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2025-05-09 18:59:23, 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 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
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