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1 to 25 of 44  Show
  1. 1
    "Complete genomic sequence of the human retinoblastoma susceptibility gene."
    Toguchida J., McGee T.L., Paterson J.C., Eagle J.R., Tucker S., Yandell D.W., Dryja T.P.
    Genomics 17:535-543(1993) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  2. 2
    "Intron 17 of the human retinoblastoma susceptibility gene encodes an actively transcribed G protein-coupled receptor gene."
    Herzog H., Darby K., Hort Y.J., Shine J.
    Genome Res. 6:858-861(1996) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  3. 3
    "The human purinergic receptor P2Y5 is encoded in intron 17 of the retinoblastoma gene."
    Bohm S.K., Trumpp A., Khitin L.M., Kong W., Payan D.G., Bunnett N.W.
    Submitted (JUL-1997) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [MRNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  4. 4
    Category: Sequences.
    Tissue: Endometrium and Heart.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2471 other entries.

  5. 5
    "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].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12927 other entries.

  6. 6
    Totoki Y., Toyoda A., Takeda T., Sakaki Y., Tanaka A., Yokoyama S.
    Submitted (APR-2005) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
    Category: Sequences.
    Tissue: Thymus.
    Source: UniProtKB/Swiss-Prot (reviewed).
  7. 7
    Kaighin V.A., Martin A.L., Aronstam R.S.
    Submitted (APR-2011) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  8. 8
    NIEHS SNPs program
    Submitted (OCT-2002) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA], VARIANT TRP-137.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  9. 9
    "The DNA sequence and analysis of human chromosome 13."
    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.
    Ross M.T.
    Nature 428:522-528(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 919 other entries.

  10. 10
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  11. 11
    "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].
    Category: Sequences.
    Tissue: Brain, Placenta and Testis.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50448 other entries.

  12. 12
    "Expression of purinergic receptors (ionotropic P2X1-7 and metabotropic P2Y1-11) during myeloid differentiation of HL60 cells."
    Adrian K., Bernhard M.K., Breitinger H.-G., Ogilvie A.
    Biochim. Biophys. Acta 1492:127-138(2000) [PubMed] [Europe PMC] [Abstract]
    Cited for: TISSUE SPECIFICITY, DEVELOPMENTAL STAGE.
    Category: Expression.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 other entries.

  13. 13
    "G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth."
    Pasternack S.M., von Kuegelgen I., Aboud K.A., Lee Y.-A., Rueschendorf F., Voss K., Hillmer A.M., Molderings G.J., Franz T., Ramirez A., Nuernberg P., Noethen M.M., Betz R.C.
    Nat. Genet. 40:329-334(2008) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, SUBCELLULAR LOCATION, TISSUE SPECIFICITY, INVOLVEMENT IN HYPT8.
    Category: Function, Subcellular Location, Pathology & Biotech, Expression.
    Source: UniProtKB/Swiss-Prot (reviewed).

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

  14. 14
    "Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair."
    Shimomura Y., Wajid M., Ishii Y., Shapiro L., Petukhova L., Gordon D., Christiano A.M.
    Nat. Genet. 40:335-339(2008) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANTS ARWH1 VAL-63; PHE-188 AND LYS-189, TISSUE SPECIFICITY.
    Category: Pathology & Biotech, Expression, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

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

  15. 15
    "Genomic organization of the human G-alpha-14 and G-alpha-Q genes and mutation analysis in chorea-acanthocytosis (CHAC)."
    Rubio J.P., Levy E.R., Dobson-Stone C., Monaco A.P.
    Genomics 57:84-93(1999) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: Pathway.
    Source: Reactome:R-HSA-417913.

    This publication is mapped to 148 other entries.

  16. 16
    "Stable association between G alpha(q) and phospholipase C beta 1 in living cells."
    Dowal L., Provitera P., Scarlata S.
    J. Biol. Chem. 281:23999-24014(2006) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: Pathway.
    Source: Reactome:R-HSA-417913.

    This publication is mapped to 152 other entries.

  17. 17
    "GPR92 as a new G12/13- and Gq-coupled lysophosphatidic acid receptor that increases cAMP, LPA5."
    Lee C.W., Rivera R., Gardell S., Dubin A.E., Chun J.
    J. Biol. Chem. 281:23589-23597(2006) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: Pathway.
    Source: Reactome:R-HSA-417913.

    This publication is mapped to 5 other entries.

  18. 18
    "Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)."
    Azeem Z., Jelani M., Naz G., Tariq M., Wasif N., Kamran-Ul-Hassan Naqvi S., Ayub M., Yasinzai M., Amin-Ud-Din M., Wali A., Ali G., Chishti M.S., Ahmad W.
    Hum. Genet. 123:515-519(2008) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: In the present study 14 of 22 families with autosomal recessive hypotrichosis show linkage to LAH3 locus on chromosome 13q14.11-q21.32. Affected individuals of all the 22 families have common clinical features.
    Source: GeneRIF:10161.

    This publication is mapped to 2 other entries.

  19. 19
    "Dissociation of heterotrimeric g proteins in cells."
    Lambert N.A.
    Sci Signal 1:re5-re5(2008) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: Pathway.
    Source: Reactome:R-HSA-417913.

    This publication is mapped to 413 other entries.

  20. 20
    "Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation."
    Petukhova L., Sousa E.C. Jr., Martinez-Mir A., Vitebsky A., Dos Santos L.G., Shapiro L., Haynes C., Gordon D., Shimomura Y., Christiano A.M.
    Genomics 92:273-278(2008) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Our findings show that mutations in P2RY5 display variable expressivity underlying both hypotrichosis and woolly hair and underscore the essential role of P2RY5 in the tissue integrity and maintenance of the hair follicle.
    Source: GeneRIF:10161.

    This publication is mapped to 2 other entries.

  21. 21
    "Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene."
    Shimomura Y., Garzon M.C., Kristal L., Shapiro L., Christiano A.M.
    Exp. Dermatol. 18:218-221(2009) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: There is an involvement of P2RY5 mutations in hereditary hair diseases.
    Source: GeneRIF:10161.

    This publication is mapped to 2 other entries.

  22. 22
    "Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis."
    Shimomura Y., Wajid M., Petukhova L., Shapiro L., Christiano A.M.
    J. Invest. Dermatol. 129:622-628(2009) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: LIPH is a second causative gene for ARWH/hypotrichosis giving rise to a phenotype clinically indistinguishable from P2RY5 mutations.
    Source: GeneRIF:10161.

    This publication is mapped to 5 other entries.

  23. 23
    "G alpha 16, a G protein alpha subunit specifically expressed in hematopoietic cells."
    Amatruda T.T. III, Steele D.A., Slepak V.Z., Simon M.I.
    Proc. Natl. Acad. Sci. U.S.A. 88:5587-5591(1991) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: Pathway.
    Source: Reactome:R-HSA-417913.

    This publication is mapped to 148 other entries.

  24. 24
    "[Involvement of receptor P2Y5 and its ligand LPA in hypotrichosis simplex and autosomal recessive wooly hair syndrome]."
    Dereure O.
    Ann Dermatol Venereol 135:794-795(2008) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: gene is involved in genetics of hypotrichosis simplex and autosomal recessive wooly hair syndrome.
    Source: GeneRIF:10161.

    This publication is mapped to 2 other entries.

  25. 25
    "Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families."
    Tariq M., Ayub M., Jelani M., Basit S., Naz G., Wasif N., Raza S.I., Naveed A.K., ullah Khan S., Azeem Z., Yasinzai M., Wali A., Ali G., Chishti M.S., Ahmad W.
    Br. J. Dermatol. 160:1006-1010(2009) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Mutations revealed in the results extend the body of evidence implicating the P2RY5 gene in the pathogenesis of human hereditary hair loss.
    Source: GeneRIF:10161.

    This publication is mapped to 2 other entries.

1 to 25 of 44  Show
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