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2024-04-26 10:04:52, GGRNA.v2 : RefSeq release 222 (Jan, 2024)

LOCUS       NM_001282469            1161 bp    mRNA    linear   PRI 25-DEC-2022
DEFINITION  Homo sapiens testis specific protein Y-linked 10 (TSPY10),
            transcript variant 1, mRNA.
ACCESSION   NM_001282469 XM_003403496
VERSION     NM_001282469.3
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 1161)
  AUTHORS   Luck K, Kim DK, Lambourne L, Spirohn K, Begg BE, Bian W, Brignall
            R, Cafarelli T, Campos-Laborie FJ, Charloteaux B, Choi D, Cote AG,
            Daley M, Deimling S, Desbuleux A, Dricot A, Gebbia M, Hardy MF,
            Kishore N, Knapp JJ, Kovacs IA, Lemmens I, Mee MW, Mellor JC,
            Pollis C, Pons C, Richardson AD, Schlabach S, Teeking B, Yadav A,
            Babor M, Balcha D, Basha O, Bowman-Colin C, Chin SF, Choi SG,
            Colabella C, Coppin G, D'Amata C, De Ridder D, De Rouck S,
            Duran-Frigola M, Ennajdaoui H, Goebels F, Goehring L, Gopal A,
            Haddad G, Hatchi E, Helmy M, Jacob Y, Kassa Y, Landini S, Li R, van
            Lieshout N, MacWilliams A, Markey D, Paulson JN, Rangarajan S,
            Rasla J, Rayhan A, Rolland T, San-Miguel A, Shen Y, Sheykhkarimli
            D, Sheynkman GM, Simonovsky E, Tasan M, Tejeda A, Tropepe V,
            Twizere JC, Wang Y, Weatheritt RJ, Weile J, Xia Y, Yang X,
            Yeger-Lotem E, Zhong Q, Aloy P, Bader GD, De Las Rivas J, Gaudet S,
            Hao T, Rak J, Tavernier J, Hill DE, Vidal M, Roth FP and Calderwood
            MA.
  TITLE     A reference map of the human binary protein interactome
  JOURNAL   Nature 580 (7803), 402-408 (2020)
   PUBMED   32296183
REFERENCE   2  (bases 1 to 1161)
  AUTHORS   Skaletsky H, Kuroda-Kawaguchi T, Minx PJ, Cordum HS, Hillier L,
            Brown LG, Repping S, Pyntikova T, Ali J, Bieri T, Chinwalla A,
            Delehaunty A, Delehaunty K, Du H, Fewell G, Fulton L, Fulton R,
            Graves T, Hou SF, Latrielle P, Leonard S, Mardis E, Maupin R,
            McPherson J, Miner T, Nash W, Nguyen C, Ozersky P, Pepin K, Rock S,
            Rohlfing T, Scott K, Schultz B, Strong C, Tin-Wollam A, Yang SP,
            Waterston RH, Wilson RK, Rozen S and Page DC.
  TITLE     The male-specific region of the human Y chromosome is a mosaic of
            discrete sequence classes
  JOURNAL   Nature 423 (6942), 825-837 (2003)
   PUBMED   12815422
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            BC121114.1 and DB545400.1.
            
            On May 17, 2019 this sequence version replaced NM_001282469.2.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC121114.1, ERR279874.771.1
                                           [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1968968, SAMEA2148093
                                           [ECO:0000348]
            ##Evidence-Data-END##
            
            ##RefSeq-Attributes-START##
            MANE Ensembl match     :: ENST00000428845.6/ ENSP00000406407.2
            RefSeq Select criteria :: based on expression, longest protein
            ##RefSeq-Attributes-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-945               BC121114.1         5-949
            946-1161            DB545400.1         280-495
FEATURES             Location/Qualifiers
     source          1..1161
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="Y"
                     /map="Yp11.2"
     gene            1..1161
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /note="testis specific protein Y-linked 10"
                     /db_xref="GeneID:100289087"
                     /db_xref="HGNC:HGNC:37473"
     exon            1..532
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /inference="alignment:Splign:2.1.0"
     variation       38
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1556185297"
     CDS             47..973
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /note="isoform 1 is encoded by transcript variant 1;
                     Testis-specific Y-encoded protein 3; Testis-specific
                     Y-encoded protein 1; Cancer/testis antigen 78"
                     /codon_start=1
                     /product="testis-specific Y-encoded protein 10 isoform 1"
                     /protein_id="NP_001269398.1"
                     /db_xref="CCDS:CCDS65365.1"
                     /db_xref="GeneID:100289087"
                     /db_xref="HGNC:HGNC:37473"
                     /translation="
MRPEGSLTYRVPERLRQGFCGVGRAAQALVCASAKEGTAFRMEAVQEGAAGVESEQAALGEEAVLLLDDIMAEVEVVAEEEGLVERREEAQRAQQAVPGPGPMTPESALEELLAVQVELEPVNAQARKAFSRQREKMERRRKPHLDRRGAVIQSVPGFWANVIANHPQMSALITDEDEDMLSYMVSLEVEEEKHPVHLCKIMLFFRSNPYFQNKVITKEYLVNITEYRASHSTPIEWYPDYEVEAYRRRHHNSSLNFFNWFSDHNFAGSNKIAEILCKDLWRNPLQYYKRMKPPEEGTETSGDSQLLS"
     misc_feature    422..910
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /note="Nucleosome assembly protein (NAP); Region: NAP;
                     cl08298"
                     /db_xref="CDD:447601"
     variation       73
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1556185309"
     variation       151
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1603145591"
     variation       258..284
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="tggcggaggtggaggtggtggcggagg"
                     /replace="tggcggaggtggaggtggtggcggaggtggaggtggtggcggagg"
                     /db_xref="dbSNP:1569407053"
     variation       267
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1603145604"
     variation       273
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1603145607"
     variation       309
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1603145614"
     variation       312
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1603145619"
     variation       372
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1353461329"
     variation       437
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1556185323"
     variation       460
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1556185338"
     variation       478
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1401946011"
     variation       485
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1556185358"
     variation       496
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1603145631"
     exon            533..610
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /inference="alignment:Splign:2.1.0"
     variation       536
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1278882587"
     variation       572..582
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="gaaga"
                     /replace="gaagatgaaga"
                     /db_xref="dbSNP:775696224"
     exon            611..722
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /inference="alignment:Splign:2.1.0"
     variation       615
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1603145682"
     exon            723..868
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /inference="alignment:Splign:2.1.0"
     variation       728
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1225448270"
     variation       757
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1556185436"
     variation       785
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1556185448"
     variation       852
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1556185461"
     exon            869..950
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /inference="alignment:Splign:2.1.0"
     variation       946
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1276818797"
     exon            951..1161
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /inference="alignment:Splign:2.1.0"
     variation       957
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:746060619"
     variation       1019
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1556185515"
     variation       1061..1062
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="tt"
                     /replace="ttt"
                     /db_xref="dbSNP:1393550796"
     variation       1064
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:2124357100"
     variation       1086
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:372116142"
     regulatory      1144..1149
                     /regulatory_class="polyA_signal_sequence"
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /note="hexamer: AATAAA"
     polyA_site      1161
                     /gene="TSPY10"
                     /gene_synonym="CT78; TSPY; TSPY1; TSPY3"
                     /note="major polyA site"
ORIGIN      
ggcccttcgcgcgcagtcccttagggggcgcctggaagcccggcgcatgcgccctgagggctcgctgacctaccgggtgccagagaggctgcggcagggtttctgtggcgtgggtcgggcagcacaggccttggtgtgtgcgagtgccaaggagggcaccgccttcaggatggaggctgtacaggagggggcggccggggtggagagtgagcaggcggctttgggggaggaggcggtgctgctgttggatgacataatggcggaggtggaggtggtggcggaggaggagggcctcgtggagcggcgggaggaggcccagcgggcacagcaggctgtgcctggccctgggcccatgaccccagagtctgcactggaggagctgctggccgttcaggtggagctggagccggttaatgcccaagccaggaaggccttttctcggcagcgggaaaagatggagcggaggcgcaagccccacctagaccgcagaggcgccgtcatccagagcgtccctggcttctgggccaatgttattgcaaaccacccccagatgtcagccctgatcactgacgaagatgaagacatgctgagctacatggtcagcctggaggtggaagaagagaagcatcctgttcatctctgcaagatcatgttgttctttcggagtaacccctacttccagaataaagtgattaccaaggaatatctggtgaacatcacagaatacagggcttctcattccactccaattgagtggtatccggattatgaagtggaggcctatcgccgcagacaccacaacagcagccttaacttcttcaactggttctctgaccacaacttcgcaggatctaacaagattgctgagatcctatgtaaggacctgtggcgcaatcccctgcaatactacaagaggatgaagccacctgaagagggaacagagacgtcaggggactcccagttgttgagttgaatatgatggagcatcagattttacctaatacagcagaactcctaaaaagttacagccatatgcaggacggcagtactcagcatggtcttatgcacaggaactaaaggaaaaacagatcgagtcacaaaaattcaggaagagggggtaaatgtggattgtatggaatgaaaaataaacattctcaagga
//

by @meso_cacase at DBCLS
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If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596. [Full Text]