LOCUS       NM_001145139            1795 bp    mRNA    linear   PRI 09-JUN-2022
DEFINITION  Homo sapiens chromosome X open reading frame 49B (CXorf49B),
            transcript variant 1, mRNA.
ACCESSION   NM_001145139 XM_001716545
VERSION     NM_001145139.2
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.
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            BX276092.9.
            
            On Sep 21, 2020 this sequence version replaced NM_001145139.1.
            
            ##Evidence-Data-START##
            Transcript exon combination :: SRR14038192.3676953.1,
                                           SRR11853567.32045.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1968968, SAMEA2148093
                                           [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000542739.3/ ENSP00000482270.1
            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
            1-1299              BX276092.9         111945-113243
            1300-1456           BX276092.9         113820-113976
            1457-1533           BX276092.9         114520-114596
            1534-1579           BX276092.9         114879-114924
            1580-1621           BX276092.9         115479-115520
            1622-1795           BX276092.9         115627-115800
FEATURES             Location/Qualifiers
     source          1..1795
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq13.1"
     gene            1..1795
                     /gene="CXorf49B"
                     /gene_synonym="CXorf49"
                     /note="chromosome X open reading frame 49B"
                     /db_xref="GeneID:100132994"
                     /db_xref="HGNC:HGNC:34229"
     exon            1..1299
                     /gene="CXorf49B"
                     /gene_synonym="CXorf49"
                     /inference="alignment:Splign:2.1.0"
     CDS             76..1620
                     /gene="CXorf49B"
                     /gene_synonym="CXorf49"
                     /codon_start=1
                     /product="uncharacterized protein CXorf49"
                     /protein_id="NP_001138611.1"
                     /db_xref="CCDS:CCDS75992.1"
                     /db_xref="GeneID:100132994"
                     /db_xref="HGNC:HGNC:34229"
                     /translation="MSSPDKVSVCGAGFDLEGGKKAGSRTASPGAPGAHSHGLDLGVP
                     GSGDGKSESGFTDPEGFSFESESELIEQGRVVLWGREGRPGTPVDDQGDVVDYSFYLA
                     DEPAAIVPPPSVQGHPFPEGAAAEGSAENWADAEVGPSGRDVLGHSPGKWQQASAGRL
                     HLCGPGPVRAWKNPERGSKSRWSLRVDPQQPSAKGPTRLPTHDSDSADESSDLPLMKV
                     GICRNEGSQAKPGSPKKRADTSRQASFHCKESYLPVPGRFLTSAPRGLTPVAERPAVG
                     ELEDSPQKKMQSRAWGKVEVRPSCSGAAAAGALPQGLSRRKMAGGKKSLGGASQLALG
                     RGFPACGERLSAAPPEPATFPPFSGVRPQGMSKKPQKPKHSSPGKKPAGRKTRESQAA
                     AREDNDPNRDEVPRAQLPTHRPGLPRLSVRRGEFSSSDPNIRAPQLPGTSEPSAYSPG
                     GLVPRRHAPSGNQQPPVHPPRPERQQQPPGAQGCPRCIWLQREIEDLTQQLAAMQFLT
                     DKFQDL"
     exon            1300..1456
                     /gene="CXorf49B"
                     /gene_synonym="CXorf49"
                     /inference="alignment:Splign:2.1.0"
     exon            1457..1533
                     /gene="CXorf49B"
                     /gene_synonym="CXorf49"
                     /inference="alignment:Splign:2.1.0"
     exon            1534..1579
                     /gene="CXorf49B"
                     /gene_synonym="CXorf49"
                     /inference="alignment:Splign:2.1.0"
     exon            1580..1621
                     /gene="CXorf49B"
                     /gene_synonym="CXorf49"
                     /inference="alignment:Splign:2.1.0"
     exon            1622..1795
                     /gene="CXorf49B"
                     /gene_synonym="CXorf49"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 ctgggctcag ctctccgctc ccgccgttac caggacgacc gtctccccgc agcccaggct
       61 gcccggactg gcgccatgag ctcccccgac aaggtgtccg tttgtggggc cggtttcgac
      121 ctggagggtg gcaaaaaggc tggctcccgc acggccagcc ccggagcccc aggggcccac
      181 agccacggcc tcgatttggg ggtgccgggc agcggcgatg gcaagagcga gagcgggttc
      241 acagatccag agggcttcag cttcgagtct gagagcgaat tgatagagca aggaagggtg
      301 gtgctctggg gccgggaagg ccggccaggc accccggtgg atgaccaagg ggacgttgtg
      361 gactactcat tctacctggc tgacgaacca gccgccatcg tgccgccgcc cagcgtccag
      421 ggacacccgt tcccagaagg tgccgctgcc gaagggtcgg ctgagaattg ggcagatgcg
      481 gaggtcggtc ccagtgggag agacgtgctg ggccacagcc ctggaaaatg gcagcaggcc
      541 tctgccggcc gtctccacct ctgcggtcct gggccagtgc gggcctggaa gaacccggaa
      601 aggggctcga agagcagatg gagcctccgc gtggatcccc agcagccctc tgcgaaaggc
      661 cccaccaggc tgcctaccca cgactctgat tccgcagatg agagcagcga cttaccactg
      721 atgaaggtag gcatttgccg caacgaagga agccaggcca agcccggcag ccccaagaag
      781 cgagcagaca catccagaca ggcaagcttc cactgcaagg agagttacct gcctgtgccg
      841 ggccgtttcc tgacctctgc tccccgcgga ctcactccag tcgcagagag gccggctgtg
      901 ggagagctgg aggactctcc ccagaagaaa atgcagagca gggcctgggg aaaggtggag
      961 gtcaggccca gctgctcagg agctgctgct gcaggggccc tgccccaggg cctttcgagg
     1021 aggaagatgg ccggggggaa gaagtcccta gggggtgcct ctcaactggc cctggggaga
     1081 ggctttcctg cctgcggaga gagactctca gccgctcccc cggagccggc caccttcccg
     1141 ccattctctg gtgtgcggcc acaggggatg tccaagaaac cccaaaagcc taagcacagc
     1201 agccctggga agaaaccagc agggaggaag accagggagt cccaggctgc ggccagagaa
     1261 gataatgacc caaatagaga tgaggtccca agagcccaac ttcccaccca caggccagga
     1321 ctgcctcgcc tgtctgtgcg tcgtggagaa ttcagcagta gcgaccccaa catcagagct
     1381 ccccaacttc cgggaacttc agagccctcg gcctacagcc cgggaggcct cgtgcccaga
     1441 cgccatgcac cctccggtaa ccagcagccg cctgtccatc ccccaagacc ggaaaggcag
     1501 cagcagcccc cgggagccca gggctgtcct cggtgcatct ggctgcagag ggaaattgag
     1561 gaccttacac agcagctagc ggccatgcag ttcctcactg acaagttcca ggacctttga
     1621 agttggagcc agcatcttcc tacaagatga acagctgcca cctttggagc tccggagctg
     1681 cagccaagcg ggttccctcc atatcctgtt cagccagggc ttcctctctt ccgctgcatt
     1741 tgcccccttc ccaacgcagt tcaaagcaat ttgaaataaa gtcgttctca tattc
//
