Homo sapiens (human): 4205 Help Entry 4205              CDS       T01001                                  Symbol MEF2A, ADCAD1, RSRFC4, RSRFC9, mef2 Name (RefSeq) myocyte enhancer factor 2A   KO K09260   MADS-box transcription enhancer factor 2A Organism hsa  Homo sapiens (human) Pathway hsa04022   cGMP-PKG signaling pathway hsa04371   Apelin signaling pathway hsa04928   Parathyroid hormone synthesis, secretion and action hsa05418   Fluid shear stress and atherosclerosis Disease H01742   Coronary artery disease H02505   Atherosclerosis Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04371 Apelin signaling pathway     4205 (MEF2A)    04022 cGMP-PKG signaling pathway     4205 (MEF2A)  09150 Organismal Systems   09152 Endocrine system    04928 Parathyroid hormone synthesis, secretion and action     4205 (MEF2A)  09160 Human Diseases   09166 Cardiovascular disease    05418 Fluid shear stress and atherosclerosis     4205 (MEF2A)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     4205 (MEF2A) Transcription factors [BR:hsa03000]  Eukaryotic type   beta-Scaffold factors with minor groove contacts    MADS-box regulators of differentiation, MEF-2     4205 (MEF2A) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SRF-TF HJURP_C Motif Other DBs NCBI-GeneID:  4205 NCBI-ProteinID:  NP_001306135 OMIM:  600660 HGNC:  6993 Ensembl:  ENSG00000068305 UniProt:  Q02078 A0A0S2Z4N0 Structure PDBPDBj LinkDB All DBs Position 15:99565417..99716488 Genome browser AA seq 505 aa AA seqDB search MGRKKIQITRIMDERNRQVTFTKRKFGLMKKAYELSVLCDCEIALIIFNSSNKLFQYAST DMDKVLLKYTEYNEPHESRTNSDIVETLRKKGLNGCESPDADDYFEHSPLSEDRFSKLNE DSDFIFKRGPPGLPPQNFSMSVTVPVTSPNALSYTNPGSSLVSPSLAASSTLTDSSMLSP PQTTLHRNVSPGAPQRPPSTGNAGGMLSTTDLTVPNGAGSSPVGNGFVNSRASPNLIGAT GANSLGKVMPTKSPPPPGGGNLGMNSRKPDLRVVIPPSSKGMMPPLSEEEELELNTQRIS SSQATQPLATPVVSVTTPSLPPQGLVYSAMPTAYNTDYSLTSADLSALQGFNSPGMLSLG QVSAWQQHHLGQAALSSLVAGGQLSQGSNLSINTNQNISIKSEPISPPRDRMTPSGFQQQ QQQQQQQQPPPPPQPQPQPPQPQPRQEMGRSPVDSLSSSSSSYDGSDREDPRGDFHSPIV LGRPPNTEDRESPSVKRMRMDAWVT NT seq 1518 nt NT seq  +upstreamnt  +downstreamnt atggggcggaagaaaatacaaatcacacgcataatggatgaaaggaaccgacaggtcact tttacaaagagaaagtttggattaatgaagaaagcctatgaacttagtgtgctctgtgac tgtgaaatagcactcatcattttcaacagctctaacaaactgtttcaatatgctagcact gatatggacaaagttcttctcaagtatacagaatataatgaacctcatgaaagcagaacc aactcggatattgttgagactttaagaaagaaaggccttaatggttgtgagagccctgat gctgacgattactttgagcacagtccactctcggaggacagattcagcaaactaaatgaa gatagtgattttattttcaaacgaggccctcctggtctgccacctcagaacttttcaatg tctgtcacagttccagtgaccagccccaatgctttgtcctacactaacccagggagttca ctggtgtccccatctttggcagccagctcaacgttaacagattcaagcatgctctctcca cctcaaaccacattacatagaaatgtgtctcctggagctcctcagagaccaccaagtact ggcaatgcaggtgggatgttgagcactacagacctcacagtgccaaatggagctggaagc agtccagtggggaatggatttgtaaactcaagagcttctccaaatttgattggagctact ggtgcaaatagcttaggcaaagtcatgcctacaaagtctccccctccaccaggtggtggt aatcttggaatgaacagtaggaaaccagatcttcgagttgtcatccccccttcaagcaag ggcatgatgcctccactatcggaggaagaggaattggagttgaatacccagaggatcagt agttctcaagccactcaacctcttgctaccccagtcgtgtctgtgacaaccccaagcttg cctccgcaaggacttgtgtactcagcaatgccgactgcctacaacactgattattcactg accagcgctgacctgtcagcccttcaaggcttcaactcgccaggaatgctgtcgctggga caggtgtcggcctggcagcagcaccacctaggacaagcagccctcagctctcttgttgct ggagggcagttatctcagggttccaatttatccattaataccaaccaaaacatcagcatc aagtccgaaccgatttcacctcctcgggatcgtatgaccccatcgggcttccagcagcag cagcagcagcagcagcagcagcagccgccgccaccaccgcagccccagccacaacccccg cagccccagccccgacaggaaatggggcgctcccctgtggacagtctgagcagctctagt agctcctatgatggcagtgatcgggaggatccacggggcgacttccattctccaattgtg cttggccgacccccaaacactgaggacagagaaagcccttctgtaaagcgaatgaggatg gacgcgtgggtgacctaa

Homo sapiens (human): 4208 Help Entry 4208              CDS       T01001                                  Symbol MEF2C, C5DELq14.3, DEL5q14.3, NEDHSIL Name (RefSeq) myocyte enhancer factor 2C   KO K04454   MADS-box transcription enhancer factor 2C Organism hsa  Homo sapiens (human) Pathway hsa04010   MAPK signaling pathway hsa04022   cGMP-PKG signaling pathway hsa04371   Apelin signaling pathway hsa04921   Oxytocin signaling pathway hsa04928   Parathyroid hormone synthesis, secretion and action hsa05202   Transcriptional misregulation in cancer hsa05418   Fluid shear stress and atherosclerosis Network nt06240  Transcription (cancer)   Element N00119   MLL-AF4 fusion to transcriptional activation Disease H00773   Autosomal dominant intellectual developmental disorder H01223   Mental retardation-stereotypic movements-epilepsy and/or cerebral malformations Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04010 MAPK signaling pathway     4208 (MEF2C)    04371 Apelin signaling pathway     4208 (MEF2C)    04022 cGMP-PKG signaling pathway     4208 (MEF2C)  09150 Organismal Systems   09152 Endocrine system    04921 Oxytocin signaling pathway     4208 (MEF2C)    04928 Parathyroid hormone synthesis, secretion and action     4208 (MEF2C)  09160 Human Diseases   09161 Cancer: overview    05202 Transcriptional misregulation in cancer     4208 (MEF2C)   09166 Cardiovascular disease    05418 Fluid shear stress and atherosclerosis     4208 (MEF2C)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     4208 (MEF2C) Transcription factors [BR:hsa03000]  Eukaryotic type   beta-Scaffold factors with minor groove contacts    MADS-box regulators of differentiation, MEF-2     4208 (MEF2C) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SRF-TF HJURP_C Motif Other DBs NCBI-GeneID:  4208 NCBI-ProteinID:  NP_001180279 OMIM:  600662 HGNC:  6996 Ensembl:  ENSG00000081189 UniProt:  Q06413 LinkDB All DBs Position 5:complement(88717117..88904105) Genome browser AA seq 473 aa AA seqDB search MGRKKIQITRIMDERNRQVTFTKRKFGLMKKAYELSVLCDCEIALIIFNSTNKLFQYAST DMDKVLLKYTEYNEPHESRTNSDIVETLRKKGLNGCDSPDPDADDSVGHSPESEDKYRKI NEDIDLMISRQRLCAVPPPNFEMPVSIPVSSHNSLVYSNPVSSLGNPNLLPLAHPSLQRN SMSPGVTHRPPSAGNTGGLMGGDLTSGAGTSAGNGYGNPRNSPGLLVSPGNLNKNMQAKS PPPMNLGMNNRKPDLRVLIPPGSKNTMPSVSEDVDLLLNQRINNSQSAQSLATPVVSVAT PTLPGQGMGGYPSAISTTYGTEYSLSSADLSSLSGFNTASALHLGSVTGWQQQHLHNMPP SALSQLGACTSTHLSQSSNLSLPSTQSLNIKSEPVSPPRDRTTTPSRYPQHTRHEAGRSP VDSLSSCSSSYDGSDREDHRNEFHSPIGLTRPSPDERESPSVKRMRLSEGWAT NT seq 1422 nt NT seq  +upstreamnt  +downstreamnt atggggagaaaaaagattcagattacgaggattatggatgaacgtaacagacaggtgaca tttacaaagaggaaatttgggttgatgaagaaggcttatgagctgagcgtgctgtgtgac tgtgagattgcgctgatcatcttcaacagcaccaacaagctgttccagtatgccagcacc gacatggacaaagtgcttctcaagtacacggagtacaacgagccgcatgagagccggaca aactcagacatcgtggagacgttgagaaagaagggccttaatggctgtgacagcccagac cccgatgcggacgattccgtaggtcacagccctgagtctgaggacaagtacaggaaaatt aacgaagatattgatctaatgatcagcaggcaaagattgtgtgctgttccacctcccaac ttcgagatgccagtctccatcccagtgtccagccacaacagtttggtgtacagcaaccct gtcagctcactgggaaaccccaacctattgccactggctcacccttctctgcagaggaat agtatgtctcctggtgtaacacatcgacctccaagtgcaggtaacacaggtggtctgatg ggtggagacctcacgtctggtgcaggcaccagtgcagggaacgggtatggcaatccccga aactcaccaggtctgctggtctcacctggtaacttgaacaagaatatgcaagcaaaatct cctcccccaatgaatttaggaatgaataaccgtaaaccagatctccgagttcttattcca ccaggcagcaagaatacgatgccatcagtgtctgaggatgtcgacctgcttttgaatcaa aggataaataactcccagtcggctcagtcattggctaccccagtggtttccgtagcaact cctactttaccaggacaaggaatgggaggatatccatcagccatttcaacaacatatggt accgagtactctctgagtagtgcagacctgtcatctctgtctgggtttaacaccgccagc gctcttcaccttggttcagtaactggctggcaacagcaacacctacataacatgccacca tctgccctcagtcagttgggagcttgcactagcactcatttatctcagagttcaaatctc tccctgccttctactcaaagcctcaacatcaagtcagaacctgtttctcctcctagagac cgtaccaccaccccttcgagatacccacaacacacgcgccacgaggcggggagatctcct gttgacagcttgagcagctgtagcagttcgtacgacgggagcgaccgagaggatcaccgg aacgaattccactcccccattggactcaccagaccttcgccggacgaaagggaaagtccc tcagtcaagcgcatgcgactttctgaaggatgggcaacatga

Homo sapiens (human): 4209 Help Entry 4209              CDS       T01001                                  Symbol MEF2D Name (RefSeq) myocyte enhancer factor 2D   KO K09262   MADS-box transcription enhancer factor 2D Organism hsa  Homo sapiens (human) Pathway hsa04022   cGMP-PKG signaling pathway hsa04371   Apelin signaling pathway hsa04928   Parathyroid hormone synthesis, secretion and action Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04371 Apelin signaling pathway     4209 (MEF2D)    04022 cGMP-PKG signaling pathway     4209 (MEF2D)  09150 Organismal Systems   09152 Endocrine system    04928 Parathyroid hormone synthesis, secretion and action     4209 (MEF2D)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     4209 (MEF2D)    04131 Membrane trafficking [BR:hsa04131]     4209 (MEF2D) Transcription factors [BR:hsa03000]  Eukaryotic type   beta-Scaffold factors with minor groove contacts    MADS-box regulators of differentiation, MEF-2     4209 (MEF2D) Membrane trafficking [BR:hsa04131]  Autophagy   Chaperone mediated autophagy (CMA)    Selective cargos     4209 (MEF2D) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  SRF-TF HJURP_C CCDC53 TFIIA Motif Other DBs NCBI-GeneID:  4209 NCBI-ProteinID:  NP_005911 OMIM:  600663 HGNC:  6997 Ensembl:  ENSG00000116604 UniProt:  Q14814 Structure PDBPDBj LinkDB All DBs Position 1:complement(156463727..156500775) Genome browser AA seq 521 aa AA seqDB search MGRKKIQIQRITDERNRQVTFTKRKFGLMKKAYELSVLCDCEIALIIFNHSNKLFQYAST DMDKVLLKYTEYNEPHESRTNADIIETLRKKGFNGCDSPEPDGEDSLEQSPLLEDKYRRA SEELDGLFRRYGSTVPAPNFAMPVTVPVSNQSSLQFSNPSGSLVTPSLVTSSLTDPRLLS PQQPALQRNSVSPGLPQRPASAGAMLGGDLNSANGACPSPVGNGYVSARASPGLLPVANG NSLNKVIPAKSPPPPTHSTQLGAPSRKPDLRVITSQAGKGLMHHLTEDHLDLNNAQRLGV SQSTHSLTTPVVSVATPSLLSQGLPFSSMPTAYNTDYQLTSAELSSLPAFSSPGGLSLGN VTAWQQPQQPQQPQQPQPPQQQPPQPQQPQPQQPQQPQQPPQQQSHLVPVSLSNLIPGSP LPHVGAALTVTTHPHISIKSEPVSPSRERSPAPPPPAVFPAARPEPGDGLSSPAGGSYET GDRDDGRGDFGPTLGLLRPAPEPEAEGSAVKRMRLDTWTLK NT seq 1566 nt NT seq  +upstreamnt  +downstreamnt atggggaggaaaaagattcagatccagcgaatcaccgacgagcggaaccgacaggtgact ttcaccaagcggaagtttggcctgatgaagaaggcgtatgagctgagcgtgctatgtgac tgcgagatcgcactcatcatcttcaaccactccaacaagctgttccagtacgccagcacc gacatggacaaggtgctgctcaagtacacggagtacaatgagccacacgagagccgcacc aacgccgacatcatcgagaccctgaggaagaagggcttcaacggctgcgacagccccgag cccgacggggaggactcgctggaacagagccccctgctggaggacaagtaccgacgcgcc agcgaggagctcgacgggctcttccggcgctatgggtcaactgtcccggcccccaacttt gccatgcctgtcacggtgcccgtgtccaatcagagctcactgcagttcagcaatcccagc ggctccctggtcaccccttccctggtgacatcatccctcacggacccgcggctcctgtcc ccccagcagccagcactacagaggaacagtgtgtctcctggcctgccccagcggccagct agtgcgggggccatgctggggggtgacctgaacagtgctaacggagcctgccccagccct gttgggaatggctacgtcagtgctcgggcttcccctggcctcctccctgtggccaatggc aacagcctaaacaaggtcatccctgccaagtctccacccccacctacccacagcacccag cttggagcccccagccgcaagcccgacctgcgagtcatcacttcccaggcaggaaagggg ttaatgcatcacttgactgaggaccatttagatctgaacaatgcccagcgccttggggtc tcccagtctactcattcgctcaccaccccagtggtttctgtggcaacgccgagtttactc agccagggcctccccttctcttccatgcccactgcctacaacacagattaccagttgacc agtgcagagctctcctccttaccagcctttagttcacctggggggctgtcgctaggcaat gtcactgcctggcaacagccacagcagccccagcagccgcagcagccacagcctccacag cagcagccaccgcagccacagcagccacagccacagcagcctcagcagccgcaacagcca cctcagcaacagtcccacctggtccctgtatctctcagcaacctcatcccgggcagcccc ctgccccacgtgggtgctgccctcacagtcaccacccacccccacatcagcatcaagtca gaaccggtgtccccaagccgtgagcgcagccctgcgcctccccctccagctgtgttccca gctgcccgccctgagcctggcgatggtctcagcagcccagccgggggatcctatgagacg ggagaccgggatgacggacggggggacttcgggcccacactgggcctgctgcgcccagcc ccagagcctgaggctgagggctcagctgtgaagaggatgcggcttgatacctggacatta aagtga

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