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2025-05-09 17:27:12, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_133379 18236 bp mRNA linear PRI 08-JUL-2013
DEFINITION Homo sapiens titin (TTN), transcript variant novex, mRNA.
ACCESSION NM_133379
VERSION NM_133379.4 GI:428980889
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 18236)
AUTHORS LeWinter,M.M. and Granzier,H.L.
TITLE Titin is a major human disease gene
JOURNAL Circulation 127 (8), 938-944 (2013)
PUBMED 23439446
REMARK GeneRIF: [review] Signal pathways of titin isoforms are described
in a major human cardiovascular disease.
Review article
REFERENCE 2 (bases 1 to 18236)
AUTHORS Hamdani,N., Krysiak,J., Kreusser,M.M., Neef,S., Dos Remedios,C.G.,
Maier,L.S., Kruger,M., Backs,J. and Linke,W.A.
TITLE Crucial role for Ca2(+)/calmodulin-dependent protein kinase-II in
regulating diastolic stress of normal and failing hearts via titin
phosphorylation
JOURNAL Circ. Res. 112 (4), 664-674 (2013)
PUBMED 23283722
REMARK GeneRIF: Human end-stage failing hearts revealed higher CaMKII
expression/activity & phosphorylation at PEVK/titin N2B-unique
sequence sites than donor hearts. Deranged CaMKII-dependent titin
phosphorylation contributes to altered diastolic stress.
REFERENCE 3 (bases 1 to 18236)
AUTHORS Somkuti,J., Martonfalvi,Z., Kellermayer,M.S. and Smeller,L.
TITLE Different pressure-temperature behavior of the structured and
unstructured regions of titin
JOURNAL Biochim. Biophys. Acta 1834 (1), 112-118 (2013)
PUBMED 23063534
REMARK GeneRIF: Different pressure-temperature behavior of the structured
and unstructured regions of titin.
REFERENCE 4 (bases 1 to 18236)
AUTHORS Tskhovrebova,L. and Trinick,J.
TITLE Roles of titin in the structure and elasticity of the sarcomere
JOURNAL J. Biomed. Biotechnol. 2010, 612482 (2010)
PUBMED 20625501
REMARK GeneRIF: Recent titin data is reviewed and its implications for
sarcomere architecture and elasticity, are discussed.
Review article
REFERENCE 5 (bases 1 to 18236)
AUTHORS Labeit,S., Lahmers,S., Burkart,C., Fong,C., McNabb,M., Witt,S.,
Witt,C., Labeit,D. and Granzier,H.
TITLE Expression of distinct classes of titin isoforms in striated and
smooth muscles by alternative splicing, and their conserved
interaction with filamins
JOURNAL J. Mol. Biol. 362 (4), 664-681 (2006)
PUBMED 16949617
REMARK GeneRIF: This suggests that the titin Z2-Zis1 domain can link
filamins and alpha-actinin together in the periphery of the
Z-line/dense bodies in a fashion that is conserved in smooth and
striated muscles.
REFERENCE 6 (bases 1 to 18236)
AUTHORS Bang,M.L., Centner,T., Fornoff,F., Geach,A.J., Gotthardt,M.,
McNabb,M., Witt,C.C., Labeit,D., Gregorio,C.C., Granzier,H. and
Labeit,S.
TITLE The complete gene sequence of titin, expression of an unusual
approximately 700-kDa titin isoform, and its interaction with
obscurin identify a novel Z-line to I-band linking system
JOURNAL Circ. Res. 89 (11), 1065-1072 (2001)
PUBMED 11717165
REFERENCE 7 (bases 1 to 18236)
AUTHORS Freiburg,A., Trombitas,K., Hell,W., Cazorla,O., Fougerousse,F.,
Centner,T., Kolmerer,B., Witt,C., Beckmann,J.S., Gregorio,C.C.,
Granzier,H. and Labeit,S.
TITLE Series of exon-skipping events in the elastic spring region of
titin as the structural basis for myofibrillar elastic diversity
JOURNAL Circ. Res. 86 (11), 1114-1121 (2000)
PUBMED 10850961
REFERENCE 8 (bases 1 to 18236)
AUTHORS Labeit,S. and Kolmerer,B.
TITLE Titins: giant proteins in charge of muscle ultrastructure and
elasticity
JOURNAL Science 270 (5234), 293-296 (1995)
PUBMED 7569978
REFERENCE 9 (bases 1 to 18236)
AUTHORS Furst,D.O., Vinkemeier,U. and Weber,K.
TITLE Mammalian skeletal muscle C-protein: purification from bovine
muscle, binding to titin and the characterization of a full-length
human cDNA
JOURNAL J. Cell. Sci. 102 (PT 4), 769-778 (1992)
PUBMED 1429890
REFERENCE 10 (bases 1 to 18236)
AUTHORS Labeit,S., Gautel,M., Lakey,A. and Trinick,J.
TITLE Towards a molecular understanding of titin
JOURNAL EMBO J. 11 (5), 1711-1716 (1992)
PUBMED 1582406
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AC023270.7 and BX537998.1.
This sequence is a reference standard in the RefSeqGene project.
On Dec 8, 2012 this sequence version replaced gi:291045226.
Summary: This gene encodes a large abundant protein of striated
muscle. The product of this gene is divided into two regions, a
N-terminal I-band and a C-terminal A-band. The I-band, which is the
elastic part of the molecule, contains two regions of tandem
immunoglobulin domains on either side of a PEVK region that is rich
in proline, glutamate, valine and lysine. The A-band, which is
thought to act as a protein-ruler, contains a mixture of
immunoglobulin and fibronectin repeats, and possesses kinase
activity. An N-terminal Z-disc region and a C-terminal M-line
region bind to the Z-line and M-line of the sarcomere,
respectively, so that a single titin molecule spans half the length
of a sarcomere. Titin also contains binding sites for muscle
associated proteins so it serves as an adhesion template for the
assembly of contractile machinery in muscle cells. It has also been
identified as a structural protein for chromosomes. Alternative
splicing of this gene results in multiple transcript variants.
Considerable variability exists in the I-band, the M-line and the
Z-disc regions of titin. Variability in the I-band region
contributes to the differences in elasticity of different titin
isoforms and, therefore, to the differences in elasticity of
different muscle types. Mutations in this gene are associated with
familial hypertrophic cardiomyopathy 9, and autoantibodies to titin
are produced in patients with the autoimmune disease scleroderma.
[provided by RefSeq, Feb 2012].
Transcript Variant: This variant (novex-3) is the shortest
transcript and encodes the shortest isoform (novex-3). Its last
exon is nearly 8 kb and is not found in the other variants. The
novex-3 isoform, which is found in all striated muscle, lacks the
PEVK region and has a C-terminal truncation compared to longer
isoforms. This variant is supported by data in PMID:11717165.
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
CCDS Note: This CCDS ID represents the TTN novex-3 isoform, which
has a novel and shorter C-terminus compared to longer isoforms.
This isoform is supported by data in PMID:11717165, but it should
be noted that the evidence for the transcript is partial on the 5'
end, and thus this CCDS representation has an inferred exon
combination.
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 ERS025082, ERS025083
[ECO:0000350]
##Evidence-Data-END##
##RefSeq-Attributes-START##
inferred exon combination :: PMID: 11717165
##RefSeq-Attributes-END##
COMPLETENESS: full length.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-212 AC023270.7 65697-65908 c
213-316 AC023270.7 63037-63140 c
317-520 AC023270.7 60623-60826 c
521-808 AC023270.7 58880-59167 c
809-894 AC023270.7 58310-58395 c
895-1139 AC023270.7 57972-58216 c
1140-1470 AC023270.7 53407-53737 c
1471-1623 AC023270.7 52884-53036 c
1624-1761 AC023270.7 51889-52026 c
1762-1887 AC023270.7 50557-50682 c
1888-2025 AC023270.7 49193-49330 c
2026-2163 AC023270.7 48463-48600 c
2164-2301 AC023270.7 47845-47982 c
2302-2595 AC023270.7 44333-44626 c
2596-2718 AC023270.7 44105-44227 c
2719-3000 AC023270.7 42555-42836 c
3001-3066 AC023270.7 42205-42270 c
3067-3325 AC023270.7 41291-41549 c
3326-3389 AC023270.7 41024-41087 c
3390-3605 AC023270.7 40697-40912 c
3606-3748 AC023270.7 39606-39748 c
3749-3954 AC023270.7 38485-38690 c
3955-4188 AC023270.7 37714-37947 c
4189-4433 AC023270.7 37359-37603 c
4434-4705 AC023270.7 36189-36460 c
4706-4870 AC023270.7 35905-36069 c
4871-5039 AC023270.7 35634-35802 c
5040-6733 AC023270.7 33841-35534 c
6734-7015 AC023270.7 33406-33687 c
7016-7282 AC023270.7 32692-32958 c
7283-7555 AC023270.7 32323-32595 c
7556-7819 AC023270.7 31947-32210 c
7820-8080 AC023270.7 31594-31854 c
8081-8341 AC023270.7 29696-29956 c
8342-8605 AC023270.7 28897-29160 c
8606-8866 AC023270.7 28545-28805 c
8867-9127 AC023270.7 28164-28424 c
9128-9388 AC023270.7 27158-27418 c
9389-9530 AC023270.7 26499-26640 c
9531-9696 AC023270.7 26244-26409 c
9697-9928 AC023270.7 24866-25097 c
9929-10213 AC023270.7 23012-23296 c
10214-10339 AC023270.7 22662-22787 c
10340-10528 AC023270.7 17469-17657 c
10529-10585 AC023270.7 11609-11665 c
10586-16531 AC023270.7 4579-10524 c
16532-18236 BX537998.1 3284-4988
FEATURES Location/Qualifiers
source 1..18236
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="2"
/map="2q31"
gene 1..18236
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="titin"
/db_xref="GeneID:7273"
/db_xref="HGNC:12403"
/db_xref="MIM:188840"
exon 1..212
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 85
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647840"
misc_feature 202..204
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="upstream in-frame stop codon"
exon 213..316
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
CDS 226..17040
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/EC_number="2.7.11.1"
/note="isoform novex-3 is encoded by transcript variant
novex; connectin; rhabdomyosarcoma antigen MU-RMS-40.14"
/codon_start=1
/product="titin isoform novex-3"
/protein_id="NP_596870.2"
/db_xref="GI:110349721"
/db_xref="CCDS:CCDS33337.1"
/db_xref="GeneID:7273"
/db_xref="HGNC:12403"
/db_xref="MIM:188840"
/translation="
MTTQAPTFTQPLQSVVVLEGSTATFEAHISGFPVPEVSWFRDGQVISTSTLPGVQISFSDGRAKLTIPAVTKANSGRYSLKATNGSGQATSTAELLVKAETAPPNFVQRLQSMTVRQGSQVRLQVRVTGIPTPVVKFYRDGAEIQSSLDFQISQEGDLYSLLIAEAYPEDSGTYSVNATNSVGRATSTAELLVQGEEEVPAKKTKTIVSTAQISESRQTRIEKKIEAHFDARSIATVEMVIDGAAGQQLPHKTPPRIPPKPKSRSPTPPSIAAKAQLARQQSPSPIRHSPSPVRHVRAPTPSPVRSVSPAARISTSPIRSVRSPLLMRKTQASTVATGPEVPPPWKQEGYVASSSEAEMRETTLTTSTQIRTEERWEGRYGVQEQVTISGAAGAAASVSASASYAAEAVATGAKEVKQDADKSAAVATVVAAVDMARVREPVISAVEQTAQRTTTTAVHIQPAQEQVRKEAEKTAVTKVVVAADKAKEQELKSRTKEVITTKQEQMHVTHEQIRKETEKTFVPKVVISAAKAKEQETRISEEITKKQKQVTQEAIRQETEITAASMVVVATAKSTKLETVPGAQEETTTQQDQMHLSYEKIMKETRKTVVPKVIVATPKVKEQDLVSRGREGITTKREQVQITQEKMRKEAEKTALSTIAVATAKAKEQETILRTRETMATRQEQIQVTHGKVDVGKKAEAVATVVAAVDQARVREPREPGHLEESYAQQTTLEYGYKERISAAKVAEPPQRPASEPHVVPKAVKPRVIQAPSETHIKTTDQKGMHISSQIKKTTDLTTERLVHVDKRPRTASPHFTVSKISVPKTEHGYEASIAGSAIATLQKELSATSSAQKITKSVKAPTVKPSETRVRAEPTPLPQFPFADTPDTYKSEAGVEVKKEVGVSITGTTVREERFEVLHGREAKVTETARVPAPVEIPVTPPTLVSGLKNVTVIEGESVTLECHISGYPSPTVTWYREDYQIESSIDFQITFQSGIARLMIREAFAEDSGRFTCSAVNEAGTVSTSCYLAVQVSEEFEKETTAVTEKFTTEEKRFVESRDVVMTDTSLTEEQAGPGEPAAPYFITKPVVQKLVEGGSVVFGCQVGGNPKPHVYWKKSGVPLTTGYRYKVSYNKQTGECKLVISMTFADDAGEYTIVVRNKHGETSASASLLEEADYELLMKSQQEMLYQTQVTAFVQEPKVGETAPGFVYSEYEKEYEKEQALIRKKMAKDTVVVRTYVEDQEFHISSFEERLIKEIEYRIIKTTLEELLEEDGEEKMAVDISESEAVESGFDSRIKNYRILEGMGVTFHCKMSGYPLPKIAWYKDGKRIKHGERYQMDFLQDGRASLRIPVVLPEDEGIYTAFASNIKGNAICSGKLYVEPAAPLGAPTYIPTLEPVSRIRSLSPRSVSRSPIRMSPARMSPARMSPARMSPARMSPGRRLEETDESQLERLYKPVFVLKPVSFKCLEGQTARFDLKVVGRPMPETFWFHDGQQIVNDYTHKVVIKEDGTQSLIIVPATPSDSGEWTVVAQNRAGRSSISVILTVEAVEHQVKPMFVEKLKNVNIKEGSRLEMKVRATGNPNPDIVWLKNSDIIVPHKYPKIRIEGTKGEAALKIDSTVSQDSAWYTATAINKAGRDTTRCKVNVEVEFAEPEPERKLIIPRGTYRAKEIAAPELEPLHLRYGQEQWEEGDLYDKEKQQKPFFKKKLTSLRLKRFGPAHFECRLTPIGDPTMVVEWLHDGKPLEAANRLRMINEFGYCSLDYGVAYSRDSGIITCRATNKYGTDHTSATLIVKDEKSLVEESQLPEGRKGLQRIEELERMAHEGALTGVTTDQKEKQKPDIVLYPEPVRVLEGETARFRCRVTGYPQPKVNWYLNGQLIRKSKRFRVRYDGIHYLDIVDCKSYDTGEVKVTAENPEGVIEHKVKLEIQQREDFRSVLRRAPEPRPEFHVHEPGKLQFEVQKVDRPVDTTETKEVVKLKRAERITHEKVPEESEELRSKFKRRTEEGYYEAITAVELKSRKKDESYEELLRKTKDELLHWTKELTEEEKKALAEEGKITIPTFKPDKIELSPSMEAPKIFERIQSQTVGQGSDAHFRVRVVGKPDPECEWYKNGVKIERSDRIYWYWPEDNVCELVIRDVTAEDSASIMVKAINIAGETSSHAFLLVQAKQLITFTQELQDVVAKEKDTMATFECETSEPFVKVKWYKDGMEVHEGDKYRMHSDRKVHFLSILTIDTSDAEDYSCVLVEDENVKTTAKLIVEGAVVEFVKELQDIEVPESYSGELECIVSPENIEGKWYHNDVELKSNGKYTITSRRGRQNLTVKDVTKEDQGEYSFVIDGKKTTCKLKMKPRPIAILQGLSDQKVCEGDIVQLEVKVSLESVEGVWMKDGQEVQPSDRVHIVIDKQSHMLLIEDMTKEDAGNYSFTIPALGLSTSGRVSVYSVDVITPLKDVNVIEGTKAVLECKVSVPDVTSVKWYLNDEQIKPDDRVQAIVKGTKQRLVINRTHASDEGPYKLIVGRVETNCNLSVEKIKIIRGLRDLTCTETQNVVFEVELSHSGIDVLWNFKDKEIKPSSKYKIEAHGKIYKLTVLNMMKDDEGKYTFYAGENMTSGKLTVAGGAISKPLTDQTVAESQEAVFECEVANPDSKGEWLRDGKHLPLTNNIRSESDGHKRRLIIAATKLDDIGEYTYKVATSKTSAKLKVEAVKIKKTLKNLTVTETQDAVFTVELTHPNVKGVQWIKNGVVLESNEKYAISVKGTIYSLRIKNCAIVDESVYGFRLGRLGASARLHVETVKIIKKPKDVTALENATVAFEVSVSHDTVPVKWFHKSVEIKPSDKHRLVSERKVHKLMLQNISPSDAGEYTAVVGQLECKAKLFVETLHITKTMKNIEVPETKTASFECEVSHFNVPSMWLKNGVEIEMSEKFKIVVQGKLHQLIIMNTSTEDSAEYTFVCGNDQVSATLTVTPIMITSMLKDINAEEKDTITFEVTVNYEGISYKWLKNGVEIKSTDKCQMRTKKLTHSLNIRNVHFGDAADYTFVAGKATSTATLYVEARHIEFRKHIKDIKVLEKKRAMFECEVSEPDITVQWMKDDQELQITDRIKIQKEKYVHRLLIPSTRMSDAGKYTVVAGGNVSTAKLFVEGRDVRIRSIKKEVQVIEKQRAVVEFEVNEDDVDAHWYKDGIEINFQVQERHKYVVERRIHRMFISETRQSDAGEYTFVAGRNRSSVTLYVNAPEPPQVLQELQPVTVQSGKPARFCAVISGRPQPKISWYKEEQLLSTGFKCKFLHDGQEYTLLLIEAFPEDAAVYTCEAKNDYGVATTSASLSVEVPEVVSPDQEMPVYPPAIITPLQDTVTSEGQPARFQCRVSGTDLKVSWYSKDKKIKPSRFFRMTQFEDTYQLEIAEAYPEDEGTYTFVASNAVGQVSSTANLSLEAPESILHERIEQEIEMEMKELFSEGESEHSERDTRDAFSDSEDIDHKSMAAKRYASRISSTSSWPEYFKPSFTQKLTFKYVLEGEPVVFTCRLIACPTPEMTWFHNNRPIPTGLRRIIKAESDLHHHSSSLEIKRVQDRDSGSYRLLAINSEGSAESTASLLVIQKGQDEKYLEFLKRAERTHENVEALVERGEDRIKVDLRFTGSPFNKKQDVEQKGMMRTIHFKTMSSAKKTDYMYDEEYLESKSDIRGWLNVGESFLDKETKVKLQRLREARKTLMEKKKLSLLDTSSEISSRTLRSEASDKDILFSREDMKIRSMSDLAESYKVDHSAESIVQNPHALSNQMDQNIESEELPTSFQTIVDEEIFQTEIRMSQEALVKESLPKDHLYGEILVNENTQARGQLEEIMANTTIGESSTYITNVCEKEEVYETPENVSQAITPHASESFGTLVNVEESEEIASERIKKDDLRELQLSASTRIDEFKTEQKEENMRFFENSFRKRPQRCPPSFLQEIESQEVYEGDSCNFVCHFQGYPQPIVTWYNNDMPIPRNQNFIIHSLENYSILTLSSVHHQNEGSITCVLFNQYGTVKTTSMLKVKAKQKHDVKAHKVPVFHDYLDEEEELALVFDQAKGAHPSMSQEGQTNLHLLKTNPPVPPSGDTELLSFPVEIQVTAATPIPEQDKESKEVFQTEELEPKAMPQDQVTQSPKHRFVFLSDITNEPPKMLQEMPKHARCREGDSIILECLISGEPQPVVTWFQNGVLLKQNQKFQFEEVNCSHQLYIKDVNSQDSGKYKCVAENNSGAVESVSDLTVEPVTYRENSQFENIGEIYGKYSRDQQLQDQGESVRAHFYDYPAGPFTPWTNVKEYSVRDYFQSLETIEQIDQKEQVRCIPSREKIPRFVHGASRTIKISKPIRAEFIQCQAEGKERHVSEKSKLHQAEGTVYPFVDDFSDVTIKKEIRNNFGKLGRSEKENVQECAQSDYLPNIHSERISDSYNTKDSSAIVYEESLGEEIHYPGKKVKHRIIEFEKLHVEKGVLEKRPTRTSIVNPPQKKIDDKAFSLKQRESRSSNLNANMYQAEKMSPNTESDSSNIAINLKLLSSQTHKEFDAQEREQQEKISLIDKPAISKRAEHESPITFDLKQFHTQIKHTDVKFQELDSGQPEEAYFKIQHPADTENIVFDLKQMYSHIGDPALEFQGQETREQQEIHYKEKIPSPETLQPDTHNISKSVQNNVFASQEISSSQELSNRTMVEKSSIDENSISLEKEVRHVQEQNLDILKTDLSLKSFSEEIYSESCALLPTSSADIEETDLSEKSCPLENGGRSSISHLKKAASEEKPLGVGEMEEECTLEPELAAFPKQDGGTQEYTDATLEDHRGDVQEADTLHRQLSLSQCFPLLMTEEQQNPGEQISTNIHASGEEKCYEEVQVQNEASFSTLEGEMIETSFSQNIPKLDEAHTTEAAESETSLTQYLLAAGKREVPETKDTRDQAKLVQSESITSMEVEEVTFNTVYEYYNQKQESLGRPLSPESDISIGVGSTTSEEISELDQFYTPPSSVEYFESPKSPDLYFNPSDITKQSSIHSGGETVERYSTPLGEVAERYSTPSEGEVGERYSTPPGETLERYSTPPGETLERYSTPPGETLERYSTPPGETLERYSTPPGETLERYSTPPGEALERYSIPTGGPNPTGTFKTYPSKIEREDGTPNEHFYTPTEERGSAYEIWRSDSFGTPNEAIEPKDNEMPPSFIEPLTKRKVYENTTLGFIVEVEGLPVPGVKWYRNKSLLEPDERIKMERVGNVCSLEISNIQKGEGGEYMCHAVNIIGEAKSFANVDIMPQEERVVALPPPVTHQHVMEFDLEHTTSSRTPSPQEIVLEVELSEKDVKEFEKQVKIVTVPEFTPDHKSMIVSLDVLPFNFVDPNMDSREGEDKELKIDLEVFEMPPRFIMPICDFKIPENSDAVFKCSVIGIPTPEVKWYKEYMCIEPDNIKYVISEEKGSHTLKIRNVCLSDSATYRCRAVNCVGEAICRGFLTMGDSEIFAVIAKKSKVTLSSLMEELVLKSNYTDSFFEFQVVEGPPRFIKGISDCYAPIGTAAYFQCLVRGSPRPTVYWYKDGKLVQGRRFTVEESGTGFHNLFITSLVKSDEGEYRCVATNKSGMAESFAALTLT
"
misc_feature 241..516
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 262..516
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin like; Region: IG_like; smart00410"
/db_xref="CDD:197708"
misc_feature 535..804
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 556..804
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin like; Region: IG_like; smart00410"
/db_xref="CDD:197708"
misc_feature 1753..1872
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Titin Z; Region: Titin_Z; pfam09042"
/db_xref="CDD:149937"
misc_feature 1879..2004
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Titin Z; Region: Titin_Z; pfam09042"
/db_xref="CDD:149937"
misc_feature 2017..2142
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Titin Z; Region: Titin_Z; pfam09042"
/db_xref="CDD:149937"
misc_feature 2155..2280
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Titin Z; Region: Titin_Z; pfam09042"
/db_xref="CDD:149937"
misc_feature 3052..3321
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 3103..3306
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 3469..3738
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 3520..3735
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 4102..4368
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 4117..4368
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 4594..4866
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 4660..4854
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 4891..5166
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 4912..5166
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin like; Region: IG_like; smart00410"
/db_xref="CDD:197708"
misc_feature <5389..5607
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cl11960"
/db_xref="CDD:213125"
misc_feature 5746..6012
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 5764..6012
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 6457..6729
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 6478..6729
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 6748..7011
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 6799..7005
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 7027..7281
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 7078..>7236
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 7330..7503
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin C-2 Type; Region: IGc2; smart00408"
/db_xref="CDD:197706"
misc_feature 7564..7815
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 7609..7782
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 7825..8076
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 8089..8337
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 8107..8337
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 8347..8601
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 8365..>8556
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 8611..8862
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 8626..8862
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 8872..9123
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 8890..9126
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin like; Region: IG_like; smart00410"
/db_xref="CDD:197708"
misc_feature 9136..9384
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 9151..9384
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 9400..9651
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 9418..9651
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin like; Region: IG_like; smart00410"
/db_xref="CDD:197708"
misc_feature <9760..9924
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 9982..10203
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 10009..10200
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 10258..10518
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 10279..10521
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 10735..11016
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 10786..11007
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 12055..12324
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 12109..12309
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin domain; Region: Ig; cd00096"
/db_xref="CDD:143165"
misc_feature 12697..12969
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 12718..12969
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin like; Region: IG_like; smart00410"
/db_xref="CDD:197708"
misc_feature 15772..16035
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 15805..16035
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 16363..16632
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 16402..16632
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin; Region: IG; smart00409"
/db_xref="CDD:197707"
misc_feature 16765..17031
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin I-set domain; Region: I-set;
pfam07679"
/db_xref="CDD:191810"
misc_feature 16795..17031
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/note="Immunoglobulin like; Region: IG_like; smart00410"
/db_xref="CDD:197708"
exon 317..520
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 381
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:72647842"
exon 521..808
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 767
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647843"
exon 809..894
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 889
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647844"
exon 895..1139
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 1140..1470
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 1195
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647845"
variation 1228
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647846"
exon 1471..1623
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 1624..1761
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 1672
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:34337578"
variation 1717
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647851"
exon 1762..1887
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 1888..2025
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 2026..2163
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 2164..2301
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 2298
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="t"
/db_xref="dbSNP:72647860"
exon 2302..2595
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 2596..2718
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 2657
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:35813871"
exon 2719..3000
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 2836
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="g"
/replace="t"
/db_xref="dbSNP:72647861"
variation 2989
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647862"
exon 3001..3066
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 3067..3325
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 3083
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="g"
/db_xref="dbSNP:72647865"
exon 3326..3389
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 3341
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647867"
variation 3358
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647868"
exon 3390..3605
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
STS 3537..3680
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/standard_name="D2S1574E"
/db_xref="UniSTS:150658"
exon 3606..3748
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 3634
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="g"
/db_xref="dbSNP:72647870"
exon 3749..3954
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 3955..4188
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 3984
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:2291308"
variation 4109
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:1552280"
exon 4189..4433
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 4209
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="c"
/db_xref="dbSNP:72647872"
exon 4434..4705
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 4471
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647875"
variation 4547
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="g"
/db_xref="dbSNP:72647876"
exon 4706..4870
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
STS 4760..4866
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/standard_name="A008T22"
/db_xref="UniSTS:24210"
variation 4855
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647877"
exon 4871..5039
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 5040..6733
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 5613
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647878"
STS 6331..6459
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/standard_name="D2S1524E"
/db_xref="UniSTS:45880"
variation 6473
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace=""
/replace="g"
/db_xref="dbSNP:72647879"
exon 6734..7015
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 6885
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647880"
variation 6998
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647881"
exon 7016..7282
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 7283..7555
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 7556..7819
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 7820..8080
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 8081..8341
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 8342..8605
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 8606..8866
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 8814
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647883"
exon 8867..9127
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 8912
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647884"
exon 9128..9388
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 9163
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647885"
variation 9375
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647886"
exon 9389..9530
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 9531..9696
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 9584
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647894"
exon 9697..9928
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 9929..10213
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 10214..10339
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 10340..10528
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 10529..10585
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
exon 10586..18220
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/inference="alignment:Splign:1.39.8"
variation 11231
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647896"
variation 12074
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647897"
variation 12341
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72647898"
variation 12749
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="c"
/db_xref="dbSNP:72647899"
variation 12869
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="t"
/db_xref="dbSNP:72647900"
variation 12941
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72647901"
variation 13348
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="g"
/replace="t"
/db_xref="dbSNP:72647902"
variation 13390
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72648903"
variation 13701
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72648904"
variation 13833
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72648905"
variation 14094
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="g"
/replace="t"
/db_xref="dbSNP:72648906"
variation 14969
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72648907"
variation 14979
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="g"
/replace="t"
/db_xref="dbSNP:72648908"
variation 15031
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="t"
/db_xref="dbSNP:72648909"
variation 15501
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72648910"
variation 15672
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="c"
/replace="t"
/db_xref="dbSNP:72648911"
variation 15859
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:72648912"
variation 16385
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72648913"
variation 16636
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72648914"
variation 16657
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72648915"
STS 16774..17386
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/standard_name="TTN_3879"
/db_xref="UniSTS:462604"
variation 17111
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="g"
/db_xref="dbSNP:72648916"
variation 17180
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="t"
/db_xref="dbSNP:3813240"
variation 17343
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
/replace="a"
/replace="c"
/db_xref="dbSNP:72648917"
polyA_site 18220
/gene="TTN"
/gene_synonym="CMD1G; CMH9; CMPD4; EOMFC; HMERF; LGMD2J;
MYLK5; TMD"
ORIGIN
gagcagtcgtgcattcccagcctcgcctcgggtgtagggattgcatagaaaagcaaaactacacagtcttgactgtgtagttttgtttttaggattagaggctcaccgattcatgtcggagatggtcagaaaaaccaactctccataggacgtcgtttcagaagcaaccttgggcttagtcccaccctttttaggcactcttgagaaatcagagtgcctagaaagatgacaactcaagcaccgacgtttacgcagccgttacaaagcgttgtggtactggagggtagtaccgcaacctttgaggctcacattagtggttttccagttcctgaggtgagctggtttagggatggccaggtgatttccacttccactctgcccggcgtgcagatctcctttagcgatggccgcgctaaactgacgatccccgccgtgactaaagccaacagtggacgatattccctgaaagccaccaatggatctggacaagcgactagtactgctgagcttctcgtgaaagctgagacagcaccacccaacttcgttcaacgactgcagagcatgaccgtgagacaaggaagccaagtgagactccaagtgagagtgactggaatccctacacctgtggtgaagttctaccgggatggagccgaaatccagagctcccttgatttccaaatttcacaagaaggcgacctctacagcttactgattgcagaagcataccctgaggactcagggacctattcagtaaatgccaccaatagcgttggaagagctacttcgactgctgaattactggttcaaggtgaagaagaagtacctgctaaaaagacaaagacaattgtttcgactgctcagatctcagaatcaagacaaacccgaattgaaaagaagattgaagcccactttgatgccagatcaattgcaacagttgagatggtcatagatggtgccgctgggcaacagctgccacataaaacacctcccaggattcctccgaagccaaagtcaagatccccaacaccaccgtctattgctgccaaagcacagctggctcggcagcagtccccatcgcccataagacactccccttccccggtcagacacgtgcgggcaccgaccccatctccggtcaggtccgtgtctccagcagcaagaatctccacatcccccatcaggtctgttaggtctccattgctcatgcgtaagactcaggcatccaccgtggccacaggtcctgaagtgcctcccccttggaagcaagagggctacgtggcctcctcatctgaggctgagatgagagagacaacgctgacaacctctactcagatcaggacagaagagagatgggaagggagatacggtgtccaggagcaagtgaccatcagtggtgctgcgggtgctgccgccagtgtgtcggccagtgctagctacgcagcagaggctgttgccactggtgctaaagaggtgaaacaagatgctgacaaaagtgcagctgttgcgactgttgttgctgccgttgatatggccagagtgagagaaccagtgatcagcgctgtagagcagactgctcagaggacaaccacgactgctgtgcacatccaacctgctcaagaacaggtaagaaaggaagcggagaagactgctgtaactaaggtagtagtggccgccgataaagccaaggaacaagaattaaaatcaagaaccaaagaagtaattaccacaaagcaagagcagatgcacgtaactcatgagcagataagaaaagaaactgaaaaaacatttgtaccaaaggtagtaatttccgcagctaaagccaaagaacaagaaactagaatttctgaagaaattactaagaaacagaaacaagtaactcaagaagcaataagacaggaaactgagataactgctgcatccatggtggtagttgccactgcaaagtccacaaaactagaaacagtcccgggagctcaagaagaaactaccacacaacaagatcaaatgcacctaagttatgaaaagataatgaaggaaactaggaaaacagttgtacctaaagtcatagttgccacacccaaagtcaaagaacaagatttagtatcaagaggtagagaaggcattactaccaaaagagaacaagtgcaaataactcaggagaagatgagaaaggaagccgagaaaactgccttgtctacaatagcagttgctactgctaaagccaaagaacaagaaacaatactgagaactagagaaactatggctactagacaagaacaaatccaagttacccatggaaaggtggacgttggaaaaaaggctgaagctgtagcaacagttgttgctgcagtagaccaggcccgagtcagagagcccagagagcctgggcatcttgaagaatcctatgctcagcagaccactttggagtacggatataaggaacgcatttccgccgcaaaggtagctgagcctccccaacgtccagcctcagaaccccacgttgtccctaaagcagtcaagcctagagtaatccaggctccttctgagactcatatcaaaactactgatcaaaagggaatgcacatatcatcacagatcaagaaaactacagatctaacaacggaaagattagtccatgtggataaacgcccccgcacagctagccctcactttactgtttcaaaaatttctgttcctaagacagaacatggatatgaggcatcaatagccggtagtgctattgccacattacaaaaagagttgtcagccacatcttctgctcagaagatcaccaaatcggtgaaggctcctactgtgaagcccagtgagactagagtaagggcagagcccacacccttgccacagttccccttcgctgacacaccagatacttacaagagtgaagctggcgttgaggtgaaaaaggaagtaggggtgagcatcactggcaccaccgtccgtgaagagcgctttgaagtactgcacggacgcgaagccaaggtaacagaaacagcaagagtaccagcacctgttgaaattcctgttactccaccaactttggtctcgggcttaaaaaatgtgactgtcatagaaggtgaatctgtcaccttggagtgccacatctctggatacccatccccgacagtgacatggtacagggaagactaccaaatcgaaagttccattgacttccagataaccttccagagtggaattgctcgtcttatgattcgcgaagcatttgcggaagacagcgggcgatttacttgcagtgctgtaaatgaggctggaaccgtcagcacatcctgctatctggctgtgcaggtgtcagaagaatttgaaaaggaaaccacagccgtgactgagaaatttactacagaagagaaacgctttgttgagtcaagagatgtggttatgactgatactagcctcacagaggaacaagcagggcctggagaacctgccgcgccttactttattacaaaaccagtggtccagaaactggtggaaggtgggagcgtggtgtttggatgccaagttggcggcaacccaaagccccatgtatactggaaaaaatctggtgttcctctaaccactggatacagatacaaagtgagttacaacaaacaaaccggtgaatgcaagctggtgatttctatgacttttgctgatgatgctggagaatacactattgttgttcgcaataagcatggagaaacttctgcatctgcttccttgcttgaagaagctgattatgagttactgatgaagtcccagcaagaaatgctttatcagacacaagtgactgcatttgttcaagaacctaaagttggagaaacagcacctggatttgtatactctgagtatgaaaaagagtatgaaaaagaacaagccttaattaggaagaaaatggccaaagatactgtagtggtcagaacttatgtagaagatcaggaattccatatttcttcctttgaagagagacttattaaagaaattgaatatagaataataaagactacattagaagaacttcttgaagaagatggagaagaaaagatggcagttgacatttctgaatctgaagctgttgaatcaggatttgattcaagaatcaagaattatagaattcttgaggggatgggtgtcacttttcattgcaagatgtctggatatccattaccaaagattgcttggtacaaagatggcaagcgcatcaaacatggagaaagataccaaatggactttctacaagatggcagagctagtctgcgtatacctgttgttcttccagaagatgaaggaatctacactgcatttgccagcaatattaaaggaaatgcaatttgctcagggaaattgtatgtggagcctgctgcaccacttggagctccgacttacattcccacactagagccagtgagcagaatcagatctctctctccacgttcagtgagcaggtctcctatacgcatgtctcctgcacggatgtcacctgcaaggatgtctcctgcacggatgtcccctgcaagaatgtcccctggacgtaggctggaggagacagatgagtcacaacttgagagactatataaaccagtctttgtgttaaaacctgtttctttcaaatgtttagaagggcaaactgccagatttgacttaaaggttgttggtagacctatgccagagacgttctggtttcatgatggccagcaaattgtcaatgactatacccataaagtagtcattaaagaagatggtactcaatcactaattattgtccctgccacacccagtgattctggggaatggactgtggttgcccaaaacagggcaggcagatcttcaatttcagtgattttaactgtggaagctgtggaacatcaggtaaaaccgatgtttgtagaaaaactgaaaaatgtcaatataaaggaaggttcccgacttgaaatgaaagtcagagctacgggtaaccccaaccctgacattgtatggttgaaaaa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//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:7273 -> Molecular function: GO:0002020 [protease binding] evidence: IPI
GeneID:7273 -> Molecular function: GO:0003676 [nucleic acid binding] evidence: IEA
GeneID:7273 -> Molecular function: GO:0004674 [protein serine/threonine kinase activity] evidence: IDA
GeneID:7273 -> Molecular function: GO:0004713 [protein tyrosine kinase activity] evidence: IEA
GeneID:7273 -> Molecular function: GO:0005509 [calcium ion binding] evidence: IDA
GeneID:7273 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
GeneID:7273 -> Molecular function: GO:0005516 [calmodulin binding] evidence: IPI
GeneID:7273 -> Molecular function: GO:0005516 [calmodulin binding] evidence: TAS
GeneID:7273 -> Molecular function: GO:0005524 [ATP binding] evidence: IEA
GeneID:7273 -> Molecular function: GO:0008307 [structural constituent of muscle] evidence: IMP
GeneID:7273 -> Molecular function: GO:0008307 [structural constituent of muscle] evidence: TAS
GeneID:7273 -> Molecular function: GO:0019899 [enzyme binding] evidence: IPI
GeneID:7273 -> Molecular function: GO:0031433 [telethonin binding] evidence: IPI
GeneID:7273 -> Molecular function: GO:0031433 [telethonin binding] evidence: ISS
GeneID:7273 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI
GeneID:7273 -> Molecular function: GO:0042805 [actinin binding] evidence: IDA
GeneID:7273 -> Molecular function: GO:0042805 [actinin binding] evidence: IPI
GeneID:7273 -> Molecular function: GO:0043621 [protein self-association] evidence: IDA
GeneID:7273 -> Molecular function: GO:0051015 [actin filament binding] evidence: IDA
GeneID:7273 -> Molecular function: GO:0051371 [muscle alpha-actinin binding] evidence: IPI
GeneID:7273 -> Biological process: GO:0001701 [in utero embryonic development] evidence: IEA
GeneID:7273 -> Biological process: GO:0002576 [platelet degranulation] evidence: TAS
GeneID:7273 -> Biological process: GO:0003300 [cardiac muscle hypertrophy] evidence: IMP
GeneID:7273 -> Biological process: GO:0006936 [muscle contraction] evidence: NAS
GeneID:7273 -> Biological process: GO:0006936 [muscle contraction] evidence: TAS
GeneID:7273 -> Biological process: GO:0006941 [striated muscle contraction] evidence: TAS
GeneID:7273 -> Biological process: GO:0007076 [mitotic chromosome condensation] evidence: IEP
GeneID:7273 -> Biological process: GO:0007512 [adult heart development] evidence: IEA
GeneID:7273 -> Biological process: GO:0007596 [blood coagulation] evidence: TAS
GeneID:7273 -> Biological process: GO:0030049 [muscle filament sliding] evidence: TAS
GeneID:7273 -> Biological process: GO:0030168 [platelet activation] evidence: TAS
GeneID:7273 -> Biological process: GO:0030240 [skeletal muscle thin filament assembly] evidence: IMP
GeneID:7273 -> Biological process: GO:0030241 [skeletal muscle myosin thick filament assembly] evidence: IMP
GeneID:7273 -> Biological process: GO:0035995 [detection of muscle stretch] evidence: TAS
GeneID:7273 -> Biological process: GO:0043056 [forward locomotion] evidence: IEA
GeneID:7273 -> Biological process: GO:0045214 [sarcomere organization] evidence: IMP
GeneID:7273 -> Biological process: GO:0045859 [regulation of protein kinase activity] evidence: IMP
GeneID:7273 -> Biological process: GO:0048739 [cardiac muscle fiber development] evidence: IMP
GeneID:7273 -> Biological process: GO:0048769 [sarcomerogenesis] evidence: IMP
GeneID:7273 -> Biological process: GO:0050790 [regulation of catalytic activity] evidence: IMP
GeneID:7273 -> Biological process: GO:0051592 [response to calcium ion] evidence: IDA
GeneID:7273 -> Biological process: GO:0055003 [cardiac myofibril assembly] evidence: IMP
GeneID:7273 -> Biological process: GO:0055008 [cardiac muscle tissue morphogenesis] evidence: IMP
GeneID:7273 -> Biological process: GO:0060048 [cardiac muscle contraction] evidence: IMP
GeneID:7273 -> Cellular component: GO:0000794 [condensed nuclear chromosome] evidence: IDA
GeneID:7273 -> Cellular component: GO:0005576 [extracellular region] evidence: TAS
GeneID:7273 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
GeneID:7273 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
GeneID:7273 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
GeneID:7273 -> Cellular component: GO:0005794 [Golgi apparatus] evidence: IDA
GeneID:7273 -> Cellular component: GO:0005829 [cytosol] evidence: TAS
GeneID:7273 -> Cellular component: GO:0005865 [striated muscle thin filament] evidence: IDA
GeneID:7273 -> Cellular component: GO:0030018 [Z disc] evidence: IDA
GeneID:7273 -> Cellular component: GO:0031430 [M band] evidence: IDA
GeneID:7273 -> Cellular component: GO:0031430 [M band] evidence: IEA
GeneID:7273 -> Cellular component: GO:0031674 [I band] evidence: IDA
ANNOTATIONS from NCBI Entrez Gene (20130726):
NP_596870 -> EC 2.7.11.1
by
@meso_cacase at
DBCLS
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