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2024-04-18 12:07:50, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001105528            3398 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens coiled-coil domain containing 178 (CCDC178),
            transcript variant 1, mRNA.
ACCESSION   NM_001105528
VERSION     NM_001105528.1  GI:157671918
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 3398)
  AUTHORS   Tao,S., Wang,Z., Feng,J., Hsu,F.C., Jin,G., Kim,S.T., Zhang,Z.,
            Gronberg,H., Zheng,L.S., Isaacs,W.B., Xu,J. and Sun,J.
  TITLE     A genome-wide search for loci interacting with known prostate
            cancer risk-associated genetic variants
  JOURNAL   Carcinogenesis 33 (3), 598-603 (2012)
   PUBMED   22219177
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            BC091517.1, AC104956.6, BC130535.1, AC025888.8 and AK000027.1.
            
            Transcript Variant: This variant (1) represents the longer
            transcript and encodes the longer isoform (1).
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC130535.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025084 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-1535              BC091517.1         42-1576
            1536-1536           AC104956.6         56342-56342         c
            1537-1942           BC130535.1         1474-1879
            1943-1943           AC025888.8         164652-164652       c
            1944-3085           BC130535.1         1881-3022
            3086-3398           AK000027.1         607-919
FEATURES             Location/Qualifiers
     source          1..3398
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="18"
                     /map="18q12.1"
     gene            1..3398
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /note="coiled-coil domain containing 178"
                     /db_xref="GeneID:374864"
                     /db_xref="HGNC:29588"
     exon            1..120
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            121..200
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    125..127
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /note="upstream in-frame stop codon"
     CDS             143..2746
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /note="isoform 1 is encoded by transcript variant 1;
                     coiled-coil domain-containing protein 178"
                     /codon_start=1
                     /product="coiled-coil domain-containing protein 178
                     isoform 1"
                     /protein_id="NP_001098998.1"
                     /db_xref="GI:157671919"
                     /db_xref="CCDS:CCDS42424.1"
                     /db_xref="GeneID:374864"
                     /db_xref="HGNC:29588"
                     /translation="
MTENKTVSSSSTRDDQTNIGLTCQEVKALREKAWSRTNEGNAMSQSLVLYGASKENSEGFHESKMTNTEGVNKGIYFSYPCRRHSCAVVNIPAPCVNKMISHIQDVESKIQEHLKRFETSFEEWSRTSSTKDLKEDWSVTTPVKEVKPGEKRDEKCPELKQEMETLLSEAIRLIKSLETDRADAEEALKQQRSRKNMINMKIDSWSVWKLQELPLAVQKEHEAYLSDVIELQWHLEDKANQLQHFEKQKTELEEANAKIQADIDYMNEHGPLLDSKQNQELQDLKNHYKKKMEVMDLHRKVNEELEEALEACENARLKAQQIKEEIDKDIYQDEKTIEAYKREIYQLNSLFDHYSSSVINVNTNIEEKEEEVTEAIRETKSSKNELHSLSKMLEDLRRVYDQLTWKQKSHENQYLEAVNDFYAAKKTWDIELSDVAKDFSAISLACTKLTEDNKKLEIDINKITVKTNESIRKKSKYESEIKYLTIMKLKNDKHLKNIYKEAYRIGTLFHLTKHKTDEMEDKIAEVRRKFKGREEFLKKLTQGEVAAGMVLQKKLYSIYEVQALERKELIKNRAICAMSLAELQEPLLQLEDEAERIRSLDKEHSVMLNNIIDQKDLIRRKVGKVKKKLRKKGKKTLDALIETESKRSAIFKDLEATKSKTMIFYAKINELNEELKAKEEEKKSFDQTLEILKNKFITMRFKREHAQTVFDHYMQEKKDCEERIFEEDQRFRVLLAVRQKTLQDTQKIIADSLEENLRLAQEYQQLQITFLKEKDNYFNIYDKQLSLDTSIRDKKQLCQLQRRMHTLWQEHFKLVVLFSQMRLANFQTDSQESIQKILAVQEESSNLMQHILGFFQTLTDGTCENDG
"
     exon            201..260
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            261..350
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            351..490
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            491..513
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            514..599
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            600..800
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            801..1021
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            1022..1164
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            1165..1318
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            1319..1414
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            1415..1551
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            1552..1735
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            1736..1798
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            1799..1960
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     variation       1941
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:457896"
     variation       1943
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:466113"
     exon            1961..2074
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            2075..2220
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            2221..2380
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            2381..2530
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            2531..2665
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     exon            2666..3355
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /inference="alignment:Splign:1.39.8"
     STS             2936..3113
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /standard_name="RH92259"
                     /db_xref="UniSTS:88116"
     variation       3053
                     /gene="CCDC178"
                     /gene_synonym="C18orf34"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1052411"
ORIGIN      
tgtctgctcaatcaagtcaaatactgaacaacttcctggcggagaggctgagaattttatacttgcttgctcgaaagcaccccaaataagatgatccacgccaacacctcccctttacaggttttaaaatattcttataactatgactgaaaacaagacagtttcctcttcttccactagagatgatcaaaccaatataggtttaacatgtcaggaagtaaaggctctcagagagaaggcatggtcaaggacaaatgaaggcaatgccatgtctcaaagtttggttctatatggagcctctaaggagaacagtgaaggttttcatgaaagtaaaatgacaaatactgaaggggtgaataaaggcatttactttagctacccatgtcgacgtcacagctgtgccgtagtaaatattccagcaccttgtgtcaacaaaatgatttcacacatccaagatgtggagtccaaaatacaggagcatttgaaaaggtttgaaacttcttttgaagaatggagcagaacttcttccacaaaagacctgaaagaagattggagtgtaactacaccagtgaaagaggtcaaaccaggagaaaagagagatgaaaagtgtccagagttaaagcaggaaatggaaacattgctctcagaggccattcgtctcattaaaagtctagaaactgaccgggcagacgctgaagaagctttaaaacaacagagatcaagaaagaatatgattaacatgaaaattgactcttggtcagtctggaaacttcaagaactcccattggctgtgcagaaagaacatgaggcctatttgagtgatgttatagaattacaatggcatcttgaagataaagctaatcaactacaacattttgaaaaacaaaagacagagttagaagaagcaaatgcaaagattcaagcagacatagactacatgaatgaacatggccctctactggactctaagcagaatcaggaacttcaagatctgaagaaccattataaaaaaaaaatggaggtaatggacctacacagaaaagttaatgaagaacttgaagaagctttagaagcctgtgaaaatgccagattgaaggctcagcaaattaaagaagagattgataaggatatttaccaggatgaaaaaaccatagaggcctacaagagagagatatatcaacttaacagtctatttgatcattactcttcatcagtgataaatgttaatactaatattgaggagaaggaagaggaagtgactgaagcaataagggaaacaaagtcatcaaaaaatgaattacattctctatcaaaaatgctggaagatttgagaagagtttatgaccaactaacctggaagcaaaaaagtcatgaaaatcagtatctggaagcagttaatgatttttatgctgcaaaaaaaacatgggatattgagctttctgatgttgcaaaagatttttcagctatttctttggcatgtacaaaactgacggaagacaataaaaaacttgagattgatattaacaaaataacagtaaaaaccaatgaaagcatacggaaaaaatcaaaatacgaatctgaaataaaatatttgacaataatgaagttaaagaatgataaacatctcaagaacatctataaggaggcttatcgcattggtactcttttccacctaaccaaacacaagacagatgaaatggaagataaaatagcagaagtgagaagaaagttcaagggtagagaagaattcctgaaaaaactcactcaaggtgaagtggctgctggaatggtgcttcagaaaaaactatattccatttacgaagtccaggcacttgagcggaaagagcttataaaaaatagagcaatatgtgccatgtcactggcagaactacaggaacctctgcttcaactagaagatgaagctgaaagaatcagaagtctcgacaaagaacattctgttatgcttaataatataattgatcagaaagatcttattagaagaaaggtgggaaaagtaaagaaaaaattacgaaaaaaggggaagaaaacccttgatgcattaatagaaactgagagtaaacgctcagcaatttttaaagacctagaagcaactaaaagtaagacaatgattttttatgcaaaaataaatgaattgaatgaggaattaaaagcaaaagaagaagaaaagaaaagttttgatcagacacttgaaatattaaagaacaaatttataactatgagatttaaaagggaacatgcacaaactgtgtttgatcattatatgcaagagaaaaaagactgtgaagagagaatctttgaggaagatcagagatttagagtgctccttgctgtaagacaaaaaactcttcaagatacccaaaaaataatagctgattcacttgaagaaaatctgcgtttagctcaagagtatcaacagctacagattacattcttaaaagaaaaggacaattatttcaatatatatgataaacagctatcacttgatacttcaattagagataagaaacagctctgtcagctgcagagaaggatgcacacactgtggcaggagcacttcaaactggtggtcctcttcagccagatgaggctggccaacttccagacagactctcaggagagtattcagaaaatattagctgtgcaggaggaatcttcaaatttaatgcaacacatcttaggtttcttccagactttgacagatggcacatgcgaaaacgatggttaagcaaacaaccaatgtatcttggatgctgaaataaaagacaagaaaagtcacacagttcagataacagtgtaattggacattcacctgtttgccatttcacacttccatgaacgaaaaactcactcacctcccagcatgctttgccactcttttactcacagcaaatccataacaatgaaacaggtgactttcatgctgctgtcaggaacgatctaatttcagctctgggtgactgattgcaattggctttgcctcatctgataattaatctatgtcaccattaattggaagagagaataattactggcggtgttgacagtgactgttcgcttccccagatttccctatcgtcttggcccaaataaaggctttgccattcagtacttaaagtttgtgtaaactgtaacaatatctatgcccatgtgacactttgagacactctgtctaatgtacttttgtttttgtgtttaccagtcttttttagctcactgagagctgtctctctcaatcactcctcaatgttctatcttaattttgtggaagtttaaagttttcaatgagctggagatgaatgattaatgaataaatttaaatgcttcattttgtccaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaaa
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