LOCUS       NM_010246               2110 bp    mRNA    linear   ROD 04-JUN-2024
DEFINITION  Mus musculus frizzled class receptor 9 (Fzd9), mRNA.
ACCESSION   NM_010246 XM_284144 XM_916560
VERSION     NM_010246.1
KEYWORDS    RefSeq; RefSeq Select.
SOURCE      Mus musculus (house mouse)
  ORGANISM  Mus musculus
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha;
            Muroidea; Muridae; Murinae; Mus; Mus.
REFERENCE   1  (bases 1 to 2110)
  AUTHORS   Murphy,P., Armit,C., Hill,B., Venkataraman,S., Frankel,P.,
            Baldock,R.A. and Davidson,D.R.
  TITLE     Integrated analysis of Wnt signalling system component gene
            expression
  JOURNAL   Development 149 (16) (2022)
   PUBMED   35831952
REFERENCE   2  (bases 1 to 2110)
  AUTHORS   Sompel,K., Dwyer-Nield,L.D., Smith,A.J., Elango,A., Backos,D.S.,
            Zhang,B., Gross,J., Ternyak,K., Matsuda,J.L., Kopf,K., Keith,R.L.
            and Tennis,M.A.
  TITLE     Iloprost requires the Frizzled-9 receptor to prevent lung cancer
  JOURNAL   iScience 25 (6), 104442 (2022)
   PUBMED   35707728
  REMARK    Publication Status: Online-Only
REFERENCE   3  (bases 1 to 2110)
  AUTHORS   Vollersen,N., Zhao,W., Rolvien,T., Lange,F., Schmidt,F.N.,
            Sonntag,S., Shmerling,D., von Kroge,S., Stockhausen,K.E.,
            Sharaf,A., Schweizer,M., Karsak,M., Busse,B., Bockamp,E.,
            Semler,O., Amling,M., Oheim,R., Schinke,T. and Yorgan,T.A.
  TITLE     The WNT1G177C mutation specifically affects skeletal integrity in a
            mouse model of osteogenesis imperfecta type XV
  JOURNAL   Bone Res 9 (1), 48 (2021)
   PUBMED   34759273
  REMARK    Publication Status: Online-Only
REFERENCE   4  (bases 1 to 2110)
  AUTHORS   Bedogni,F. and Hevner,R.F.
  TITLE     Cell-Type-Specific Gene Expression in Developing Mouse Neocortex:
            Intermediate Progenitors Implicated in Axon Development
  JOURNAL   Front Mol Neurosci 14, 686034 (2021)
   PUBMED   34321999
  REMARK    Publication Status: Online-Only
REFERENCE   5  (bases 1 to 2110)
  AUTHORS   Zacarias-Fluck,M.F., Jauset,T., Martinez-Martin,S., Kaur,J.,
            Casacuberta-Serra,S., Masso-Valles,D., Serrano Del Pozo,E.,
            Martin-Fernandez,G., Gonzalez-Larreategui,I., Lopez-Estevez,S.,
            Brown-Swigart,L., Beaulieu,M.E., Whitfield,J.R., Madan,B.,
            Virshup,D.M., Evan,G.I. and Soucek,L.
  TITLE     The Wnt signaling receptor Fzd9 is essential for Myc-driven
            tumorigenesis in pancreatic islets
  JOURNAL   Life Sci Alliance 4 (5), e201900490 (2021)
   PUBMED   33653688
  REMARK    GeneRIF: The Wnt signaling receptor Fzd9 is essential for
            Myc-driven tumorigenesis in pancreatic islets.
            Publication Status: Online-Only
REFERENCE   6  (bases 1 to 2110)
  AUTHORS   Xu,L., Tan,L., Goldring,M.B., Olsen,B.R. and Li,Y.
  TITLE     Expression of frizzled genes in mouse costochondral chondrocytes
  JOURNAL   Matrix Biol 20 (2), 147-151 (2001)
   PUBMED   11334716
REFERENCE   7  (bases 1 to 2110)
  AUTHORS   Valero,M.C., de Luis,O., Cruces,J. and Perez Jurado,L.A.
  TITLE     Fine-scale comparative mapping of the human 7q11.23 region and the
            orthologous region on mouse chromosome 5G: the low-copy repeats
            that flank the Williams-Beuren syndrome deletion arose at
            breakpoint sites of an evolutionary inversion(s)
  JOURNAL   Genomics 69 (1), 1-13 (2000)
   PUBMED   11013070
REFERENCE   8  (bases 1 to 2110)
  AUTHORS   Borello,U., Buffa,V., Sonnino,C., Melchionna,R., Vivarelli,E. and
            Cossu,G.
  TITLE     Differential expression of the Wnt putative receptors Frizzled
            during mouse somitogenesis
  JOURNAL   Mech Dev 89 (1-2), 173-177 (1999)
   PUBMED   10559494
REFERENCE   9  (bases 1 to 2110)
  AUTHORS   Wang,Y.K., Sporle,R., Paperna,T., Schughart,K. and Francke,U.
  TITLE     Characterization and expression pattern of the frizzled gene Fzd9,
            the mouse homolog of FZD9 which is deleted in Williams-Beuren
            syndrome
  JOURNAL   Genomics 57 (2), 235-248 (1999)
   PUBMED   10198163
REFERENCE   10 (bases 1 to 2110)
  AUTHORS   Perez Jurado,L.A., Wang,Y.K., Francke,U. and Cruces,J.
  TITLE     TBL2, a novel transducin family member in the WBS deletion:
            characterization of the complete sequence, genomic structure,
            transcriptional variants and the mouse ortholog
  JOURNAL   Cytogenet Cell Genet 86 (3-4), 277-284 (1999)
   PUBMED   10575226
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            BE985819.1, AF033585.2 and AK021164.1.
            
            On or before Mar 2, 2008 this sequence version replaced
            XM_916560.2, XM_284144.5.
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript is intronless :: AK021164.1 [ECO:0000345]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            RefSeq Select criteria :: based on single protein-coding transcript
            ##RefSeq-Attributes-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-218               BE985819.1         1-218
            219-940             AF033585.2         74-795
            941-1792            AK021164.1         1125-1976
            1793-2093           AF033585.2         1648-1948
            2094-2110           AK021164.1         2278-2294
FEATURES             Location/Qualifiers
     source          1..2110
                     /organism="Mus musculus"
                     /mol_type="mRNA"
                     /strain="C57BL/6"
                     /db_xref="taxon:10090"
                     /chromosome="5"
                     /map="5 75.08 cM"
     gene            1..2110
                     /gene="Fzd9"
                     /gene_synonym="Fz9; mfz9"
                     /note="frizzled class receptor 9"
                     /db_xref="GeneID:14371"
                     /db_xref="MGI:MGI:1313278"
     exon            1..2110
                     /gene="Fzd9"
                     /gene_synonym="Fz9; mfz9"
                     /inference="alignment:Splign:2.1.0"
     polyA_site      2110
                     /gene="Fzd9"
                     /gene_synonym="Fz9; mfz9"
                     /note="putative"
ORIGIN      
        1 cggccgcgcc gcggggcgat ggccgtgcca ccgctgctcc gcggggcgct gctgctgtgg
       61 cagctgctgg cgacgggcgg cgcggcgctg gagatcggcc gcttcgatcc ggagcgtggc
      121 cgtggccccg caccgtgcca agcgatggag atccccatgt gccggggcat tggctacaac
      181 ctgacccgca tgcccaacct actgggccac acgtcgcagg gcgaggcggc ggcgcagctg
      241 gccgagttct cgcccctcgt gcagtacggc tgccacagcc acctgcgctt cttcctctgc
      301 tcgctctacg ccccaatgtg caccgaccag gtctccactc ccatcccagc ctgccggccc
      361 atgtgcgagc aggctcgcct gcgctgcgcc cccatcatgg agcaattcaa tttcggctgg
      421 cccgactcac tcgactgtgc ccggctcccc acgcgcaacg acccgcacgc actctgtatg
      481 gaggcacccg agaacgctac agcaggcccc acagaacccc acaagggcct gggcatgctc
      541 cctgtggcac ctcggcccgc gaggccaccg ggagattcag ccccaggtcc cggcagcggt
      601 ggcacctgcg acaaccccga gaagttccag tacgtggaga agagtcgctc gtgcgctccg
      661 cgctgcgggc caggcgtcga ggtgttctgg tctcggcgcg ataaggactt cgcgctggtt
      721 tggatggctg tgtggtccgc gttgtgtttc ttctccacgg ccttcaccgt gttcaccttc
      781 ctgctggagc ctcaccggtt ccagtaccca gagcgcccga ttatcttcct ttctatgtgc
      841 tacaatgtct actccttggc cttcctgatc agagcggtgg caggtgcaca gagtgtggca
      901 tgcgaccagg aggcaggggc tctgtatgtg atccaggagg gtctggaaaa cacaggctgc
      961 accctggtct tcctgttgct ctattatttc gggatggcca gctcactttg gtgggtggtt
     1021 ttgactctaa cctggttcct ggctgcaggc aaaaaatggg gccacgaggc catcgaggct
     1081 cacggcagct acttccacat ggcagcgtgg ggcctgccag cactcaaaac tatcgtggtc
     1141 ctgactctgc gcaaggtggc tggcgatgaa ctgactgggc tctgctatgt agccagcatg
     1201 gacccggcag ccctcactgg ctttgtgttg gtacccctat cttgctacct ggtactgggt
     1261 accagtttcc tcctgaccgg ttttgtggct ctcttccata tccgcaaaat catgaagacg
     1321 ggaggcacca atacggagaa gctggagaag ctgatggtca aaatcggagt cttttccatc
     1381 ctttacacag tgccggccac ctgcgtcatt gtctgctacg tttatgaacg cctcaacatg
     1441 gacttctggc ggcttcgggc cacagagcaa ccatgtactg ctgccaccgt gcctggaggc
     1501 cggagagact gctcgctgcc agggggctcg gtgcccactg tggctgtctt catgctcaaa
     1561 atcttcatgt ccttggtggt gggcatcacc agtggagtct gggtatggag ttccaagact
     1621 tttcagactt ggcagagcct gtgctaccga aaaatggcag ctggccgagc ccgggccaag
     1681 gcctgccgaa ccccaggggg ctatggccgg ggtacccact gccactacaa agcccccacg
     1741 gtggtcttgc acatgactaa gacagacccc tctctggaga accccacaca cctctagaac
     1801 ataggctagg ctgtgagtta tggttgctcc ctccttgccc tcccctcccc ccttcagaga
     1861 cagctgacta acagctgccc agctgtcaag gtcagacaag tgagacacag ggggctgagg
     1921 actagggtgg ggacccagta aagctcaggg ccttgacctt ctgtctcatg cagggagtgg
     1981 tcctagtcca cagagggtcc caggataaga aggggcagaa gggggcaggg tccagtgcag
     2041 agttatttaa tgatgtaatt tattgtggca tttctctgga agctgtgact ggaataaacc
     2101 ctcgtgtggc
//
