LOCUS       XM_047420683            1348 bp    mRNA    linear   PRI 25-AUG-2024
DEFINITION  PREDICTED: Homo sapiens replication factor C subunit 2 (RFC2),
            transcript variant X1, mRNA.
ACCESSION   XM_047420683
VERSION     XM_047420683.1
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_000007.14) 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..1348
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
     gene            1..1348
                     /gene="RFC2"
                     /gene_synonym="RFC40"
                     /note="replication factor C subunit 2; Derived by
                     automated computational analysis using gene prediction
                     method: Gnomon. Supporting evidence includes similarity
                     to: 22 ESTs, 308 long SRA reads, and 89% coverage of the
                     annotated genomic feature by RNAseq alignments, including
                     32 samples with support for all annotated introns"
                     /db_xref="GeneID:5982"
                     /db_xref="HGNC:HGNC:9970"
                     /db_xref="MIM:600404"
     CDS             91..744
                     /gene="RFC2"
                     /gene_synonym="RFC40"
                     /codon_start=1
                     /product="replication factor C subunit 2 isoform X1"
                     /protein_id="XP_047276639.1"
                     /db_xref="GeneID:5982"
                     /db_xref="HGNC:HGNC:9970"
                     /db_xref="MIM:600404"
                     /translation="MCPTSSLRMTDGAQQALRRTMEIYSKTTRFALACNASDKIIEPI
                     QSRCAVLRYTKLTDAQILTRLMNVIEKERVPYTDDGLEAIIFTAQGDMRQALNNLQST
                     FSGFGFINSENVFKVCDEPHPLLVKEMIQHCVNANIDEAYKILAHLWHLGYSPEDIIG
                     NIFRVCKTFQMAEYLKLEFIKEIGYTHMKIAEGVNSLLQMAGLLARLCQKTMAPVAS"
ORIGIN      
        1 gggttgaaaa atataggcca gtaaagctga atgaaattgt cgggaatgaa gacaccgtga
       61 gcaggctaga ggtctttgca agggaaggaa atgtgcccaa catcatcatt gcgcatgacc
      121 gacggagccc agcaagcctt gaggagaacc atggaaatct actctaaaac cactcgcttc
      181 gcccttgctt gtaatgcttc ggataagatc atcgagccca ttcagtcccg ctgtgcagtc
      241 ctccggtaca caaagctgac cgacgcccag atcctcacca ggctgatgaa tgttatcgag
      301 aaggagaggg taccctacac tgatgacggc ctagaagcca tcatcttcac ggcccaggga
      361 gacatgaggc aggcgctgaa caacctgcag tccaccttct caggatttgg cttcattaac
      421 agtgagaacg tgttcaaggt ctgtgacgag ccccacccac tgctggtaaa ggagatgatc
      481 cagcactgtg tgaatgccaa cattgacgaa gcctacaaga ttcttgctca cttgtggcat
      541 ctgggctact caccagaaga tatcattggc aacatctttc gagtgtgtaa aactttccaa
      601 atggcagaat acctgaaact ggagtttatc aaggaaattg gatacactca catgaaaata
      661 gcggaaggag tgaactctct tttgcagatg gcaggcctcc tggcaaggct gtgtcagaag
      721 acaatggccc cggtggccag ttagagcaga gacttcactg actgacttac aggtgcccta
      781 ttctgaggta caggagccgc ggctttctga tgggggaaaa tgccgcctta ggctggagcc
      841 aacatgactg tcctttaaac tccagtggct ggccaggcac ggtagctcac gcctgtaatc
      901 ccaacacttt gggaggccga ggcaggtgga tcacctgagg tcagaagttc aagaccagcc
      961 tggccaacat ggggaaaccc tgtctttact aaaaatataa aaattagctg ggtgtggtgg
     1021 cgggcacctg taatcccagc tactcgggag gctgtggcag gagaatcgct tgaacccagg
     1081 aggtggaggt tgcagtgagc caagatcaca ccattgcact ccagcctggg cgacagagtc
     1141 tccatctggg gaaaaaaatt aaataaataa actcccgtga cttgcatgtt tgcttctggg
     1201 acgtctgtgc cccgcaagtg tttgagtttg gcctccaccc cattgatgcg gtgacggggc
     1261 ggaaaggcgc agagaagctg agggcggtct ctgatctgtg tgtgggttga cattttagct
     1321 aataaagcct tgcagtgttt gttggcaa
//
