LOCUS       NM_001393655            1587 bp    mRNA    linear   PRI 08-APR-2024
DEFINITION  Homo sapiens 5'-nucleotidase domain containing 4 (NT5DC4),
            transcript variant 1, mRNA.
ACCESSION   NM_001393655
VERSION     NM_001393655.1
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 1587)
  AUTHORS   Gaudet,P., Livstone,M.S., Lewis,S.E. and Thomas,P.D.
  TITLE     Phylogenetic-based propagation of functional annotations within the
            Gene Ontology consortium
  JOURNAL   Brief Bioinform 12 (5), 449-462 (2011)
   PUBMED   21873635
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AC079922.5.
            
            Transcript Variant: This variant (1) encodes the longer isoform
            (1).
            
            ##Evidence-Data-START##
            RNAseq introns :: single sample supports all introns SAMEA2148874,
                              SAMEA2151119 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            inferred exon combination :: based on alignments, homology
            MANE Ensembl match        :: ENST00000688554.1/ ENSP00000509504.1
            RefSeq Select criteria    :: based on manual assertion,
                                         conservation, expression
            ##RefSeq-Attributes-END##
            COMPLETENESS: full length.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-134               AC079922.5         103412-103545
            135-208             AC079922.5         104210-104283
            209-326             AC079922.5         104378-104495
            327-422             AC079922.5         104575-104670
            423-529             AC079922.5         104875-104981
            530-587             AC079922.5         105106-105163
            588-681             AC079922.5         105473-105566
            682-732             AC079922.5         105810-105860
            733-816             AC079922.5         106111-106194
            817-849             AC079922.5         106486-106518
            850-975             AC079922.5         107173-107298
            976-1042            AC079922.5         107566-107632
            1043-1213           AC079922.5         107774-107944
            1214-1265           AC079922.5         108630-108681
            1266-1326           AC079922.5         109070-109130
            1327-1404           AC079922.5         112019-112096
            1405-1587           AC079922.5         121305-121487
FEATURES             Location/Qualifiers
     source          1..1587
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="2"
                     /map="2q14.1"
     gene            1..1587
                     /gene="NT5DC4"
                     /note="5'-nucleotidase domain containing 4"
                     /db_xref="GeneID:284958"
                     /db_xref="HGNC:HGNC:27678"
     exon            1..134
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     CDS             61..1428
                     /gene="NT5DC4"
                     /note="isoform 1 is encoded by transcript variant 1;
                     5'-nucleotidase domain-containing protein 4"
                     /codon_start=1
                     /product="5'-nucleotidase domain-containing protein 4
                     isoform 1"
                     /protein_id="NP_001380584.1"
                     /db_xref="CCDS:CCDS92846.1"
                     /db_xref="GeneID:284958"
                     /db_xref="HGNC:HGNC:27678"
                     /translation="MASVDWREPEGLVSPQGPKQDWHQRIFVNRSLALGKIRCFGFDM
                     DYTLAAYKSPAYEALTFELLLERLVCIGYPHEILRYTYDPTFPTRRLVFDELYGNLLK
                     VDAHGNVLLGAYGFTFLSDLPLLRAEIWSFYPSKFIQRDDLQCFYILNMLFNLPETYL
                     YACLVDFFSGCSRYTNCDTGYQHGNLFMSFRSLFQDVTDAMNNIHQSGCLKKTLEDLE
                     KYVKKDPRLPILLGKMKEVGKVFLATNSSYNYTNAIMTYLFSISEAEASGRPWRSYFD
                     LIVVDTQKPHFFAEGLVLRQVNTVMAGAEDSGKLHVGTYTGPHQHCAVYSGGSSDMVC
                     ELLGVRGMDILYIGDHIFGDILKSKKRQGWRTCLVVPELSWELDIWAQEKERLEELKR
                     LDTHLADIYQHMDGSSCELQVINFTKREIQMPHESVVEQEQANLDPASCLLSCNQRFI
                     KRSHY"
     exon            135..208
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            209..326
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            327..422
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            423..529
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            530..587
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            588..681
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            682..732
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            733..816
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            817..849
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            850..975
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            976..1042
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            1043..1213
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            1214..1265
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            1266..1326
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            1327..1404
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
     exon            1405..1587
                     /gene="NT5DC4"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 actgatagtg tgcaggaggc tgaggaaggg acacttgcct cctcctcact ctgggtgacg
       61 atggccagtg tagactggag agagccggag ggactggtct cccctcaagg cccgaagcag
      121 gactggcacc agcggatttt tgtcaaccgc agcctggcgc tggggaagat tcgttgcttt
      181 ggcttcgaca tggactacac tctggctgcc tacaagtccc cagcttatga ggccctgacc
      241 ttcgagctgc tgctggagcg cctggtgtgc attgggtacc cgcatgagat cctgcgctac
      301 acctacgacc ccaccttccc caccaggcgg ctggtgttcg atgaactcta tgggaacctg
      361 ctgaaggtgg acgcccacgg gaatgtgctg ctgggtgcct atggcttcac cttcctctcg
      421 gacctacccc tcctcagggc agagatctgg agcttctacc ccagcaagtt cattcagagg
      481 gacgacctgc agtgtttcta catactcaac atgctcttca acctgcctga aacctacctc
      541 tatgcctgct tggtggactt cttctctggc tgctcccgtt acactaattg tgacaccggc
      601 tatcagcatg ggaacctctt catgtccttc cgaagcctct tccaggatgt gactgatgcc
      661 atgaataaca tccaccagtc gggctgtctc aagaagaccc tggaggactt ggagaaatat
      721 gtgaagaagg atccacgcct ccccatcctg ctggggaaga tgaaggaggt tgggaaagtg
      781 tttctggcca ccaacagcag ctacaactac accaatgcca tcatgaccta cctgttcagc
      841 atcagtgagg ctgaagcctc gggcaggccc tggaggtcct actttgacct gatcgtggtg
      901 gacacgcaga agccccactt ctttgcagag gggttggtcc tgaggcaggt caacacggta
      961 atggcaggtg cagaggactc aggaaagctc cacgtgggca cctacacagg gccccaccag
     1021 cactgtgctg tctactctgg aggctcttcg gacatggtgt gcgagctgct tggggttcgg
     1081 gggatggaca tcctgtacat tggggaccac atttttgggg acattctcaa gtccaagaag
     1141 cgtcagggct ggcggacttg cctggtggtt cctgagctgt cctgggagct ggacatctgg
     1201 gcccaggaga aggagcggtt ggaggagctg aagagactgg acacgcacct ggcagacata
     1261 taccagcaca tggatgggag cagttgtgag ctgcaagtca tcaacttcac caagagagag
     1321 atccagatgc cacatgagtc agttgtggag caagaacagg ccaatctaga ccctgcctcc
     1381 tgcctcctct cctgcaacca gaggttcatc aagagaagcc actactaaat cgtgttcctg
     1441 cagcatttct gggtagcggg acactgctcg ctcaatcctc gacgaacgcc gtacaggagt
     1501 gataaatttc atgtcttgca cttccggcat cccatttatt ctgagagaca gcaagagatg
     1561 cattaaaaac cttatcattt aaaaaaa
//
