LOCUS       NM_001395229             949 bp    mRNA    linear   PRI 17-FEB-2024
DEFINITION  Homo sapiens CFAP97 domain containing 2 (CFAP97D2), transcript
            variant 2, mRNA.
ACCESSION   NM_001395229
VERSION     NM_001395229.1
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 949)
  AUTHORS   Kim,J.M., Lee,K.H., Jeon,Y.J., Oh,J.H., Jeong,S.Y., Song,I.S.,
            Kim,J.M., Lee,D.S. and Kim,N.S.
  TITLE     Identification of genes related to Parkinson's disease using
            expressed sequence tags
  JOURNAL   DNA Res 13 (6), 275-286 (2006)
   PUBMED   17213182
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AL160396.33.
            
            ##Evidence-Data-START##
            RNAseq introns :: mixed sample support SAMEA2144333, SAMEA2145774
                              [ECO:0006172]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            inferred exon combination :: based on alignments, homology
            MANE Ensembl match        :: ENST00000636692.2/ ENSP00000489989.1
            RefSeq Select criteria    :: based on manual assertion,
                                         conservation
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-164               AL160396.33        32028-32191
            165-245             AL160396.33        49167-49247
            246-364             AL160396.33        53096-53214
            365-949             AL160396.33        75272-75856
FEATURES             Location/Qualifiers
     source          1..949
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="13"
                     /map="13q34"
     gene            1..949
                     /gene="CFAP97D2"
                     /note="CFAP97 domain containing 2"
                     /db_xref="GeneID:101929355"
                     /db_xref="HGNC:HGNC:53789"
     exon            1..164
                     /gene="CFAP97D2"
                     /inference="alignment:Splign:2.1.0"
     CDS             75..371
                     /gene="CFAP97D2"
                     /note="isoform 2 is encoded by transcript variant 2;
                     uncharacterized protein C17orf105 homolog; CFAP97
                     domain-containing protein 2"
                     /codon_start=1
                     /product="uncharacterized protein CFAP97D2 isoform 2"
                     /protein_id="NP_001382158.1"
                     /db_xref="CCDS:CCDS91845.1"
                     /db_xref="GeneID:101929355"
                     /db_xref="HGNC:HGNC:53789"
                     /translation="MHGAPRLTFPCASEYLWHAREKAYQDHRRKVQSAQPLVDTRAPL
                     TFRHLHLKLKRLKLEEERLSVIERDNRLLLEKVASVMRTRGQTDSKNNSKHRRK"
     exon            165..245
                     /gene="CFAP97D2"
                     /inference="alignment:Splign:2.1.0"
     exon            246..364
                     /gene="CFAP97D2"
                     /inference="alignment:Splign:2.1.0"
     exon            365..949
                     /gene="CFAP97D2"
                     /inference="alignment:Splign:2.1.0"
     regulatory      922..927
                     /regulatory_class="polyA_signal_sequence"
                     /gene="CFAP97D2"
                     /note="hexamer: ATTAAA"
     polyA_site      949
                     /gene="CFAP97D2"
                     /note="major polyA site"
ORIGIN      
        1 acagcgtctc caggtctgca ccaggcccca gctgctcctc tgtctggaat gagcaagacg
       61 attttgttgc tgagatgcac ggagcccccc ggctgacctt tccctgtgcc agtgagtacc
      121 tgtggcatgc aagggagaaa gcctatcagg accacaggag aaaggtccag agcgcccagc
      181 cgctggtaga cacccgcgcc ccgctgacgt tccgccatct ccacctgaaa ctcaagaggc
      241 tgaagctgga ggaggaacgg ctctccgtca tcgagaggga caaccgcctg ctcctggaga
      301 aggtggcctc tgtcatgagg accaggggac agactgacag caaaaacaac tccaagcaca
      361 ggaggaagtg aaactggatt agcaagcgca cagccaagcc tggaccctaa aagagaagtg
      421 aggaagggta aggattcaga acacaaatcc agaaagaaga caagtgtgat gagggagtca
      481 caaggaagac ccacaaggcc agccatgagc tcccccaggc taacacagcc agcggtctca
      541 gggcagtgtg gggaatcagc cttgcccagg gccggggcca gggcagcccc gctgtcttcc
      601 tctcttcact gttatcacag ccggagcagc tgtgaagtgc ccaggaggca gctcctcaaa
      661 cggtgtttca acaatgtgcc cgagcagatg acgcagcaaa actattttct gtgcttcttg
      721 gactctgata actggaaaca aactatgcag agtcatgtta ggaggtgagg gtttgaatta
      781 gattgttttc tctagctatg aagacttatt ctgttactgt attttgagct gtggtggatt
      841 tgtctataat tcctaggtgg atttttaact taccttaaaa gctctgtgat tgttccttta
      901 acaaatatct aaataaatca gattaaaatt tttgaacgtg atgaaacta
//
