LOCUS       NM_152325               1523 bp    mRNA    linear   PRI 09-FEB-2025
DEFINITION  Homo sapiens testis expressed 26 (TEX26), transcript variant 1,
            mRNA.
ACCESSION   NM_152325
VERSION     NM_152325.3
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 1523)
  AUTHORS   Dunham,A., Matthews,L.H., Burton,J., Ashurst,J.L., Howe,K.L.,
            Ashcroft,K.J., Beare,D.M., Burford,D.C., Hunt,S.E.,
            Griffiths-Jones,S., Jones,M.C., Keenan,S.J., Oliver,K., Scott,C.E.,
            Ainscough,R., Almeida,J.P., Ambrose,K.D., Andrews,D.T.,
            Ashwell,R.I., Babbage,A.K., Bagguley,C.L., Bailey,J., Bannerjee,R.,
            Barlow,K.F., Bates,K., Beasley,H., Bird,C.P., Bray-Allen,S.,
            Brown,A.J., Brown,J.Y., Burrill,W., Carder,C., Carter,N.P.,
            Chapman,J.C., Clamp,M.E., Clark,S.Y., Clarke,G., Clee,C.M.,
            Clegg,S.C., Cobley,V., Collins,J.E., Corby,N., Coville,G.J.,
            Deloukas,P., Dhami,P., Dunham,I., Dunn,M., Earthrowl,M.E.,
            Ellington,A.G., Faulkner,L., Frankish,A.G., Frankland,J.,
            French,L., Garner,P., Garnett,J., Gilbert,J.G., Gilson,C.J.,
            Ghori,J., Grafham,D.V., Gribble,S.M., Griffiths,C., Hall,R.E.,
            Hammond,S., Harley,J.L., Hart,E.A., Heath,P.D., Howden,P.J.,
            Huckle,E.J., Hunt,P.J., Hunt,A.R., Johnson,C., Johnson,D., Kay,M.,
            Kimberley,A.M., King,A., Laird,G.K., Langford,C.J., Lawlor,S.,
            Leongamornlert,D.A., Lloyd,D.M., Lloyd,C., Loveland,J.E.,
            Lovell,J., Martin,S., Mashreghi-Mohammadi,M., McLaren,S.J.,
            McMurray,A., Milne,S., Moore,M.J., Nickerson,T., Palmer,S.A.,
            Pearce,A.V., Peck,A.I., Pelan,S., Phillimore,B., Porter,K.M.,
            Rice,C.M., Searle,S., Sehra,H.K., Shownkeen,R., Skuce,C.D.,
            Smith,M., Steward,C.A., Sycamore,N., Tester,J., Thomas,D.W.,
            Tracey,A., Tromans,A., Tubby,B., Wall,M., Wallis,J.M., West,A.P.,
            Whitehead,S.L., Willey,D.L., Wilming,L., Wray,P.W., Wright,M.W.,
            Young,L., Coulson,A., Durbin,R., Hubbard,T., Sulston,J.E., Beck,S.,
            Bentley,D.R., Rogers,J. and Ross,M.T.
  TITLE     The DNA sequence and analysis of human chromosome 13
  JOURNAL   Nature 428 (6982), 522-528 (2004)
   PUBMED   15057823
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            AL353680.8 and BC030277.1.
            
            On Nov 23, 2018 this sequence version replaced NM_152325.2.
            
            Transcript Variant: This variant (1) encodes the longer isoform
            (a).
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            ##Evidence-Data-START##
            Transcript exon combination :: SRR5189667.226642.1,
                                           SRR5189667.347037.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1968968, SAMEA2148093
                                           [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000380473.8/ ENSP00000369840.3
            RefSeq Select criteria :: based on conservation, expression,
                                      longest protein
            ##RefSeq-Attributes-END##
            COMPLETENESS: full length.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-41                AL353680.8         78735-78775
            42-1039             BC030277.1         1-998
            1040-1523           AL353680.8         121096-121579
FEATURES             Location/Qualifiers
     source          1..1523
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="13"
                     /map="13q12.3"
     gene            1..1523
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /note="testis expressed 26"
                     /db_xref="GeneID:122046"
                     /db_xref="HGNC:HGNC:28622"
     exon            1..121
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /inference="alignment:Splign:2.1.0"
     CDS             61..930
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /note="isoform a is encoded by transcript variant 1;
                     testis-expressed sequence 26 protein; testis-expressed
                     protein 26"
                     /codon_start=1
                     /product="testis-expressed protein 26 isoform a"
                     /protein_id="NP_689538.1"
                     /db_xref="CCDS:CCDS9339.1"
                     /db_xref="GeneID:122046"
                     /db_xref="HGNC:HGNC:28622"
                     /translation="MEQPGPRAPDPSLCHHNLQPTDDPNWDSYATTMRTAFTPKTGAV
                     PALIRQNGIRRLGYTYSLSDPILNQTQYSDEYTWKSHSKEDLIKTETSRGIKSHKSHL
                     NEDIFLWTLPHCQQTGTLKNCLPWKIPASMKEVNKALSNQFISLTKRDFVDRSKAQKI
                     KKSSHLSLEWKKLLPQPPDTEFRRNYQIPAKIPELQDFSFKYGCYSSLPVASQGLVPS
                     VLHSYLRNQEHTKKQTTYQSDYDKTYPDFLMLLNSFTSSQVKEYLQSLSYKDRQIIDR
                     FIRTHCDTNKKKK"
     exon            122..206
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /inference="alignment:Splign:2.1.0"
     exon            207..372
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /inference="alignment:Splign:2.1.0"
     exon            373..529
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /inference="alignment:Splign:2.1.0"
     exon            530..706
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /inference="alignment:Splign:2.1.0"
     exon            707..868
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /inference="alignment:Splign:2.1.0"
     exon            869..1523
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /inference="alignment:Splign:2.1.0"
     regulatory      1018..1023
                     /regulatory_class="polyA_signal_sequence"
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /note="hexamer: AATAAG"
     polyA_site      1039
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /note="major polyA site"
     regulatory      1093..1098
                     /regulatory_class="polyA_signal_sequence"
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /note="hexamer: AATAAA"
     polyA_site      1113
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /note="major polyA site"
     regulatory      1504..1509
                     /regulatory_class="polyA_signal_sequence"
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /note="hexamer: AATAAA"
     polyA_site      1523
                     /gene="TEX26"
                     /gene_synonym="C13orf26"
                     /note="major polyA site"
ORIGIN      
        1 ggctcccgca agcgctgaga tagctggagc cagggccccg cggccgcctc ctggggcaga
       61 atggaacagc ctgggcccag ggctccggat ccctctctct gccaccacaa cctccagcca
      121 acagatgacc ccaactggga ttcctatgct accactatga ggactgcatt cacgcctaaa
      181 acaggagcag tgcctgcctt aattcgccaa aacggtatca gaagattagg atatacatat
      241 tcacttagtg atcctattct caatcagaca caatatagtg atgagtacac ttggaaatca
      301 cactctaaag aagatttgat caaaactgag acttcaagag gaatcaagag ccacaaatct
      361 catctcaatg aagacatttt cctgtggaca ctacctcact gtcaacaaac ggggacacta
      421 aagaactgcc tcccttggaa aatcccggct tcaatgaaag aagttaacaa ggcactatca
      481 aatcagttta tttcccttac taagagagac tttgtggaca gatcaaaagc tcagaagatt
      541 aagaaaagtt ctcacttgtc tctggaatgg aaaaagttac ttccccaacc tccagacact
      601 gaattccgaa ggaattacca aattccagct aaaattcctg agcttcaaga tttcagtttc
      661 aaatatggat gctactcaag cttgcctgtt gcttctcagg gtctagtgcc ttctgtgctg
      721 cacagctacc tgaggaacca agagcacaca aagaaacaga ccacatacca aagtgactac
      781 gacaaaacct acccagattt cttaatgctt ttaaactcat ttacttcctc tcaagtcaaa
      841 gagtaccttc agagtctttc ctacaaagat agacaaatta ttgatcgctt tattcgtact
      901 cactgtgaca ctaacaaaaa gaagaaatga aaagggaaaa tagtacaaat gaagaaaatc
      961 tgaaaatcaa tggaagcacg aggacattcc tagtcatttt ctcaattatc aaggaaaaat
     1021 aagatgcaaa tagcttcaag tatgatgtga tagtcatgaa tttgtgtctt ttgctccgct
     1081 ttatttttaa acaataaaat taaggctaca aaattttccc tgaacatagc tttagctgta
     1141 tccaatagtt tttgatacaa tgtttttttc ttttcccttt tggatactta atttgtagtt
     1201 tcaattttga tttctcctgt gaactaggaa ttatgtggaa gagatttctt aatgtcccat
     1261 taatcagaga cttaagaaat cattttattg ccttatctct tctttgaatg aatgaaagtt
     1321 taaaaatctg cttttgggaa atcaattgca gttttattta atgccattaa tcaagtatat
     1381 gattaatttg tgtgttacgt gaatatgaga aaaaaattat agtttattgt attttttaat
     1441 cccttatatc tttaattgta tacttgaatt gttcaattct gaaagaatat tggaacctcc
     1501 cacaataaat atatttttat caa
//
