LOCUS       XM_047445742             971 bp    mRNA    linear   PRI 25-AUG-2024
DEFINITION  PREDICTED: Homo sapiens regulatory factor X8 (RFX8), transcript
            variant X11, mRNA.
ACCESSION   XM_047445742
VERSION     XM_047445742.1
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_000002.12) 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..971
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="2"
     gene            1..971
                     /gene="RFX8"
                     /note="regulatory factor X8; Derived by automated
                     computational analysis using gene prediction method:
                     Gnomon. Supporting evidence includes similarity to: 1 EST,
                     1 long SRA read, and 100% coverage of the annotated
                     genomic feature by RNAseq alignments, including 4 samples
                     with support for all annotated introns"
                     /db_xref="GeneID:731220"
                     /db_xref="HGNC:HGNC:37253"
     CDS             4..870
                     /gene="RFX8"
                     /codon_start=1
                     /product="DNA-binding protein RFX8 isoform X9"
                     /protein_id="XP_047301698.1"
                     /db_xref="GeneID:731220"
                     /db_xref="HGNC:HGNC:37253"
                     /translation="MAEGVPASPSSGEGSRGPHSGVIQWLVDNFCICEECSVPRCLMY
                     EIYVETCGQNTENQVNPATFGKLVRLVFPDLGTRRLGTRGSARYHYDGICIKKSSFFY
                     AQYCYLIGEKRYHSGDAIAFEKSTNYNSIIQQEATCEDHSPMKTDPVGSPLSEFRRCP
                     FLEQEQAKKYSCNMMAFLADEYCNYCRDILRNVEDLLTSFWKSLQQDTVMLMSLPDVC
                     QLFKCYDVQLYKGIEDVLLHDFLEDVSIQYLKSVQLFSKKFKLWLLNALEGVPALLQI
                     SKLKDYANGIEK"
ORIGIN      
        1 gccatggccg agggggtgcc ggcctcgccg tcgagcggcg agggtagccg gggcccgcac
       61 agcggcgtca tccagtggtt ggtcgacaac ttctgcattt gcgaagagtg cagcgtccct
      121 cgctgtctca tgtatgagat ttacgtggag acctgtgggc aaaacactga gaaccaagtc
      181 aacccggcca cctttgggaa gcttgtgaga ttggtttttc cggaccttgg cacccggagg
      241 ctgggcacta gaggaagtgc caggtatcat tatgatggaa tctgtatcaa gaaaagctct
      301 ttcttctatg cccagtattg ctacctgata ggtgaaaaaa ggtatcacag tggagatgcc
      361 attgcctttg aaaaatctac taattataac agcattatcc aacaagaagc aacatgtgaa
      421 gatcattcac cgatgaagac agacccagtt ggatcccctt tgtctgaatt caggagatgt
      481 ccatttctgg agcaagaaca ggcaaagaaa tactcctgta atatgatggc cttccttgct
      541 gacgaatact gcaactattg tcgagacatt ttacgaaatg tggaggactt gcttacttcc
      601 ttctggaagt ctctgcagca agacacagtc atgctgatgt cattgcctga cgtgtgccag
      661 ctctttaaat gctacgacgt ccagctgtac aagggaattg aggatgttct ccttcatgac
      721 ttcttggaag atgtttctat tcagtacctg aaatctgtgc agttatttag taagaaattt
      781 aagctgtggc tccttaatgc tttggaaggt gttccagccc tcttgcagat ctccaaactc
      841 aaagactatg cgaatggtat tgaaaagtaa gaggcgtgtc agcgttttga agtcagatct
      901 acaggccatc atcaatcaag gcactttggc tacttctaag aaagccctgg caagtgaccg
      961 gagtggcgca g
//
