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1 to 22 of 22  Show
  1. 1
    "Novel genes expressed in hematopoietic stem/progenitor cells from myelodysplastic syndrome patients."
    Zhao M., Gu J., Li N., Peng Y., Han Z., Chen Z.
    Submitted (DEC-1999) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  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] (ISOFORMS 1; 2; 3 AND 4).
    Category: Sequences.
    Tissue: Lung, Placenta, Testis, Trachea and Uterus.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12927 other entries.

  3. 3
    "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.

  4. 4
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  5. 5
    "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 2), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 592-1137 (ISOFORM 4).
    Category: Sequences.
    Tissue: Colon and Urinary bladder.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50448 other entries.

  6. 6
    Suzuki Y., Sugano S., 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] OF 591-1137 (ISOFORM 4).
    Category: Sequences.
    Tissue: Lung.
    Source: UniProtKB/Swiss-Prot (reviewed).
  7. 7
    "Alg14 recruits Alg13 to the cytoplasmic face of the endoplasmic reticulum to form a novel bipartite UDP-N-acetylglucosamine transferase required for the second step of N-linked glycosylation."
    Gao X.-D., Tachikawa H., Sato T., Jigami Y., Dean N.
    J. Biol. Chem. 280:36254-36262(2005) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION (ISOFORM 2).
    Category: Function.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3 and mapped to 2 other entries.

  8. 8
    "OTU deubiquitinases reveal mechanisms of linkage specificity and enable ubiquitin chain restriction analysis."
    Mevissen T.E., Hospenthal M.K., Geurink P.P., Elliott P.R., Akutsu M., Arnaudo N., Ekkebus R., Kulathu Y., Wauer T., El Oualid F., Freund S.M., Ovaa H., Komander D.
    Cell 154:169-184(2013) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 16 and mapped to 2 other entries.

  9. 9
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 18117 other entries.

  10. 10
    Cited for: INVOLVEMENT IN EIEE36, VARIANT EIEE36 GLU-94, CHARACTERIZATION OF VARIANT EIEE36 GLU-94.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  11. 11
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 other entries.

  12. 12
    Cited for: INVOLVEMENT IN EIEE36, VARIANT EIEE36 SER-107.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 4 other entries.

  13. 13
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 70 other entries.

  14. 14
    "De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies."
    Epi4K Consortium
    Am. J. Hum. Genet. 99:287-298(2016) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT EIEE36 SER-107.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 5 and mapped to 13 other entries.

  15. 15
    "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration."
    Lim J., Hao T., Shaw C., Patel A.J., Szabo G., Rual J.F., Fisk C.J., Li N., Smolyar A., Hill D.E., Barabasi A.L., Vidal M., Zoghbi H.Y.
    Cell 125:801-814(2006) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q9NP73.

    This publication is mapped to 566 other entries.

  16. 16
    Category: Interaction.
    Source: IntAct:Q9NP73.

    This publication is mapped to 271 other entries.

  17. 17
    "The human-bacterial pathogen protein interaction networks of Bacillus anthracis, Francisella tularensis, and Yersinia pestis."
    Dyer M.D., Neff C., Dufford M., Rivera C.G., Shattuck D., Bassaganya-Riera J., Murali T.M., Sobral B.W.
    PLoS ONE 5:e12089-e12089(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q9NP73.

    This publication is mapped to 4890 other entries.

  18. 18
    Category: Function.
    Annotation: Pathway.
    Source: Reactome:R-HSA-449329.

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

  19. 19
    "Protein interaction network of the mammalian Hippo pathway reveals mechanisms of kinase-phosphatase interactions."
    Couzens A.L., Knight J.D., Kean M.J., Teo G., Weiss A., Dunham W.H., Lin Z.Y., Bagshaw R.D., Sicheri F., Pawson T., Wrana J.L., Choi H., Gingras A.C.
    Sci Signal 6:rs15-rs15(2013) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q9NP73.

    This publication is mapped to 457 other entries.

  20. 20
    "X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblings."
    Bissar-Tadmouri N., Donahue W.L., Al-Gazali L., Nelson S.F., Bayrak-Toydemir P., Kantarci S.
    Am. J. Med. Genet. A 164A:164-169(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: We report on a novel missense variant in the ALG13 gene in a nonconsanguineous Arab family that co-segregates with nonsyndromic intellectual disability.
    Source: GeneRIF:79868.

    This publication is mapped to 3 other entries.

  21. 21
    "Dysregulation of the Expression of Asparagine-Linked Glycosylation 13 Short Isoform 2 Affects Nephrin Function by Altering Its N-Linked Glycosylation."
    Esposito T., De Stefano G., Reccia M.G., Di Lorenzo I., Napolitano F., Scalabri F., Lombardi A., Saleem M.A., Griffiths L.R., Gianfrancesco F.
    Nephron 136:143-150(2017) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: ALG13-is2 could be an important modifier of renal filtration defects.
    Source: GeneRIF:79868.

    This publication is mapped to 3 other entries.

  22. 22
    "Exome sequence identified a c.320A > G ALG13 variant in a female with infantile epileptic encephalopathy with normal glycosylation and random X inactivation: Review of the literature."
    Hamici S., Bastaki F., Khalifa M.
    Eur J Med Genet 60:541-547(2017) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: A female patient heterozygous for ALG13 Asn107Ser variant presented with infantile spasms developmental delay and dysmorphic features. The patient showed normal pattern of glycosylated transferrin and random pattern of X-inactivation.
    Source: GeneRIF:79868.

    This publication is mapped to 3 other entries.

1 to 22 of 22  Show
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