LOCUS       NM_001080140            1294 bp    mRNA    linear   PRI 02-FEB-2024
DEFINITION  Homo sapiens cancer/testis antigen family 47 member A7 (CT47A7),
            mRNA.
ACCESSION   NM_001080140 XM_926686
VERSION     NM_001080140.1
KEYWORDS    RefSeq; MANE Select.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 1294)
  AUTHORS   Chen,Y.T., Iseli,C., Venditti,C.A., Old,L.J., Simpson,A.J. and
            Jongeneel,C.V.
  TITLE     Identification of a new cancer/testis gene family, CT47, among
            expressed multicopy genes on the human X chromosome
  JOURNAL   Genes Chromosomes Cancer 45 (4), 392-400 (2006)
   PUBMED   16382448
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AL670379.17.
            This sequence is a reference standard in the RefSeqGene project.
            
            On Jan 13, 2007 this sequence version replaced XM_926686.2.
            
            Summary: This locus represents a member of the cancer/testis gene
            family 47. This family, also known as CT47, is comprised of 13
            nearly identical loci clustered at Xq24. [provided by RefSeq, Sep
            2010].
            
            ##Evidence-Data-START##
            Transcript exon combination :: CA417843.1, DB539785.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1968968, SAMEA2148093
                                           [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000434883.3/ ENSP00000392283.2
            RefSeq Select criteria :: based on single protein-coding transcript
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-997               AL670379.17        26223-27219         c
            998-1153            AL670379.17        25180-25335         c
            1154-1294           AL670379.17        23901-24041         c
FEATURES             Location/Qualifiers
     source          1..1294
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq24"
     gene            1..1294
                     /gene="CT47A7"
                     /gene_synonym="CT47.7"
                     /note="cancer/testis antigen family 47 member A7"
                     /db_xref="GeneID:653282"
                     /db_xref="HGNC:HGNC:33288"
                     /db_xref="MIM:300786"
     exon            1..997
                     /gene="CT47A7"
                     /gene_synonym="CT47.7"
                     /inference="alignment:Splign:2.1.0"
     CDS             256..1122
                     /gene="CT47A7"
                     /gene_synonym="CT47.7"
                     /note="cancer/testis CT47 family, member 7"
                     /codon_start=1
                     /product="cancer/testis antigen 47A"
                     /protein_id="NP_001073609.1"
                     /db_xref="CCDS:CCDS35385.1"
                     /db_xref="GeneID:653282"
                     /db_xref="HGNC:HGNC:33288"
                     /db_xref="MIM:300786"
                     /translation="MSATGDRHPTQGDQEAPVSQEGAQAEAAGAGNQEGGDSGPDSSD
                     VVPAAEVVGVAGPVEGLGEEEGEQAAGLAAVPRGGSAEEDSDIGPATEEEEEEEGNEA
                     ANFDLAVVARRYPASGIHFVLLDMVHSLLHRLSHNDHILIENRQLSRLMVGPHAAARN
                     LWGNLPPLLLPQRLGAGAAARAGEGLGLIQEAASVPEPAVPADLAEMAREPAEEAAEE
                     KLSEEATEEPDAEEPATEEPTAQEATAPEEVTKSQPEKWDEEAQDAAGEEEKEQEKEK
                     DAENKVKNSKGT"
     exon            998..1153
                     /gene="CT47A7"
                     /gene_synonym="CT47.7"
                     /inference="alignment:Splign:2.1.0"
     exon            1154..1294
                     /gene="CT47A7"
                     /gene_synonym="CT47.7"
                     /inference="alignment:Splign:2.1.0"
     regulatory      1262..1267
                     /regulatory_class="polyA_signal_sequence"
                     /gene="CT47A7"
                     /gene_synonym="CT47.7"
     polyA_site      1288
                     /gene="CT47A7"
                     /gene_synonym="CT47.7"
ORIGIN      
        1 accagaatct ttcccgcctt atctaagtcc tctcaggcca gacttggtgg gaggttccta
       61 ggattcgctc cctgcccttc ccaccttagg gtgtcctctg agacagactc ttatttcctc
      121 aataaagaga aagactctta ttccctcagc ggccagctcc tcgcctcccc tcggccgtag
      181 ccacctcagt ggtcaccgtc ttcaccgtgg tcgcctcagc ccgctcgcca ccccagttga
      241 ggcgctgctg gtgtcatgtc tgccacaggg gaccgacacc cgacccaagg ggaccaggag
      301 gccccggtaa gccaggaggg agcacaggcc gaggcggccg gagctggtaa ccaggagggc
      361 ggcgactccg gccccgacag cagcgacgtg gtgcctgcgg ccgaggtggt cggagtcgca
      421 gggcccgtgg aaggcctcgg ggaggaggag ggtgagcagg cggcaggcct ggccgcagtc
      481 ccccggggcg ggagcgccga ggaggactca gatatcgggc ccgcgacgga ggaagaggag
      541 gaggaagagg ggaacgaggc ggccaacttc gacttggcgg tggtcgcccg tcgctacccg
      601 gcgtcgggca ttcacttcgt gctcctggac atggtccact cccttctcca ccgcctctct
      661 cacaacgacc acatcctcat agagaaccgt caactcagcc gcctgatggt ggggccacac
      721 gctgctgcgc gcaacctctg gggcaacctc cccccgctgc tgctgcccca gaggctgggt
      781 gcaggggccg cagcccgggc gggcgagggc ctgggcctga tccaggaggc cgcatcggtc
      841 ccagagcctg cagtgccagc tgacctggcc gagatggcca gggagcccgc ggaggaggcc
      901 gcagaggaga agctctcaga ggaggccaca gaggaaccag acgcagagga accggccaca
      961 gaagaaccga ccgcacagga ggccacggcc ccagaggaag tcactaaatc tcagcccgaa
     1021 aagtgggatg aagaggccca agatgctgca ggcgaggaag agaaagaaca agaaaaagag
     1081 aaggatgcgg aaaacaaggt gaagaactcc aaagggacct agacgcagca gaggtgaagc
     1141 caagaaaatc cagatgcctg tgggaattgt aacacatatc attccaaagt tcgttacatc
     1201 aaaagtgata tccagtgaca tctaactttc atggatgtat gtgacagtgt tcaagttaaa
     1261 aaataaaagt ttgttttaaa tgaataaact gaaa
//
