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2024-04-25 06:35:39, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001271629            5694 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens myocyte enhancer factor 2D (MEF2D), transcript variant
            2, mRNA.
ACCESSION   NM_001271629
VERSION     NM_001271629.1  GI:410442514
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 5694)
  AUTHORS   She,H., Yang,Q., Shepherd,K., Smith,Y., Miller,G., Testa,C. and
            Mao,Z.
  TITLE     Direct regulation of complex I by mitochondrial MEF2D is disrupted
            in a mouse model of Parkinson disease and in human patients
  JOURNAL   J. Clin. Invest. 121 (3), 930-940 (2011)
   PUBMED   21393861
  REMARK    GeneRIF: direct regulation of complex I by mitochondrial MEF2D
            underlies its neuroprotective effects, and dysregulation of this
            pathway may contribute to Parkinson disease
REFERENCE   2  (bases 1 to 5694)
  AUTHORS   Aude-Garcia,C., Collin-Faure,V., Bausinger,H., Hanau,D.,
            Rabilloud,T. and Lemercier,C.
  TITLE     Dual roles for MEF2A and MEF2D during human macrophage terminal
            differentiation and c-Jun expression
  JOURNAL   Biochem. J. 430 (2), 237-244 (2010)
   PUBMED   20590529
  REMARK    GeneRIF: MEF2A and MEF2D play dual roles in human macrophages
            differentiation, as activators and as repressors of c-jun
            transcription.
REFERENCE   3  (bases 1 to 5694)
  AUTHORS   Czubryt,M.P., Lamoureux,L., Ramjiawan,A., Abrenica,B.,
            Jangamreddy,J. and Swan,K.
  TITLE     Regulation of cardiomyocyte Glut4 expression by ZAC1
  JOURNAL   J. Biol. Chem. 285 (22), 16942-16950 (2010)
   PUBMED   20363751
  REMARK    GeneRIF: ZAC1 is a novel and previously unknown regulator of
            cardiomyocyte Glut4 expression and glucose uptake; MEF2 is a
            regulator of ZAC1 expression in response to induction of
            hypertrophy
REFERENCE   4  (bases 1 to 5694)
  AUTHORS   Yang,Q., She,H., Gearing,M., Colla,E., Lee,M., Shacka,J.J. and
            Mao,Z.
  TITLE     Regulation of neuronal survival factor MEF2D by chaperone-mediated
            autophagy
  JOURNAL   Science 323 (5910), 124-127 (2009)
   PUBMED   19119233
  REMARK    GeneRIF: MEF2D levels were increased in the brains patients with
            Parkinson's disease
REFERENCE   5  (bases 1 to 5694)
  AUTHORS   Liu,G., Han,J., Profirovic,J., Strekalova,E. and
            Voyno-Yasenetskaya,T.A.
  TITLE     Galpha13 regulates MEF2-dependent gene transcription in endothelial
            cells: role in angiogenesis
  JOURNAL   Angiogenesis 12 (1), 1-15 (2009)
   PUBMED   19093215
  REMARK    GeneRIF: MEF2 proteins are an important component in
            Galpha13-mediated angiogenesis.
REFERENCE   6  (bases 1 to 5694)
  AUTHORS   Zhao,M., New,L., Kravchenko,V.V., Kato,Y., Gram,H., di Padova,F.,
            Olson,E.N., Ulevitch,R.J. and Han,J.
  TITLE     Regulation of the MEF2 family of transcription factors by p38
  JOURNAL   Mol. Cell. Biol. 19 (1), 21-30 (1999)
   PUBMED   9858528
REFERENCE   7  (bases 1 to 5694)
  AUTHORS   Yang,C.C., Ornatsky,O.I., McDermott,J.C., Cruz,T.F. and Prody,C.A.
  TITLE     Interaction of myocyte enhancer factor 2 (MEF2) with a
            mitogen-activated protein kinase, ERK5/BMK1
  JOURNAL   Nucleic Acids Res. 26 (20), 4771-4777 (1998)
   PUBMED   9753748
REFERENCE   8  (bases 1 to 5694)
  AUTHORS   Ornatsky,O.I. and McDermott,J.C.
  TITLE     MEF2 protein expression, DNA binding specificity and complex
            composition, and transcriptional activity in muscle and non-muscle
            cells
  JOURNAL   J. Biol. Chem. 271 (40), 24927-24933 (1996)
   PUBMED   8798771
REFERENCE   9  (bases 1 to 5694)
  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   10 (bases 1 to 5694)
  AUTHORS   Breitbart,R.E., Liang,C.S., Smoot,L.B., Laheru,D.A., Mahdavi,V. and
            Nadal-Ginard,B.
  TITLE     A fourth human MEF2 transcription factor, hMEF2D, is an early
            marker of the myogenic lineage
  JOURNAL   Development 118 (4), 1095-1106 (1993)
   PUBMED   8269842
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BC040949.1, AL139412.10 and
            R42560.1.
            
            Summary: This gene is a member of the myocyte-specific enhancer
            factor 2 (MEF2) family of transcription factors. Members of this
            family are involved in control of muscle and neuronal cell
            differentiation and development, and are regulated by class II
            histone deacetylases. Fusions of the encoded protein with Deleted
            in Azoospermia-Associated Protein 1 (DAZAP1) due to a translocation
            have been found in an acute lymphoblastic leukemia cell line,
            suggesting a role in leukemogenesis. The encoded protein may also
            be involved in Parkinson disease and myotonic dystrophy.
            Alternative splicing results in multiple transcript variants.
            [provided by RefSeq, Oct 2012].
            
            Transcript Variant: This variant (2) contains an alternate exon and
            splice site in the 5' UTR, and lacks an internal in-frame exon in
            the coding region, compared to variant 1. The resulting isoform (2,
            also known as hMEF2Da0), is shorter than isoform 1.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            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 :: BC040949.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-83                BC040949.1         1-83
            84-84               AL139412.10        51073-51073         c
            85-495              BC040949.1         85-495
            496-496             AL139412.10        41505-41505         c
            497-969             BC040949.1         497-969
            970-970             AL139412.10        37668-37668         c
            971-3194            BC040949.1         971-3194
            3195-5490           AL139412.10        24471-26766         c
            5491-5694           R42560.1           1-204               c
FEATURES             Location/Qualifiers
     source          1..5694
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="1"
                     /map="1q12-q23"
     gene            1..5694
                     /gene="MEF2D"
                     /note="myocyte enhancer factor 2D"
                     /db_xref="GeneID:4209"
                     /db_xref="HGNC:6997"
                     /db_xref="MIM:600663"
     exon            1..88
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     variation       84
                     /gene="MEF2D"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:947660"
     exon            89..268
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     STS             142..317
                     /gene="MEF2D"
                     /standard_name="MARC_16813-16814:1033503049:1"
                     /db_xref="UniSTS:268128"
     misc_feature    197..199
                     /gene="MEF2D"
                     /note="upstream in-frame stop codon"
     variation       203
                     /gene="MEF2D"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:28730744"
     CDS             215..1759
                     /gene="MEF2D"
                     /note="isoform 2 is encoded by transcript variant 2; MADS
                     box transcription enhancer factor 2, polypeptide D;
                     myocyte-specific enhancer factor 2D"
                     /codon_start=1
                     /product="myocyte-specific enhancer factor 2D isoform 2"
                     /protein_id="NP_001258558.1"
                     /db_xref="GI:410442515"
                     /db_xref="GeneID:4209"
                     /db_xref="HGNC:6997"
                     /db_xref="MIM:600663"
                     /translation="
MGRKKIQIQRITDERNRQVTFTKRKFGLMKKAYELSVLCDCEIALIIFNHSNKLFQYASTDMDKVLLKYTEYNEPHESRTNADIIETLRKKGFNGCDSPEPDGEDSLEQSPLLEDKYRRASEELDGLFRRYGSTVPAPNFAMPVTVPVSNQSSLQFSNPSGSLVTPSLVTSSLTDPRLLSPQQPALQRNSVSPGLPQRPASAGAMLGGDLNSANGACPSPVGNGYVSARASPGLLPVANGNSLNKVIPAKSPPPPTHSTQLGAPSRKPDLRVITSQAGKGLMHHLNNAQRLGVSQSTHSLTTPVVSVATPSLLSQGLPFSSMPTAYNTDYQLTSAELSSLPAFSSPGGLSLGNVTAWQQPQQPQQPQQPQPPQQQPPQPQQPQPQQPQQPQQPPQQQSHLVPVSLSNLIPGSPLPHVGAALTVTTHPHISIKSEPVSPSRERSPAPPPPAVFPAARPEPGDGLSSPAGGSYETGDRDDGRGDFGPTLGLLRPAPEPEAEGSAVKRMRLDTWTLK
"
     misc_feature    218..448
                     /gene="MEF2D"
                     /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(218..226,230..232,236..238,251..253,257..259,
                     269..274,281..286,290..295,302..307,311..316,326..328)
                     /gene="MEF2D"
                     /note="DNA binding site [nucleotide binding]"
                     /db_xref="CDD:29020"
     misc_feature    order(275..277,296..301,308..313,317..322,329..331,
                     344..346,350..352,356..358,374..376,380..382,398..400,
                     407..412,419..421,428..433)
                     /gene="MEF2D"
                     /note="dimerization interface [polypeptide binding]; other
                     site"
                     /db_xref="CDD:29020"
     misc_feature    389..391
                     /gene="MEF2D"
                     /note="putative phosphorylation site [posttranslational
                     modification]; other site"
                     /db_xref="CDD:29020"
     misc_feature    497..679
                     /gene="MEF2D"
                     /note="Holliday junction regulator protein family
                     C-terminal repeat; Region: HJURP_C; pfam12347"
                     /db_xref="CDD:152782"
     misc_feature    575..577
                     /gene="MEF2D"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine, by PKA; propagated from
                     UniProtKB/Swiss-Prot (Q14814.1); phosphorylation site"
     misc_feature    752..754
                     /gene="MEF2D"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine, by MAPK7; propagated from
                     UniProtKB/Swiss-Prot (Q14814.1); phosphorylation site"
     misc_feature    905..907
                     /gene="MEF2D"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q14814.1); phosphorylation site"
     misc_feature    947..949
                     /gene="MEF2D"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N6-acetyllysine; propagated from
                     UniProtKB/Swiss-Prot (Q14814.1); acetylation site"
     misc_feature    965..967
                     /gene="MEF2D"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q14814.1); phosphorylation site"
     misc_feature    1508..1510
                     /gene="MEF2D"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="N6-acetyllysine, alternate; propagated from
                     UniProtKB/Swiss-Prot (Q14814.1); acetylation site"
     misc_feature    1523..1525
                     /gene="MEF2D"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (Q14814.1); phosphorylation site"
     STS             215..733
                     /gene="MEF2D"
                     /standard_name="Mef2d"
                     /db_xref="UniSTS:265605"
     exon            269..472
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     STS             370..733
                     /gene="MEF2D"
                     /standard_name="Mef2d"
                     /db_xref="UniSTS:238138"
     exon            473..610
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     exon            611..821
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     exon            822..878
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     exon            879..1069
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     STS             935..1045
                     /gene="MEF2D"
                     /standard_name="D1S262E"
                     /db_xref="UniSTS:147387"
     exon            1070..1199
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     exon            1200..1440
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     exon            1441..1747
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     exon            1748..5683
                     /gene="MEF2D"
                     /inference="alignment:Splign:1.39.8"
     STS             2295..3176
                     /gene="MEF2D"
                     /standard_name="MEF2D_2065"
                     /db_xref="UniSTS:280845"
     STS             2852..3009
                     /gene="MEF2D"
                     /standard_name="RH70462"
                     /db_xref="UniSTS:33507"
     STS             2966..3178
                     /gene="MEF2D"
                     /standard_name="RH81006"
                     /db_xref="UniSTS:89519"
     polyA_site      3187
                     /gene="MEF2D"
     STS             4348..4423
                     /gene="MEF2D"
                     /standard_name="1996"
                     /db_xref="UniSTS:56140"
     STS             5459..5674
                     /gene="MEF2D"
                     /standard_name="HSC1IB102"
                     /db_xref="UniSTS:25334"
     polyA_signal    5647..5652
                     /gene="MEF2D"
     polyA_site      5683
                     /gene="MEF2D"
ORIGIN      
ggggcctgagaccacccctgccctaggcccagctttcctggactgcctgcccccacaaaccaacagcccgcccccaggtccccagtcgaaggtatcctgcagaccatgaactgagcactgttcccagaccgttcatgagcacagtgtaaggtgtgccgagacccaccacccagcgagcccctcccctccgtagcactgaggacccccggagaagatggggaggaaaaagattcagatccagcgaatcaccgacgagcggaaccgacaggtgactttcaccaagcggaagtttggcctgatgaagaaggcgtatgagctgagcgtgctatgtgactgcgagatcgcactcatcatcttcaaccactccaacaagctgttccagtacgccagcaccgacatggacaaggtgctgctcaagtacacggagtacaatgagccacacgagagccgcaccaacgccgacatcatcgagaccctgaggaagaagggcttcaacggctgcgacagccccgagcccgacggggaggactcgctggaacagagccccctgctggaggacaagtaccgacgcgccagcgaggagctcgacgggctcttccggcgctatgggtcaactgtcccggcccccaactttgccatgcctgtcacggtgcccgtgtccaatcagagctcactgcagttcagcaatcccagcggctccctggtcaccccttccctggtgacatcatccctcacggacccgcggctcctgtccccccagcagccagcactacagaggaacagtgtgtctcctggcctgccccagcggccagctagtgcgggggccatgctggggggtgacctgaacagtgctaacggagcctgccccagccctgttgggaatggctacgtcagtgctcgggcttcccctggcctcctccctgtggccaatggcaacagcctaaacaaggtcatccctgccaagtctccacccccacctacccacagcacccagcttggagcccccagccgcaagcccgacctgcgagtcatcacttcccaggcaggaaaggggttaatgcatcacttgaacaatgcccagcgccttggggtctcccagtctactcattcgctcaccaccccagtggtttctgtggcaacgccgagtttactcagccagggcctccccttctcttccatgcccactgcctacaacacagattaccagttgaccagtgcagagctctcctccttaccagcctttagttcacctggggggctgtcgctaggcaatgtcactgcctggcaacagccacagcagccccagcagccgcagcagccacagcctccacagcagcagccaccgcagccacagcagccacagccacagcagcctcagcagccgcaacagccacctcagcaacagtcccacctggtccctgtatctctcagcaacctcatcccgggcagccccctgccccacgtgggtgctgccctcacagtcaccacccacccccacatcagcatcaagtcagaaccggtgtccccaagccgtgagcgcagccctgcgcctccccctccagctgtgttcccagctgcccgccctgagcctggcgatggtctcagcagcccagccgggggatcctatgagacgggagaccgggatgacggacggggggacttcgggcccacactgggcctgctgcgcccagccccagagcctgaggctgagggctcagctgtgaagaggatgcggcttgatacctggacattaaagtgacgattcccactcccctcctctcagcctccctgatgaagagttgacaatctcaccgcccgcccttccctgccccgggctcctcccgctcgacccccacttcctttcttgtgcttcgtgtcctgttgacggttacatttgtgtataattattatattattattattattattatattttttttaatttggattctcgctttggagagggggatgctctcatcccctctttctgtaccccccaccattttcactggctggggggctctctttttcgcgggaaggggggacactttgcacgttgtacacatatgctgcaggaagggggtggggggcccaataaggcctttgggaaaggacaggtgccgagccctgcatgtggagccctcccaccccacccccagatagagggaaataaccaaaaaactaccaaacaacagaaacccacactctagactgaaaccccaaagtgggcttgatgggtgggtttgtgtttcaaggggaaagtgaggcagaggttctgaaaagggtctctgtttttgtgttcatgtagccataggcacatggagcagaatacttaagcctggcccccaaatgcccctgcacacacacgtgccacacctgcgctgattcttgtgtgtgctgcacccccaaggtgtgtgggtgctggctgagctttgggccgggaaggcagcctgggaatctgaggctggagacaggggtttgaggtgggggcctctctggaagcacatttggagggaaagacaagagagccatgaggagagggctgaggagggcagaagggctaggcagggggcaaattgagcccctcccttccccagtttttctctaagatatacagtgcaatagctccccacccctcagttgacgccagccctgtaaagctggccacagtgtgcagggagaatggggagagggtcttcagtgaggtggctggggcgagagtcggcctggacttccctggggtgctccaggccagagctctttcattggggcgagtgtggtgaggggacgtccttggtcttgcacgcacactacctgggggagtcaacactgggatggtctgtggggtgggagggcctacggatgggtccgtagaggtcccacctccctcattcctccttggcccctctccctagcttctcctgttagctccttctgctcctgaccccacctccttgctcttggcgcccctattgtctctggctacctccttgtcccaccacctccaggctgcatcccaccttccctcttggctactgtaattgtaaatagcgacctttggaaaacgttagcggtgtaacagtccaggaaactgtttttttttgttgttgttgtattgatatgaaatgagattctatttttgtcaaagtatattgtaataataatgactcaaacggcccgtactgtacagacgagattcttctgctgttgttcttgctcccctcccctcctctgagtccgcccctccctgctgcctcctcagtggggcagtgggcaaggggcccaggggcagccgaagcacggggtcctgagacctcaggcaggattggagatcaaaccagagggggcaggcccccagcctgctctctaggatcaccccccgccctaaggggcctggcctggggtgacgtggccaggcagactgtctgccccactccttcacacaagcccagctcctctgcccaaggggtgcggcgcccccttggggtttcctcccagttggagagtagagttaagacaaggcccagttttgtgttagccgaccgtctttgcccacctctatgacccagcctcttgcagtattcccatacttgatgcagggaaggaaccagaagcagaggggcctctacgcaggtacacacgtgtacctgagtgtgttcatgagggcatctggtgtttatgtgtctgagtgtagctttgtatttatgtgtgtgtgtgtgtgtatgtctgattgcacgggtgtacttttgtatttatgtgtgtgtgtggttgcacgggtgtgcctctgtgtgtctctgaccctggctgggtgtgtgtgcaaatctgtgtgactggagctctaggggcatctctgtgtctgagtgtgcctggtgtgtgtttacaaagggagagttggctgctccagctccacagccctgggaccccaactcctgtcttccctgctcctttccctgtgttcaccctcagctctgacacattgaactgcagttggggggattggcagttagccctctgtgcttctccctgcagccctacctctgccaaggtctctccctccagggacctctgcttccacccacatatgtccacttagtcacccacacttgacacagttcctggagtaccctcttcccccaaccccagacctgctttcagagcaaaactcaagtccctcttcctccgtgaagcttctccctcagctgagcagtgatcacttactcactcttaaccccaatccgctgactgggtggggacagcacgtccagccttcccacctctcctgcaggcttctagacggagtttcaaaaactgatgagcctcgatccagggcttgaaagaagccagggtgtaatcttgttcatgcatgcgtccccagagcctcgcccagtgcctggcacatagtaggcactcaataaatgctgaatgggtgaatagttgaatgataggtgctcaataaatgaatgaatggccttcccttctcaggctattcccaccattagtctgcccacctttctaggctgggcttggccaccattaaacacggggtgggggtgagggcccctgcaattcacggtgcaatattcaccagttttgccctctgcctcataaaggcaaacctggcttttgattaccatgtgtggatgtttcagtgtcctttcttctctgtccctggggatggggtggtctgtgaatatgtgacatttctgcagttcagtatccgaaggtttctcttgggggtaggggctcctgggcggccagatgaatgggtccctgggaacccagacctcagatgaggacttaatgtcttcttcctctcaagccaaattcgcctccacccactccctctgaagaactgggcatttgccaaagtaaccactggagtcatctaatggccctccccctccccaggtttcccacagctttcagggacagtgggcaagaggacacccccccccaccacctcagtggaacacaccattctccccccctcaacagcacactcagtgcagcaagactgacccctgaccccctcccagccctccctaccttggacaggaaggaagtaatgcaccttctcttgctgattatttatttgtttggagagacagaaatgtaaaagtgtatctagaaatatctatatctctatatatttttaactgactctttggaatcccctggggtggggtgaggggtaagtttaggctttcgcggaggggaggagacatggagcctgggaactccttgttctcccctctgctgcctctccccaccccttaaagcagttggtagaaggaatggtatttgtatggggggagggaggctggaatggagaatctggattctctcctcttccccattctccagagggagggaggtggtgaggaagaggaagggaggggcaggatgggccatggaggtgccccacccccacacctgacaatcacccacactcctggggctcttcctgggtcctggggcagggcgagtccaagtgtgaggctgttgatttgttttcaatatttcttttcgtgctgtatggtgatgctttcttagtattctacacaataagaaaagacaaagtcctcgagattcttatgagttttgtttgaaaactctttcactatatttgttgtaaagaggtttactattaaaagaaaaagaatacacgtttctgatacttcggaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:4209 -> Molecular function: GO:0000977 [RNA polymerase II regulatory region sequence-specific DNA binding] evidence: IDA
            GeneID:4209 -> Molecular function: GO:0000981 [sequence-specific DNA binding RNA polymerase II transcription factor activity] evidence: IDA
            GeneID:4209 -> Molecular function: GO:0003700 [sequence-specific DNA binding transcription factor activity] evidence: NAS
            GeneID:4209 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:4209 -> Molecular function: GO:0033613 [activating transcription factor binding] evidence: IPI
            GeneID:4209 -> Molecular function: GO:0042826 [histone deacetylase binding] evidence: IPI
            GeneID:4209 -> Molecular function: GO:0046983 [protein dimerization activity] evidence: IEA
            GeneID:4209 -> Biological process: GO:0001649 [osteoblast differentiation] evidence: IEA
            GeneID:4209 -> Biological process: GO:0001958 [endochondral ossification] evidence: IEA
            GeneID:4209 -> Biological process: GO:0002062 [chondrocyte differentiation] evidence: IEA
            GeneID:4209 -> Biological process: GO:0006366 [transcription from RNA polymerase II promoter] evidence: IDA
            GeneID:4209 -> Biological process: GO:0006915 [apoptotic process] evidence: IEA
            GeneID:4209 -> Biological process: GO:0007399 [nervous system development] evidence: IEA
            GeneID:4209 -> Biological process: GO:0007512 [adult heart development] evidence: IEP
            GeneID:4209 -> Biological process: GO:0007517 [muscle organ development] evidence: TAS
            GeneID:4209 -> Biological process: GO:0035914 [skeletal muscle cell differentiation] evidence: IEA
            GeneID:4209 -> Biological process: GO:0045944 [positive regulation of transcription from RNA polymerase II promoter] evidence: IDA
            GeneID:4209 -> Cellular component: GO:0005634 [nucleus] evidence: IDA
            GeneID:4209 -> Cellular component: GO:0005730 [nucleolus] evidence: IDA
            GeneID:4209 -> Cellular component: GO:0043231 [intracellular membrane-bounded organelle] evidence: IDA

by @meso_cacase at DBCLS
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