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2024-03-28 21:02:03, GGRNA : RefSeq release 60 (20130726)

LOCUS       NR_046375                810 bp    RNA     linear   PRI 16-JUL-2013
DEFINITION  Homo sapiens MRVI1 antisense RNA 1 (MRVI1-AS1), transcript variant
            2, non-coding RNA.
ACCESSION   NR_046375
VERSION     NR_046375.1  GI:378548185
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 810)
  AUTHORS   Kimura,K., Wakamatsu,A., Suzuki,Y., Ota,T., Nishikawa,T.,
            Yamashita,R., Yamamoto,J., Sekine,M., Tsuritani,K., Wakaguri,H.,
            Ishii,S., Sugiyama,T., Saito,K., Isono,Y., Irie,R., Kushida,N.,
            Yoneyama,T., Otsuka,R., Kanda,K., Yokoi,T., Kondo,H., Wagatsuma,M.,
            Murakawa,K., Ishida,S., Ishibashi,T., Takahashi-Fujii,A.,
            Tanase,T., Nagai,K., Kikuchi,H., Nakai,K., Isogai,T. and Sugano,S.
  TITLE     Diversification of transcriptional modulation: large-scale
            identification and characterization of putative alternative
            promoters of human genes
  JOURNAL   Genome Res. 16 (1), 55-65 (2006)
   PUBMED   16344560
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            DB071465.1, BU569149.1 and AI075905.1.
            
            Transcript Variant: This variant (2) lacks an internal exon,
            compared to variant 1.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BU569149.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025083, ERS025084 [ECO:0000350]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-76                DB071465.1         4-79
            77-731              BU569149.1         4-658
            732-810             AI075905.1         1-79                c
FEATURES             Location/Qualifiers
     source          1..810
                     /organism="Homo sapiens"
                     /mol_type="transcribed RNA"
                     /db_xref="taxon:9606"
                     /chromosome="11"
                     /map="11p15.4"
     gene            1..810
                     /gene="MRVI1-AS1"
                     /note="MRVI1 antisense RNA 1"
                     /db_xref="GeneID:100129827"
                     /db_xref="HGNC:43434"
     misc_RNA        1..810
                     /gene="MRVI1-AS1"
                     /product="MRVI1 antisense RNA 1, transcript variant 2"
                     /db_xref="GeneID:100129827"
                     /db_xref="HGNC:43434"
     exon            1..307
                     /gene="MRVI1-AS1"
                     /inference="alignment:Splign:1.39.8"
     variation       16
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:113869643"
     variation       48
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:367611654"
     variation       154
                     /gene="MRVI1-AS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1462940"
     variation       195
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:16907957"
     variation       274
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1979367"
     variation       280
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:16907959"
     exon            308..446
                     /gene="MRVI1-AS1"
                     /inference="alignment:Splign:1.39.8"
     variation       397
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:183636382"
     exon            447..558
                     /gene="MRVI1-AS1"
                     /inference="alignment:Splign:1.39.8"
     variation       449
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:375605649"
     variation       463
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:368923760"
     variation       470
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200472330"
     variation       479
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:375909923"
     variation       486
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:368228015"
     variation       496
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:373545447"
     variation       502
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376790854"
     variation       506
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:371383883"
     variation       507
                     /gene="MRVI1-AS1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:376079865"
     exon            559..800
                     /gene="MRVI1-AS1"
                     /inference="alignment:Splign:1.39.8"
     variation       601
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:185808082"
     variation       663
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375132397"
     variation       727
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:149429287"
     variation       771
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:189927339"
     variation       778
                     /gene="MRVI1-AS1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:144853682"
     variation       782
                     /gene="MRVI1-AS1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:78994316"
ORIGIN      


aaagccccgccccccgcgcgttgccgggagacggcgcccaaccttcctctgcagcgcccctaccgacccgcgctccgcagctcctgagggctttcgagcccagatggtcatctgagacgagaggtggcggcgaaggagagtctcgcctgtcacgctcccggagcaggggcttcatgaggtggccatggaaacagcctggcagactcccatctctcctggtgccatctccggagcggaaagtggagcgccccgctggcgaccaaggccgcactgagagccctggtttggtcaacagttgggctccaagtctacaggtttctaggcccttggtgagtgaagagcagttcattacgaaatgacctccaagaacaaggctcagcattctctgaaatctcatgaagcagtgtaaccagctctcaagtatcttcctgtgaactagccacagggagccctggtattccttgaacatgcatacctttcccagcgtgagggacatggaccgtgccgtgcgagggaccccatcttctgcagcaggagggagcagagaagagaacacagggattcctgttgctaaaaggtctgttttctcctgctagccaccctcatcagccagagttcaaaccctgacagtgcccatggagagatctggtccaaggcaccaacctcttcctgctggactgagaaagagcctcctactgtgtctctctttacctcagcttttgcacacctccaatatattgtccactgaagtcagaataatctaaaaataaaggctgattacctcatgtggtataaacttaaaaaaaaaaa
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