LOCUS       XM_047438839            1684 bp    mRNA    linear   PRI 25-AUG-2024
DEFINITION  PREDICTED: Homo sapiens IgLON family member 5 (IGLON5), transcript
            variant X2, mRNA.
ACCESSION   XM_047438839
VERSION     XM_047438839.1
DBLINK      BioProject: PRJNA168
KEYWORDS    RefSeq; includes ab initio.
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_000019.10) 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##
            
            ##RefSeq-Attributes-START##
            ab initio :: 40% of CDS bases
            ##RefSeq-Attributes-END##
FEATURES             Location/Qualifiers
     source          1..1684
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="19"
     gene            1..1684
                     /gene="IGLON5"
                     /note="IgLON family member 5; Derived by automated
                     computational analysis using gene prediction method:
                     Gnomon. Supporting evidence includes similarity to: 2
                     ESTs, and 87% coverage of the annotated genomic feature by
                     RNAseq alignments, including 3 samples with support for
                     all annotated introns"
                     /db_xref="GeneID:402665"
                     /db_xref="HGNC:HGNC:34550"
                     /db_xref="MIM:618861"
     CDS             205..735
                     /gene="IGLON5"
                     /codon_start=1
                     /product="igLON family member 5 isoform X1"
                     /protein_id="XP_047294795.1"
                     /db_xref="GeneID:402665"
                     /db_xref="HGNC:HGNC:34550"
                     /db_xref="MIM:618861"
                     /translation="MPPPAPGARLRLLAAAALAGLAVISRGLLSQSLEFNSPADNYTV
                     CEGDNATLSCFIDEHVTRVAWLNRSNILYAGNDRWTSDPRVRLLINTPEEFSILITEV
                     GLGDEGLYTCSFQTRHQPYTTQVYLIVHVPARIVNISSPVTVNEGGNVNLLCLAVGRP
                     EPTVTWRQLRDHKPQT"
ORIGIN      
        1 gtcagcgccg cccccctccc cgggtctgca gcagctccag ccgcctcgtc gcgccccccc
       61 agccccctcc ccccgccccc gccgcccccc gggccggtgc agcgcaggcg gggtccccct
      121 ccccctcccc cctctccccc caggcctcgc gcgccccgga ccggcccccc ctttcccctc
      181 cccctccgcg ccgcctctgc cgcgatgccc ccccctgcgc ccggggcccg gctccggctt
      241 ctcgccgccg ccgccctggc cggcttggcc gtcatcagcc gagggctgct ctcccagagc
      301 ctggagttca actctcctgc cgacaactac acagtgtgtg aaggtgacaa cgccaccctc
      361 agctgcttca tcgacgagca cgtgacccgc gtggcctggc tgaaccgctc caacatcctg
      421 tatgccggca atgaccgctg gaccagcgac ccgcgggtgc ggctgctcat caacaccccc
      481 gaggagttct ccatcctcat caccgaggtg gggctcggcg acgagggcct ctacacctgc
      541 tccttccaga cccgccacca gccgtacacc actcaggtct acctcattgt ccacgtccct
      601 gcccgcattg tgaacatctc gtcgcctgtg acggtgaatg aggggggcaa tgtgaacctg
      661 ctttgcctgg ccgtggggcg gccagagccc acggtcacct ggagacagct ccgagaccac
      721 aaaccccaga cctaagaggc gtcaccactg gctttccacc tgccgtccta ggcctgggcc
      781 actgcttctg cgtcacttgc caaaccccag cctgcgtcac ttccccaacc ccagtgtccc
      841 cgatgtctcc ccacgcgctc acagcattct cctgggctga gatcccctgc cactaggtgc
      901 cctaagccag gctgcaccag cggtcctgcg tacatctctg cctctctctt ctgctggacg
      961 ctctagccca gcgggcctca tggtgtgggc cccagacccg aagcatcagc ataccttggg
     1021 aacttgccag gaatgcactt tcccaggctc caaccaagac ctgctaaatc caaagctccc
     1081 tctcgctcca caagccccaa gaaccagtgc tcaaggttac ccacaaacgg cgccagagtg
     1141 cccatatatg acagtccagg tcctagacat cacccaccag cccttttatg tggatctcca
     1201 ccaccagatc ccagatccct ggatcctcat tctcagggtc tttgaagacc catggtgcca
     1261 gtcactagat cccattccct gaatccctgg atcttacccc actgggtcat ctgagcccca
     1321 tgagcctggt cttgacatct gggaatctct ggatgcccta agtcccagag ggtcttctga
     1381 gactgctgct gtgttatgag acccccatat acttggattg ctgatcccaa tcaccagatc
     1441 ctgattccct agaccccatg aatcagatcc cagaacgagg gaccctgccc cactggttct
     1501 gtatttgcta gatccttctg agacctaaca tcctgggatc cccctcccca ttggggtcct
     1561 ccccacggag ctccatgatc tgagtcagat tcctggaggg atctcctgaa cccttagatt
     1621 ctctaaccca ccccactggg ttccaggaac tgagtcccag acctcactcc ttcccccacc
     1681 ccca
//
