LOCUS       XM_005254677             799 bp    mRNA    linear   PRI 25-AUG-2024
DEFINITION  PREDICTED: Homo sapiens sorting nexin 22 (SNX22), transcript
            variant X1, mRNA.
ACCESSION   XM_005254677
VERSION     XM_005254677.4
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,
            supported by EST evidence.
            Also see:
                Documentation of NCBI's Annotation Process
            
            On Apr 5, 2022 this sequence version replaced XM_005254677.3.
            
            ##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..799
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="15"
     gene            1..799
                     /gene="SNX22"
                     /note="sorting nexin 22; Derived by automated
                     computational analysis using gene prediction method:
                     Gnomon. Supporting evidence includes similarity to: 1 EST,
                     1 Protein, and 100% coverage of the annotated genomic
                     feature by RNAseq alignments, including 39 samples with
                     support for all annotated introns"
                     /db_xref="GeneID:79856"
                     /db_xref="HGNC:HGNC:16315"
     CDS             46..570
                     /gene="SNX22"
                     /codon_start=1
                     /product="sorting nexin-22 isoform X1"
                     /protein_id="XP_005254734.1"
                     /db_xref="GeneID:79856"
                     /db_xref="HGNC:HGNC:16315"
                     /translation="MLEVHIPSVGPEAEGPRQSPEKSHMIKKLYKVPDFPSKRLPNWR
                     TRGLEQRRQGLEAYIQGILYLNQEVPKELLEFLRLRHFPTDPKASNWGTLREFLPGDS
                     SSQQHQRPVLSFHVDPYVCNPSPGEEVPRYGATGLGCGLCISRLLGPSDSISFLLPTS
                     GATTSCSCPLEPAL"
ORIGIN      
        1 agggctccga gccgagcgcg cggagcagct ggggccgggg cgcggatgct ggaagttcac
       61 atcccgtcgg tggggcccga ggccgagggg cccaggcaga gcccggagaa aagccacatg
      121 atcaagaagc tgtacaaagt gcccgacttc ccctcgaaac gcctgcccaa ctggaggacc
      181 agagggttgg aacagcgccg gcagggcttg gaggcttaca tccagggcat cctgtacctg
      241 aaccaggagg tgcccaagga gttactggaa ttcctgagac ttcggcactt ccccacagac
      301 cccaaggcta gcaactgggg caccctgagg gagttcctgc ctggcgacag cagctcccag
      361 cagcaccagc ggcctgtcct gagcttccat gtggatccct atgtttgcaa cccctcccca
      421 ggtgaggagg tgcctagata tggggctaca gggctgggtt gtgggctttg catttctcgg
      481 ctcctgggac cctcagacag catctccttc ctgctgccca cctctggagc cactacctcc
      541 tgctcctgtc ccctggagcc tgctttgtag acacaaggaa aacaagtttg gcttccctgg
      601 tctccatttc ttcagcagcc tgacttcttt accaagctga tgtgaaaaga atgtgacctg
      661 ggaatgcgga ggcttcattt ggggtggaca gctgctgtct gctgccttgg caggggctcc
      721 tactcccaag tgggggctga gcccatgagc aggagctcaa ggagctgcag gtctgaggcc
      781 agacctgttt aattctatc
//
