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2024-04-18 17:42:03, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001130928 5100 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens myocyte enhancer factor 2A (MEF2A), transcript variant
4, mRNA.
ACCESSION NM_001130928
VERSION NM_001130928.1 GI:195972804
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 5100)
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 5100)
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 5100)
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 5100)
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 5100)
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 5100)
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 5100)
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 5100)
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 5100)
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 5100)
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 BC013437.2, BC053871.2,
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 (4) lacks an in-frame coding exon
compared to transcript variant 1, resulting in a shorter isoform
(4) missing an internal protein segment, compared to isoform 1.
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 :: BC053871.2 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025081, ERS025082 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-28 BC013437.2 178-205
29-798 BC053871.2 1-770
799-1583 BC013437.2 1186-1970
1584-2421 AB208985.1 2232-3069
2422-4887 AC022692.11 153286-155751
4888-5100 N93079.1 1-213 c
FEATURES Location/Qualifiers
source 1..5100
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="15"
/map="15q26"
gene 1..5100
/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..196
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/inference="alignment:Splign:1.39.8"
misc_feature 134..136
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/note="upstream in-frame stop codon"
CDS 143..1432
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/note="isoform 4 is encoded by transcript variant 4; 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 4"
/protein_id="NP_001124400.1"
/db_xref="GI:195972805"
/db_xref="CCDS:CCDS58401.1"
/db_xref="GeneID:4205"
/db_xref="HGNC:6993"
/db_xref="MIM:600660"
/translation="
MGRKKIQITRIMDERNRQTLRKKGLNGCESPDADDYFEHSPLSEDRFSKLNEDSDFIFKRGPPGLPPQNFSMSVTVPVTSPNALSYTNPGSSLVSPSLAASSTLTDSSMLSPPQTTLHRNVSPGAPQRPPSTGNAGGMLSTTDLTVPNGAGSSPVGNGFVNSRASPNLIGATGANSLGKVMPTKSPPPPGGGNLGMNSRKPDLRVVIPPSSKGMMPPLNTQRISSSQATQPLATPVVSVTTPSLPPQGLVYSAMPTAYNTDYSLTSADLSALQGFNSPGMLSLGQVSAWQQHHLGQAALSSLVAGGQLSQGSNLSINTNQNISIKSEPISPPRDRMTPSGFQQQQQQQQQQQPPPPPQPQPQPPQPQPRQEMGRSPVDSLSSSSSSYDGSDREDPRGDFHSPIVLGRPPNTEDRESPSVKRMRMDAWVT
"
misc_feature 146..>217
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/note="MADS: MCM1, Agamous, Deficiens, and SRF (serum
response factor) box family of eukaryotic transcriptonal
regulators. Binds DNA and exists as hetero and
homo-dimers. Composed of 2 main subgroups: SRF-like/Type
I and MEF2-like (myocyte enhancer factor 2)/...; Region:
MADS; cl00109"
/db_xref="CDD:198517"
misc_feature 221..397
/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 152..359
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/standard_name="Mef2a"
/db_xref="UniSTS:265600"
STS 152..308
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/standard_name="Mef2a"
/db_xref="UniSTS:265601"
variation 166
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:370523988"
exon 197..328
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/inference="alignment:Splign:1.39.8"
variation 197
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:17423081"
variation 204
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:3205682"
variation 219
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:368757733"
variation 220
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1135555"
variation 226
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1135556"
variation 229
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1135557"
variation 235
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1135558"
variation 238
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1135559"
variation 239
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1135560"
variation 244
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1135561"
variation 251
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1135562"
variation 255
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:3208173"
variation 261
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1135563"
variation 268
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1136937"
variation 271
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:3198317"
variation 274
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1135564"
variation 277
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1135565"
variation 283
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1135566"
variation 285
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1135567"
variation 286
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1135568"
variation 290
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1135569"
variation 298
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1135570"
variation 303
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1135571"
variation 308
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1135572"
variation 309
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1135574"
variation 324
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1135575"
variation 328
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:17420057"
exon 329..548
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/inference="alignment:Splign:1.39.8"
variation 399
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:374058145"
variation 449
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:189538320"
variation 451
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:3803420"
variation 484
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:146192119"
variation 495
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:370083199"
variation 530
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:373867888"
exon 549..608
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/inference="alignment:Splign:1.39.8"
variation 561
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:199820037"
variation 577
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:376779827"
variation 590
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:377207410"
exon 609..796
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/inference="alignment:Splign:1.39.8"
variation 675
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:189526729"
variation 689
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:199751824"
variation 694
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:369943942"
variation 720
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:121918530"
variation 728
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:79454361"
variation 739
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:200748600"
variation 766
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:369552532"
variation 767
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:373219260"
variation 768
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:121918529"
variation 780
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:121918531"
variation 793
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:376183174"
exon 797..923
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/inference="alignment:Splign:1.39.8"
variation 799..800
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:17854846"
variation 799
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:325408"
variation 805
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:325407"
variation 844
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:3730283"
variation 880
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:372479689"
variation 902
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:373204094"
exon 924..1050
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/inference="alignment:Splign:1.39.8"
variation 937
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:373943430"
variation 940
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:368107439"
variation 941
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:373128826"
exon 1051..5086
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/inference="alignment:Splign:1.39.8"
variation 1051
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:199613639"
variation 1080
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:375108417"
variation 1093
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:369483642"
STS 1110..1267
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/standard_name="G64293"
/db_xref="UniSTS:158672"
variation 1146
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:372533601"
variation 1156
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:144461661"
variation 1158
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:369579124"
variation 1159
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:3730059"
variation 1165..1166
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="cagcag"
/db_xref="dbSNP:374033278"
variation 1166..1171
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="cagcag"
/db_xref="dbSNP:3138597"
variation 1166..1168
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="cag"
/db_xref="dbSNP:373652230"
variation 1170..1175
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="agcagc"
/db_xref="dbSNP:58424802"
variation 1174..1179
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="gcagca"
/db_xref="dbSNP:72276751"
variation 1175..1176
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="cagcag"
/db_xref="dbSNP:72236998"
variation 1176..1177
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="agcagc"
/db_xref="dbSNP:72416294"
variation 1182
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:200861006"
variation 1185..1190
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="agcagc"
/db_xref="dbSNP:72198683"
variation 1194
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:201861701"
variation 1197
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:199811207"
variation 1203
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:369815961"
variation 1213
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:367780642"
variation 1261
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:325400"
variation 1277
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:370921147"
variation 1348
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:34851361"
variation 1349
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:111748677"
variation 1362
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:370778860"
variation 1577..1578
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:145618675"
variation 1577
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:201277440"
variation 1578..1579
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:144020290"
variation 1579..1580
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:10628004"
variation 1584..1585
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="gtgt"
/db_xref="dbSNP:34507751"
variation 1584
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:28444186"
variation 1624
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:374107493"
variation 1671
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:376220587"
variation 1935
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:75665175"
variation 1946
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:140014502"
variation 1958
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:72760574"
variation 2000
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:190007997"
variation 2007
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:201784078"
variation 2007
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="g"
/db_xref="dbSNP:34756453"
variation 2072
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:145205421"
variation 2084
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11635271"
STS 2087..2436
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/standard_name="D15S907"
/db_xref="UniSTS:279"
variation 2297
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:182261693"
variation 2448
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:1059750"
variation 2449
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:186608671"
variation 2474
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:1454315"
variation 2624
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:190999757"
variation 2854..2858
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="gttaa"
/db_xref="dbSNP:71982844"
variation 2861
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="aactt"
/db_xref="dbSNP:67611863"
variation 2864
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1059755"
variation 2865
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:149125295"
variation 2869
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:1059756"
variation 2875
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1059757"
variation 2899..2900
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:1059758"
variation 2900
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:325399"
variation 2905
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1136940"
variation 3090
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:142460833"
variation 3091
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:184041593"
variation 3116
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:368872347"
variation 3181
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:897074"
variation 3409
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:188542083"
variation 3428
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:372386338"
variation 3460
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:375267826"
variation 3467
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:59420387"
variation 3469
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:12902459"
variation 3470..3471
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="a"
/db_xref="dbSNP:67644135"
variation 3471
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="c"
/db_xref="dbSNP:58267790"
variation 3473..3474
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="cc"
/db_xref="dbSNP:141367967"
variation 3473
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="c"
/db_xref="dbSNP:144314500"
variation 3475
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:11550216"
variation 3476
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:75869168"
variation 3477
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:148429386"
variation 3482
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="c"
/replace="cc"
/db_xref="dbSNP:58849948"
variation 3490
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:1059759"
variation 3502
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:325383"
variation 3560
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="g"
/db_xref="dbSNP:325382"
variation 3628
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:1059760"
variation 3641
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:11550217"
variation 3646
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:193162969"
variation 3665
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:184981047"
variation 3668
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:187250165"
variation 3751
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:372383636"
variation 3808
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:146891523"
variation 3998
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:191660882"
variation 4107
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:41303617"
variation 4188
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:140716704"
variation 4270
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:325381"
variation 4271
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="g"
/db_xref="dbSNP:200152842"
variation 4289
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:183911417"
variation 4367
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:113970475"
variation 4395
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:188188955"
variation 4400
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="a"
/db_xref="dbSNP:34602555"
variation 4479
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:182321371"
variation 4481
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:113827147"
variation 4521
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:145829205"
variation 4528..4529
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="cat"
/db_xref="dbSNP:374735275"
variation 4528
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:77710130"
variation 4529..4530
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace=""
/replace="atc"
/db_xref="dbSNP:371572866"
variation 4548
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:28377673"
variation 4562
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="t"
/db_xref="dbSNP:138403437"
variation 4673
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="g"
/db_xref="dbSNP:74033759"
STS 4811..5083
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/standard_name="D15S901"
/db_xref="UniSTS:13157"
variation 4934
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="c"
/replace="t"
/db_xref="dbSNP:150316263"
variation 4996
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="a"
/replace="c"
/db_xref="dbSNP:12442844"
polyA_site 5014
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
polyA_signal 5038..5043
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
polyA_site 5067
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
variation 5074
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
/replace="g"
/replace="t"
/db_xref="dbSNP:325380"
polyA_site 5086
/gene="MEF2A"
/gene_synonym="ADCAD1; mef2; RSRFC4; RSRFC9"
ORIGIN
atcttgtagaaaatttcagctgtagcccttggactagaagctgaaataacagaagctgtgtacgatgcattagggtattgaagaaaattaacttttgaattaaatatttggaatataaggaaataaggaaagttgactgaaaatggggcggaagaaaatacaaatcacacgcataatggatgaaaggaaccgacagactttaagaaagaaaggccttaatggttgtgagagccctgatgctgacgattactttgagcacagtccactctcggaggacagattcagcaaactaaatgaagatagtgattttattttcaaacgaggccctcctggtctgccacctcagaacttttcaatgtctgtcacagttccagtgaccagccccaatgctttgtcctacactaacccagggagttcactggtgtccccatctttggcagccagctcaacgttaacagattcaagcatgctctctccacctcaaaccacattacatagaaatgtgtctcctggagctcctcagagaccaccaagtactggcaatgcaggtgggatgttgagcactacagacctcacagtgccaaatggagctggaagcagtccagtggggaatggatttgtaaactcaagagcttctccaaatttgattggagctactggtgcaaatagcttaggcaaagtcatgcctacaaagtctccccctccaccaggtggtggtaatcttggaatgaacagtaggaaaccagatcttcgagttgtcatccccccttcaagcaagggcatgatgcctccactaaatacccaaaggatcagtagttctcaagccactcaacctcttgctaccccagtcgtgtctgtgacaaccccaagcttgcctccgcaaggacttgtgtactcagcaatgccgactgcctacaacactgattattcactgaccagcgctgacctgtcagcccttcaaggcttcaactcgccaggaatgctgtcgctgggacaggtgtcggcctggcagcagcaccacctaggacaagcagccctcagctctcttgttgctggagggcagttatctcagggttccaatttatccattaataccaaccaaaacatcagcatcaagtccgaaccgatttcacctcctcgggatcgtatgaccccatcgggcttccagcagcagcagcagcagcagcagcagcagcagccgccgccaccaccgcagccccagccacaacccccgcagccccagccccgacaggaaatggggcgctcccctgtggacagtctgagcagctctagtagctcctatgatggcagtgatcgggaggatccacggggcgacttccattctccaattgtgcttggccgacccccaaacactgaggacagagaaagcccttctgtaaagcgaatgaggatggacgcgtgggtgacctaaggcttccaagctgatgtttgtacttttgtgttactgcagtgacctgccctacatatctaaatcggtaaataaggacatgagttaaatatatttatatgtacatacatatatatatccctttacatatatatgtatgtgggtgtgagtgtgtatgtgtgggtgtgtgttacatacacagaatcaggcacttacctgcaaactccttgtaggtctgcagatgtgtgtcccatggcagacaaagcaccctgtaggcacagacaagtctggcacttccttggactacttgtttcgtaaagataaccagtttttgcagagaaacgtgtacccatatataattctcccacactagcttgcagaaacctagagggccccctacttgttttatttaactgtgcagtgactgtagttacttaagagaaaatgctttgtagaacagagcagtagaaaagcaggaaccaagaaagcaatactgtacataaaatgtcatttatattttccaacctggcatgggtgtctgttgcaaaggggtgcatgggaaagggctgttgatattaaaaacaaacaaaacaaaaaagccccacacataactgttttgcacgtgcaaaaatgtattgggtcaagaagtgatctttagctaataaagaaagagaatagaaaacacgcatgagatattcagaaaatactagcctagaaatatagagcattaacaaagtaaaattaatatattaagttataattggaatatgtcagaagtttctttttacattcatatcttaaaaattaaagaaactgattttagctcatgtatattttatatgaaagaaaacacccttatgaattgatgactatatataaaattatattcactacttttgaacacattctgctatgaattatttatataagccaaagctatatgttgtaacttttttttagagaatagctttatcttggtttaactctttagttttattttaagaggggaaaacaaaaatatcttgcaagcagaaccttggaaaaaaaaagccatgaacacttattctaaatgtaaattaaaagttgagccaaactctttgtgtatatagcatcttaaatatattatcacctttgatgtaagtacctatgtattgtatggtcaccagattaaaaagtatatttttgtggattgccgccaatctggggggaaaaggcgaggtcctttattaagtattcactgtttaatatttactattttgttaaatatactgtactttggattttaattattagcccagttttttcagaggattgtataaaggggtttctcccctcactggtggtgaatgtgtgatgttacattgtaatctttgtgctgtatgggttgagcatcattatatattttgtatgtgtacataaatagcaaagtggcaaaaaaaattggtgttaagttcatcctgcataagtataaaatgtgttgtaacagattttgtaaggcattatttaaaacttgccttttgtgaggaaaaaatgtagtagaaaaagctgacctaatttaattaatattagagaaaatggcaaaatagtagatgagcacaaaggttttataagtggtaaatgattaggggaaaataatcatggggaaagggatcttttttccttgaccctctgaaaacagaacgatgcagctggttacaaaatcctaccgttatcagctcttctgcacattgcagtgatgctttggtatgcggggagaaacactcttagggtgctggtccttggcatgactcttgccattctaattggaattagtgccaccctcagcttggattttgaacaaggccttattctttcaggaagacaactaatggatgatagcaagttcatccacttactgggcttgtgccatgagcaaaattcaaagtcctgtatatctttcattgtagatttttaaatactccttttcctaaaaaactcaagggtttaaaaattgctattttatattttaaatgatattgagcagctacctacaatttctatgtacattttgttcccccccccccaccccccccccaaattacgttccttttgacattttcctcatctgctgtttgtgacaagtcatcagccagatttcctgactgacacataggtatgatcagtgcaggagagacctgcgcaccacaggctgcaaactggaggttctgttctcatggcagtttgggcagtaacttttgagagaggccaaaaaaaggaggatgacatgctgtctcctctcttcagtatagacattaggctcttattcagaaaggatttttctttaaaaatgtacttactttactgaactacttacaggcacatttcttcataaggccacacctaatccaaacaagacagtctcccaacactgaagttccaaaataatccttaccactttgtaaaccatttatagctttgaaagtgttaagtgattccttcgttattatttatgcatgttcatgaacttctgctgtacattggaataggagttaacacattcacatttactgtctattttcttgtgtgccttatgagatggcttttctgactgtatctcaatagtctttctttctatgcaggtttataatcagtacaactactgttttctaaaatactactactcaaggctcggagtttgtatttaaattacactgaccaagtaacaatgtattccatttcaggaactgaatatttgactgttaacctttttcccatacgtccagtgtggcatggagcatatggacttgacagacatctctcacccagacgcccacgtgtgaacacacccacatccacatctctgggtggaaaccagcctagagaggggacgacgctaatggtgttgctttagaaccgtcttttcttacccttttagactcgtgttttgtatgagacaccattgcaagaaaattttatccctccagaagtattttattactaaagaacaaaagcaaaaaaagcttaaattgcactggttaaagtacagtttccaacagctgtccttcctcagtactctaatggccactccaccgcgagtggaagtcactgttgtgtgtacacaggtggtcccaatcaaaactccatcttttgagcccaattatgtccattttgttatagactaaatcaggggtttgttctacaagaacaatacatgttttaccctttcctttaactagaaggataactagtaatgcatcaacataatttctgtattaaccatcatgcgcacaagaaatacatagtaaataaggaagctgaaaactcctggcattggatcttaagctagatgattagaatgtgaaaaagattttacaaatgtaaaacttctatttctctgtagaaactttcttcactttgctgtgcaagaagacactgctttgctatatttaaaatggcttttttaaaagagatttatgtatttggtaaatgtttgtagtcaacagttcacacaagaagctgtacacggtttgatcatgtaaaaccgtttggcggcacaagctggactttgttgccatccttgagatgaaccttttaagaaaaataagttaatctcaatttttccctgaatgtgttgtttttcttcattatacaataaatataatagtgaactttttatcaaatggtgaagacaatgctaaaaaaaaaaaaaaaaa
//
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
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