LOCUS AF109733 2746 bp mRNA linear HUM 06-APR-1999 DEFINITION Homo sapiens SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin D1 (SMARCD1) mRNA, complete cds. ACCESSION AF109733 VERSION AF109733.1 KEYWORDS . 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 2746) AUTHORS Wang,W., Xue,Y., Zhou,S., Kuo,A., Cairns,B.R. and Crabtree,G.R. TITLE Diversity and specialization of mammalian SWI/SNF complexes JOURNAL Genes Dev. 10 (17), 2117-2130 (1996) PUBMED 8804307 REFERENCE 2 (bases 1 to 2746) AUTHORS Ring,H.Z., Vameghi-Meyers,V., Wang,W., Crabtree,G.R. and Francke,U. TITLE Five SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin (SMARC) genes are dispersed in the human genome JOURNAL Genomics 51 (1), 140-143 (1998) PUBMED 9693044 REFERENCE 3 (bases 1 to 2746) AUTHORS Ring,H.Z. and Francke,U. TITLE Direct Submission JOURNAL Submitted (25-NOV-1998) Genetics and HHMI, Stanford University School of Medicine, B205 Beckman Center, Stanford, CA 94305, USA FEATURES Location/Qualifiers source 1..2746 /db_xref="H-InvDB:HIT000069614" /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="12" /map="12q13-q14" /tissue_type="peripheral blood" /note="from two individuals" gene 1..2746 /gene="SMARCD1" CDS 145..1506 /gene="SMARCD1" /note="BAF60a; similar to sequences presented in GenBank Accession Numbers U66617, U66618, U66619 and U66620" /codon_start=1 /product="SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin D1" /protein_id="AAD23390.1" /translation="MLPGSRMTPQGPSMGPPGYGGNPSVRPGLAQSGMDQSRKRPAPQ QIQQVQQQAVQNRNHNAKKKKMADKILPQRIRELVPESQAYMDLLAFERKLDQTIMRK RLDIQEALKRPIKQKRKLRIFISNTFNPAKSDAEDGEGTVASWELRVEGRLLEDSALS KYDATKQKRKFSSFFKSLVIELDKDLYGPDNHLVEWHRTATTQETDGFQVKRPGDVNV RCTVLLMLDYQPPQFKLDPRLARLLGIHTQTRPVIIQALWQYIKTHKLQDPHEREFVI CDKYLQQIFESQRMKFSEIPQRLHALLMPPEPIIINHVISVDPNDQKKTACYDIDVEV DDTLKTQMNSFLLSTASQQEIATLDNKIHETIETINQLKTQREFMLSFARDPQGFIND WLQSQCRDLKTMTDVVGNPEEERRAEFYFQPWAQEAVCRYFYSKVQQRRQELEQALGI RNT" misc_difference 1228..1350 /gene="SMARCD1" /note="difference between this sequence and Homo sapiens sequence presented in GenBank Accession Number U66617" /replace="" BASE COUNT 628 a 777 c 686 g 655 t ORIGIN 1 ggcgccggag cctcaggagg ggcgggcgcg gctgctgcct tgggcccggg cggaactccg 61 gggcctcctg tgcgaatggg cccggctccg ggtcaagggc tgtaccgctc cccgatgccc 121 ggagcggcct atccgagacc aggtatgttg ccaggcagcc gaatgacacc tcagggacct 181 tccatgggac cccctggcta tggggggaac ccttcagtcc gacctggcct ggcccagtca 241 gggatggatc agtcccgcaa gagacctgcc cctcagcaga tccagcaggt ccagcagcag 301 gcggtccaaa atcgaaacca caatgcaaag aaaaagaaga tggctgacaa aattctacct 361 caaaggattc gtgaactggt accagaatcc caggcctata tggatctctt ggcttttgaa 421 aggaaactgg accagactat catgaggaaa cggctagata tccaagaggc cttgaaacgt 481 cccatcaagc aaaaacggaa gctgcgaatt ttcatttcta acactttcaa tccggctaag 541 tcagatgccg aggatgggga agggacggtg gcttcctggg agcttcgggt agaaggacgg 601 ctcctggagg attcagcctt gtccaaatat gatgccacta aacaaaagag gaagttctct 661 tcctttttta agtccttggt gattgaactg gacaaagacc tgtatgggcc agacaaccat 721 ctggtagaat ggcacaggac cgccactacc caggagaccg atggctttca ggtgaagcgg 781 ccgggagacg tgaatgtacg gtgtactgtc ctactgatgc tggattacca gcctccccag 841 tttaaattag acccccgcct agctcgactc ctgggcatcc atacccagac tcgtccagtg 901 atcatccaag cactgtggca atatattaag acacataagc tccaggaccc tcacgagcgg 961 gagtttgtca tctgtgacaa gtacctgcag cagatctttg agtctcaacg tatgaagttt 1021 tcagagatcc ctcagcggct ccatgccttg cttatgccac cagaacctat catcattaat 1081 catgtcatca gtgttgaccc gaatgatcag aaaaagacag cttgttatga cattgatgtt 1141 gaagtggatg acaccttgaa gacccagatg aattcttttc tgctgtccac tgccagccaa 1201 caggagattg ctactctaga caacaagatc catgagacaa tagaaaccat caaccagctg 1261 aagactcagc gggagttcat gctgagcttt gccagagacc ctcagggttt catcaatgac 1321 tggcttcagt cccagtgcag ggacctcaag acaatgactg atgtggtggg taacccagag 1381 gaggagcgcc gagctgagtt ctacttccag ccctgggctc aggaggctgt gtgccgatac 1441 ttctactcca aggtgcagca gagacgacaa gaattagagc aagccctggg aatccggaat 1501 acatagggcc tctcccacag ccctgattcg actgcaccaa ttcttgattt gggccctgtg 1561 ctgcctgcct catagtatct gccttggtct tgcttggggc gttccagggg atgctgttgg 1621 ttcaaggaca acaccagaat gaagagggtc tcacaagaca cctgttatcc tcttctttca 1681 ccctatctct tcccaccccc agcttccctt tgccccacaa agttcccatg tgcctgtacc 1741 ctcccctggt ctacatagga cctctagata gtgttagaga gagaacatgt agtggtaatg 1801 agtgcttgga atggattggc ctcaggccag gtggtcttca aggggaccag ctaactgatc 1861 ctacccttca gagacccagg agttgggagc tttcgctcct tctccaagac tcaggcctgt 1921 gggcactcta taagctagtt gatcttggct ctcctgataa cagaatccaa tttccttcct 1981 tccctccaca ggtttggaac aaactctccc ttcacttgtt gccctgtagc actacagaaa 2041 ccctggttct tggctccact gagccccagg tcagtcccca gcctctgggt tggcctgctg 2101 tcagtgcttc tctcactcct tagttggggt ccacatcagt attggagttt tgttctttat 2161 tgctccctcc cagacactcc ctgtggctgc cctttgtgat tccctcagat ctgccctaat 2221 cccgggcatt tgggtggggg aatcttgcct ttccctttca gagccccagg gatctcatct 2281 ggggaactgt cattgccagc agaggctgtt ccttcctgct gtttggagat gtgactcatt 2341 cattcactca ctccaccctg cctctgcatc ccttaatgga gaaacgggcc taaaaccaaa 2401 cgggtaaaaa gccctgggcc atccctgtct tcctgtccct tgtctgccca gttgacacct 2461 actggtgact tctagggcac tgaggagtga aagcgcctag ggctggagaa tagcgctgag 2521 ttgggtttgt gactcttccc tctccctgcc tcacaggatt gtgactcccc agcccctgcc 2581 ctcaaagctt cagacccctc aggtagcagc aggaccttgt gatcttggcc ccttggatct 2641 gagatggttt ttgcatcttt ccaggagagc ctcacattct tcttccaggt tgtatcaccc 2701 ccgagttagc atatcccagg ctcgcagact caacacagca agggtg //