LOCUS       XM_047426132             779 bp    mRNA    linear   PRI 25-AUG-2024
DEFINITION  PREDICTED: Homo sapiens wiskott-Aldrich syndrome protein family
            member 1-like (LOC124902536), mRNA.
ACCESSION   XM_047426132
VERSION     XM_047426132.1
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_000010.11) annotated using gene prediction method: Gnomon,
            supported by mRNA 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..779
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="10"
     gene            1..779
                     /gene="LOC124902536"
                     /note="wiskott-Aldrich syndrome protein family member
                     1-like; Derived by automated computational analysis using
                     gene prediction method: Gnomon. Supporting evidence
                     includes similarity to: 1 mRNA, and 90% coverage of the
                     annotated genomic feature by RNAseq alignments"
                     /db_xref="GeneID:124902536"
     CDS             134..571
                     /gene="LOC124902536"
                     /codon_start=1
                     /product="wiskott-Aldrich syndrome protein family member
                     1-like"
                     /protein_id="XP_047282088.1"
                     /db_xref="GeneID:124902536"
                     /translation="MGPGNGSFVMAQPATLTFSHHLEDPLSVRPSRPQAAEETWGRGS
                     RKPSPEAPSAAPGGILRATRSCARGRARPPQRPERPGLPRASASRWGLRAPIPPLPAI
                     GAPRNCGVSTRPGARAHSRSPSPPREMLPAFYPAPPWRAPQTM"
ORIGIN      
        1 actctgactt tccagcgccc aggccggggc gccgccaggg cgtctctgag ggtcgcgccc
       61 cgataccttc ctccacccca cggcttcttc cccccaaggg cggggctggg ggcccaggag
      121 caccacagcc cccatgggcc cgggaaatgg cagcttcgtc atggcccagc ccgccacgct
      181 caccttttcc caccacctgg aggatccact ctccgtccgt ccttcccgac ctcaggctgc
      241 agaggaaacc tgggggcggg ggtcgaggaa gccgagcccc gaggctccca gcgccgcccc
      301 aggaggaatc ttgcgggcca ctagaagctg tgcgcgcggc cgggctcggc ccccacaacg
      361 gcccgagcgg ccgggcctgc cgcgagcctc cgcgtccagg tggggtctcc gcgcccccat
      421 tccacccctc cccgccatcg gcgctccccg caactgcggg gtttccaccc gccccggcgc
      481 tcgcgcccac tcacggtctc cctcgccccc ccgggagatg ctcccggcgt tctatcccgc
      541 cccgccctgg cgcgccccgc aaacgatgtg accccggccc cctgcggtct cccctcctcc
      601 ggacgctgcc cctgccccac ctgtggcgct cccgtcatct ctagagcccc caaccagagt
      661 cctccagccc acccgcgagg ctcgcgcacc tgcgatgcgg ccccactagc agggacccgc
      721 ccacctgtgg cgctacccct gcctctgccg cctcccgcac cgctagcgcg gcccccacc
//
