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1 to 16 of 16  Show
  1. 1
    "Complete sequencing and characterization of 21,243 full-length human cDNAs."
    Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.
    Sugano S.
    Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1; 2 AND 3).
    Category: Sequences.
    Tissue: Testis.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12927 other entries.

  2. 2
    "The DNA sequence of the human X chromosome."
    Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P., Frankish A., Lovell F.L., Howe K.L., Ashurst J.L., Fulton R.S., Sudbrak R., Wen G., Jones M.C.
    Bentley D.R.
    Nature 434:325-337(2005) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2134 other entries.

  3. 3
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  4. 4
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3), VARIANT LYS-451.
    Category: Sequences.
    Tissue: Testis.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50448 other entries.

  5. 5
    "An abundance of X-linked genes expressed in spermatogonia."
    Wang P.J., McCarrey J.R., Yang F., Page D.C.
    Nat. Genet. 27:422-426(2001) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 20-940 (ISOFORM 3).
    Category: Sequences.
    Tissue: Testis.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 37 and mapped to 70 other entries.

  6. 6
    "ZIP4H (TEX11) deficiency in the mouse impairs meiotic double strand break repair and the regulation of crossing over."
    Adelman C.A., Petrini J.H.
    PLoS Genet. 4:E1000042-E1000042(2008) [PubMed] [Europe PMC] [Abstract]
    Cited for: TISSUE SPECIFICITY.
    Category: Expression.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  7. 7
    Cited for: INVOLVEMENT IN SPGFX2, VARIANTS SPGFX2 VAL-171 AND THR-698.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  8. 8
    "SHOC1 is a ERCC4-(HhH)2-like protein, integral to the formation of crossover recombination intermediates during mammalian meiosis."
    Guiraldelli M.F., Felberg A., Almeida L.P., Parikh A., de Castro R.O., Pezza R.J.
    PLoS Genet. 14:E1007381-E1007381(2018) [PubMed] [Europe PMC] [Abstract]
    Cited for: INTERACTION WITH SHOC1.
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 and mapped to 1 other entries.

  9. 9
    "Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations."
    Nakamura S., Miyado M., Saito K., Katsumi M., Nakamura A., Kobori Y., Tanaka Y., Ishikawa H., Yoshida A., Okada H., Hata K., Nakabayashi K., Okamura K., Ogata H., Matsubara Y., Ogata T., Nakai H., Fukami M.
    Andrology 5:824-831(2017) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT SPGFX2 VAL-171.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 4 other entries.

  10. 10
    Category: Interaction.
    Source: IntAct:Q8IYF3.

    This publication is mapped to 1504 other entries.

  11. 11
    "Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent."
    Aston K.I., Krausz C., Laface I., Ruiz-Castane E., Carrell D.T.
    Hum. Reprod. 25:1383-1397(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator).
    Source: GeneRIF:56159.

    This publication is mapped to 351 other entries.

  12. 12
    Category: Interaction.
    Source: IntAct:Q8IYF3.

    This publication is mapped to 121 other entries.

  13. 13
    Category: Interaction.
    Source: IntAct:Q8IYF3.

    This publication is mapped to 4105 other entries.

  14. 14
    "TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse."
    Yang F., Silber S., Leu N.A., Oates R.D., Marszalek J.D., Skaletsky H., Brown L.G., Rozen S., Page D.C., Wang P.J.
    EMBO Mol Med 7:1198-1210(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Genetic screening of a large cohort of idiopathic infertile men reveals that TEX11 mutations including frameshift and splicing acceptor site mutations cause infertility in 1% of azoospermic men; TEX11 mutations including frameshift and splicing acceptor site mutations cause infertility in 1% of non-obstructive azoospermic men.
    Source: GeneRIF:56159.

    This publication is mapped to 3 other entries.

  15. 15
    "RNA immunoprecipitation identifies novel targets of DAZL in human foetal ovary."
    Rosario R., Smith R.W., Adams I.R., Anderson R.A.
    Mol. Hum. Reprod. 23:177-186(2017) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: Through the translational regulation of novel RNA targets SMC1B and TEX11 DAZL may have a key role in regulating chromosome cohesion and DNA recombination; two processes fundamental in determining oocyte quality and whose establishment in foetal life may support lifelong fertility.
    Source: GeneRIF:56159.

    This publication is mapped to 4 other entries.

  16. 16
    "A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review."
    Sha Y., Zheng L., Ji Z., Mei L., Ding L., Lin S., Wang X., Yang X., Li P.
    BMC Med. Genet. 19:63-63(2018) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Data identified one novel TEX11 mutation in two brothers. The missense mutation is associated with male infertility especially azoospermia.
    Source: GeneRIF:56159.
1 to 16 of 16  Show
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