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1 to 15 of 15  Show
  1. 1
    "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] (ISOFORMS 1 AND 2).
    Category: Sequences.
    Tissue: Lymph and Placenta.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50448 other entries.

  2. 2
    "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 1-166 (ISOFORM 1).
    Category: Sequences.
    Tissue: Mammary gland.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12927 other entries.

  3. 3
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 18117 other entries.

  4. 4
    "A Gly-zipper motif mediates homodimerization of the transmembrane domain of the mitochondrial kinase ADCK3."
    Khadria A.S., Mueller B.K., Stefely J.A., Tan C.H., Pagliarini D.J., Senes A.
    J. Am. Chem. Soc. 136:14068-14077(2014) [PubMed] [Europe PMC] [Abstract]
    Cited for: SUBUNIT.
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

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

  5. 5
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 6320 other entries.

  6. 6
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 10 other entries.

  7. 7
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 452 other entries.

  8. 8
    Cited for: VARIANTS NPHS9 TRP-178; GLY-286; TRP-320; TRP-343 AND GLN-477, FUNCTION, INTERACTION WITH COQ6 AND COQ7, SUBCELLULAR LOCATION, TISSUE SPECIFICITY.
    Category: Function, Subcellular Location, Pathology & Biotech, Expression, Interaction, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 5 and mapped to 1 other entries.

  9. 9
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 1 other entry.

  10. 10
    Category: Function.
    Annotation: Observational study of gene-disease association. (HuGE Navigator).
    Source: GeneRIF:79934.

    This publication is mapped to 3063 other entries.

  11. 11
    Category: Interaction.
    Source: IntAct:Q96D53.

    This publication is mapped to 65 other entries.

  12. 12
    "A human interactome in three quantitative dimensions organized by stoichiometries and abundances."
    Hein M.Y., Hubner N.C., Poser I., Cox J., Nagaraj N., Toyoda Y., Gak I.A., Weisswange I., Mansfeld J., Buchholz F., Hyman A.A., Mann M.
    Cell 163:712-723(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q96D53.

    This publication is mapped to 5376 other entries.

  13. 13
    "Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations."
    Park E., Kang H.G., Choi Y.H., Lee K.B., Moon K.C., Jeong H.J., Nagata M., Cheong H.I.
    Pediatr. Nephrol. 32:1547-1554(2017) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Study in Korean cohort revealed that ADCK4 mutations should be considered in older children presenting with steroid resistant focal segmental glomerulosclerosis. The association with medullary nephrocalcinosis may be an additional diagnostic indicator.
    Source: GeneRIF:79934.

    This publication is mapped to 1 other entry.

  14. 14
    "Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function."
    Vazquez Fonseca L., Doimo M., Calderan C., Desbats M.A., Acosta M.J., Cerqua C., Cassina M., Ashraf S., Hildebrandt F., Sartori G., Navas P., Trevisson E., Salviati L.
    Hum. Mutat. 39:406-414(2018) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Subcellular Location, Pathology & Biotech, Sequences.
    Annotation: a COQ8B polymorphism present in 50% of the European population (NM_024876.3:c.521A > G p.His174Arg) affects stability of the protein and could represent a risk factor for secondary Coenzyme Q deficiencies or for other complex traits.
    Source: GeneRIF:79934.

    This publication is mapped to 1 other entry.

  15. 15
    "A novel ADCK4 mutation in a Chinese family with ADCK4-Associated glomerulopathy."
    Yang J., Yang Y., Hu Z.
    Biochem. Biophys. Res. Commun. 506:444-449(2018) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: a novel ABC1 domain-localized pathogenic mutation responsible for ADCK4-glomerulopathy was identified further supporting the importance of the C-terminal portion of ADCK4.
    Source: GeneRIF:79934.

    This publication is mapped to 1 other entry.

1 to 15 of 15  Show
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