LOCUS       NM_001396485            1194 bp    mRNA    linear   PRI 29-OCT-2022
DEFINITION  Homo sapiens nuclear pore complex interacting protein family member
            B2 (NPIPB2), transcript variant 6, mRNA.
ACCESSION   NM_001396485
VERSION     NM_001396485.1
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 1194)
  AUTHORS   Saiga A, Uozumi N, Ono T, Seno K, Ishimoto Y, Arita H, Shimizu T
            and Hanasaki K.
  TITLE     Group X secretory phospholipase A2 can induce arachidonic acid
            release and eicosanoid production without activation of cytosolic
            phospholipase A2 alpha
  JOURNAL   Prostaglandins Other Lipid Mediat 75 (1-4), 79-89 (2005)
   PUBMED   15789617
  REMARK    GeneRIF: sPLA2-X induces potent arachidonic acid release without
            activation of cytosolic phospholipase A2 alpha.
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC007216.2.
            
            ##Evidence-Data-START##
            RNAseq introns :: mixed sample support SAMEA1965299, SAMEA1966682
                              [ECO:0006172]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000399147.8/ ENSP00000382101.4
            RefSeq Select criteria :: based on manual assertion, longest
                                      protein
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-63                AC007216.2         85646-85708
            64-192              AC007216.2         90023-90151
            193-292             AC007216.2         93767-93866
            293-488             AC007216.2         93979-94174
            489-590             AC007216.2         97140-97241
            591-651             AC007216.2         98246-98306
            652-687             AC007216.2         98416-98451
            688-1194            AC007216.2         99812-100318
FEATURES             Location/Qualifiers
     source          1..1194
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="16"
                     /map="16p13.13"
     gene            1..1194
                     /gene="NPIPB2"
                     /note="nuclear pore complex interacting protein family
                     member B2"
                     /db_xref="GeneID:729978"
                     /db_xref="HGNC:HGNC:37451"
     CDS             1..1194
                     /gene="NPIPB2"
                     /note="isoform 3 is encoded by transcript variant 6;
                     putative NPIP-like protein LOC729978; putative nuclear
                     pore complex-interacting protein family member B2"
                     /codon_start=1
                     /product="putative nuclear pore complex-interacting
                     protein family member B2 isoform 3"
                     /protein_id="NP_001383414.1"
                     /db_xref="CCDS:CCDS92110.1"
                     /db_xref="GeneID:729978"
                     /db_xref="HGNC:HGNC:37451"
                     /translation="MFCCLGYEWLSGGCKTWHSAWVINTLADHHHRGTDFGGSPWLRI
                     IIAFPRSYKVVLTLWTVYLWLSFLKTIFQSENGHDVSTDVQQRARRSNRRRQEGLRSI
                     CMHTKKRVSSFPGNKIGLKDVITLRRHVETKGRAKIRKMKVTTKINHHDKINGKRKTA
                     KKQKLSVKECEHAEKERQVSEAEENGKLDMKEIHTYMKMFQRAQELRRRAEDYHKCKI
                     PPSARKALCNWVRMAAAEHRHSSGLPYWPYLTAETLKNRMGHQPPPPTQQHSITDNSL
                     SLKTPPECLLTPLPPSADDNLKTPPECLLTPLPPSAPPSADDNLKTPPLATQEAEAEK
                     PPKPKRWRAAEMESPPEPKRRRAAEVESPPEPKRRRAAEVEPSSPEPKRRRLSKLRTG
                     HCTQA"
     exon            1..63
                     /gene="NPIPB2"
                     /inference="alignment:Splign:2.1.0"
     exon            64..192
                     /gene="NPIPB2"
                     /inference="alignment:Splign:2.1.0"
     exon            193..292
                     /gene="NPIPB2"
                     /inference="alignment:Splign:2.1.0"
     exon            293..488
                     /gene="NPIPB2"
                     /inference="alignment:Splign:2.1.0"
     exon            489..590
                     /gene="NPIPB2"
                     /inference="alignment:Splign:2.1.0"
     exon            591..651
                     /gene="NPIPB2"
                     /inference="alignment:Splign:2.1.0"
     exon            652..687
                     /gene="NPIPB2"
                     /inference="alignment:Splign:2.1.0"
     exon            688..1194
                     /gene="NPIPB2"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 atgttttgtt gcttaggata tgaatggctg agcggaggct gtaaaacctg gcactctgct
       61 tgggttatca atactctggc tgaccatcat catcgtggga ctgactttgg tggaagtcct
      121 tggttacgta tcattattgc atttccgaga agttataaag ttgtccttac cctctggaca
      181 gtttaccttt ggttgtcttt cctgaagact atcttccagt ctgaaaatgg acatgatgta
      241 tccacagatg tacagcagag agccaggagg tccaaccgcc gtagacagga agggctgagg
      301 tccatttgta tgcacacaaa gaaaagagtt tcttcctttc caggaaataa aattggcctg
      361 aaagacgtca ttactctacg gagacatgtg gaaacaaaag gtagagctaa aatccgtaag
      421 atgaaggtga caacgaaaat caaccatcat gacaaaatca atggaaagag gaagaccgcc
      481 aaaaaacaga aactaagcgt gaaagaatgt gagcatgcag aaaaggagag gcaggtgtca
      541 gaggcagagg aaaatgggaa attggatatg aaagaaatac acacctacat gaaaatgttt
      601 caacgtgcgc aagagttgcg gcggcgggca gaggactacc acaaatgcaa aatcccccct
      661 tctgcaagaa aggctctttg caactgggtc agaatggcgg cagcggagca tcgtcattct
      721 tcaggattgc cctactggcc ctacctcaca gctgaaactt taaaaaacag gatgggccac
      781 cagccacctc ctccaactca acaacattct ataactgata actccctgag cctcaagaca
      841 cctcccgagt gtctgctcac tccccttcca ccctcagcgg atgataatct caagacacct
      901 cccgagtgtc tgctcactcc ccttccaccc tcagctccac cctcagcgga tgataatctc
      961 aagacacctc ccttagctac tcaggaggct gaggcagaaa aaccacccaa acccaagagg
     1021 tggagagcgg ctgagatgga atcaccaccc gaacccaaga ggcggagggc cgctgaggtg
     1081 gaatcaccac ccgaacccaa gaggcggagg gccgctgagg tggaaccatc atcacccgag
     1141 cccaagaggc ggaggttgag taagctgaga acaggccatt gcactcaagc ctga
//
