LOCUS       NR_003135               1091 bp    RNA     linear   PRI 16-JUL-2013
DEFINITION  Homo sapiens centrosomal protein 170kDa pseudogene 1 (CEP170P1),
            non-coding RNA.
ACCESSION   NR_003135 XR_015931 XR_017916
VERSION     NR_003135.2  GI:195539370
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 1091)
  AUTHORS   Xin,X., Rual,J.F., Hirozane-Kishikawa,T., Hill,D.E., Vidal,M.,
            Boone,C. and Thierry-Mieg,N.
  TITLE     Shifted Transversal Design smart-pooling for high coverage
            interactome mapping
  JOURNAL   Genome Res. 19 (7), 1262-1269 (2009)
   PUBMED   19447967
COMMENT     PROVISIONAL REFSEQ: This record has not yet been subject to final
            NCBI review. The reference sequence was derived from BC014590.2.
            On Aug 2, 2008 this sequence version replaced gi:112734796.
            
            Summary: This locus appears to be a transcribed pseudogene similar
            to centrosomal protein 170kDa (CEP170). An approximately 50 kb
            region upstream of this locus also is homologous to CEP170, but is
            not transcribed. [provided by RefSeq, Jul 2008].
FEATURES             Location/Qualifiers
     source          1..1091
                     /organism="Homo sapiens"
                     /mol_type="transcribed RNA"
                     /db_xref="taxon:9606"
                     /chromosome="4"
                     /map="4q26"
     gene            1..1091
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /note="centrosomal protein 170kDa pseudogene 1"
                     /pseudo
                     /db_xref="GeneID:645455"
                     /db_xref="HGNC:28364"
     misc_RNA        1..1091
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /product="centrosomal protein 170kDa pseudogene 1"
                     /pseudo
                     /db_xref="GeneID:645455"
                     /db_xref="HGNC:28364"
     exon            1..46
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       4
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2631170"
     variation       8
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:2728186"
     exon            47..173
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       62
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:200676170"
     variation       72
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185507101"
     exon            174..270
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       260
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:56219159"
     exon            271..441
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       308
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2728244"
     variation       343
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:200079270"
     variation       346
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:200878100"
     exon            442..530
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       520
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201967574"
     exon            531..624
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       554
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:7686065"
     variation       554
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:74916465"
     variation       618
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:2787261"
     exon            625..676
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       639
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:185234365"
     variation       672
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1415901"
     exon            677..1070
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /inference="alignment:Splign:1.39.8"
                     /pseudo
     variation       712
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:201105783"
     variation       865
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:192196158"
     variation       960
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:3109971"
     variation       1037
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:12182"
     variation       1041
                     /gene="CEP170P1"
                     /gene_synonym="CEP170L; FAM68B; KIAA0470L"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:147547300"
ORIGIN      

aactgacttgaagatgtgtgattattttcagtaggcagacatctaaccctgaaaaccactcgcttgcagagcgctggatcagcaatgcctactagttcttcattcaaacaccggattaaagagcaggaagactacatccgagattggactgctcatcgagaagagatagccaggatcagccaagatcttgctctcattgctcgggagatcaacgatgtagcaggagagatagattcagtgacttcatcaggcactgcccctagtaccacattggttgatcgtgtttttgatgaaagcctcaacttccaaaagattcctccattagttcattccaaaacaccagaaggaaacaacggtcgatctggtgatccaagacctcaagcagcagagcctcccgatcacttaacaattacaaggcggagaacctggagcagggatgaagtcatgggagataatctgctgctgtcatccgtctttcagttctctaagaagataagacaatctatagataagacagctggaaagatcagaatattatttaaagacaaagatcggaattgggatgacatagaaagcaaattaagagccgaaagtgaagtccctattgtgaaaacctcgagcatggagatttcttctatcttacaggaactgaaaagagtagaaaagcagctacaagcaatcaatgctatgattgatcctgatggaactttggaggctctgaacaacatgggatttcccagtgctatgttgccatctccaccgaaacagaagtccagccctgtgaataaccaccacagcccgggtcagacaccaacacttggccaaccagaagctagggctcttcatcctgctgctgtttcagccgcagctgaatttgagaatgctgaatctgaggctgatttcagtatacatttcaatagagtcaaccctgatggggaagaggaagatgttacagtacataaatgactttctcttgattgttgaaaaatcattacctgtggaatgactaggaatattggaagcagcatagtgttgacgtacgcaaaacaagacagcttggtcagctacaaaaaacaaaaaaaaaaaaaaaa

//

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:645455 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI