LOCUS       XM_017022809            1262 bp    mRNA    linear   PRI 25-AUG-2024
DEFINITION  PREDICTED: Homo sapiens putative golgin subfamily A member 8I
            (LOC101930434), transcript variant X1, mRNA.
ACCESSION   XM_017022809
VERSION     XM_017022809.1
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_000015.10) annotated using gene prediction method: Gnomon.
            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..1262
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="15"
     gene            1..1262
                     /gene="LOC101930434"
                     /note="putative golgin subfamily A member 8I; Derived by
                     automated computational analysis using gene prediction
                     method: Gnomon. Supporting evidence includes similarity
                     to: 100% coverage of the annotated genomic feature by
                     RNAseq alignments, including 2 samples with support for
                     all annotated introns"
                     /db_xref="GeneID:101930434"
     CDS             152..661
                     /gene="LOC101930434"
                     /codon_start=1
                     /product="putative golgin subfamily A member 8I isoform
                     X1"
                     /protein_id="XP_016878298.1"
                     /db_xref="GeneID:101930434"
                     /translation="MALPGEGHGGEHLDSDGEEAPRPMPSVPEDLESREAMSSFMDQL
                     EEKADLSELVKKKELCFIHHWRDRCHQKIHHLLSEPGGRAKDAALVGGHHQAGAQGGD
                     EGEAAGAAADGVAAYSNYNNGHRKFLATAQNPADEPGPGAPAPQELGAAGKHGGYLFQ
                     IPVCSYLHS"
ORIGIN      
        1 gccacagagc atcttcaagg agctgaacaa tgagaacaag agcgcactgc agttggagca
       61 gcaagtaaag gagctacagg agaagcttgg tgaggagcac ctggaagcgg ccagccagca
      121 gaaccagcag ctaacggccc agctgagcct catggctctc cctggggaag gacacggagg
      181 agaacatctg gacagtgacg gggaggaggc acctcggccc atgccgagtg tcccagagga
      241 cctggagagc agggaggcca tgagcagctt tatggaccaa ctggaggaga aggcagacct
      301 gagtgagctg gtgaagaaaa aagaactttg cttcatccac cactggcgag atagatgcca
      361 tcagaaaatc catcaccttt tatcagaacc agggggccgt gccaaagatg cggcactggt
      421 aggaggacac catcaggctg gagctcaggg aggagatgaa ggtgaagctg ctggagctgc
      481 agcagatggt gttgcggctt atagcaacta caacaatggg cacagaaaat tcctggccac
      541 tgcccagaac cctgctgatg agcccggtcc aggagcccca gccccccagg agcttggggc
      601 tgcaggcaag catggtggtt atctatttca gatacctgtt tgctcatatt tacattccta
      661 actgaacaat gtctgaagag gtacttaaac ctgtcataaa acacaaatga gcttatgacc
      721 aaatgcttag tgccagaaaa aacttcaaac tgcaatatga gtctctccaa atacagaaag
      781 gaccagtatt ttaagaggta tgttaactaa aatgttgcag tgtatggagc agagcaggaa
      841 gaacctttaa gtccgaaact tacaagtaaa tttcatagtt tccgtggtcc ttccacaaca
      901 acctctggca tctgtttttt ctacaatgga ggtaacagta gctctttcag agcaggaaaa
      961 ggcttagagc agtgctagaa gagggtggtg gctatataaa gtttagctat ttgtatattg
     1021 taacaaacca cctttttttt ttttttaagt cagtagtaga tttcttttgg aaaagtagcc
     1081 gcctcctgtc tagagatacc tgcagttcca ctaagtgaac attggtgtct gctcaccttt
     1141 gcctctattt ctctcaataa tatactctta agctgttccc tgatttagca attttataca
     1201 ctttcttttt ctttattttt ttttcctttc ccttttcctg agacactgtc ccgctctgtc
     1261 gc
//
