LOCUS       NM_001205259            1462 bp    mRNA    linear   PRI 17-FEB-2024
DEFINITION  Homo sapiens TP53 target 3C (TP53TG3C), transcript variant 1, mRNA.
ACCESSION   NM_001205259 XM_001725812
VERSION     NM_001205259.3
KEYWORDS    RefSeq; MANE Select.
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 1462)
  AUTHORS   Kim,J.M., Lee,K.H., Jeon,Y.J., Oh,J.H., Jeong,S.Y., Song,I.S.,
            Kim,J.M., Lee,D.S. and Kim,N.S.
  TITLE     Identification of genes related to Parkinson's disease using
            expressed sequence tags
  JOURNAL   DNA Res 13 (6), 275-286 (2006)
   PUBMED   17213182
REFERENCE   2  (bases 1 to 1462)
  AUTHORS   Ng,C.C., Koyama,K., Okamura,S., Kondoh,H., Takei,Y. and Nakamura,Y.
  TITLE     Isolation and characterization of a novel TP53-inducible gene,
            TP53TG3
  JOURNAL   Genes Chromosomes Cancer 26 (4), 329-335 (1999)
   PUBMED   10534768
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC138869.2.
            
            On Jul 30, 2021 this sequence version replaced NM_001205259.2.
            
            Sequence Note:.
            
            ##Evidence-Data-START##
            Transcript exon combination :: DT215671.1, SRR14038197.2321194.1
                                           [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1968968, SAMEA2142853
                                           [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000561509.3/ ENSP00000455132.1
            RefSeq Select criteria :: based on manual assertion
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-430               AC138869.2         19941-20370         c
            431-1462            AC138869.2         17738-18769         c
FEATURES             Location/Qualifiers
     source          1..1462
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="16"
                     /map="16p11.2"
     gene            1..1462
                     /gene="TP53TG3C"
                     /gene_synonym="TP53TG3; TP53TG3E; TP53TG3F"
                     /note="TP53 target 3C"
                     /db_xref="GeneID:653550"
                     /db_xref="HGNC:HGNC:42962"
     exon            1..430
                     /gene="TP53TG3C"
                     /gene_synonym="TP53TG3; TP53TG3E; TP53TG3F"
                     /inference="alignment:Splign:2.1.0"
     CDS             69..443
                     /gene="TP53TG3C"
                     /gene_synonym="TP53TG3; TP53TG3E; TP53TG3F"
                     /note="TP53-inducible gene 3 protein"
                     /codon_start=1
                     /product="TP53-target gene 3 protein"
                     /protein_id="NP_001192188.1"
                     /db_xref="CCDS:CCDS58458.1"
                     /db_xref="GeneID:653550"
                     /db_xref="HGNC:HGNC:42962"
                     /translation="MRASPCISQPAASWHPRPSALRPTAGSGPDTRTPGTVEDGSAPC
                     PAFRSPAVSPCGEEPCCFQISPAEETLELGRLVSPGNCDTLSPRAAGFYACHVRSLIP
                     CRSTKGRWPLTASAAGLSSFSG"
     exon            431..1462
                     /gene="TP53TG3C"
                     /gene_synonym="TP53TG3; TP53TG3E; TP53TG3F"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 tcctcctgta gccccaccat ccaccgtggg gaacggtgga gagactacaa ctcccagtat
       61 gcaccgcgat gcgcgcctca ccctgcatct cccagcccgc agccagctgg catcctagac
      121 cctctgccct gcgaccaaca gccgggagcg gaccagacac cagaactccc ggaacggttg
      181 aagacggttc cgctccctgt cccgcctttc gcagcccagc agtttcgccc tgcggagagg
      241 agccttgctg tttccaaatc tctcctgctg aagagacatt ggagctaggg cggctagttt
      301 cacctggtaa ttgtgacacc ctgtctcctc gagctgcagg cttttatgct tgtcatgttc
      361 gaagtttgat accttgcaga tcaacaaagg gccggtggcc tctcactgcc tccgcggcag
      421 ggttgtcaag tttttcaggt taagtactgc acgactactc gcttctgaaa ctgatagaca
      481 ctgcctcagc tccgtgcagg gcagacgcac aagagcagaa tctccgtggg acatctctct
      541 ggagcatcaa tattactgca gtatttggaa gaaacaaatt taaataagtt ctaaggtgaa
      601 gaatggaaca tttaagacaa gtctggaaag tcatctgcct ttaataactg tcgtttgtcc
      661 ttaacgtcag actttctcca agaccaaaac tctaagaact tatttccatt cttacaaata
      721 gtaaaaatga taaatcatat caagtcaatt gaaagtcctg cctgctgctt tcctaaattg
      781 caatatggcc ttggtatggt tttatttgta cttttgtggg ggattcgtgg atctttagat
      841 taaaaaaaaa aaaataggtt tttgaacaat ttttgcaagt ttgcagctgt tagttattga
      901 tttatttttc caacccatct aattcttctg tctctctcct caggctcaat aattccatgg
      961 gtctctaagg ctgtgtttat tttctttaaa ttttgttgat ttacttttat actccatttg
     1021 attttttcta tctctcacct tttctcagac tcagtcatcc cacaggtctg taaggctctg
     1081 ttcattttct ttaaacttct tttttttttc ctctcctcag attggataaa ttatattgct
     1141 atgtctctgt ttctgaacta tagaaaagct caaaattatt atttttattt ctcatttttt
     1201 atatggctat tttttctctg ctgatgtttc acatctattc atttatgaga atattttcct
     1261 ttgccctcat gagcgtgttt ataatagctg ccttcaaatt cttgtctgcc gtttacatct
     1321 tggacatctt ggagatggct actgcctgct ttttatcttg tgtatttatt acattttcac
     1381 gtgtcttcac gcatcccttg aattggaaat tgtgccctgg agactgtata caagactgga
     1441 ttaaaaagac tggattctgt tt
//
