megalencephalic leukodystrophy with cysts is caused by a common MLC1 mutation". Neurology. 62 (6): 878–82. doi:10.1212/01.wnl.0000115106.88813.5b. PMID 15037685. S2CID 6463695.
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