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2024-03-28 22:47:42, GGRNA : RefSeq release 60 (20130726)

LOCUS       NR_002311                983 bp    RNA     linear   PRI 16-JUL-2013
DEFINITION  Homo sapiens VENT homeobox pseudogene 7 (VENTXP7), non-coding RNA.
ACCESSION   NR_002311
VERSION     NR_002311.1  GI:63025197
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 983)
  AUTHORS   Moretti,P.A., Davidson,A.J., Baker,E., Lilley,B., Zon,L.I. and
            D'Andrea,R.J.
  TITLE     Molecular cloning of a human Vent-like homeobox gene
  JOURNAL   Genomics 76 (1-3), 21-29 (2001)
   PUBMED   11549314
REFERENCE   2  (bases 1 to 983)
  AUTHORS   Moretti,P., Simmons,P., Thomas,P., Haylock,D., Rathjen,P., Vadas,M.
            and D'Andrea,R.
  TITLE     Identification of homeobox genes expressed in human haemopoietic
            progenitor cells
  JOURNAL   Gene 144 (2), 213-219 (1994)
   PUBMED   7518789
COMMENT     PROVISIONAL REFSEQ: This record is based on preliminary annotation
            provided by NCBI staff in collaboration with Anne Booth and Peter
            Holland. The reference sequence was derived from AC104183.2.
            
            Summary: Homeobox genes encode DNA-binding proteins, many of which
            are thought to be involved in early embryonic development. Homeobox
            genes encode a DNA-binding domain of 60 to 63 amino acids referred
            to as the homeodomain. This pseudogene is a member of the Vent
            homeobox gene family. [provided by RefSeq, Jul 2008].
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-983               AC104183.2         107865-108847
FEATURES             Location/Qualifiers
     source          1..983
                     /organism="Homo sapiens"
                     /mol_type="transcribed RNA"
                     /db_xref="taxon:9606"
                     /chromosome="3"
                     /map="3p24.3"
     gene            1..983
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /note="VENT homeobox pseudogene 7"
                     /pseudo
                     /db_xref="GeneID:391518"
                     /db_xref="HGNC:13638"
     misc_RNA        1..983
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /product="VENT homeobox pseudogene 7"
                     /pseudo
                     /db_xref="GeneID:391518"
                     /db_xref="HGNC:13638"
     exon            1..983
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       57
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:409972"
     variation       80
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:375267013"
     variation       119
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:409974"
     variation       120
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:371532"
     variation       137
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:181960475"
     variation       152
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:74754190"
     variation       153
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:79026794"
     variation       190
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:35986875"
     variation       204
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:186114023"
     variation       207..227
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace=""
                     /replace="gctagctcgtcaaatctgcat"
                     /db_xref="dbSNP:376007300"
     variation       220
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:138634288"
     variation       275
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:4857993"
     variation       308
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:366161"
     variation       416
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:190591886"
     variation       430
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:142715866"
     variation       456
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:147375591"
     variation       507
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:11718548"
     variation       518
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:138058311"
     variation       582
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:430387"
     variation       617
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:440905"
     variation       664
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:141708999"
     variation       665
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:180877648"
     variation       679
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:800605"
     variation       684..685
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace=""
                     /replace="cc"
                     /db_xref="dbSNP:112237068"
     variation       740
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:776644"
     variation       748
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:372420655"
     variation       773
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:377531093"
     variation       780
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11129005"
     variation       799..800
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace=""
                     /replace="acat"
                     /db_xref="dbSNP:371788955"
     variation       818
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:72625843"
     variation       819
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:150567334"
     variation       833
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:376847119"
     variation       958
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:74878128"
     variation       964
                     /gene="VENTXP7"
                     /gene_synonym="HPX42; VENTX1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:77654249"
ORIGIN      


acctgaccgccatgtgtctctcctcctccccacctcgtggctggcagcagccctccagctttggctccgtggactggctctgcctgagcagctgctcagggtcgacccacacccccaggcctgccgacgtctcccccgggagcctccctggcccgggccagacgttcggcacccgggagccccctcaggctgtcagtaccaaggaggctagctcgtcaaatctgcatgcgccggagaggactgtggctgggttgagtaaggagccaaacccctagctggctcccggtgtccgcacagccttcaccacggagcaggtccgtgccttggagggcgtcttccggcaccaccagtacctgggccctctggagcggaattggctggccagggagatgcagctctcagaggtccagataaaaacctggtttcaaaatcgccggatgaaacacaaacggcaaatgcaggactcccagctaaacggccccttatcggggtctctccacgggccccctgctttccactcaccatcttctggccttgccaatggcctgcagctgctgtgcccttgggcacccctgcctgggtcccctggctgccccttggctccttctggggtctccgacaaatggatcaagaggccctggcctcttcgtgggcttcctgctgcgggcagcctctggcataccaccccccacgcccaggaagtggtgcgcataagctgggaccagccctgtccacggggccccggggcctgtgtgctctgccagagacaggggatgcatttgaggaaacgcctccgactacatgcctcccacacaagcggtctgtgcagatcgcatctgacgcctacccggaggactcagctgttctgtttacatcgtggcggcacctctcaccctgaccctcgcaaaggttctggagatttctggagaatatatttgttaaagtcacctcttcacttaaaaaaaaaaaaaaaaaaaaaaaaa
//

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