LOCUS       NM_001405026            1758 bp    mRNA    linear   PRI 08-APR-2024
DEFINITION  Homo sapiens t-complex 11 family, X-linked 1 (TCP11X1), transcript
            variant 1, mRNA.
ACCESSION   NM_001405026
VERSION     NM_001405026.1
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 1758)
  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
            AC234791.5.
            
            ##Evidence-Data-START##
            RNAseq introns :: single sample supports all introns SAMEA1968968,
                              SAMEA2158569 [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            inferred exon combination :: based on alignments, homology
            MANE Ensembl match        :: ENST00000622971.4/ ENSP00000494553.1
            RefSeq Select criteria    :: based on manual assertion,
                                         conservation, expression, longest
                                         protein
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-40                AC234791.5         44167-44206
            41-178              AC234791.5         44694-44831
            179-281             AC234791.5         46844-46946
            282-402             AC234791.5         50407-50527
            403-623             AC234791.5         51261-51481
            624-760             AC234791.5         52248-52384
            761-981             AC234791.5         52631-52851
            982-1163            AC234791.5         52950-53131
            1164-1327           AC234791.5         53893-54056
            1328-1758           AC234791.5         55231-55661
FEATURES             Location/Qualifiers
     source          1..1758
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="X"
                     /map="Xq22.1"
     gene            1..1758
                     /gene="TCP11X1"
                     /note="t-complex 11 family, X-linked 1"
                     /db_xref="GeneID:100996631"
                     /db_xref="HGNC:HGNC:48369"
     exon            1..40
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     exon            41..178
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     CDS             52..1560
                     /gene="TCP11X1"
                     /note="isoform 1 is encoded by transcript variant 1;
                     T-complex protein 11 homolog; T-complex protein 11
                     X-linked protein 1; T-complex protein 11-like X-linked
                     protein 1"
                     /codon_start=1
                     /product="T-complex protein 11-like X-linked protein 1
                     isoform 1"
                     /protein_id="NP_001391955.1"
                     /db_xref="GeneID:100996631"
                     /db_xref="HGNC:HGNC:48369"
                     /translation="MPKTEETVLQNDPSVAENGAPEPKTPGQSQKSKSFCLDDQSPDL
                     IETVNEVSKLSISHEIVVNQDFYVEETILPPNSVEGRFAEAMYNAFWNHLKEQLLSTP
                     PDFTCALELLKDVKETLLSLLLPWQNRLRNEIEEALDTDLLKQEAEHGALDVPHLSNY
                     ILNLMALLCAPVRDEAIQKLETIRDPVQLLRGILRVLGLMKMDMVNYTIQSFRPYLQE
                     HSIQYEQAKFQELLDKQPSLLDYTTKWLTKAATDITTLCPSSPDSPSSSCSMVCSLPS
                     GAGNNSEPPSPTMVLYQGYLNLLLWDLENVEFPETLLMDRIRLQELAFQLHQLTVLAS
                     VLLVARSFSGEVLFRSPEFVDRLKCTTKALTEEFISRPEETMLSVSEQVSQEVHQGLK
                     DMGLTTLSSENTASLLGQLQNITKKENCIRSIVDQWIRFFLKCCLLHGMQESLLHFPG
                     GLILIEKELAELGWKFLNLMHHNQQVFGPYYAEILKHIIHPAQAQETDVEPN"
     exon            179..281
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     exon            282..402
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     exon            403..623
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     exon            624..760
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     exon            761..981
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     exon            982..1163
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     exon            1164..1327
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
     exon            1328..1758
                     /gene="TCP11X1"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 agacgcagag gcgaggccgc cagtcgagga cgaggaggag ataacatcaa gatgccgaag
       61 actgaggaaa ctgtgctcca gaatgatccc agtgtagcag agaatggggc ccctgagcct
      121 aaaacaccag ggcagagcca gaaaagcaag agtttctgtt tagatgacca gtctcctgat
      181 ctgatagaga cagttaatga agtttccaag ctgagcattt cacatgaaat tgtagtaaac
      241 caagatttct atgtggaaga gaccattttg cctccaaaca gtgtagaagg caggtttgcg
      301 gaggcaatgt acaatgcttt ttggaaccat ctgaaagaac agctattgag tactcctcct
      361 gacttcactt gtgcccttga acttctaaaa gatgttaagg agaccttgct atcactgcta
      421 ttaccatggc agaaccgcct aagaaatgag atagaagaag ctctggacac agatctcctc
      481 aagcaggaag cagaacatgg ggccctggat gtccctcatc tttctaacta cattctcaat
      541 ttgatggctc tgctatgtgc accggttcga gatgaagcga tacagaaact agagaccata
      601 agagatccag tgcagttact gaggggcatc ctccgtgttc tgggcctaat gaaaatggac
      661 atggtgaact ataccatcca gagctttcga ccctacctgc aggaacattc catccagtat
      721 gaacaagcta aattccagga actccttgat aaacagccca gtctcctcga ttataccaca
      781 aaatggctaa ccaaagcagc cacagacatc actacactat gtccgagttc tcctgactca
      841 cctagctcct cctgcagcat ggtgtgttca cttccaagcg gggcaggtaa caattcagag
      901 ccccccagtc caacaatggt gctataccaa ggttacctga acctcctcct ctgggatctt
      961 gaaaacgtag aattcccaga gactctgctg atggacagaa tccggctcca ggaactggca
     1021 ttccagttgc accagttaac tgtcctggcc tcagtcttgc tagtggccag aagcttctct
     1081 ggtgaagttt tattcagatc acctgaattt gtggatagac tgaaatgcac caccaaggcc
     1141 ctaactgagg aatttatctc caggcctgaa gagactatgc tgagtgtgag tgaacaggtg
     1201 tctcaggaag tccatcaagg ccttaaggac atgggcctca ctactctgag cagtgaaaac
     1261 acagcatctc ttctaggcca actccagaac atcaccaaga aagagaactg cattcgtagc
     1321 attgttgatc agtggatccg tttttttctc aaatgctgtt tgcttcatgg catgcaggag
     1381 tctctgctac actttcctgg aggcctcatt ctcattgaaa aggagttggc agaactgggc
     1441 tggaagtttc tcaatctgat gcatcataat cagcaggtat ttggcccata ctatgctgag
     1501 atcctaaaac acatcatcca tccagctcaa gcacaagaaa cagatgtgga gcctaactga
     1561 tagtgctgga ccccagctat ggcaacaggg actcaggaga gagaggtcag catgtttctg
     1621 ggaggacatc acctgtggtt agtcgaacag tcagccctct tcctcgctat agccaggaca
     1681 cagggatgca ggggtcaagc atgtaagcac caactggccc aatccccttc actaataaac
     1741 ctctgagctg caagaaaa
//
