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2024-03-29 18:00:08, GGRNA.v2 : RefSeq release 222 (Jan, 2024)

LOCUS       NM_001320964             900 bp    mRNA    linear   PRI 30-DEC-2022
DEFINITION  Homo sapiens testis specific protein Y-linked 1 (TSPY1), transcript
            variant 3, mRNA.
ACCESSION   NM_001320964
VERSION     NM_001320964.2
KEYWORDS    RefSeq.
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 900)
  AUTHORS   Paladhi P, Dutta S, Pal S, Bose G, Ghosh P, Chattopadhyay R,
            Chakravarty B, Saha I and Ghosh S.
  TITLE     Novel Mutations of TSPY1 Gene Associate Spermatogenic Failure Among
            Men
  JOURNAL   Reprod Sci 29 (4), 1241-1261 (2022)
   PUBMED   35041134
  REMARK    GeneRIF: Novel Mutations of TSPY1 Gene Associate Spermatogenic
            Failure Among Men.
REFERENCE   2  (bases 1 to 900)
  AUTHORS   Leng X, Liu M, Tao D, Yang B, Zhang Y, He T, Xie S, Wang Z, Liu Y
            and Yang Y.
  TITLE     Epigenetic modification-dependent androgen receptor occupancy
            facilitates the ectopic TSPY1 expression in prostate cancer cells
  JOURNAL   Cancer Sci 112 (2), 691-702 (2021)
   PUBMED   33185915
  REMARK    GeneRIF: Epigenetic modification-dependent androgen receptor
            occupancy facilitates the ectopic TSPY1 expression in prostate
            cancer cells.
REFERENCE   3  (bases 1 to 900)
  AUTHORS   Giguere K, Leblond FA, Goma-Matsetse E, Dave V, Behanzin L, Guedou
            FA and Alary M.
  TITLE     A novel nested polymerase chain reaction targeting the
            testis-specific protein Y-encoded family of genes for high
            sensitivity of recent semen exposure detection: Comparison with
            four other assays of semen detection
  JOURNAL   PLoS One 14 (7), e0220326 (2019)
   PUBMED   31344101
  REMARK    GeneRIF: Compared to n-TSPY, all other PCR assays had poor
            performance to detect semen exposure. The n-TSPY is an accessible
            assay that may have great utility in assessing semen exposure in
            studies where many factors are expected to accelerate biomarkers'
            clearance.
            Publication Status: Online-Only
REFERENCE   4  (bases 1 to 900)
  AUTHORS   Tu W, Yang B, Leng X, Pei X, Xu J, Liu M, Dong Q, Tao D, Lu Y, Liu
            Y and Yang Y.
  TITLE     Testis-specific protein, Y-linked 1 activates PI3K/AKT and RAS
            signaling pathways through suppressing IGFBP3 expression during
            tumor progression
  JOURNAL   Cancer Sci 110 (5), 1573-1586 (2019)
   PUBMED   30815935
  REMARK    GeneRIF: Experimental evidence establishes TSPY1 as an oncogenic
            factor that facilitates tumor progression and causes poor prognosis
            in male patients with lung adenocarcinoma or hepatocellular
            carcinoma. These findings revealed that TSPY1 strongly promotes the
            activation of the PI3K/AKT and RAS signaling pathways through
            suppressing IGFBP3 gene transcription.
REFERENCE   5  (bases 1 to 900)
  AUTHORS   Xue Y and Tyler-Smith C.
  TITLE     An Exceptional Gene: Evolution of the TSPY Gene Family in Humans
            and Other Great Apes
  JOURNAL   Genes (Basel) 2 (1), 36-47 (2011)
   PUBMED   24710137
  REMARK    Publication Status: Online-Only
REFERENCE   6  (bases 1 to 900)
  AUTHORS   Krick R, Jakubiczka S and Arnemann J.
  TITLE     Expression, alternative splicing and haplotype analysis of
            transcribed testis specific protein (TSPY) genes
  JOURNAL   Gene 302 (1-2), 11-19 (2003)
   PUBMED   12527192
REFERENCE   7  (bases 1 to 900)
  AUTHORS   Zhang JS, Yang-Feng TL, Muller U, Mohandas TK, de Jong PJ and Lau
            YF.
  TITLE     Molecular isolation and characterization of an expressed gene from
            the human Y chromosome
  JOURNAL   Hum Mol Genet 1 (9), 717-726 (1992)
   PUBMED   1284595
REFERENCE   8  (bases 1 to 900)
  AUTHORS   Guttenbach M, Muller U and Schmid M.
  TITLE     A human moderately repeated Y-specific DNA sequence is
            evolutionarily conserved in the Y chromosome of the great apes
  JOURNAL   Genomics 13 (2), 363-367 (1992)
   PUBMED   1612595
REFERENCE   9  (bases 1 to 900)
  AUTHORS   Arnemann J, Jakubiczka S, Thuring S and Schmidtke J.
  TITLE     Cloning and sequence analysis of a human Y-chromosome-derived,
            testicular cDNA, TSPY
  JOURNAL   Genomics 11 (1), 108-114 (1991)
   PUBMED   1765369
REFERENCE   10 (bases 1 to 900)
  AUTHORS   Arnemann J, Epplen JT, Cooke HJ, Sauermann U, Engel W and Schmidtke
            J.
  TITLE     A human Y-chromosomal DNA sequence expressed in testicular tissue
  JOURNAL   Nucleic Acids Res 15 (21), 8713-8724 (1987)
   PUBMED   3479749
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BC121113.1 and AI002165.1.
            
            On Aug 14, 2020 this sequence version replaced NM_001320964.1.
            
            Summary: The protein encoded by this gene is found only in
            testicular tissue and may be involved in spermatogenesis. Many
            functional paralogs and pseudogenes of this gene are present in a
            cluster in humans, but only a single, nonfunctional orthologous
            gene is found in mouse. Alternative splicing results in multiple
            transcript variants. [provided by RefSeq, Mar 2016].
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: BC121113.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           SAMEA1968968, SAMEA2148093
                                           [ECO:0000348]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-779               BC121113.1         5-783
            780-900             AI002165.1         11-131              c
FEATURES             Location/Qualifiers
     source          1..900
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="Y"
                     /map="Yp11.2"
     gene            1..900
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /note="testis specific protein Y-linked 1"
                     /db_xref="GeneID:7258"
                     /db_xref="HGNC:HGNC:12381"
                     /db_xref="MIM:480100"
     exon            1..133
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /inference="alignment:Splign:2.1.0"
     variation       8
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1556182097"
     variation       17
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1603142441"
     variation       21
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1379118618"
     variation       22
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1603142449"
     variation       29
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1394730875"
     variation       30
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1603142459"
     variation       38
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1290917158"
     CDS             47..712
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /note="isoform 3 is encoded by transcript variant 3;
                     cancer/testis antigen 78; testis-specific Y-encoded
                     protein 1; testis specific protein, Y-linked"
                     /codon_start=1
                     /product="testis-specific Y-encoded protein 1 isoform 3"
                     /protein_id="NP_001307893.1"
                     /db_xref="GeneID:7258"
                     /db_xref="HGNC:HGNC:12381"
                     /db_xref="MIM:480100"
                     /translation="
MRPEGSLTYRVPERLRQGFCGVGRAAQALVELEPVNAQARKAFSRQREKMERRRKPHLDRRGAVIQSVPGFWANVIANHPQMSALITDEDEDMLSYMVSLEVGEEKHPVHLCKIMLFFRSNPYFQNKVITKEYLVNITEYRASHSTPIEWYPDYEVEAYRRRHHNSSLNFFNWFSDHNFAGSNKIAEILCKDLWRNPLQYYKRMKPPEEGTETSGDSQLLS"
     misc_feature    161..649
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /note="Nucleosome assembly protein (NAP); Region: NAP;
                     cl08298"
                     /db_xref="CDD:447601"
     variation       58
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1603142470"
     variation       60
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1556182135"
     variation       67
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1603142485"
     variation       73
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:754351883"
     variation       85
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1603142497"
     exon            134..271
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /inference="alignment:Splign:2.1.0"
     variation       137
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1311462417"
     variation       139
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1208423297"
     variation       140
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1288137239"
     variation       145
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1488548781"
     variation       146
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:745768816"
     variation       149
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:1240362123"
     variation       150
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:201424738"
     variation       155
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1192052574"
     variation       161
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:775446628"
     variation       164
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:749030159"
     variation       199
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1556182495"
     variation       217
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:772185599"
     variation       224
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1556182525"
     variation       235
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1603142681"
     variation       236
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1431837856"
     exon            272..349
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /inference="alignment:Splign:2.1.0"
     variation       290
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1603142738"
     exon            350..461
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /inference="alignment:Splign:2.1.0"
     variation       354
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1297059542"
     variation       355
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1342988681"
     variation       357
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:756757652"
     variation       361
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:780785122"
     variation       364
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:745321922"
     variation       374
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:756131625"
     variation       376
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:780067981"
     variation       377
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1275117981"
     variation       380
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1603142783"
     variation       381
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:749157835"
     variation       383
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1366442282"
     variation       388
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1603142795"
     variation       392
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:768481082"
     variation       394
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:773349562"
     variation       401
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:747291345"
     variation       402
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:771012234"
     variation       408
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:776707915"
     variation       412
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:759547669"
     variation       420
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1231837592"
     variation       427
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:770355301"
     variation       438
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1486450497"
     exon            462..607
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /inference="alignment:Splign:2.1.0"
     variation       471
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1215732327"
     variation       496
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1556182856"
     variation       501
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1603142842"
     variation       520
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1282047748"
     variation       524
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1453465763"
     variation       527
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1363870448"
     variation       543
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1246391705"
     variation       584
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:763277112"
     variation       591
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1556182928"
     exon            608..689
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /inference="alignment:Splign:2.1.0"
     variation       622
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1603142880"
     variation       629
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:751830669"
     variation       635
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:761547400"
     variation       638
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1333134024"
     variation       645
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:767219205"
     variation       648
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1377437524"
     variation       653
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace=""
                     /replace="a"
                     /db_xref="dbSNP:1239149611"
     variation       665
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1277739251"
     variation       680
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1358351478"
     variation       684
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1228984985"
     variation       685
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:749954093"
     variation       687
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1332965070"
     exon            690..900
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /inference="alignment:Splign:2.1.0"
     variation       696
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:771192571"
     variation       754
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1172453097"
     variation       758
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:781388283"
     variation       800..801
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="tt"
                     /replace="ttt"
                     /db_xref="dbSNP:2124353821"
     variation       803
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1603143019"
     variation       825
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:2124353832"
     variation       884
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:1603143024"
     variation       894
                     /gene="TSPY1"
                     /gene_synonym="CT78; DYS14; pJA923; TSPY"
                     /replace="a"
                     /replace="t"
                     /db_xref="dbSNP:1603143026"
ORIGIN      
ggcccttcgcgcgcagtcccttagggggcgcctggaagcccggcgcatgcgccctgagggctcgctgacctaccgggtgccagagaggctgcggcagggtttctgtggcgtgggtcgggcagcacaggccttggtggagctggagccggttaatgcccaagccaggaaggccttttctcggcagcgggaaaagatggagcggaggcgcaagccccacctagaccgcagaggcgccgtcatccagagcgtccctggcttctgggccaatgttattgcaaaccacccccagatgtcagccctgatcactgacgaagatgaagacatgctgagctacatggtcagcctggaggtgggagaagagaagcatcctgttcatctctgcaagatcatgttgttctttcggagtaacccctacttccagaataaagtgattaccaaggaatatctggtgaacatcacagaatacagggcttctcattccactccaattgagtggtatccggattatgaagtggaggcctatcgccgcagacaccacaacagcagccttaacttcttcaactggttctctgaccacaacttcgcaggatctaacaagattgctgagatcctatgtaaggacctgtggcgcaatcccctgcaatactacaagaggatgaagccacctgaagagggaacagagacgtcaggggactcccagttgttgagttgaatatgatggagcatcagattttacctaatacagcagaactcctaaaaagttacagccatatgcaggacggcagtactcagcatggtcttatgcacaggaactaaaggaaaaagagatcgagtcacaaaaattcaggaagagggggtaaatgtggattgtatggaatgaaaaataaacattctcaagga
//

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).

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]