LOCUS       NM_001170741            2675 bp    mRNA    linear   PRI 09-JUN-2024
DEFINITION  Homo sapiens NUT family member 2G (NUTM2G), transcript variant 2,
            mRNA.
ACCESSION   NM_001170741
VERSION     NM_001170741.3
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 2675)
  AUTHORS   Humphray,S.J., Oliver,K., Hunt,A.R., Plumb,R.W., Loveland,J.E.,
            Howe,K.L., Andrews,T.D., Searle,S., Hunt,S.E., Scott,C.E.,
            Jones,M.C., Ainscough,R., Almeida,J.P., Ambrose,K.D., Ashwell,R.I.,
            Babbage,A.K., Babbage,S., Bagguley,C.L., Bailey,J., Banerjee,R.,
            Barker,D.J., Barlow,K.F., Bates,K., Beasley,H., Beasley,O.,
            Bird,C.P., Bray-Allen,S., Brown,A.J., Brown,J.Y., Burford,D.,
            Burrill,W., Burton,J., Carder,C., Carter,N.P., Chapman,J.C.,
            Chen,Y., Clarke,G., Clark,S.Y., Clee,C.M., Clegg,S., Collier,R.E.,
            Corby,N., Crosier,M., Cummings,A.T., Davies,J., Dhami,P., Dunn,M.,
            Dutta,I., Dyer,L.W., Earthrowl,M.E., Faulkner,L., Fleming,C.J.,
            Frankish,A., Frankland,J.A., French,L., Fricker,D.G., Garner,P.,
            Garnett,J., Ghori,J., Gilbert,J.G., Glison,C., Grafham,D.V.,
            Gribble,S., Griffiths,C., Griffiths-Jones,S., Grocock,R., Guy,J.,
            Hall,R.E., Hammond,S., Harley,J.L., Harrison,E.S., Hart,E.A.,
            Heath,P.D., Henderson,C.D., Hopkins,B.L., Howard,P.J., Howden,P.J.,
            Huckle,E., Johnson,C., Johnson,D., Joy,A.A., Kay,M., Keenan,S.,
            Kershaw,J.K., Kimberley,A.M., King,A., Knights,A., Laird,G.K.,
            Langford,C., Lawlor,S., Leongamornlert,D.A., Leversha,M., Lloyd,C.,
            Lloyd,D.M., Lovell,J., Martin,S., Mashreghi-Mohammadi,M.,
            Matthews,L., McLaren,S., McLay,K.E., McMurray,A., Milne,S.,
            Nickerson,T., Nisbett,J., Nordsiek,G., Pearce,A.V., Peck,A.I.,
            Porter,K.M., Pandian,R., Pelan,S., Phillimore,B., Povey,S.,
            Ramsey,Y., Rand,V., Scharfe,M., Sehra,H.K., Shownkeen,R.,
            Sims,S.K., Skuce,C.D., Smith,M., Steward,C.A., Swarbreck,D.,
            Sycamore,N., Tester,J., Thorpe,A., Tracey,A., Tromans,A.,
            Thomas,D.W., Wall,M., Wallis,J.M., West,A.P., Whitehead,S.L.,
            Willey,D.L., Williams,S.A., Wilming,L., Wray,P.W., Young,L.,
            Ashurst,J.L., Coulson,A., Blocker,H., Durbin,R., Sulston,J.E.,
            Hubbard,T., Jackson,M.J., Bentley,D.R., Beck,S., Rogers,J. and
            Dunham,I.
  TITLE     DNA sequence and analysis of human chromosome 9
  JOURNAL   Nature 429 (6990), 369-374 (2004)
   PUBMED   15164053
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AL158827.27.
            
            On Jan 3, 2020 this sequence version replaced NM_001170741.2.
            
            Sequence Note:.
            
            ##Evidence-Data-START##
            RNAseq introns :: single sample supports all introns SAMEA1968968,
                              SAMEA2148093 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000372322.4/ ENSP00000361397.3
            RefSeq Select criteria :: based on conservation, expression,
                                      longest protein
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-198               AL158827.27        128480-128677
            199-895             AL158827.27        131359-132055
            896-1024            AL158827.27        134965-135093
            1025-1164           AL158827.27        136062-136201
            1165-1505           AL158827.27        136701-137041
            1506-1622           AL158827.27        137522-137638
            1623-2675           AL158827.27        138001-139053
FEATURES             Location/Qualifiers
     source          1..2675
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="9"
                     /map="9q22.33"
     gene            1..2675
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /note="NUT family member 2G"
                     /db_xref="GeneID:441457"
                     /db_xref="HGNC:HGNC:23449"
     exon            1..198
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /inference="alignment:Splign:2.1.0"
     CDS             183..2408
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /note="isoform 2 is encoded by transcript variant 2;
                     family with sequence similarity 22, pseudogene; protein
                     FAM22G; family with sequence similarity 22, member G"
                     /codon_start=1
                     /product="NUT family member 2G isoform 2"
                     /protein_id="NP_001164212.1"
                     /db_xref="CCDS:CCDS55329.1"
                     /db_xref="GeneID:441457"
                     /db_xref="HGNC:HGNC:23449"
                     /translation="MASNGAYPVLGPGVTVNPGTSLSVFTALPFATPSPGPTHRPPLV
                     TAVVPPAGPLVLSAFPSTPLVAGQDGRGPSGAGASNVFVQMRTEVGPVKPPQAQTLIL
                     TQAPLVWQAPGTLCGGVMCPPPLLLAAAPGVPVTSAQVVGGTQACEGGWSHGLPLPPP
                     PPAAQVAPIVSPGNAGPWPQGAHGEGSLAPSQAKARPDDSCKPKSVYENFRLWQHYKP
                     LARRHLPQSPDTEALSCFLIPVLRSLARRKPTMTLEEGLWRAMREWQHTSNFDRMIFY
                     EMAAKFLEFEAEEEMQIQKSQWMKGPQSLPPPAPPRLEPRGPPAPEVVKQPVYLPSKD
                     GPKAPTACLPPPRPQRPAETKAHLPPPRPPRPAETKVPEEIPPEVVQEYVDIMEELLG
                     SHPGDTGEPEGQREKGKVEQPQEEDGMTSDPGLLSYIDKLCSQEDFVTKVEAVIHPRF
                     LEELLSPDPQMDFLALSQELEQEEGLTLAQLVEKRLLSLKEKGCGRAAPRHGTARLDS
                     SPSEFAAGQEAAREVPDPQQRVSVETSPPQTAAQDPQGQGRVRTGMARSEDPAVLLGC
                     QDSPRLKAVRPTSPPQDHRPTCPGLGTKDALGLPGESPVKESHGLAKGSSEETELPGM
                     VYVVGSHHRLRPWRLSQSPVPSSGLLSPGGRGPQGALQSPSAQKRGLSPSPSPASKSK
                     KRPLFGSPSPAEKTPHPGPGLRVSGEQSLAWGLGGPSQSQKRKGDPLASRRKKKRHCS
                     Q"
     exon            199..895
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /inference="alignment:Splign:2.1.0"
     exon            896..1024
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /inference="alignment:Splign:2.1.0"
     exon            1025..1164
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /inference="alignment:Splign:2.1.0"
     exon            1165..1505
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /inference="alignment:Splign:2.1.0"
     exon            1506..1622
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /inference="alignment:Splign:2.1.0"
     exon            1623..2675
                     /gene="NUTM2G"
                     /gene_synonym="FAM22G; NUTMG"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 gcccctcccc ctctgcagaa tgtctggggt cctgtgttcc aaacctgttt atatgcaaat
       61 tatccctgct ccacttggac tcaggaggat ctgctgagtc aggtcactct ctgggtcctg
      121 cccttgactt ttttcattgc ggaagctgcc agacagtggt ggtcagtgcc cagcctgagg
      181 ggatggcttc aaatggagca tacccagtgc tgggacccgg cgtgaccgtg aaccctggca
      241 cctccctgtc tgtgttcacg gctctgccct ttgccacacc ctctcccggc ccaacacaca
      301 ggccgcccct cgtgactgca gtggttcctc cagccggccc tctggtgctc tctgccttcc
      361 ccagcacccc tctagtggca ggacaggatg gccgcggccc aagtggggct ggggcttcca
      421 acgtctttgt ccagatgagg acagaagtgg ggcctgtgaa gccccctcag gcacagacct
      481 tgatcctaac tcaggccccc ctcgtctggc aggctccagg caccctctgt ggaggtgtca
      541 tgtgtccacc tcccctactc ctggcagctg ctcctggggt gcccgttacc tctgcccagg
      601 tggttggggg cacccaggcc tgtgagggag gctggtccca tggccttcct cttccaccac
      661 caccaccggc tgcccaggtg gcccccatcg tgtccccagg gaacgctggg ccatggccac
      721 aaggggctca tggagagggc agcctggctc cctcccaggc caaggcccgg ccggacgact
      781 cctgtaaacc caagagtgtc tatgagaact tccgactctg gcagcactac aagcccctgg
      841 cccggaggca ccttccccag agtcctgaca ctgaagcgct ttcctgcttc ctcatcccag
      901 ttctccgatc cctggcccgg cggaagccca ccatgacgct ggaggaggga ctgtggcggg
      961 ccatgcggga atggcagcac acgagcaact ttgaccggat gattttctac gagatggcgg
     1021 caaagttcct ggagtttgag gctgaggagg agatgcagat tcagaaatcg cagtggatga
     1081 aggggcccca gagcctgcct cctccagccc cgccgaggct tgaacctcga ggaccccctg
     1141 cccctgaggt ggtcaagcag ccagtgtacc ttcccagcaa ggatggcccc aaggccccga
     1201 ctgcctgcct gccaccaccc aggccccaga ggccagcgga gaccaaggcc cacctgccac
     1261 cacccaggcc cccgaggcca gcagagacca aggtccctga ggagatcccc cctgaagtgg
     1321 tgcaggagta tgtggacatc atggaggagc tgctggggtc tcaccctggg gacacagggg
     1381 agcctgaggg acaacgggaa aagggcaaag tggagcagcc gcaggaagag gacgggatga
     1441 cctcagaccc gggcctcctg agctacattg acaagctgtg ttcccaggaa gactttgtca
     1501 ccaaggtgga ggccgtcatt cacccccgat tcctggaaga attgctttcc ccagatccac
     1561 agatggattt cttggcccta agccaggagc tggagcagga ggaaggactc acccttgccc
     1621 agctagtgga gaagcgcctc ctgtccttga aggagaaagg gtgcgggagg gcagcccctc
     1681 gacatggcac ggccaggttg gactcaagtc cttctgagtt tgcagctggc caagaagcag
     1741 cgagagaggt ccctgacccc caacaaaggg tcagcgtgga aacctcccca ccccagacgg
     1801 ctgcccagga ccctcaggga cagggcagag tgcgcactgg catggccagg tccgaagacc
     1861 ctgctgtgct tttgggatgt caggactccc ccaggctgaa ggctgtccgg ccaacctctc
     1921 ctccccagga ccacagaccc acctgccccg gcctggggac caaggacgcc ttgggtctcc
     1981 ctggagagtc tcctgtcaag gagtcacatg ggctggctaa ggggtcaagt gaggagacgg
     2041 aactccctgg catggtctat gtcgtgggtt cccaccacag gctgaggccc tggaggctgt
     2101 cccagagccc tgtcccttcc tcgggccttc tcagcccagg agggagagga ccccagggag
     2161 ctcttcaatc tccatctgct cagaaaagag gcctcagccc atcaccttct cctgccagca
     2221 agtccaagaa gcgacctctc tttggaagcc catcccctgc tgaaaagaca ccgcacccag
     2281 ggcctgggct cagggtctct ggggagcaat ccctggcttg ggggctgggt ggcccctcac
     2341 agtctcaaaa gagaaagggt gaccccttgg cctccaggag gaagaagaag cggcattgta
     2401 gccagtaggg gccgccatgg ggcagactct ctgatgccag tccccaaaag tggggctctg
     2461 aagtctcgga ccctcatggc acccggtgcc ccaaagcaaa ggctgcttct cctccagtgc
     2521 tgatcttgct gggccttagc tttggagggt aggggaagga ggggagggag aaggtggctg
     2581 aacggggagg gcaggaaggg agggcctggg gggtgggaag cagtgccttg ggggccttgt
     2641 gtgtaaatgt gaataaatgt agttgttttg gaaaa
//
