LOCUS       NM_001366559            1687 bp    mRNA    linear   PRI 17-APR-2022
DEFINITION  Homo sapiens ATF7-NPFF readthrough (ATF7-NPFF), transcript variant
            1, mRNA.
ACCESSION   NM_001366559
VERSION     NM_001366559.1
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC073594.31 and AC023509.42.
            
            ##Evidence-Data-START##
            RNAseq introns :: mixed sample support SAMEA1965299, SAMEA1966682
                              [ECO:0006172]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-104               AC073594.31        5524-5627           c
            105-173             AC023509.42        21749-21817
            174-270             AC023509.42        70133-70229
            271-389             AC023509.42        79322-79440
            390-527             AC023509.42        85218-85355
            528-685             AC023509.42        88111-88268
            686-785             AC023509.42        89511-89610
            786-899             AC023509.42        90147-90260
            900-1052            AC023509.42        90874-91026
            1053-1250           AC023509.42        98009-98206
            1251-1359           AC023509.42        99386-99494
            1360-1481           AC023509.42        115628-115749
            1482-1687           AC023509.42        115877-116082
FEATURES             Location/Qualifiers
     source          1..1687
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="12"
                     /map="12q13.13"
     gene            1..1687
                     /gene="ATF7-NPFF"
                     /note="ATF7-NPFF readthrough"
                     /db_xref="GeneID:114108587"
                     /db_xref="HGNC:HGNC:55073"
     exon            1..104
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            105..173
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     CDS             126..1517
                     /gene="ATF7-NPFF"
                     /note="isoform 1 is encoded by transcript variant 1"
                     /codon_start=1
                     /product="ATF7-NPFF readthrough protein isoform 1"
                     /protein_id="NP_001353488.1"
                     /db_xref="GeneID:114108587"
                     /db_xref="HGNC:HGNC:55073"
                     /translation="MGDDRPFVCNAPGCGQRFTNEDHLAVHKHKHEMTLKFGPARTDS
                     VIIADQTPTPTRFLKNCEEVGLFNELASSFEHEFKKAADEDEKKAAAGPLDMSLPSTP
                     DIKIKEEEPVEVDSSPPDSPASSPCSPPLKEKEVTPKPVLISTPTPTIVRPGSLPLHL
                     GYDPLHPTLPSPTSVITQAPPSNRQMGSPTGSLPLVMHLANGQTMPVLPGPPVQMPSV
                     ISLARPVSMVPNIPGIPGPPVNSSGSISPSGHPIPSEAKMRLKATLTHQVSSINGGCG
                     MVVGTASTMVTARPEQSQILIQHPDAPSPAQPQVSPAQPTPSTGGRRRRTVDEDPDER
                     RQRFLERNRAAASRCRQKRKLWVSSLEKKAEELTSQNIQLSNEVTLLRNEVAQLKQLL
                     LAHKDCPVTALQKKTQGYLGGRQRTPPTTGCPDLWVTVALPAPGNGETWPEPSLPVSA
                     PEVWQKYPGILEE"
     exon            174..270
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            271..389
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            390..527
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            528..685
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            686..785
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            786..899
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            900..1052
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            1053..1250
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            1251..1359
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            1360..1481
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     exon            1482..1687
                     /gene="ATF7-NPFF"
                     /inference="alignment:Splign:2.1.0"
     regulatory      1665..1670
                     /regulatory_class="polyA_signal_sequence"
                     /gene="ATF7-NPFF"
                     /note="hexamer: AATAAA"
     polyA_site      1687
                     /gene="ATF7-NPFF"
                     /note="major polyA site"
ORIGIN      
        1 ggacgggagg aaagtatccg ttccgccaag gggggaaagg aggagctgga gacagattgt
       61 aggaccgagc gcgggcaggc gggaggcaac ggagctacca gccgctcctc tctgctatat
      121 gaaatatggg agacgacaga ccgtttgtgt gcaatgcccc gggctgtgga cagagattta
      181 caaacgagga ccacctggca gttcataaac acaagcatga gatgacattg aaatttggcc
      241 cagcccgaac tgactcagtc atcattgcag atcaaacgcc tactccaact agattcctga
      301 agaactgtga ggaggtggga ctcttcaatg aactagctag ctcctttgaa catgaattca
      361 agaaagctgc agatgaggat gagaaaaagg ctgctgctgg gccccttgac atgtctctgc
      421 cttccacacc agacatcaaa atcaaagaag aagagccagt ggaggtagac tcatccccac
      481 ctgatagccc tgcctctagt ccctgttccc caccactgaa ggagaaggag gttaccccaa
      541 agcctgttct gatctctacc cccacaccca ccattgtacg tcctggctcc ctgcctctcc
      601 acttgggcta tgatccactt catccaaccc ttccctcccc aacctctgtc atcacacagg
      661 ctccaccatc caacaggcaa atggggtctc ccactggctc cctccctctt gtcatgcatc
      721 ttgctaatgg acagaccatg cctgtgttgc cagggcctcc agtacagatg ccgtctgtta
      781 tatcgctggc cagacctgtg tccatggtgc ccaacattcc tggtatccct ggcccaccag
      841 ttaacagtag tggctccatt tctccctctg gccaccctat accatcagaa gccaagatga
      901 gactgaaagc caccctaact caccaagtct cctcaatcaa tggtggttgt ggaatggtgg
      961 tgggtactgc cagcaccatg gtgacagccc gcccagagca gagccagatt ctcatccagc
     1021 accctgatgc cccatcccct gcccagccac aggtctcacc agctcagccc acccctagta
     1081 ctggggggcg acggcggcgc acagtagatg aagatccaga tgagcgacgg cagcgctttc
     1141 tggagcgcaa ccgggctgca gcctcccgct gccgccaaaa gcgaaagctg tgggtgtcct
     1201 ccctagagaa gaaggccgaa gaactcactt ctcagaacat tcagctgagt aatgaagtca
     1261 cattactacg caatgaggtg gcccagttga aacagctact gttagctcat aaagactgcc
     1321 cagtcactgc actacagaaa aagactcaag gctatttagg aggaagacag cgaacccctc
     1381 ccaccacagg atgcccagac ctctgggtca ctgttgcact acctgctcca ggcaatggag
     1441 agacctggcc ggagccaagc cttcctgttt cagccccaga ggtttggcag aaatacccag
     1501 ggatcctgga ggaatgaatg gctgagtccc cgggctggag aggggctgaa ttcccagttc
     1561 tggagcctgg ctgcccctca acgctttggg aagaagtgac atgtcatccc ttgatatgtc
     1621 tgcatgcaag gtccacaccc aaaagtgtca atgtttgccc cccaaataaa attgtctggc
     1681 ttctgaa
//
