2024-05-08 11:45:39, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001164296 14893 bp mRNA linear ROD 31-DEC-2022 DEFINITION Rattus norvegicus plectin (Plec), transcript variant 1, mRNA. ACCESSION NM_001164296 VERSION NM_001164296.2 KEYWORDS RefSeq. SOURCE Rattus norvegicus (Norway rat) ORGANISM Rattus norvegicus Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus. REFERENCE 1 (bases 1 to 14893) AUTHORS Ni Y, Wang X, Yin X, Li Y, Liu X, Wang H, Liu X, Zhang J, Gao H, Shi B and Zhao S. TITLE Plectin protects podocytes from adriamycin-induced apoptosis and F-actin cytoskeletal disruption through the integrin alpha6beta4/FAK/p38 MAPK pathway JOURNAL J Cell Mol Med 22 (11), 5450-5467 (2018) PUBMED 30187999 REMARK GeneRIF: these findings indicated that plectin protects podocytes from ADR-induced apoptosis and F-actin cytoskeletal disruption by inhibiting integrin alpha6beta4/FAK/p38 pathway activation and that plectin may be a therapeutic target for podocyte injury-related glomerular diseases. REFERENCE 2 (bases 1 to 14893) AUTHORS Guo Z, Neilson LJ, Zhong H, Murray PS, Zanivan S and Zaidel-Bar R. TITLE E-cadherin interactome complexity and robustness resolved by quantitative proteomics JOURNAL Sci Signal 7 (354), rs7 (2014) PUBMED 25468996 REMARK Publication Status: Online-Only REFERENCE 3 (bases 1 to 14893) AUTHORS Zanivan S, Maione F, Hein MY, Hernandez-Fernaud JR, Ostasiewicz P, Giraudo E and Mann M. TITLE SILAC-based proteomics of human primary endothelial cell morphogenesis unveils tumor angiogenic markers JOURNAL Mol Cell Proteomics 12 (12), 3599-3611 (2013) PUBMED 23979707 REFERENCE 4 (bases 1 to 14893) AUTHORS Rezniczek GA, Walko G and Wiche G. TITLE Plectin gene defects lead to various forms of epidermolysis bullosa simplex JOURNAL Dermatol Clin 28 (1), 33-41 (2010) PUBMED 19945614 REMARK Review article Erratum:[Dermatol Clin. 2010 Apr;28(2):439-41] REFERENCE 5 (bases 1 to 14893) AUTHORS Zhang T, Haws P and Wu Q. TITLE Multiple variable first exons: a mechanism for cell- and tissue-specific gene regulation JOURNAL Genome Res 14 (1), 79-89 (2004) PUBMED 14672974 REFERENCE 6 (bases 1 to 14893) AUTHORS Rezniczek GA, Abrahamsberg C, Fuchs P, Spazierer D and Wiche G. TITLE Plectin 5'-transcript diversity: short alternative sequences determine stability of gene products, initiation of translation and subcellular localization of isoforms JOURNAL Hum Mol Genet 12 (23), 3181-3194 (2003) PUBMED 14559777 REFERENCE 7 (bases 1 to 14893) AUTHORS Fuchs P, Zorer M, Rezniczek GA, Spazierer D, Oehler S, Castanon MJ, Hauptmann R and Wiche G. TITLE Unusual 5' transcript complexity of plectin isoforms: novel tissue-specific exons modulate actin binding activity JOURNAL Hum Mol Genet 8 (13), 2461-2472 (1999) PUBMED 10556294 REFERENCE 8 (bases 1 to 14893) AUTHORS Elliott CE, Becker B, Oehler S, Castanon MJ, Hauptmann R and Wiche G. TITLE Plectin transcript diversity: identification and tissue distribution of variants with distinct first coding exons and rodless isoforms JOURNAL Genomics 42 (1), 115-125 (1997) PUBMED 9177781 REFERENCE 9 (bases 1 to 14893) AUTHORS Liu CG, Maercker C, Castanon MJ, Hauptmann R and Wiche G. TITLE Human plectin: organization of the gene, sequence analysis, and chromosome localization (8q24) JOURNAL Proc Natl Acad Sci U S A 93 (9), 4278-4283 (1996) PUBMED 8633055 REFERENCE 10 (bases 1 to 14893) AUTHORS Wiche G, Becker B, Luber K, Weitzer G, Castanon MJ, Hauptmann R, Stratowa C and Stewart M. TITLE Cloning and sequencing of rat plectin indicates a 466-kD polypeptide chain with a three-domain structure based on a central alpha-helical coiled coil JOURNAL J Cell Biol 114 (1), 83-99 (1991) PUBMED 2050743 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff in collaboration with Gunther Rezniczek, Gerhard Wiche. The reference sequence was derived from JACYVU010000186.1. On Feb 10, 2021 this sequence version replaced NM_001164296.1. Summary: Plectin is a prominent member of an important family of structurally and in part functionally related proteins, termed plakins or cytolinkers, that are capable of interlinking different elements of the cytoskeleton. Plakins, with their multi-domain structure and enormous size, not only play crucial roles in maintaining cell and tissue integrity and orchestrating dynamic changes in cytoarchitecture and cell shape, but also serve as scaffolding platforms for the assembly, positioning, and regulation of signaling complexes (for reviews see PMID: 9701547, 11854008, and 17499243). Plectin is expressed as several protein isoforms in a wide range of cell types and tissues from a single gene located on chromosome 8 in humans (PMID: 8633055, 8698233). Until 2010, this locus was named plectin 1 (symbol PLEC1 in human; Plec1 in mouse and rat) and the gene product had been referred to as 'hemidesmosomal protein 1' or 'plectin 1, intermediate filament binding 500kDa'. These names were replaced by plectin. The plectin gene locus in mouse on chromosome 15 has been analyzed in detail (PMID: 10556294, 14559777), revealing a genomic exon-intron organization with well over 40 exons spanning over 62 kb and an unusual 5' transcript complexity of plectin isoforms. Eleven exons (1-1j) have been identified that alternatively splice directly into a common exon 2 which is the first exon to encode plectin's highly conserved actin binding domain (ABD). Three additional exons (-1, 0a, and 0) splice into an alternative first coding exon (1c), and two additional exons (2alpha and 3alpha) are optionally spliced within the exons encoding the acting binding domain (exons 2-8). Analysis of the human locus has identified eight of the eleven alternative 5' exons found in mouse and rat (PMID: 14672974); exons 1i, 1j and 1h have not been confirmed in human. Furthermore, isoforms lacking the central rod domain encoded by exon 31 have been detected in mouse (PMID:10556294), rat (PMID: 9177781), and human (PMID: 11441066, 10780662, 20052759). The short alternative amino-terminal sequences encoded by the different first exons direct the targeting of the various isoforms to distinct subcellular locations (PMID: 14559777). As the expression of specific plectin isoforms was found to be dependent on cell type (tissue) and stage of development (PMID: 10556294, 12542521, 17389230) it appears that each cell type (tissue) contains a unique set (proportion and composition) of plectin isoforms, as if custom-made for specific requirements of the particular cells. Concordantly, individual isoforms were found to carry out distinct and specific functions (PMID: 14559777, 12542521, 18541706). In 1996, a number of groups reported that patients suffering from epidermolysis bullosa simplex with muscular dystrophy (EBS-MD) lacked plectin expression in skin and muscle tissues due to defects in the plectin gene (PMID: 8698233, 8941634, 8636409, 8894687, 8696340). Two other subtypes of plectin-related EBS have been described: EBS-pyloric atresia (PA) and EBS-Ogna. For reviews of plectin-related diseases see PMID: 15810881, 19945614. Mutations in the plectin gene related to human diseases should be named based on the position in NM_000445 (human variant 1, isoform 1c), unless the mutation is located within one of the other alternative first exons, in which case the position in the respective Reference Sequence should be used. [provided by RefSeq, Aug 2011]. Transcript Variant: This variant (1) contains the 5'-most coding exon (exon 1c) and encodes isoform 1c. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## RNAseq introns :: mixed/partial sample support SAMD00132261, SAMD00132262 [ECO:0000350] ##Evidence-Data-END## ##RefSeq-Attributes-START## gene product(s) localized to mito. :: PMID: 18541706, 17389230 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-205 JACYVU010000186.1 1189949-1190153 c 206-267 JACYVU010000186.1 1154007-1154068 c 268-357 JACYVU010000186.1 1153608-1153697 c 358-435 JACYVU010000186.1 1152740-1152817 c 436-528 JACYVU010000186.1 1152541-1152633 c 529-695 JACYVU010000186.1 1151539-1151705 c 696-811 JACYVU010000186.1 1150779-1150894 c 812-918 JACYVU010000186.1 1150601-1150707 c 919-1038 JACYVU010000186.1 1150388-1150507 c 1039-1134 JACYVU010000186.1 1150220-1150315 c 1135-1262 JACYVU010000186.1 1149844-1149971 c 1263-1356 JACYVU010000186.1 1149483-1149576 c 1357-1511 JACYVU010000186.1 1148624-1148778 c 1512-1821 JACYVU010000186.1 1148207-1148516 c 1822-1899 JACYVU010000186.1 1148046-1148123 c 1900-2061 JACYVU010000186.1 1147811-1147972 c 2062-2166 JACYVU010000186.1 1147533-1147637 c 2167-2262 JACYVU010000186.1 1147327-1147422 c 2263-2388 JACYVU010000186.1 1146987-1147112 c 2389-2541 JACYVU010000186.1 1145996-1146148 c 2542-2696 JACYVU010000186.1 1145747-1145901 c 2697-2823 JACYVU010000186.1 1145528-1145654 c 2824-3007 JACYVU010000186.1 1145241-1145424 c 3008-3165 JACYVU010000186.1 1145003-1145160 c 3166-3344 JACYVU010000186.1 1144733-1144911 c 3345-3483 JACYVU010000186.1 1143473-1143611 c 3484-3840 JACYVU010000186.1 1143029-1143385 c 3841-3924 JACYVU010000186.1 1142873-1142956 c 3925-4029 JACYVU010000186.1 1142597-1142701 c 4030-4128 JACYVU010000186.1 1142407-1142505 c 4129-7509 JACYVU010000186.1 1138026-1141406 c 7510-14893 JACYVU010000186.1 1130507-1137890 c FEATURES Location/Qualifiers source 1..14893 /organism="Rattus norvegicus" /mol_type="mRNA" /strain="BN" /db_xref="taxon:10116" /chromosome="7" /map="7q34" gene 1..14893 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="plectin" /db_xref="GeneID:64204" /db_xref="RGD:621649" exon 1..205 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" CDS 7..13728 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="isoform 1c is encoded by transcript variant 1; plectin 1" /codon_start=1 /product="plectin isoform 1c" /protein_id="NP_001157768.1" /db_xref="GeneID:64204" /db_xref="RGD:621649" /translation="
MSGEDSEVRPVAVAEGSSNGSSGSPSPGDTLPWNLGKTQRSRRSGGGSVGNGSVLDPAERAVIRIADERDRVQKKTFTKWVNKHLIKAQRHISDLYEDLRDGHNLISLLEVLSGDSLPREKGRMRFHKLQNVQIALDYLRHRQVKLVNIRNDDIADGNPKLTLGLIWTIILHFQISDIQVSGQSEDMTAKEKLLLWSQRMVEGYQGLRCDNFTTSWRDGRLFNAIIHRHKPMLIDMNKVYRQTNLENLDQAFSVAERDLGVTRLLDPEDVDVPQPDEKSIITYVSSLYDAMPRVPGAQDGVRANELQLRWQEYRELVLLLLQWIRHHTAAFEERKFPSSFEEIEILWCQFLKFKETELPAKEADKNRSKGIYQSLEGAVQAGQLKIPPGYHPLDVEKEWGKLHVAILEREKQLRSEFERLECLQRIVSKLQMEAGLCEEQLNQADSLLQSDIRLLASGKAAQRAGEVERDLDKADGMIRLLFNDVQTLKDGRHPQGEQMYRRVYRLHERLVAIRTEYNLRLKAGVGAPVTQVTLQSTQRRPELEDSTLRYLHDLLAWVEENQRRIDGAEWGVDLPSVEAQLGSHRGMHQSIEEFRAKIERARNDESQLSPATRGAYRDCLGRLDLQYAKLLNSSKARLRSLESLHGFVAAATKELMWLNEKEEEEVGFDWSDRNTNMAAKKESYSALMRELEMKEKKIKEIQNTGDRLLREDHPARPTVESFQAALQTQWSWMLQLCCCIEAHLKENTAYFQFFSDVREAEEQLQKLQETLRRKYSCDRSITVTRLEDLLQDAQDEKEQLNEYKGHLSGLAKRAKAIVQLKPRNPAHPVRGHVPLLAVCDYKQVEVTVHKGDQCQLVGPAQPFHWKVLGGSSSEAAVPSVCFLVPPPNQEAQEAVARLEAQHQALVTLWHQLHVDMKSLLAWQSLNRDIQLIRSWSLVTFRTLKPEEQRQALRNLELHYQAFLRDSQDAGGFGPEDRLVAEREYGSCSRHYQQLLQSLEQGEQEESRCQRCISELKDIRLQLEACETRTVHRLRLPLDKDPARECAQRIAEQQKAQAEVEGLGKGVARLSAEAEKVLALPEPSPAAPTLRSELELTLGKLEQVRSLSAIYLEKLKTISLVIRSTQGAEEVLKTHEEHLKEAQAVPATLQELEVTKASLKKLRAQAEAQQPVFNTLRDELRGAQEVGERLQQRHGERDVEVERWRERVTQLLERWQAVLAQTDVRQRELEQLGRQLRYYRESADPLSSWLQDAKSRQEQIQAVPIANSQAAREQLRQEKALLEEIERHGEKVEECQKFAKQYINAIKDYELQLITYKAQLEPVASPAKKPKVQSGSESVIQEYVDLRTRYSELTTLTSQYIKFISETLRRMEEEERLAEQQRAEERERLAEVEAALEKQRQLAEAHAQAKAQAELEARELQRRMQEEVTRREEAAVDAQQQKRSIQEELQHLRQSSEAEIQAKAQQVEAAERSRMRIEEEIRVVRLQLETTERQRGGAEDELQALRARAEEAEAQKRQAQEEAERLRRQVQDESQRKRQAEAELALRVKAEAEAAREKQRALQALDELKLQAEEAERRLRQAEAERARQVQVALETAQRSAEVELQSKRASFAEKTAQLERTLQEEHVTVTQLREEAERRAQQQAEAERAREEAERELERWQLKANEALRLRLQAEEVAQQKSLAQADAEKQKEEAEREARRRGKAEEQAVRQRELAEQELEKQRQLAEGTAQQRLAAEQELIRLRAETEQGEQQRQLLEEELARLQHEATAATQKRQELEAELAKVRAEMEVLLASKARAEEESRSTSEKSKQRLEAEAGRFRELAEEAARLRALAEEAKRQRQLAEEDAARQRAEAERVLTEKLAAISEATRLKTEAEIALKEKEAENERLRRLAEDEAFQRRRLEEQAAQHKADIEERLAQLRKASESELERQKGLVEDTLRQRRQVEEEIMALKASFEKAAAGKAELELELGRIRSNAEDTMRSKELAEQEAARQRQLAAEEEQRRREAEERVQRSLAAEEEAARQRKVALEEVERLKAKVEEARRLRERAEQESARQLQLAQEAAQKRLQAEEKAHAFVVQQREEELQQTLQQEQNMLERLRSEAEAARRAAEEAEEAREQAEREAAQSRKQVEEAERLKQSAEEQAQAQAQAQAAAEKLRKEAEQEAARRAQAEQAALKQKQAADAEMEKHKKFAEQTLRQKAQVEQELTTLRLQLEETDHQKSILDEELQRLKAEVTEAARQRSQVEEELFSVRVQMEELGKLKARIEAENRALILRDKDNTQRFLEEEAEKMKQVAEEAARLSVAAQEAARLRQLAEEDLAQQRALAEKMLKEKMQAVQEATRLKAEAELLQQQKELAQEQARRLQEDKEQMAQQLVEETQGFQRTLEAERQRQLEMSAEAERLKLRMAEMSRAQARAEEDAQRFRKQAEEIGEKLHRTELATQEKVTLVQTLEIQRQQSDQDAERLREAIAELEREKEKLKQEAKLLQLKSEEMQTVQQEQILQETQALQKSFLSEKDSLLQRERFIEQEKAKLEQLFQDEVAKAKQLQEEQQRQQQQMEQEKQELVASMEEARRRQREAEEGVRRKQEELQRLEQQRQQQEKLLAEENQRLRERLQRLEEEHRAALAHSEEIATSQAAATKALPNGRDALDGPSMEAEPEYTFEGLRQKVPAQQLQEAGILSMEELQRLTQGHTTVAELTQREDVHRYLKGGSSIAGLLLKPTNEKLSVYTALQRQLLSPGTALILLEAQAASGFLLDPVRNRRLTVNEAVKEGVVGPELHHKLLSAERAVTGYKDPYTGEQISLFQAMKKDLIVRDHGIRLLEAQIATGGIIDPVHSHRVPVDVAYQRGYFDEEMNRVLADPSDDTKGFFDPNTHENLTYLQLLERCVEDPETGLRLLPLTDKAAKGGELVYTDTEARDVFEKATVSAPFGKFQGKTVTIWEIINSEYFTAEQRRDLLRQFRTGRITVEKIIKIVITVVEEHERKGQLCFEGLRALVPAAELLDSGVISHEVYQQLQRGERSVREVAEADEVRQALRGTSVIAGVWLEEAGQKLSIYEALRRDLLQPEVAVALLEAQAGTGHIIDPATSARLTVDEAVRAGLVGPEMHEKLLSAEKAVTGYRDPYSGQSVSLFQALKKGLIPREQGLRLLDAQLSTGGIVDPSKSHRVPLDVAYARGYLDKETNRALTSPRDDARVYLDPSTREPVTYSQLQQRCRSDQLTGLSLLPLSEKAVRARQEEVYSELQARETLEKAKVEVPVGGFKGRALTVWELISSEYFTEEQRQELLRQFRTGKVTVEKVIKILITIVEEVETQRQERLSFSGLRAPVPASELLASKILSRTQFEQLKDGKTSVKDLSEVGSVRTLLQGSGCLAGIYLEDSKEKVTIYEAMRRGLLRPSTATLLLEAQAATGFLVDPVRNQRLYVHEAVKAGVVGPELHEKLLSAEKAVTGYKDPYSGSTISLFQAMKKGLVLRDHAIRLLEAQIATGGIIDPVHSHRLPVDVAYQRGYFDEEMNRVLADPSDDTKGFFDPNTHENLTYLQLLERCVEDPETGLRLLPLRGAEKTEVVETTQVYTEEETRRAFEETQIDIPGGGSHGGSSMSLWEVMQSDMIPEDQRARLMADFQAGRVTKERMIIIIIEIIEKTEIIRQQNLASYDYVRRRLTAEDLYEARIISLETYNLFREGTKSLREVLEMESAWRYLYGTGSVAGVYLPGSRQTLTIYQALKKGLLSAEVARLLLEAQAATGFLLDPVKGERLTVDEAVRKGLVGPELHDRLLSAERAVTGYRDPYTEQPISLFQAMKKELIPAEEALRLLDAQLATGGIVDPRLGFHLPLEVAYQRGYLNKDTHDQLSEPSEVRSYVDPSTDERLSYTQLLKRCRRDDNSGQMLLPLSDARKLTFRGLRKQITVEELVRSQVMDEATALQLQEGLTSIEEVTKNLQKFLEGTSCIAGVFVDATKERLSVYQAMKKGIIRPGTAFELLEAQAATGYVIDPIKGLKLTVEEAVRMGIVGPEFKDKLLSAERAVTGYKDPYSGKLISLFQAMKKGLILKDHGIRLLEAQIATGGIIDPEESHRLPVEVAYKRGLFDEEMNEILTDPSDDTKGFFDPNTEENLTYLQLMERCITDPQTGLCLLPLKEKKRERKTSSKSSVRKRRVVIVDPETGKEMSVYEAYRKGLIDHQTYLELSEQECEWEEITISSSDGVVKSMIIDRRSGRQYDIDDAITKNLIDRSALDQYRAGTLSITEFADMLSGNAGGFRSRSSSVGSSSSYPISSAVPRTQLASWSDPTEETGPVAGILDTETLEKVSITEAMHRNLVDNITGQRLLEAQACTGGIIDPSTGERFPVTEAVNKGLVDKIMVDRINLAQKAFCGFEDPRTKTKMSAAQALKKGWLYYEAGQRFLEVQYLTGGLIEPDTPGRVSLDEALQRGTVDARTAQKLRDVSAYSKYLTCPKTKLKISYKDALDRSMVEEGTGLRLLEAAAQSSKGYYSPYSVSGSGSTAGSRTGSRTGSRAGSRRGSFDATGSGFSMTFSSSSYSSSGYGRRYASGPSASLGGPESAVA"
misc_feature 214..528 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="first calponin homology (CH) domain found in the plectin/dystonin/MACF1 family; Region: CH_PLEC-like_rpt1; cd21188" /db_xref="CDD:409037" misc_feature order(223..225,235..237,385..387,391..396,403..408, 412..414,439..465,478..480,484..489,493..498,505..510, 517..519) /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="putative actin binding site [polypeptide binding]; other site" /db_xref="CDD:409037" misc_feature 565..882 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="second calponin homology (CH) domain found in plectin and similar proteins; Region: CH_PLEC_rpt2; cd21238" /db_xref="CDD:409087" misc_feature order(571..573,583..585,733..735,739..744,751..756, 760..762,787..813,832..834,838..843,847..852,859..864, 871..873) /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="putative actin binding site [polypeptide binding]; other site" /db_xref="CDD:409087" misc_feature order(655..657,664..666,724..735,739..744) /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="polypeptide substrate binding site [polypeptide binding]; other site" /db_xref="CDD:409087" misc_feature 1936..2472 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Spectrin repeats, found in several proteins involved in cytoskeletal structure; family members include spectrin, alpha-actinin and dystrophin; the spectrin repeat forms a three helix bundle with the second helix interrupted by proline in some sequences; Region: SPEC; cd00176" /db_xref="CDD:238103" misc_feature 2245..2262 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="linker region [active]" /db_xref="CDD:238103" misc_feature 2461..2661 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="SH3 domain; Region: SH3_10; pfam17902" /db_xref="CDD:407754" misc_feature 2764..2997 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Spectrin like domain; Region: Spectrin_like; pfam18373" /db_xref="CDD:436447" misc_feature <3160..4770 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="DNA repair exonuclease SbcCD ATPase subunit [Replication, recombination and repair]; Region: SbcC; COG0419" /db_xref="CDD:223496" misc_feature <4117..6237 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="MAEBL; Provisional; Region: PTZ00121" /db_xref="CDD:173412" misc_feature <5248..7791 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="MAEBL; Provisional; Region: PTZ00121" /db_xref="CDD:173412" misc_feature 8155..8271 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 8269..8385 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 8380..8490 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: PLEC; smart00250" /db_xref="CDD:197605" misc_feature 8497..8613 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 9133..9246 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: PLEC; smart00250" /db_xref="CDD:197605" misc_feature 9253..9369 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 9364..9474 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: PLEC; smart00250" /db_xref="CDD:197605" misc_feature 9481..9597 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 10132..10248 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 10246..10362 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 10357..10452 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: PLEC; smart00250" /db_xref="CDD:197605" misc_feature 10474..10590 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 11134..11244 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: PLEC; smart00250" /db_xref="CDD:197605" misc_feature 11251..11367 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 11362..11472 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: PLEC; smart00250" /db_xref="CDD:197605" misc_feature 11479..11595 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 11860..11973 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: PLEC; smart00250" /db_xref="CDD:197605" misc_feature 11980..12096 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 12208..12324 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature <12511..12597 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 12907..13008 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: PLEC; smart00250" /db_xref="CDD:197605" misc_feature 13015..13131 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" misc_feature 13243..13359 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /note="Plectin repeat; Region: Plectin; pfam00681" /db_xref="CDD:425816" exon 206..267 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 268..357 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 358..435 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 436..528 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 529..695 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 696..811 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 812..918 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 919..1038 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 1039..1134 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 1135..1262 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 1263..1356 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 1357..1511 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 1512..1821 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 1822..1899 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 1900..2061 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 2062..2166 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 2167..2262 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 2263..2388 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 2389..2541 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 2542..2696 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 2697..2823 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 2824..3007 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 3008..3165 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 3166..3344 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 3345..3483 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 3484..3840 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 3841..3924 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 3925..4029 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 4030..4128 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 4129..7509 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" exon 7510..14893 /gene="Plec" /gene_synonym="Pcn; Plec1; Pltn" /inference="alignment:Splign:2.1.0" ORIGIN
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//
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Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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