LOCUS       NM_001419771            1336 bp    mRNA    linear   ROD 31-MAR-2024
DEFINITION  Rattus norvegicus similar to human chromosome 19 open reading frame
            67 (C19h19orf67), mRNA.
ACCESSION   NM_001419771 XM_006255325
VERSION     NM_001419771.1
KEYWORDS    RefSeq; RefSeq Select.
SOURCE      Rattus norvegicus (Norway rat)
  ORGANISM  Rattus norvegicus
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha;
            Muroidea; Muridae; Murinae; Rattus.
REFERENCE   1  (bases 1 to 1336)
  AUTHORS   Wilson,R., Geyer,S.H., Reissig,L., Rose,J., Szumska,D., Hardman,E.,
            Prin,F., McGuire,C., Ramirez-Solis,R., White,J., Galli,A.,
            Tudor,C., Tuck,E., Mazzeo,C.I., Smith,J.C., Robertson,E.,
            Adams,D.J., Mohun,T. and Weninger,W.J.
  TITLE     Highly variable penetrance of abnormal phenotypes in embryonic
            lethal knockout mice
  JOURNAL   Wellcome Open Res 1, 1 (2017)
   PUBMED   27996060
  REMARK    Publication Status: Online-Only
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            JAXUCZ010000019.1.
            
            On Apr 18, 2023 this sequence version replaced XM_006255325.4.
            
            ##Evidence-Data-START##
            Transcript exon combination :: SRR26360181.570302.1,
                                           SRR26360186.1760224.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA5760383, SAMEA5760389
                                           [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            RefSeq Select criteria :: based on conservation, expression,
                                      longest protein
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-448               JAXUCZ010000019.1  41054428-41054875   c
            449-593             JAXUCZ010000019.1  41053269-41053413   c
            594-694             JAXUCZ010000019.1  41053055-41053155   c
            695-880             JAXUCZ010000019.1  41052795-41052980   c
            881-1015            JAXUCZ010000019.1  41052270-41052404   c
            1016-1336           JAXUCZ010000019.1  41051577-41051897   c
FEATURES             Location/Qualifiers
     source          1..1336
                     /organism="Rattus norvegicus"
                     /mol_type="mRNA"
                     /strain="BN"
                     /db_xref="taxon:10116"
                     /chromosome="19"
                     /map="19q11"
     gene            1..1336
                     /gene="C19h19orf67"
                     /note="similar to human chromosome 19 open reading frame
                     67"
                     /db_xref="GeneID:686013"
                     /db_xref="RGD:1586683"
     exon            1..448
                     /gene="C19h19orf67"
                     /inference="alignment:Splign:2.1.0"
     CDS             120..1190
                     /gene="C19h19orf67"
                     /note="rCG51246-like"
                     /codon_start=1
                     /product="UPF0575 protein C19orf67 homolog"
                     /protein_id="NP_001406700.1"
                     /db_xref="GeneID:686013"
                     /db_xref="RGD:1586683"
                     /translation="MAAESWFAGSLALGPGEAPPSEELGPGPQPYGDPSWSPAGRPEG
                     STELEPQRAQSMMEAPTSTSSREPLAAELGAAPARLPLDSMFSPITDQLRYLLRKADD
                     FQSYLLYSRDRVQKEQLAKAMPTFLTMCEPYFLYLEAAARSVPPIYGALQELVRKGLL
                     EISQQLTLRLEQLVLMYASFGFVDLEETNPLSISCFFCGRFSISPSHDVSIFRYCTPA
                     AYTASHFPRYLYKKMRWNLETTTEASSQGADAHVDYYFLCYRDTWEDAGQGPANSCPQ
                     IQKLWSIGRWMPLGPAEDDLDSWILCPQPPGDYQQLLTIGFEEPSHVLATDLLVQILM
                     GQAGPARPPSSAGPAAWAAPAS"
     exon            449..593
                     /gene="C19h19orf67"
                     /inference="alignment:Splign:2.1.0"
     exon            594..694
                     /gene="C19h19orf67"
                     /inference="alignment:Splign:2.1.0"
     exon            695..880
                     /gene="C19h19orf67"
                     /inference="alignment:Splign:2.1.0"
     exon            881..1015
                     /gene="C19h19orf67"
                     /inference="alignment:Splign:2.1.0"
     exon            1016..1336
                     /gene="C19h19orf67"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 agagacgtcg aggctgggct gagagggctg cggctgcgct cactgcccaa gccggtcggc
       61 cccaggtgtg tgcgctcccg ggacgccgaa ggggctggag gagcctgctg tggacgtgga
      121 tggctgcgga gtcctggttc gcggggtcgc tggccctggg cccaggagaa gcaccgccct
      181 cggaggaatt gggacccggg ccgcagcctt atggagaccc ctcgtggtcg ccggccggga
      241 gacctgaggg ttcaacagag ctggagcccc agcgagcaca gtccatgatg gaagctccca
      301 cctccacgtc ctcccgggag ccactggcag cggagctcgg ggcggcccca gctcgcctcc
      361 cgctggactc catgttcagt ccgatcactg accagctccg ttacctgctc agaaaggcgg
      421 atgactttca aagctacttg ctctacagca gggaccgagt ccagaaagaa cagctagcca
      481 aggctatgcc caccttctta acaatgtgcg aaccttactt cctatacctt gaggctgcgg
      541 caaggagtgt ccctcccatc tacggagccc tgcaagagtt ggtccggaag gggttgctgg
      601 agatctccca gcagctaacc ctgcgcttgg aacagttagt tctcatgtat gcctcctttg
      661 ggttcgtgga cctggaggaa actaaccctt tgagcatctc ctgcttcttc tgcgggaggt
      721 tctccattag cccctcccac gatgtgtcca tcttccggta ctgcacacca gccgcgtaca
      781 ctgccagcca cttcccaaga tacctctata agaagatgcg ctggaacctg gaaaccacca
      841 cagaggccag cagccaagga gcagatgccc atgtggatta ctacttcttg tgttatcgag
      901 atacatggga ggacgcaggc cagggaccag ccaattcgtg cccccagatc cagaaactct
      961 ggtccattgg ccgatggatg cccctgggac cggcagagga tgatcttgat tcatggattt
     1021 tgtgcccaca gccacccggg gactaccagc agctactaac catcggcttc gaggagccgt
     1081 cgcacgtgct ggccaccgac ctgctggtgc agattctcat gggccaggca ggccccgccc
     1141 ggccccccag ctctgctggg cccgcggctt gggcagcccc ggcatcctaa gtcccaggag
     1201 aaggcgccag ttggagcctg acaaccccaa actccaggca ggaagaagtg cggtctgcac
     1261 tgagtacgcc caggcaagag ccaccgaaca ccaagtgcgg gctgactttt ctgttaataa
     1321 aagagcaagg tcagag
//
