호모사피엔스 종의 단백질 코딩 유전자
메켈린 은 인간에게 TMEM67 유전자 에 의해 암호화된 단백질 이다.[5] [6] [7]
함수 이 유전자에 의해 인코딩된 단백질은 1차 실륨 과 혈장 막에 국소화된다. 그 유전자는 무정막으로의 구심점 이동과 일차적 실륨의 형성에 기능한다. 이 유전자에 대해 서로 다른 ISO 양식 을 인코딩하는 다중 대본 변형이 발견되었다.[7]
임상적 유의성 이 유전자의 결함은 메켈 증후군 타입 3([6] 네프로노피시스 [8] [9] 주버트 증후군 타입 6(JBTS6)의 원인이다.[10]
참고 항목 참조 ^ a b c GRCh38: 앙상블 릴리스 89: ENSG00000164953 - 앙상블 , 2017년 5월^ a b c GRCm38: 앙상블 릴리스 89: ENSMUSG000049488 - 앙상블 , 2017년 5월^ "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 .^ Morgan NV, Gissen P, Sharif SM, Baumber L, Sutherland J, Kelly DA, Aminu K, Bennett CP, Woods CG, Mueller RF, Trembath RC, Maher ER, Johnson CA (Oct 2002). "A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24" . Hum Genet . 111 (4–5): 456–61. doi :10.1007/s00439-002-0817-0 . PMID 12384791 . S2CID 31669120 . ^ a b Smith UM, Consugar M, Tee LJ, McKee BM, Maina EN, Whelan S, Morgan NV, Goranson E, Gissen P, Lilliquist S, Aligianis IA, Ward CJ, Pasha S, Punyashthiti R, Malik SS, Batman PA, Bennett CP, Woods CG, McKeown C, Bucourt M, Miller CA, Cox P, Algazali L, Trembath RC, Torres VE, Attie-Bitach T, Kelly DA, Maher ER, Gattone VH II, Harris PC, Johnson CA (Jan 2006). "The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat". Nat Genet . 38 (2): 191–6. doi :10.1038/ng1713 . PMID 16415887 . S2CID 975892 . ^ a b "Entrez Gene: TMEM67 transmembrane protein 67" .^ Boichis H, Passwell J, David R, Miller H (January 1973). "Congenital hepatic fibrosis and nephronophthisis. A family study". Q. J. Med . 42 (165): 221–33. PMID 4688793 . ^ Otto EA, Tory K, Attanasio M, Zhou W, Chaki M, Paruchuri Y, Wise EL, Wolf MT, Utsch B, Becker C, Nürnberg G, Nürnberg P, Nayir A, Saunier S, Antignac C, Hildebrandt F (October 2009). "Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)" . J. Med. Genet . 46 (10): 663–70. doi :10.1136/jmg.2009.066613 PMID 19508969 . ^ Baala L, Romano S, Khaddour R, Saunier S, Smith UM, Audollent S, Ozilou C, Faivre L, Laurent N, Foliguet B, Munnich A, Lyonnet S, Salomon R, Encha-Razavi F, Gubler MC, Boddaert N, de Lonlay P, Johnson CA, Vekemans M, Antignac C, Attie-Bitach T (January 2007). "The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome" . Am. J. Hum. Genet . 80 (1): 186–94. doi :10.1086/510499 . PMC 1785313 PMID 17160906 .
추가 읽기 Khaddour R, Smith U, Baala L, et al. (2007). "Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online" . Hum. Mutat . 28 (5): 523–4. doi :10.1002/humu.9489 PMID 17397051 . S2CID 6528744 . Consugar MB, Kubly VJ, Lager DJ, et al. (2007). "Molecular diagnostics of Meckel-Gruber syndrome highlights phenotypic differences between MKS1 and MKS3". Hum. Genet . 121 (5): 591–9. doi :10.1007/s00439-007-0341-3 . PMID 17377820 . S2CID 11815792 . Dawe HR, Smith UM, Cullinane AR, et al. (2007). "The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation" . Hum. Mol. Genet . 16 (2): 173–86. doi :10.1093/hmg/ddl459 PMID 17185389 . Baala L, Romano S, Khaddour R, et al. (2007). "The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome" . Am. J. Hum. Genet . 80 (1): 186–94. doi :10.1086/510499 . PMC 1785313 PMID 17160906 . Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)" . Genome Res . 14 (10B): 2121–7. doi :10.1101/gr.2596504 . PMC 528928 PMID 15489334 . 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 . 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 .
