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1 to 23 of 23  Show
  1. 1
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 3), VARIANT MET-107.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2470 other entries.

  2. 2
    "Generation and annotation of the DNA sequences of human chromosomes 2 and 4."
    Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P., Wagner-McPherson C., Layman D., Wylie K., Sekhon M., Becker M.C., Fewell G.A., Delehaunty K.D., Miner T.L., Nash W.E., Kremitzki C., Oddy L., Du H.
    Wilson R.K.
    Nature 434:724-731(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 7181 other entries.

  3. 3
    "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] OF 1-545 (ISOFORM 2), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 123-660 (ISOFORMS 1/2).
    Category: Sequences.
    Tissue: Ovary and Thalamus.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12928 other entries.

  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] OF 43-660 (ISOFORM 1).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50454 other entries.

  5. 5
    "Proteomic characterization of the human centrosome by protein correlation profiling."
    Andersen J.S., Wilkinson C.J., Mayor T., Mortensen P., Nigg E.A., Mann M.
    Nature 426:570-574(2003) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY.
    Category: Sequences.
    Tissue: Lymphoblast.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 291 other entries.

  6. 6
    Cited for: INVOLVEMENT IN RP28, TISSUE SPECIFICITY.
    Category: Pathology & Biotech, Expression.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 12 other entries.

  7. 7
    "Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa."
    Bandah-Rozenfeld D., Mizrahi-Meissonnier L., Farhy C., Obolensky A., Chowers I., Pe'er J., Merin S., Ben-Yosef T., Ashery-Padan R., Banin E., Sharon D.
    Am. J. Hum. Genet. 87:382-391(2010) [PubMed] [Europe PMC] [Abstract]
    Cited for: INVOLVEMENT IN RP28, TISSUE SPECIFICITY.
    Category: Pathology & Biotech, Expression.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 11 other entries.

  8. 8
    "FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies."
    Di Gioia S.A., Letteboer S.J., Kostic C., Bandah-Rozenfeld D., Hetterschijt L., Sharon D., Arsenijevic Y., Roepman R., Rivolta C.
    Hum. Mol. Genet. 21:5174-5184(2012) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, SUBCELLULAR LOCATION, INTERACTION WITH LCA5; CEP290 AND SDCCAG8.
    Category: Function, Subcellular Location, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 6 and mapped to 9 other entries.

  9. 9
    "The retinitis pigmentosa 28 protein FAM161A is a novel ciliary protein involved in intermolecular protein interaction and microtubule association."
    Zach F., Grassmann F., Langmann T., Sorusch N., Wolfrum U., Stohr H.
    Hum. Mol. Genet. 21:4573-4586(2012) [PubMed] [Europe PMC] [Abstract]
    Cited for: INTERACTION WITH MICROTUBULES AND FAM161B.
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 and mapped to 6 other entries.

  10. 10
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 6 other entries.

  11. 11
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

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

  12. 12
    "Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation."
    Hendriks I.A., Lyon D., Young C., Jensen L.J., Vertegaal A.C., Nielsen M.L.
    Nat. Struct. Mol. Biol. 24:325-336(2017) [PubMed] [Europe PMC] [Abstract]
    Cited for: SUMOYLATION [LARGE SCALE ANALYSIS] AT LYS-468 AND LYS-484, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: PTM / Processing, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3602 other entries.

  13. 13
    Category: Interaction.
    Source: IntAct:Q3B820.

    This publication is mapped to 1656 other entries.

  14. 14
    "Homozygosity mapping reveals new nonsense mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in a Palestinian family."
    Zobor D., Balousha G., Baumann B., Wissinger B.
    Mol. Vis. 20:178-182(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: an RP28 (an autosomal recessive form of retinitis pigmentosa)-linked RP family in the Palestinian population caused by a novel nonsense mutation in FAM161A was identified.Imported.
    Source: GeneRIF:84140.
  15. 15
    "Molecular genetics of FAM161A in North American patients with early-onset retinitis pigmentosa."
    Venturini G., Di Gioia S.A., Harper S., Weigel-DiFranco C., Rivolta C., Berson E.L.
    PLoS ONE 9:e92479-e92479(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Our data indicate that mutations in FAM161A are responsible for 1% of recessive RP cases in North America similar to the prevalence detected in Germany and unlike the data from Israel and the Palestinian territories.Imported.
    Source: GeneRIF:84140.
  16. 16
    "FAM161A, a novel centrosomal-ciliary protein implicated in autosomal recessive retinitis pigmentosa."
    Zach F., Stohr H.
    Adv. Exp. Med. Biol. 801:185-190(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Subcellular Location.
    Annotation: FAM161A is a novel centrosomal-ciliary protein that likely is implicated in the regulation of microtubule-based cellular processes in the retina.Imported.
    Source: GeneRIF:84140.
  17. 17
    Category: Pathology & Biotech, Sequences.
    Annotation: Exome analysis revealed a nonsense homozygous mutation in FAM161A segregating with retinal degeneration with severe vision loss and a range of disease onset and progression.Imported.
    Source: GeneRIF:84140.
  18. 18
    Category: Interaction.
    Source: IntAct:Q3B820.

    This publication is mapped to 4109 other entries.

  19. 19
    "Interactome analysis reveals that FAM161A, deficient in recessive retinitis pigmentosa, is a component of the Golgi-centrosomal network."
    Di Gioia S.A., Farinelli P., Letteboer S.J., Arsenijevic Y., Sharon D., Roepman R., Rivolta C.
    Hum. Mol. Genet. 24:3359-3371(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Subcellular Location.
    Annotation: FAM161A's activities are probably not limited to ciliary tasks but also extend to more general cellular functions highlighting possible novel mechanisms for the molecular pathology of retinal disease.Imported.
    Source: GeneRIF:84140.
  20. 20
    Category: Sequences.
    Annotation: We screened a panel of 120 probands with recessive Retinitis Pigmentosa and two were found to harbour biallelic FAM161A variants.Imported.
    Source: GeneRIF:84140.
  21. 21
    "Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population."
    Zhou Y., Saikia B.B., Jiang Z., Zhu X., Liu Y., Huang L., Kim R., Yang Y., Qu C., Hao F., Gong B., Tai Z., Niu L., Yang Z., Sundaresan P., Zhu X.
    J. Hum. Genet. 60:625-630(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: novel homozygous frameshift mutations of RP28-linked RP gene FAM161A in Indian population.Imported.
    Source: GeneRIF:84140.
  22. 22
    "A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa."
    Van Schil K., Klevering B.J., Leroy B.P., Pott J.W., Bandah-Rozenfeld D., Zonneveld-Vrieling M.N., Sharon D., den Hollander A.I., Cremers F.P., De Baere E., Collin R.W., van den Born L.I.
    Invest. Ophthalmol. Vis. Sci. 56:7418-7426(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: founder mutation in FAM161A p.(Arg437*) underlies approximately 2% of arRP cases in the Dutch and Belgian populations.Imported.
    Source: GeneRIF:84140.
  23. 23
    Category: Interaction.
    Source: IntAct:Q3B820.

    This publication is mapped to 1812 other entries.

1 to 23 of 23  Show
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