LOCUS       NR_000039                625 bp    RNA     linear   PRI 16-JUL-2013
DEFINITION  Homo sapiens RAB9B, member RAS oncogene family pseudogene 1
            (RAB9BP1), non-coding RNA.
ACCESSION   NR_000039
VERSION     NR_000039.2  GI:208022627
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 625)
  AUTHORS   Davies,J.P., Cotter,P.D. and Ioannou,Y.A.
  TITLE     Cloning and mapping of human Rab7 and Rab9 cDNA sequences and
            identification of a Rab9 pseudogene
  JOURNAL   Genomics 41 (1), 131-134 (1997)
   PUBMED   9126495
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC091987.2.
            On Oct 2, 2008 this sequence version replaced gi:24371441.
            
            ##Evidence-Data-START##
            Transcript is intronless :: U44105.1 [ECO:0000345]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-625               AC091987.2         26344-26968         c
FEATURES             Location/Qualifiers
     source          1..625
                     /organism="Homo sapiens"
                     /mol_type="transcribed RNA"
                     /db_xref="taxon:9606"
                     /chromosome="5"
                     /map="5q21.2"
     gene            1..625
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /note="RAB9B, member RAS oncogene family pseudogene 1"
                     /pseudo
                     /db_xref="GeneID:9366"
                     /db_xref="HGNC:9793"
     misc_RNA        1..625
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /product="RAB9B, member RAS oncogene family pseudogene 1"
                     /pseudo
                     /db_xref="GeneID:9366"
                     /db_xref="HGNC:9793"
     exon            1..625
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       44
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:192568215"
     variation       63
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:148531807"
     variation       81
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184856961"
     variation       97
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:113754985"
     variation       148
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:188741095"
     variation       202
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:4571441"
     variation       324
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:112353592"
     variation       338
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:142876485"
     variation       340
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:146533723"
     variation       414
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:181452503"
     variation       428
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:184447296"
     variation       434
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:113231648"
     variation       562
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="a"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:4264921"
     variation       576
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:189183142"
     variation       613
                     /gene="RAB9BP1"
                     /gene_synonym="RAB9P1"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:141242683"
ORIGIN      

acggcaggaaaatcatcactttttaaagtaattctctttggagatggtggagttggaaagagttatcttatgcacagatatgtaattaataagtttgatacccagctctttcatacaataggtgtggaatttttaagtaaagatttggaagtggatggacattttggtaccaagtagaattgggacacagcaggtcaggagtgattctgaagcctgaggatgccattttacagaggttctgactgctgcctgcttacttttagtgttgacaattccaaagcttccagaacttaagtaactggaagaaagaattcttatatttcgctgatgtgaaagaacccaaaagctttccttttgtaattttgggtaacaagactgacagtgaacagcaggtgtctgcagaagaagcccaagcctggtgcagggacggcagcgactatccttaatttgaaacaagtgcaaaagatgccacaaatgtggcagtagcatttgaaaagggggttccaagagttcttactaccagggataggtcagatcacttgactcagagagtgatggtctgacttcatcgaaaccattggtcaatcttcattgaaagcccaagcctagctcatcttaatgttga

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