LOCUS       XM_047416832             692 bp    mRNA    linear   PRI 25-AUG-2024
DEFINITION  PREDICTED: Homo sapiens PRELI domain containing 2 (PRELID2),
            transcript variant X13, mRNA.
ACCESSION   XM_047416832
VERSION     XM_047416832.1
DBLINK      BioProject: PRJNA168
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
COMMENT     MODEL REFSEQ:  This record is predicted by automated computational
            analysis. This record is derived from a genomic sequence
            (NC_000005.10) annotated using gene prediction method: Gnomon,
            supported by EST evidence.
            Also see:
                Documentation of NCBI's Annotation Process
            
            ##Genome-Annotation-Data-START##
            Annotation Provider         :: NCBI RefSeq
            Annotation Status           :: Updated annotation
            Annotation Name             :: GCF_000001405.40-RS_2024_08
            Annotation Pipeline         :: NCBI eukaryotic genome annotation
                                           pipeline
            Annotation Software Version :: 10.3
            Annotation Method           :: Best-placed RefSeq; Gnomon;
                                           RefSeqFE; cmsearch; tRNAscan-SE
            Features Annotated          :: Gene; mRNA; CDS; ncRNA
            Annotation Date             :: 08/23/2024
            ##Genome-Annotation-Data-END##
FEATURES             Location/Qualifiers
     source          1..692
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="5"
     gene            1..692
                     /gene="PRELID2"
                     /note="PRELI domain containing 2; Derived by automated
                     computational analysis using gene prediction method:
                     Gnomon. Supporting evidence includes similarity to: 4
                     ESTs, 5 long SRA reads, and 89% coverage of the annotated
                     genomic feature by RNAseq alignments, including 1 sample
                     with support for all annotated introns"
                     /db_xref="GeneID:153768"
                     /db_xref="HGNC:HGNC:28306"
                     /db_xref="MIM:620750"
     CDS             92..523
                     /gene="PRELID2"
                     /codon_start=1
                     /product="PRELI domain-containing protein 2 isoform X6"
                     /protein_id="XP_047272788.1"
                     /db_xref="GeneID:153768"
                     /db_xref="HGNC:HGNC:28306"
                     /db_xref="MIM:620750"
                     /translation="MGVSVDVHQVYKYPFEQVVASFLRKYPNPMDKNVISVKIMEEKR
                     DESTGVIYRKRIAICQNVVPEILRKSLSTLVILCWKKVSILKVPNIQLEEESWLNPRE
                     RNMAIRSHCLTWTQYASMKEESVFRESMENPNWELESWRCC"
ORIGIN      
        1 gagtgtgggc gcctccgggc ctctgcggag ccctgggcag ctctgagctc gcggaggcgt
       61 ggccggtgcg cggggcccgc ggcgcgcggg gatgggggtc tcggtggatg tgcaccaggt
      121 gtacaagtac cccttcgagc aggtggtcgc cagctttctc cgaaagtacc ccaaccccat
      181 ggataaaaat gtcatctcag taaaaatcat ggaggaaaaa agagatgaat caacaggggt
      241 catctacaga aagaggattg caatctgtca gaacgtggtt ccagaaattt taaggaagtc
      301 cttaagcact ctggtgattc tttgttggaa aaaggtgagc attttgaaag tacctaatat
      361 ccaattagaa gaggagtcat ggctcaatcc tcgggaaaga aacatggcca tacggagtca
      421 ctgccttacg tggacacagt atgcatccat gaaggaagag tctgtcttcc gggaaagtat
      481 ggaaaaccca aattgggaat tagaatcatg gagatgctgc taaaggaaca gtgtggtgcc
      541 cccttagctg aataaagaat catcagtatg ctgaaccagg cttgcgtccc agggatgaag
      601 gcgacttgat cgtggtggat aagcttcttg atgtgctgct gcattcggtt tcccagtatt
      661 ttattgagga tttttgcatt gatgttcatc ag
//
