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2024-03-28 20:24:30, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_003802               5992 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens myosin, heavy chain 13, skeletal muscle (MYH13), mRNA.
ACCESSION   NM_003802
VERSION     NM_003802.2  GI:110624780
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 5992)
  AUTHORS   Chen,Z., Zhao,T.J., Li,J., Gao,Y.S., Meng,F.G., Yan,Y.B. and
            Zhou,H.M.
  TITLE     Slow skeletal muscle myosin-binding protein-C (MyBPC1) mediates
            recruitment of muscle-type creatine kinase (CK) to myosin
  JOURNAL   Biochem. J. 436 (2), 437-445 (2011)
   PUBMED   21426302
  REMARK    GeneRIF: Domain-mapping experiments indicated that muscle-type
            creatine kinase binds to the C-terminal domains of MyBPC1, which is
            also the binding site of myosin.
REFERENCE   2  (bases 1 to 5992)
  AUTHORS   Trynka,G., Zhernakova,A., Romanos,J., Franke,L., Hunt,K.A.,
            Turner,G., Bruinenberg,M., Heap,G.A., Platteel,M., Ryan,A.W., de
            Kovel,C., Holmes,G.K., Howdle,P.D., Walters,J.R., Sanders,D.S.,
            Mulder,C.J., Mearin,M.L., Verbeek,W.H., Trimble,V., Stevens,F.M.,
            Kelleher,D., Barisani,D., Bardella,M.T., McManus,R., van Heel,D.A.
            and Wijmenga,C.
  TITLE     Coeliac disease-associated risk variants in TNFAIP3 and REL
            implicate altered NF-kappaB signalling
  JOURNAL   Gut 58 (8), 1078-1083 (2009)
   PUBMED   19240061
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   3  (bases 1 to 5992)
  AUTHORS   Schjeide,B.M., McQueen,M.B., Mullin,K., DiVito,J., Hogan,M.F.,
            Parkinson,M., Hooli,B., Lange,C., Blacker,D., Tanzi,R.E. and
            Bertram,L.
  TITLE     Assessment of Alzheimer's disease case-control associations using
            family-based methods
  JOURNAL   Neurogenetics 10 (1), 19-25 (2009)
   PUBMED   18830724
  REMARK    GeneRIF: Meta-analysis of gene-disease association. (HuGE
            Navigator)
REFERENCE   4  (bases 1 to 5992)
  AUTHORS   Lehner,B. and Sanderson,C.M.
  TITLE     A protein interaction framework for human mRNA degradation
  JOURNAL   Genome Res. 14 (7), 1315-1323 (2004)
   PUBMED   15231747
REFERENCE   5  (bases 1 to 5992)
  AUTHORS   Schachat,F. and Briggs,M.M.
  TITLE     Phylogenetic implications of the superfast myosin in extraocular
            muscles
  JOURNAL   J. Exp. Biol. 205 (PT 15), 2189-2201 (2002)
   PUBMED   12110653
  REMARK    GeneRIF: phylogenic imlications in extraocular muscles (REVIEW)
REFERENCE   6  (bases 1 to 5992)
  AUTHORS   Weiss,A., Schiaffino,S. and Leinwand,L.A.
  TITLE     Comparative sequence analysis of the complete human sarcomeric
            myosin heavy chain family: implications for functional diversity
  JOURNAL   J. Mol. Biol. 290 (1), 61-75 (1999)
   PUBMED   10388558
REFERENCE   7  (bases 1 to 5992)
  AUTHORS   Weiss,A., McDonough,D., Wertman,B., Acakpo-Satchivi,L.,
            Montgomery,K., Kucherlapati,R., Leinwand,L. and Krauter,K.
  TITLE     Organization of human and mouse skeletal myosin heavy chain gene
            clusters is highly conserved
  JOURNAL   Proc. Natl. Acad. Sci. U.S.A. 96 (6), 2958-2963 (1999)
   PUBMED   10077619
REFERENCE   8  (bases 1 to 90)
  AUTHORS   Weiss,A.
  TITLE     Sequences and Genomic Organization of the Human Myosin Heavy Chain
            Gene Family
  JOURNAL   Thesis (1999) Albert Einstein College of Medicine, Bronx, NY, USA
REFERENCE   9  (bases 1 to 5992)
  AUTHORS   Winters,L.M., Briggs,M.M. and Schachat,F.
  TITLE     The human extraocular muscle myosin heavy chain gene (MYH13) maps
            to the cluster of fast and developmental myosin genes on chromosome
            17
  JOURNAL   Genomics 54 (1), 188-189 (1998)
   PUBMED   9806854
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AF111782.2 and AC005291.1.
            On Jul 22, 2006 this sequence version replaced gi:11321578.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AF111782.2 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025084, ERS025085 [ECO:0000350]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-1434              AF111782.2         1-1434
            1435-1503           AC005291.1         134453-134521       c
            1504-1674           AC005291.1         134188-134358       c
            1675-1984           AC005291.1         132786-133095       c
            1985-2058           AC005291.1         129314-129387       c
            2059-2146           AC005291.1         129136-129223       c
            2147-2264           AC005291.1         122060-122177       c
            2265-2388           AC005291.1         121085-121208       c
            2389-2525           AC005291.1         119373-119509       c
            2526-2781           AC005291.1         116852-117107       c
            2782-3024           AC005291.1         113008-113250       c
            3025-3201           AC005291.1         110518-110694       c
            3202-3347           AC005291.1         109337-109482       c
            3348-3438           AC005291.1         109139-109229       c
            3439-3828           AC005291.1         107776-108165       c
            3829-3955           AC005291.1         104885-105011       c
            3956-4074           AC005291.1         104679-104797       c
            4075-4271           AC005291.1         102144-102340       c
            4272-4455           AC005291.1         101560-101743       c
            4456-4621           AC005291.1         100897-101062       c
            4622-4746           AC005291.1         100089-100213       c
            4747-5055           AC005291.1         98508-98816         c
            5056-5259           AC005291.1         98220-98423         c
            5260-5385           AC005291.1         95925-96050         c
            5386-5556           AC005291.1         95445-95615         c
            5557-5661           AC005291.1         92380-92484         c
            5662-5676           AC005291.1         92263-92277         c
            5677-5992           AF111782.2         5677-5992
FEATURES             Location/Qualifiers
     source          1..5992
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="17"
                     /map="17p13"
     gene            1..5992
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="myosin, heavy chain 13, skeletal muscle"
                     /db_xref="GeneID:8735"
                     /db_xref="HGNC:7571"
                     /db_xref="MIM:603487"
     exon            1..27
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    25..27
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="upstream in-frame stop codon"
     exon            28..78
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            79..294
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     CDS             91..5907
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="myosin, heavy polypeptide 13, skeletal muscle;
                     extraocular muscle myosin heavy chain; extraocular myosin
                     heavy chain; myosin heavy chain 13; myosin heavy chain,
                     skeletal muscle, extraocular"
                     /codon_start=1
                     /product="myosin-13"
                     /protein_id="NP_003793.2"
                     /db_xref="GI:110624781"
                     /db_xref="CCDS:CCDS45613.1"
                     /db_xref="GeneID:8735"
                     /db_xref="HGNC:7571"
                     /db_xref="MIM:603487"
                     /translation="
MSSDAEMAIFGEAAPYLRKPEKERIEAQNRPFDSKKACFVADNKEMYVKGMIQTRENDKVIVKTLDDRMLTLNNDQVFPMNPPKFDKIEDMAMMTHLHEPAVLYNLKERYAAWMIYTYSGLFCVTVNPYKWLPVYKPEVVAAYRGKKRQEAPPHIFSISDNAYQFMLTDRDNQSILITGESGAGKTVNTKRVIQYFATIAVTGDKKKETQPGKMQGTLEDQIIQANPLLEAFGNAKTVRNDNSSRFGKFIRIHFGATGKLASADIETYLLEKSRVTFQLSSERSYHIFYQIMSNKKPELIDLLLISTNPFDFPFVSQGEVTVASIDDSEELLATDNAIDILGFSSEEKVGIYKLTGAVMHYGNMKFKQKQREEQAEPDGTEVADKAGYLMGLNSAEMLKGLCCPRVKVGNEYVTKGQNVQQVTNSVGALAKAVYEKMFLWMVTRINQQLDTKQPRQYFIGVLDIAGFEIFDFNSLEQLCINFTNEKLQQFFNHHMFVLEQEEYKKEGIEWEFIDFGMDLAACIELIEKPMGIFSILEEECMFPKATDTSFKNKLYDQHLGKSNNFQKPKPAKGKAEAHFSLVHYAGTVDYNIAGWLDKNKDPLNETVVGLYQKSSLKLLSFLFSNYAGAETGDSGGSKKGGKKKGSSFQTVSAVFRENLNKLMTNLRSTHPHFVRCLIPNETKTPGVMDHYLVMHQLRCNGVLEGIRICRKGFPSRILYADFKQRYRILNASAIPEGQFIDSKNASEKLLNSIDVDREQFRFGNTKVFFKAGLLGLLEEMRDEKLVTLMTSTQAVCRGYLMRVEFKKMMERRDSIFCIQYNIRSFMNVKHWPWMNLFFKIKPLLKSAEAEKEMATMKEDFERTKEELARSEARRKELEEKMVSLLQEKNDLQLQVQSETENLMDAEERCEGLIKSKILLEAKVKELTERLEEEEEMNSELVAKKRNLEDKCSSLKRDIDDLELTLTKVEKEKHATENKVKNLSEEMTALEENISKLTKEKKSLQEAHQQTLDDLQVEEDKVNGLIKINAKLEQQTDDLEGSLEQEKKLRADLERAKRKLEGDLKMSQESIMDLENDKQQIEEKLKKKEFELSQLQAKIDDEQVHSLQFQKKIKELQARIEELEEEIEAEHTLRAKIEKQRSDLARELEEISERLEEASGATSAQIEMNKKREAEFQKMRRDLEEATLQHEATAATLRKKQADSVAELGEQIDNLQRVKQKLEKEKSELKMEIDDMASNIEALSKSKSNIERTCRTVEDQFSEIKAKDEQQTQLIHDLNMQKARLQTQNGELSHRVEEKESLISQLTKSKQALTQQLEELKRQMEEETKAKNAMAHALQSSRHDCDLLREQYEEEQEAKAELQRALSKANSEVAQWRTKYETDAIQRTEELEEAKKKLAQRLQEAEENTETANSKCASLEKTKQRLQGEVEDLMRDLERSHTACATLDKKQRNFDKVLAEWKQKLDESQAELEAAQKESRSLSTELFKMRNAYEEVVDQLETLRRENKNLQEEISDLTEQIAETGKNLQEAEKTKKLVEQEKSDLQVALEEVEGSLEHEESKILRVQLELSQVKSELDRKVIEKDEEIEQLKRNSQRAAEALQSVLDAEIRSRNDALRLKKKMEGDLNEMEIQLGHSNRQMAETQKHLRTVQGQLKDSQLHLDDALRSNEDLKEQLAIVERRNGLLLEELEEMKVALEQTERTRRLSEQELLDASDRVQLLHSQNTSLINTKKKLEADIAQCQAEVENSIQESRNAEEKAKKAITDAAMMAEELKKEQDTSAHLERMKKNLEQTVKDLQHRLDEAEQLALKGGKKQIQKLENRVRELENELDVEQKRGAEALKGAHKYERKVKEMTYQAEEDHKNILRLQDLVDKLQAKVKSYKRQAEEAEEQANTQLSRCRRVQHELEEAAERADIAESQVNKLRAKSRDVGSQKMEE
"
     misc_feature    193..318
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="Myosin N-terminal SH3-like domain; Region:
                     Myosin_N; pfam02736"
                     /db_xref="CDD:111612"
     misc_feature    331..2436
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="Myosin. Large ATPases; Region: MYSc; smart00242"
                     /db_xref="CDD:197599"
     misc_feature    334..2433
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="Myosin motor domain, type II myosins. Myosin II
                     mediates cortical contraction in cell motility, and is the
                     motor in smooth and skeletal muscle. This catalytic (head)
                     domain has ATPase activity and belongs to the larger group
                     of P-loop NTPases. Myosins...; Region: MYSc_type_II;
                     cd01377"
                     /db_xref="CDD:30099"
     misc_feature    order(469..480,484..489,631..654)
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="ATP-binding site [chemical binding]; other site"
                     /db_xref="CDD:30099"
     misc_feature    814..831
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="switch I region; other site"
                     /db_xref="CDD:30099"
     misc_feature    1480..1503
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="switch II region; other site"
                     /db_xref="CDD:30099"
     misc_feature    order(1564..1599,1606..1635)
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="relay loop; other site"
                     /db_xref="CDD:30099"
     misc_feature    2065..2133
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UKX3.2);
                     Region: Actin-binding (By similarity)"
     misc_feature    2185..2229
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="SH1 helix; other site"
                     /db_xref="CDD:30099"
     misc_feature    order(2224..2229,2236..2238,2254..2256,2263..2268,
                     2275..2277,2368..2370,2377..2379,2383..2388,2392..2400,
                     2410..2412,2419..2427)
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="converter subdomain; other site"
                     /db_xref="CDD:30099"
     misc_feature    2371..2415
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (Q9UKX3.2);
                     Region: Actin-binding (By similarity)"
     misc_feature    3379..5880
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /note="Myosin tail; Region: Myosin_tail_1; pfam01576"
                     /db_xref="CDD:144972"
     variation       102
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:34042358"
     exon            295..438
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            439..595
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            596..623
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            624..735
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            736..828
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            829..892
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     variation       860
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:34416201"
     exon            893..991
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            992..1095
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            1096..1234
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     variation       1199
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:35222064"
     exon            1235..1353
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            1354..1503
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            1504..1674
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            1675..1984
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            1985..2058
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            2059..2146
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            2147..2264
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            2265..2388
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            2389..2525
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            2526..2781
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            2782..3024
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            3025..3201
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            3202..3347
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     variation       3222
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:35783712"
     exon            3348..3438
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            3439..3828
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            3829..3955
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            3956..4074
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            4075..4271
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            4272..4455
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            4456..4621
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            4622..4746
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            4747..5055
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            5056..5259
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            5260..5385
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            5386..5556
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            5557..5661
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            5662..5757
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            5758..5892
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
     exon            5893..5992
                     /gene="MYH13"
                     /gene_synonym="MyHC-eo"
                     /inference="alignment:Splign:1.39.8"
ORIGIN      
aaattgctgtgaccgcagcatctctaggaagacgctttattcctgaaggacactgactgtcacttgggaaccaagaagccctctgcagtcatgagctctgacgcagaaatggccatttttggagaagcagctccctacctccggaaaccagagaaggagagaatcgaggctcaaaatcgtccattcgattccaagaaagcctgctttgtagcggataataaggaaatgtatgtgaaaggcatgatccagactagggaaaatgacaaagtcatagtcaagaccctcgatgaccggatgctcactctgaacaatgaccaggtcttccccatgaaccctcccaaatttgacaagatcgaggacatggccatgatgactcacctgcatgaacctgctgttctgtacaacctcaaagagcgctatgcagcctggatgatctacacctactcaggcctcttctgtgtcaccgtcaacccctacaagtggctgccggtgtacaagcccgaggtggtggctgcctacagaggcaaaaagcgccaggaggccccgccccacatcttctccatctctgacaatgcctatcagttcatgctgactgatcgagacaaccagtctatcctcatcaccggagaatccggggctgggaagactgtgaacaccaagcgtgtcatccagtattttgcaacaattgcagttaccggggacaagaagaaggagacacagccaggcaaaatgcagggaaccctagaggatcagatcatccaggccaacccactgctggaggcctttggaaatgccaagactgtgaggaatgacaactcctcaagatttgggaagttcattcggattcattttggagccacaggaaagctggcatcggcagacatcgaaacttatctgttagaaaaatccagagtgacgtttcaattatccagtgagagaagctatcatattttctaccaaattatgtcaaacaagaagccagaactaattgacctgcttctgatctccaccaaccccttcgacttccccttcgtgagccaaggagaggtcacggtagccagtatcgatgacagtgaagaactgctggcgacagataatgccattgacatcctgggcttcagctcagaggagaaagtcgggatctacaaactgacgggagccgtgatgcattatgggaacatgaagttcaagcagaagcagcgtgaggagcaggcggagccagacggcaccgaagtggctgacaaagccggatacctgatgggactgaattctgcagaaatgctgaagggcctgtgctgtccaagggtgaaggttggcaatgaatatgtcactaaagggcaaaatgtccagcaggtgaccaattcggtgggtgctctggccaaagccgtctacgagaagatgttcctgtggatggtcacccgcatcaaccagcagctggacaccaagcagcccaggcagtacttcatcggggtcttggacattgctggctttgagatctttgatttcaacagcctggagcagctgtgcatcaacttcaccaatgagaaactgcaacagtttttcaaccaccacatgttcgtgctggagcaggaagagtacaagaaggaaggcatcgagtgggagttcattgacttcggaatggacctggctgcctgcatcgagctcatcgagaagcctatgggcatcttctccatcctggaagaggagtgcatgttccccaaggcaacagacacctccttcaagaacaagctgtatgaccagcatcttggaaaatccaacaacttccagaagcccaagcctgccaaaggcaaggctgaggctcacttctcgctggtgcactatgccggcaccgtggactacaacatcgccggctggctggacaaaaacaaggaccccctgaacgagactgtggtggggctgtaccagaagtcttcgctgaagcttctctccttccttttttccaactatgctggtgcagagacaggcgactccggaggaagcaagaagggcgggaagaagaagggctcctctttccagaccgtgtcggccgtgttcagggaaaatttaaacaaattgatgactaacttaaggagcacccaccctcactttgtacgatgtctgattcccaatgagaccaagactcctggtgtgatggaccactacttggtcatgcaccagctgcgctgtaacggggtcctcgagggcatccggatttgcaggaagggattccccagccggatcctctatgctgacttcaagcagcggtaccggatcctcaatgccagtgctatccctgaagggcagttcattgacagcaaaaatgcctcagagaagctcctcaactccatcgatgtggaccgggagcagttcaggttcggcaacaccaaggtgtttttcaaagctgggctcctgggacttttggaggagatgagagatgagaagctggtgacgctgatgacaagcacgcaggcggtgtgcagggggtacctgatgcgggtggagttcaagaagatgatggagaggagggactccatcttctgcatccagtacaacatccgctcttttatgaacgtcaagcactggccctggatgaacctgttcttcaaaatcaagcccctgctgaagagtgcagaggccgagaaggagatggccaccatgaaggaagactttgagaggaccaaggaagaactggcccgatctgaggctcgccggaaggagctggaggagaaaatggtctccctcctgcaggagaagaatgacctccaattgcaggtccagtctgaaacagaaaatctgatggacgctgaggaacggtgtgaaggactcatcaaaagcaagatcctactggaagcaaaagtcaaggagctgacggagagattggaagaggaagaggagatgaattctgaattggttgccaagaagaggaatctggaagataaatgctcctctctcaagagagacattgatgacctggagctgaccttgacgaaagttgaaaaggagaagcatgccacagagaacaaggtaaagaatctttccgaagaaatgacagcacttgaagaaaacatttccaaattgaccaaagaaaagaaatctctacaggaggcccatcagcaaacactggatgatcttcaggtggaagaagataaagtcaatggtctaatcaaaataaatgccaagcttgaacagcaaacagatgatcttgagggttccttagagcaggagaagaaactgcgggcggacttggaaagggcgaagaggaagctggaaggagatctgaaaatgtcccaggaatccattatggatctagaaaatgacaagcagcaaatagaagagaaattgaaaaagaaggagtttgaactcagtcagttacaagccaaaatagatgacgaacaagtccacagtttgcagtttcaaaagaagattaaagaactgcaagcccgcatagaagagctggaggaggaaattgaagcggaacacacgctcagagccaagattgagaagcagcgctcagatctggccagggaactggaggagatcagcgagaggctggaagaagccagtggggccacttcagcccagattgagatgaacaagaagagggaggctgagttccagaaaatgcgcagggacctggaggaggccaccctgcagcacgaagccacagcagccaccctgaggaagaagcaagcagatagtgtggccgagcttggggagcagattgacaacctgcagcgggtgaagcagaagctggagaaggagaagagcgagctgaagatggagattgacgacatggccagcaacatcgaggctctctccaagtcaaagagtaacatagaaagaacgtgccggacggtagaagatcaatttagtgaaatcaaagccaaggacgagcaacagacacagttgatccatgatctgaacatgcagaaagcaagactgcagacccaaaatggggagctgagccaccgagtggaagagaaggagtctctgatttcacagctgaccaaaagcaagcaggccctcacccagcagctggaggagcttaagaggcaaatggaagaagaaaccaaggccaagaacgccatggcgcacgccctgcagtcctcccgccacgactgtgacctgctgcgggaacagtatgaggaggagcaggaagccaaggccgagctgcagagggcgctgtccaaggccaacagtgaggttgcccagtggaggaccaaatacgagacggacgccattcagcgcacagaggagctggaggaggccaagaaaaaactggcccagaggctccaggaagcagaggagaacacggagacggcgaactccaagtgcgcatcgttggagaaaaccaagcagaggctgcagggagaggtggaggatctgatgcgggatctggagcgctcccacaccgcctgtgccacactggacaagaagcagaggaacttcgacaaggtccttgcagagtggaagcaaaagctggacgaaagccaggctgagttggaagctgctcagaaggagtccaggtcactcagcactgaactcttcaagatgaggaatgcctatgaggaggtggtggaccagttagagacactgaggcgagagaacaaaaatctgcaagaagagatttccgacttaactgagcagattgcagaaactggcaagaatcttcaggaagcggaaaagaccaagaagctagtggagcaggaaaagtcagatctgcaggtcgccttagaagaagtggagggttccttggaacacgaggagagcaagatcttgcgcgtgcagctagagctgagccaggtgaaatccgagctagaccgcaaggtcattgagaaggatgaagaaatcgagcagctaaaaagaaacagccagcgggcagcagaggccctgcagagcgtgctggatgctgaaatccgcagccggaacgacgccctgaggctaaagaagaagatggagggagaccttaatgagatggagattcagctgggccactccaaccgccagatggcagagacccagaagcatctgcgcacggtccagggccagctcaaggactcccagctgcatctcgatgacgccctgaggagcaatgaggacctcaaggagcagctggccatcgtggagcgcaggaatggcctcctgctggaggagctggaggaaatgaaggtggccctggaacagacggagcggacccgcaggctgtcagagcaggagctgctggacgccagcgaccgcgtgcagctcctgcactcccagaacacaagcctgataaataccaagaaaaaactggaggctgacatagctcagtgccaggcagaggtggagaactcgatccaggagtccaggaacgcagaggagaaggccaagaaggccatcacggatgctgccatgatggctgaggagctaaagaaggaacaggacaccagcgcccacctggagcggatgaagaagaacctggagcagacggtgaaggacctgcagcaccgtctagatgaggctgaacaactggcgctgaagggcgggaagaagcagatccagaaactggagaaccgggtgcgggagctggaaaatgagcttgatgtggaacagaagaggggagctgaagccctgaagggagcccacaagtacgaacgcaaagtcaaggagatgacttaccaggctgaggaggaccacaagaatatccttaggctccaggacctggtggacaagctgcaggccaaagtgaagtcttacaagaggcaggctgaggaggcggaggagcaggccaacacgcagctgtccagatgccggagagtccagcatgagctagaggaggccgcggagagggcggacatcgctgagtcccaggtcaacaagctgagggccaagagccgagacgtgggcagccagaagatggaagaatgaggctcacctgatgctcgttgccatgggacacctccgagagagtggagggaaaatgtgtgagaaataaattctcctaaatactcgg
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:8735 -> Molecular function: GO:0000146 [microfilament motor activity] evidence: TAS
            GeneID:8735 -> Molecular function: GO:0003779 [actin binding] evidence: NAS
            GeneID:8735 -> Molecular function: GO:0005516 [calmodulin binding] evidence: NAS
            GeneID:8735 -> Molecular function: GO:0005524 [ATP binding] evidence: NAS
            GeneID:8735 -> Biological process: GO:0006936 [muscle contraction] evidence: TAS
            GeneID:8735 -> Biological process: GO:0009267 [cellular response to starvation] evidence: IEA
            GeneID:8735 -> Cellular component: GO:0005859 [muscle myosin complex] evidence: TAS
            GeneID:8735 -> Cellular component: GO:0030016 [myofibril] evidence: IEA
            GeneID:8735 -> Cellular component: GO:0032982 [myosin filament] evidence: IEA

by @meso_cacase at DBCLS
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