2024-04-27 10:06:18, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001130926 5481 bp mRNA linear PRI 17-APR-2013 DEFINITION Homo sapiens myocyte enhancer factor 2A (MEF2A), transcript variant 2, mRNA. ACCESSION NM_001130926 VERSION NM_001130926.1 GI:195972800 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 5481) AUTHORS Nitert,M.D., Dayeh,T., Volkov,P., Elgzyri,T., Hall,E., Nilsson,E., Yang,B.T., Lang,S., Parikh,H., Wessman,Y., Weishaupt,H., Attema,J., Abels,M., Wierup,N., Almgren,P., Jansson,P.A., Ronn,T., Hansson,O., Eriksson,K.F., Groop,L. and Ling,C. TITLE Impact of an exercise intervention on DNA methylation in skeletal muscle from first-degree relatives of patients with type 2 diabetes JOURNAL Diabetes 61 (12), 3322-3332 (2012) PUBMED 23028138 REMARK GeneRIF: DNA methylation of genes in retinol metabolism and calcium signaling pathways (P < 3 x 10-6) and with known functions in muscle and T2D including MEF2A, RUNX1, NDUFC2, and THADA decreased after exercise REFERENCE 2 (bases 1 to 5481) AUTHORS Zhao,W., Zhao,S.P. and Peng,D.Q. TITLE The effects of myocyte enhancer factor 2A gene on the proliferation, migration and phenotype of vascular smooth muscle cells JOURNAL Cell Biochem. Funct. 30 (2), 108-113 (2012) PUBMED 22028303 REMARK GeneRIF: MEF2A dominant negative mutation enhanced cell proliferation and cell migration. REFERENCE 3 (bases 1 to 5481) AUTHORS Liu,Y., Niu,W., Wu,Z., Su,X., Chen,Q., Lu,L. and Jin,W. TITLE Variants in exon 11 of MEF2A gene and coronary artery disease: evidence from a case-control study, systematic review, and meta-analysis JOURNAL PLoS ONE 7 (2), E31406 (2012) PUBMED 22363637 REMARK GeneRIF: The rare 21-bp deletion might have a more compelling effect on coronary artery disease (CAD) than the common (CAG)(n) polymorphism, and MEF2A genetic variant might be a rare but specific cause of CAD/myocardial infarction. Review article REFERENCE 4 (bases 1 to 5481) AUTHORS Katsarou,K., Tsitoura,P. and Georgopoulou,U. TITLE MEK5/ERK5/mef2: a novel signaling pathway affected by hepatitis C virus non-enveloped capsid-like particles JOURNAL Biochim. Biophys. Acta 1813 (10), 1854-1862 (2011) PUBMED 21767578 REMARK GeneRIF: HCVne particles are capable of inducing the recently discovered ERK5 pathway, in a dose dependent way. REFERENCE 5 (bases 1 to 5481) AUTHORS She,H. and Mao,Z. TITLE Regulation of myocyte enhancer factor-2 transcription factors by neurotoxins JOURNAL Neurotoxicology 32 (5), 563-566 (2011) PUBMED 21741404 REMARK GeneRIF: [review] In this work, the mechanisms of regulation of MEF2 function by several well-known neurotoxins and their implications in various neurodegenerative diseases are reviewed. Review article REFERENCE 6 (bases 1 to 5481) AUTHORS Molkentin,J.D., Black,B.L., Martin,J.F. and Olson,E.N. TITLE Cooperative activation of muscle gene expression by MEF2 and myogenic bHLH proteins JOURNAL Cell 83 (7), 1125-1136 (1995) PUBMED 8548800 REFERENCE 7 (bases 1 to 5481) AUTHORS Hobson,G.M., Krahe,R., Garcia,E., Siciliano,M.J. and Funanage,V.L. TITLE Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23 JOURNAL Genomics 29 (3), 704-711 (1995) PUBMED 8575763 REFERENCE 8 (bases 1 to 5481) AUTHORS Funk,W.D. and Wright,W.E. TITLE Cyclic amplification and selection of targets for multicomponent complexes: myogenin interacts with factors recognizing binding sites for basic helix-loop-helix, nuclear factor 1, myocyte-specific enhancer-binding factor 2, and COMP1 factor JOURNAL Proc. Natl. Acad. Sci. U.S.A. 89 (20), 9484-9488 (1992) PUBMED 1329097 REFERENCE 9 (bases 1 to 5481) AUTHORS Yu,Y.T., Breitbart,R.E., Smoot,L.B., Lee,Y., Mahdavi,V. and Nadal-Ginard,B. TITLE Human myocyte-specific enhancer factor 2 comprises a group of tissue-restricted MADS box transcription factors JOURNAL Genes Dev. 6 (9), 1783-1798 (1992) PUBMED 1516833 REFERENCE 10 (bases 1 to 5481) AUTHORS Pollock,R. and Treisman,R. TITLE Human SRF-related proteins: DNA-binding properties and potential regulatory targets JOURNAL Genes Dev. 5 (12A), 2327-2341 (1991) PUBMED 1748287 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA778137.1, Y16312.1, BC013437.2, AB208985.1, AC022692.11 and N93079.1. Summary: The protein encoded by this gene is a DNA-binding transcription factor that activates many muscle-specific, growth factor-induced, and stress-induced genes. The encoded protein can act as a homodimer or as a heterodimer and is involved in several cellular processes, including muscle development, neuronal differentiation, cell growth control, and apoptosis. Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010]. Transcript Variant: This variant (2) uses an alternate coding exon, and is missing a 5' non-coding exon, compared to transcript variant 1. This results in a shorter isoform (2) with a varied internal 43 aa segment compared to isoform 1. Variants 2 and 5 both encode isoform 2. Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AK291835.1 [ECO:0000332] RNAseq introns :: single sample supports all introns ERS025082, ERS025083 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-177 DA778137.1 1-177 178-1179 Y16312.1 87-1088 1180-1964 BC013437.2 1186-1970 1965-2802 AB208985.1 2232-3069 2803-5268 AC022692.11 153286-155751 5269-5481 N93079.1 1-213 c FEATURES Location/Qualifiers source 1..5481 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="15" /map="15q26" gene 1..5481 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /note="myocyte enhancer factor 2A" /db_xref="GeneID:4205" /db_xref="HGNC:6993" /db_xref="MIM:600660" exon 1..177 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" exon 178..373 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" misc_feature 311..313 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /note="upstream in-frame stop codon" CDS 320..1813 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /note="isoform 2 is encoded by transcript variant 2; MADS box transcription enhancer factor 2, polypeptide A (myocyte enhancer factor 2A); myocyte-specific enhancer factor 2A; serum response factor-like protein 1" /codon_start=1 /product="myocyte-specific enhancer factor 2A isoform 2" /protein_id="NP_001124398.1" /db_xref="GI:195972801" /db_xref="CCDS:CCDS53978.1" /db_xref="GeneID:4205" /db_xref="HGNC:6993" /db_xref="MIM:600660" /translation="
MGRKKIQITRIMDERNRQVTFTKRKFGLMKKAYELSVLCDCEIALIIFNSSNKLFQYASTDMDKVLLKYTEYNEPHESRTNSDIVETLRKKGLNGCESPDADDYFEHSPLSEDRFSKLNEDSDFIFKRGPPGLPPQNFSMSVTVPVTSPNALSYTNPGSSLVSPSLAASSTLTDSSMLSPPQTTLHRNVSPGAPQRPPSTGNAGGMLSTTDLTVPNGAGSSPVGNGFVNSRASPNLIGATGANSLGKVMPTKSPPPPGGGNLGMNSRKPDLRVVIPPSSKGMMPPLNTQRISSSQATQPLATPVVSVTTPSLPPQGLVYSAMPTAYNTDYSLTSADLSALQGFNSPGMLSLGQVSAWQQHHLGQAALSSLVAGGQLSQGSNLSINTNQNISIKSEPISPPRDRMTPSGFQQQQQQQQQQQPPPPPQPQPQPPQPQPRQEMGRSPVDSLSSSSSSYDGSDREDPRGDFHSPIVLGRPPNTEDRESPSVKRMRMDAWVT
" misc_feature 323..553 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /note="MEF2 (myocyte enhancer factor 2)-like/Type II subfamily of MADS ( MCM1, Agamous, Deficiens, and SRF (serum response factor) box family of eukaryotic transcriptional regulators. Binds DNA and exists as hetero and homo-dimers. Differs from SRF-like/Type I...; Region: MADS_MEF2_like; cd00265" /db_xref="CDD:29020" misc_feature order(323..331,335..337,341..343,356..358,362..364, 374..379,386..391,395..400,407..412,416..421,431..433) /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /note="DNA binding site [nucleotide binding]" /db_xref="CDD:29020" misc_feature order(380..382,401..406,413..418,422..427,434..436, 449..451,455..457,461..463,479..481,485..487,503..505, 512..517,524..526,533..538) /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /note="dimerization interface [polypeptide binding]; other site" /db_xref="CDD:29020" misc_feature 494..496 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /note="putative phosphorylation site [posttranslational modification]; other site" /db_xref="CDD:29020" misc_feature 602..778 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /note="Holliday junction regulator protein family C-terminal repeat; Region: HJURP_C; pfam12347" /db_xref="CDD:152782" STS 329..740 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /standard_name="Mef2a" /db_xref="UniSTS:265600" STS 329..689 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /standard_name="Mef2a" /db_xref="UniSTS:265601" variation 343 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:370523988" exon 374..577 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" variation 433 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:191032083" variation 461 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:368747387" variation 484 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:372436031" variation 487 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:200687749" exon 578..709 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" variation 578 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:17423081" variation 585 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:3205682" variation 600 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:368757733" variation 601 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:1135555" variation 607 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:1135556" variation 610 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:1135557" variation 616 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:1135558" variation 619 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:1135559" variation 620 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:1135560" variation 625 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:1135561" variation 632 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:1135562" variation 636 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:3208173" variation 642 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:1135563" variation 649 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:1136937" variation 652 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:3198317" variation 655 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:1135564" variation 658 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:1135565" variation 664 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:1135566" variation 666 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:1135567" variation 667 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:1135568" variation 671 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:1135569" variation 679 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:1135570" variation 684 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:1135571" variation 689 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:1135572" variation 690 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:1135574" variation 705 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:1135575" variation 709 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:17420057" exon 710..929 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" variation 780 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:374058145" variation 830 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:189538320" variation 832 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:3803420" variation 865 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:146192119" variation 876 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:370083199" variation 911 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:373867888" exon 930..989 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" variation 942 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:199820037" variation 958 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:376779827" variation 971 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:377207410" exon 990..1177 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" variation 1056 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:189526729" variation 1070 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:199751824" variation 1075 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:369943942" variation 1101 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:121918530" variation 1109 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:79454361" variation 1120 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:200748600" variation 1147 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:369552532" variation 1148 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:373219260" variation 1149 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:121918529" variation 1161 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:121918531" variation 1174 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:376183174" exon 1178..1304 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" variation 1180..1181 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:17854846" variation 1180 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:325408" variation 1186 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:325407" variation 1225 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:3730283" variation 1261 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:372479689" variation 1283 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:373204094" exon 1305..1431 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" variation 1318 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:373943430" variation 1321 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:368107439" variation 1322 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:373128826" exon 1432..5467 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /inference="alignment:Splign:1.39.8" variation 1432 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:199613639" variation 1461 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:375108417" variation 1474 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:369483642" STS 1491..1648 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /standard_name="G64293" /db_xref="UniSTS:158672" variation 1527 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:372533601" variation 1537 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:144461661" variation 1539 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:369579124" variation 1540 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:3730059" variation 1546..1547 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="cagcag" /db_xref="dbSNP:374033278" variation 1547..1552 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="cagcag" /db_xref="dbSNP:3138597" variation 1547..1549 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="cag" /db_xref="dbSNP:373652230" variation 1551..1556 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="agcagc" /db_xref="dbSNP:58424802" variation 1555..1560 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="gcagca" /db_xref="dbSNP:72276751" variation 1556..1557 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="cagcag" /db_xref="dbSNP:72236998" variation 1557..1558 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="agcagc" /db_xref="dbSNP:72416294" variation 1563 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:200861006" variation 1566..1571 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="agcagc" /db_xref="dbSNP:72198683" variation 1575 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:201861701" variation 1578 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:199811207" variation 1584 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:369815961" variation 1594 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:367780642" variation 1642 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:325400" variation 1658 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:370921147" variation 1729 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:34851361" variation 1730 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:111748677" variation 1743 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:370778860" variation 1958..1959 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="gtgt" /db_xref="dbSNP:145618675" variation 1958 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:201277440" variation 1959..1960 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="gtgt" /db_xref="dbSNP:144020290" variation 1960..1961 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="gtgt" /db_xref="dbSNP:10628004" variation 1965..1966 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="gtgt" /db_xref="dbSNP:34507751" variation 1965 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:28444186" variation 2005 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:374107493" variation 2052 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:376220587" variation 2316 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:75665175" variation 2327 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:140014502" variation 2339 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:72760574" variation 2381 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:190007997" variation 2388 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:201784078" variation 2388 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="g" /db_xref="dbSNP:34756453" variation 2453 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:145205421" variation 2465 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:11635271" STS 2468..2817 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /standard_name="D15S907" /db_xref="UniSTS:279" variation 2678 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:182261693" variation 2829 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:1059750" variation 2830 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:186608671" variation 2855 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:1454315" variation 3005 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:190999757" variation 3235..3239 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="gttaa" /db_xref="dbSNP:71982844" variation 3242 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="aactt" /db_xref="dbSNP:67611863" variation 3245 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:1059755" variation 3246 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:149125295" variation 3250 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:1059756" variation 3256 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:1059757" variation 3280..3281 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:1059758" variation 3281 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:325399" variation 3286 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:1136940" variation 3471 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:142460833" variation 3472 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:184041593" variation 3497 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:368872347" variation 3562 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:897074" variation 3790 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:188542083" variation 3809 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:372386338" variation 3841 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:375267826" variation 3848 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:59420387" variation 3850 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:12902459" variation 3851..3852 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="a" /db_xref="dbSNP:67644135" variation 3852 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="c" /db_xref="dbSNP:58267790" variation 3854..3855 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="cc" /db_xref="dbSNP:141367967" variation 3854 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="c" /db_xref="dbSNP:144314500" variation 3856 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:11550216" variation 3857 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:75869168" variation 3858 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:148429386" variation 3863 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="c" /replace="cc" /db_xref="dbSNP:58849948" variation 3871 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:1059759" variation 3883 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:325383" variation 3941 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="g" /db_xref="dbSNP:325382" variation 4009 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:1059760" variation 4022 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:11550217" variation 4027 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:193162969" variation 4046 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:184981047" variation 4049 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:187250165" variation 4132 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:372383636" variation 4189 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:146891523" variation 4379 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:191660882" variation 4488 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:41303617" variation 4569 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:140716704" variation 4651 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:325381" variation 4652 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="g" /db_xref="dbSNP:200152842" variation 4670 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:183911417" variation 4748 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:113970475" variation 4776 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:188188955" variation 4781 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="a" /db_xref="dbSNP:34602555" variation 4860 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:182321371" variation 4862 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:113827147" variation 4902 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:145829205" variation 4909..4910 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="cat" /db_xref="dbSNP:374735275" variation 4909 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:77710130" variation 4910..4911 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="" /replace="atc" /db_xref="dbSNP:371572866" variation 4929 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:28377673" variation 4943 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="t" /db_xref="dbSNP:138403437" variation 5054 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="g" /db_xref="dbSNP:74033759" STS 5192..5464 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /standard_name="D15S901" /db_xref="UniSTS:13157" variation 5315 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="c" /replace="t" /db_xref="dbSNP:150316263" variation 5377 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="a" /replace="c" /db_xref="dbSNP:12442844" polyA_site 5395 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" polyA_signal 5419..5424 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" polyA_site 5448 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" variation 5455 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" /replace="g" /replace="t" /db_xref="dbSNP:325380" polyA_site 5467 /gene="MEF2A" /gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9" ORIGIN
agaacgagttccggtctggccgaggcttgtctcctaaaaatagccccggtgtggggatccgtgcgcggatgtcccggcgagtcccgggctgaaagaggcggctccgggcggcgcgaagcgctggtggcgggcccgggctgcggcgtgtgcgcgcccgccagctgctccggagatacgatcttgtagaaaatttcagctgtagcccttggactagaagctgaaataacagaagctgtgtacgatgcattagggtattgaagaaaattaacttttgaattaaatatttggaatataaggaaataaggaaagttgactgaaaatggggcggaagaaaatacaaatcacacgcataatggatgaaaggaaccgacaggtcacttttacaaagagaaagtttggattaatgaagaaagcctatgaacttagtgtgctctgtgactgtgaaatagcactcatcattttcaacagctctaacaaactgtttcaatatgctagcactgatatggacaaagttcttctcaagtatacagaatataatgaacctcatgaaagcagaaccaactcggatattgttgagactttaagaaagaaaggccttaatggttgtgagagccctgatgctgacgattactttgagcacagtccactctcggaggacagattcagcaaactaaatgaagatagtgattttattttcaaacgaggccctcctggtctgccacctcagaacttttcaatgtctgtcacagttccagtgaccagccccaatgctttgtcctacactaacccagggagttcactggtgtccccatctttggcagccagctcaacgttaacagattcaagcatgctctctccacctcaaaccacattacatagaaatgtgtctcctggagctcctcagagaccaccaagtactggcaatgcaggtgggatgttgagcactacagacctcacagtgccaaatggagctggaagcagtccagtggggaatggatttgtaaactcaagagcttctccaaatttgattggagctactggtgcaaatagcttaggcaaagtcatgcctacaaagtctccccctccaccaggtggtggtaatcttggaatgaacagtaggaaaccagatcttcgagttgtcatccccccttcaagcaagggcatgatgcctccactaaatacccaaaggatcagtagttctcaagccactcaacctcttgctaccccagtcgtgtctgtgacaaccccaagcttgcctccgcaaggacttgtgtactcagcaatgccgactgcctacaacactgattattcactgaccagcgctgacctgtcagcccttcaaggcttcaactcgccaggaatgctgtcgctgggacaggtgtcggcctggcagcagcaccacctaggacaagcagccctcagctctcttgttgctggagggcagttatctcagggttccaatttatccattaataccaaccaaaacatcagcatcaagtccgaaccgatttcacctcctcgggatcgtatgaccccatcgggcttccagcagcagcagcagcagcagcagcagcagcagccgccgccaccaccgcagccccagccacaacccccgcagccccagccccgacaggaaatggggcgctcccctgtggacagtctgagcagctctagtagctcctatgatggcagtgatcgggaggatccacggggcgacttccattctccaattgtgcttggccgacccccaaacactgaggacagagaaagcccttctgtaaagcgaatgaggatggacgcgtgggtgacctaaggcttccaagctgatgtttgtacttttgtgttactgcagtgacctgccctacatatctaaatcggtaaataaggacatgagttaaatatatttatatgtacatacatatatatatccctttacatatatatgtatgtgggtgtgagtgtgtatgtgtgggtgtgtgttacatacacagaatcaggcacttacctgcaaactccttgtaggtctgcagatgtgtgtcccatggcagacaaagcaccctgtaggcacagacaagtctggcacttccttggactacttgtttcgtaaagataaccagtttttgcagagaaacgtgtacccatatataattctcccacactagcttgcagaaacctagagggccccctacttgttttatttaactgtgcagtgactgtagttacttaagagaaaatgctttgtagaacagagcagtagaaaagcaggaaccaagaaagcaatactgtacataaaatgtcatttatattttccaacctggcatgggtgtctgttgcaaaggggtgcatgggaaagggctgttgatattaaaaacaaacaaaacaaaaaagccccacacataactgttttgcacgtgcaaaaatgtattgggtcaagaagtgatctttagctaataaagaaagagaatagaaaacacgcatgagatattcagaaaatactagcctagaaatatagagcattaacaaagtaaaattaatatattaagttataattggaatatgtcagaagtttctttttacattcatatcttaaaaattaaagaaactgattttagctcatgtatattttatatgaaagaaaacacccttatgaattgatgactatatataaaattatattcactacttttgaacacattctgctatgaattatttatataagccaaagctatatgttgtaacttttttttagagaatagctttatcttggtttaactctttagttttattttaagaggggaaaacaaaaatatcttgcaagcagaaccttggaaaaaaaaagccatgaacacttattctaaatgtaaattaaaagttgagccaaactctttgtgtatatagcatcttaaatatattatcacctttgatgtaagtacctatgtattgtatggtcaccagattaaaaagtatatttttgtggattgccgccaatctggggggaaaaggcgaggtcctttattaagtattcactgtttaatatttactattttgttaaatatactgtactttggattttaattattagcccagttttttcagaggattgtataaaggggtttctcccctcactggtggtgaatgtgtgatgttacattgtaatctttgtgctgtatgggttgagcatcattatatattttgtatgtgtacataaatagcaaagtggcaaaaaaaattggtgttaagttcatcctgcataagtataaaatgtgttgtaacagattttgtaaggcattatttaaaacttgccttttgtgaggaaaaaatgtagtagaaaaagctgacctaatttaattaatattagagaaaatggcaaaatagtagatgagcacaaaggttttataagtggtaaatgattaggggaaaataatcatggggaaagggatcttttttccttgaccctctgaaaacagaacgatgcagctggttacaaaatcctaccgttatcagctcttctgcacattgcagtgatgctttggtatgcggggagaaacactcttagggtgctggtccttggcatgactcttgccattctaattggaattagtgccaccctcagcttggattttgaacaaggccttattctttcaggaagacaactaatggatgatagcaagttcatccacttactgggcttgtgccatgagcaaaattcaaagtcctgtatatctttcattgtagatttttaaatactccttttcctaaaaaactcaagggtttaaaaattgctattttatattttaaatgatattgagcagctacctacaatttctatgtacattttgttcccccccccccaccccccccccaaattacgttccttttgacattttcctcatctgctgtttgtgacaagtcatcagccagatttcctgactgacacataggtatgatcagtgcaggagagacctgcgcaccacaggctgcaaactggaggttctgttctcatggcagtttgggcagtaacttttgagagaggccaaaaaaaggaggatgacatgctgtctcctctcttcagtatagacattaggctcttattcagaaaggatttttctttaaaaatgtacttactttactgaactacttacaggcacatttcttcataaggccacacctaatccaaacaagacagtctcccaacactgaagttccaaaataatccttaccactttgtaaaccatttatagctttgaaagtgttaagtgattccttcgttattatttatgcatgttcatgaacttctgctgtacattggaataggagttaacacattcacatttactgtctattttcttgtgtgccttatgagatggcttttctgactgtatctcaatagtctttctttctatgcaggtttataatcagtacaactactgttttctaaaatactactactcaaggctcggagtttgtatttaaattacactgaccaagtaacaatgtattccatttcaggaactgaatatttgactgttaacctttttcccatacgtccagtgtggcatggagcatatggacttgacagacatctctcacccagacgcccacgtgtgaacacacccacatccacatctctgggtggaaaccagcctagagaggggacgacgctaatggtgttgctttagaaccgtcttttcttacccttttagactcgtgttttgtatgagacaccattgcaagaaaattttatccctccagaagtattttattactaaagaacaaaagcaaaaaaagcttaaattgcactggttaaagtacagtttccaacagctgtccttcctcagtactctaatggccactccaccgcgagtggaagtcactgttgtgtgtacacaggtggtcccaatcaaaactccatcttttgagcccaattatgtccattttgttatagactaaatcaggggtttgttctacaagaacaatacatgttttaccctttcctttaactagaaggataactagtaatgcatcaacataatttctgtattaaccatcatgcgcacaagaaatacatagtaaataaggaagctgaaaactcctggcattggatcttaagctagatgattagaatgtgaaaaagattttacaaatgtaaaacttctatttctctgtagaaactttcttcactttgctgtgcaagaagacactgctttgctatatttaaaatggcttttttaaaagagatttatgtatttggtaaatgtttgtagtcaacagttcacacaagaagctgtacacggtttgatcatgtaaaaccgtttggcggcacaagctggactttgttgccatccttgagatgaaccttttaagaaaaataagttaatctcaatttttccctgaatgtgttgtttttcttcattatacaataaatataatagtgaactttttatcaaatggtgaagacaatgctaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726): GeneID:4205 -> Molecular function: GO:0000977 [RNA polymerase II regulatory region sequence-specific DNA binding] evidence: IDA GeneID:4205 -> Molecular function: GO:0000981 [sequence-specific DNA binding RNA polymerase II transcription factor activity] evidence: IDA GeneID:4205 -> Molecular function: GO:0001077 [RNA polymerase II core promoter proximal region sequence-specific DNA binding transcription factor activity involved in positive regulation of transcription] evidence: IEA GeneID:4205 -> Molecular function: GO:0001085 [RNA polymerase II transcription factor binding] evidence: IPI GeneID:4205 -> Molecular function: GO:0001105 [RNA polymerase II transcription coactivator activity] evidence: IDA GeneID:4205 -> Molecular function: GO:0003682 [chromatin binding] evidence: IDA GeneID:4205 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: IDA GeneID:4205 -> Molecular function: GO:0003705 [RNA polymerase II distal enhancer sequence-specific DNA binding transcription factor activity] evidence: IEA GeneID:4205 -> Molecular function: GO:0005515 [protein binding] evidence: IPI GeneID:4205 -> Molecular function: GO:0019901 [protein kinase binding] evidence: IEA GeneID:4205 -> Molecular function: GO:0033613 [activating transcription factor binding] evidence: IPI GeneID:4205 -> Molecular function: GO:0035035 [histone acetyltransferase binding] evidence: IPI GeneID:4205 -> Molecular function: GO:0042826 [histone deacetylase binding] evidence: IPI GeneID:4205 -> Molecular function: GO:0043565 [sequence-specific DNA binding] evidence: IDA GeneID:4205 -> Molecular function: GO:0046332 [SMAD binding] evidence: IPI GeneID:4205 -> Molecular function: GO:0046982 [protein heterodimerization activity] evidence: IPI GeneID:4205 -> Biological process: GO:0000002 [mitochondrial genome maintenance] evidence: ISS GeneID:4205 -> Biological process: GO:0000122 [negative regulation of transcription from RNA polymerase II promoter] evidence: IDA GeneID:4205 -> Biological process: GO:0000165 [MAPK cascade] evidence: IDA GeneID:4205 -> Biological process: GO:0002224 [toll-like receptor signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0002755 [MyD88-dependent toll-like receptor signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0002756 [MyD88-independent toll-like receptor signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IDA GeneID:4205 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: IDA GeneID:4205 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA GeneID:4205 -> Biological process: GO:0007507 [heart development] evidence: IEP GeneID:4205 -> Biological process: GO:0007517 [muscle organ development] evidence: NAS GeneID:4205 -> Biological process: GO:0034134 [toll-like receptor 2 signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0034138 [toll-like receptor 3 signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0034142 [toll-like receptor 4 signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0034146 [toll-like receptor 5 signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0034162 [toll-like receptor 9 signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0034166 [toll-like receptor 10 signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0035666 [TRIF-dependent toll-like receptor signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0038123 [toll-like receptor TLR1:TLR2 signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0038124 [toll-like receptor TLR6:TLR2 signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0042692 [muscle cell differentiation] evidence: TAS GeneID:4205 -> Biological process: GO:0045087 [innate immune response] evidence: TAS GeneID:4205 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IDA GeneID:4205 -> Biological process: GO:0048011 [neurotrophin TRK receptor signaling pathway] evidence: TAS GeneID:4205 -> Biological process: GO:0048311 [mitochondrion distribution] evidence: ISS GeneID:4205 -> Biological process: GO:0048813 [dendrite morphogenesis] evidence: ISS GeneID:4205 -> Biological process: GO:0051149 [positive regulation of muscle cell differentiation] evidence: TAS GeneID:4205 -> Biological process: GO:0051403 [stress-activated MAPK cascade] evidence: TAS GeneID:4205 -> Biological process: GO:0055005 [ventricular cardiac myofibril assembly] evidence: ISS GeneID:4205 -> Biological process: GO:0061337 [cardiac conduction] evidence: ISS GeneID:4205 -> Biological process: GO:0070375 [ERK5 cascade] evidence: IMP GeneID:4205 -> Biological process: GO:0071277 [cellular response to calcium ion] evidence: IDA GeneID:4205 -> Cellular component: GO:0000790 [nuclear chromatin] evidence: ISS GeneID:4205 -> Cellular component: GO:0005634 [nucleus] evidence: IDA GeneID:4205 -> Cellular component: GO:0005654 [nucleoplasm] evidence: TAS
by
@meso_cacase at
DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.