TMEM67
(Preusmjereno sa Mekelin)
Mekelin je protein koji je kod ljudi kodiran genom TMEM67.[5][6][7]
Aminokiselinska sekvenca uredi
Dužina polipeptidnog lanca je 995 aminokiselina, а molekulska težina 111.745 Da.[8]
| 10 | 20 | 30 | 40 | 50 | ||||
|---|---|---|---|---|---|---|---|---|
| MATRGGAGVA | MAVWSLLSAR | AVTAFLLLFL | PRFLQAQTFS | FPFQQPEKCD | ||||
| NNQYFDISAL | SCVPCGANQR | QDARGTSCVC | LPGFQMISNN | GGPAIICKKC | ||||
| PENMKGVTED | GWNCISCPSD | LTAEGKCHCP | IGHILVERDI | NGTLLSQATC | ||||
| ELCDGNENSF | MVVNALGDRC | VRCEPTFVNT | SRSCACSEPN | ILTGGLCFSS | ||||
| TGNFPLRRIS | AARYGEVGMS | LTSEWFAKYL | QSSAAACWVY | ANLTSCQALG | ||||
| NMCVMNMNSY | DFATFDACGL | FQFIFENTAG | LSTVHSISFW | RQNLPWLFYG | ||||
| DQLGLAPQVL | SSTSLPTNFS | FKGENQNTKL | KFVAASYDIR | GNFLKWQTLE | ||||
| GGVLQLCPDT | ETRLNAAYSF | GTTYQQNCEI | PISKILIDFP | TPIFYDVYLE | ||||
| YTDENQHQYI | LAVPVLNLNL | QHNKIFVNQD | SNSGKWLLTR | RIFLVDAVSG | ||||
| RENDLGTQPR | VIRVATQISL | SVHLVPNTIN | GNIYPPLITI | AYSDIDIKDA | ||||
| NSQSVKVSFS | VTYEMDHGEA | HVQTDIALGV | LGGLAVLASL | LKTAGWKRRI | ||||
| GSPMIDLQTV | VKFLVYYAGD | LANVFFIITV | GTGLYWLIFF | KAQKSVSVLL | ||||
| PMPIQEERFV | TYVGCAFALK | ALQFLHKLIS | QITIDVFFID | WERPKGKVLK | ||||
| AVEGEGGVRS | ATVPVSIWRT | YFVANEWNEI | QTVRKINSLF | QVLTVLFFLE | ||||
| VVGFKNLALM | DSSSSLSRNP | PSYIAPYSCI | LRYAVSAALW | LAIGIIQVVF | ||||
| FAVFYERFIE | DKIRQFVDLC | SMSNISVFLL | SHKCFGYYIH | GRSVHGHADT | ||||
| NMEEMNMNLK | REAENLCSQR | GLVPNTDGQT | FEIAISNQMR | QHYDRIHETL | ||||
| IRKNGPARLL | SSSASTFEQS | IKAYHMMNKF | LGSFIDHVHK | EMDYFIKDKL | ||||
| LLERILGMEF | MEPMEKSIFY | NDEGYSFSSV | LYYGNEATLL | IFDLLFFCVV | ||||
| DLACQNFILA | SFLTYLQQEI | FRYIRNTVGQ | KNLASKTLVD | QRFLI |
Funkcija uredi
Protein kodiran ovim genom nalazi se u primarnom cilijumu i u plazmamembrani. Gen funkcionira u migraciji centriola na apikalnu membranu i formiranje primarne cilije. Za ovaj gen je pronađeno više varijanti transkripta koje kodiraju različite izoforme.[7]
Klinički značaj uredi
Defekti ovog gena su uzrok Meckelovog sindroma tipa 3 (MKS3),[6] nefronoftize[9][10] i Joubertovog sindroma tip 6 (JBTS6).[11]
Također pogledajte uredi
Reference uredi
- ^ a b c GRCh38: Ensembl release 89: ENSG00000164953 - Ensembl, maj 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000049488 - Ensembl, maj 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.
- ^ 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".
- ^ "UniProt, Q5HYA8" (jezik: engleski). Pristupljeno 22. 9. 2021.
- ^ Boichis H, Passwell J, David R, Miller H (januar 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 (oktobar 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 (januar 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.
Dopunska literatura uredi
- 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.