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  1. 1
    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.
    , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
    Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 367-974 (ISOFORM 2).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12930 other entries.

  3. 3
    "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks."
    Olsen J.V., Blagoev B., Gnad F., Macek B., Kumar C., Mortensen P., Mann M.
    Cell 127:635-648(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3173 other entries.

  4. 4
    "Lysine acetylation targets protein complexes and co-regulates major cellular functions."
    Choudhary C., Kumar C., Gnad F., Nielsen M.L., Rehman M., Walther T.C., Olsen J.V., Mann M.
    Science 325:834-840(2009) [PubMed] [Europe PMC] [Abstract]
    Cited for: ACETYLATION [LARGE SCALE ANALYSIS] AT LYS-398, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: PTM / Processing, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3088 other entries.

  5. 5
    "Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis."
    Olsen J.V., Vermeulen M., Santamaria A., Kumar C., Miller M.L., Jensen L.J., Gnad F., Cox J., Jensen T.S., Nigg E.A., Brunak S., Mann M.
    Sci. Signal. 3:RA3-RA3(2010) [PubMed] [Europe PMC] [Abstract]
    Cited for: PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-576, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: PTM / Processing, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 7257 and mapped to 5 other entries.

  6. 6
    "Two mutations in human BICC1 resulting in Wnt pathway hyperactivity associated with cystic renal dysplasia."
    Kraus M.R., Clauin S., Pfister Y., Di Maio M., Ulinski T., Constam D., Bellanne-Chantelot C., Grapin-Botton A.
    Hum. Mutat. 33:86-90(2012) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION AS NEGATIVE REGULATOR OF WNT SIGNALING, VARIANT CYSRD GLY-932, VARIANT THR-711, CHARACTERIZATION OF VARIANT CYSRD GLY-932.
    Category: Function, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  7. 7
    "Toward a comprehensive characterization of a human cancer cell phosphoproteome."
    Zhou H., Di Palma S., Preisinger C., Peng M., Polat A.N., Heck A.J., Mohammed S.
    J. Proteome Res. 12:260-271(2013) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 13305 other entries.

  8. 8
    "Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation."
    Lee H., Lin M.C., Kornblum H.I., Papazian D.M., Nelson S.F.
    Hum. Mol. Genet. 23:3481-3489(2014) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT VAL-270.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3 other entries.

  9. 9
    "Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer's disease."
    Riemenschneider M., Mahmoodzadeh S., Eisele T., Klopp N., Schwarz S., Wagenpfeil S., Diehl J., Mueller U., Foerstl H., Illig T., Kurz A.
    Neurobiol. Aging 25:1305-1308(2004) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Not Associated with NEUROLOGICAL: Alzheimer's Disease.Imported, Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GAD:117820, GeneRIF:80114.

    This publication is mapped to 8 other entries.

  10. 10
    Category: Pathology & Biotech.
    Annotation: Not Associated with NEUROLOGICAL: Alzheimer's disease.Imported, Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GAD:567610, GeneRIF:80114.

    This publication is mapped to 1674 other entries.

  11. 11
    "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."
    Rose J.E., Behm F.M., Drgon T., Johnson C., Uhl G.R.
    Mol. Med. 16:247-253(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)Imported.
    Source: GeneRIF:80114.

    This publication is mapped to 11552 other entries.

  12. 12
    Annotation: Observational study meta-analysis and genome-wide association study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:80114.

    This publication is mapped to 2 other entries.

  13. 13
    "Effect of genetic variant in BICC1 on functional and structural brain changes in depression."
    Bermingham R., Carballedo A., Lisiecka D., Fagan A., Morris D., Fahey C., Donohoe G., Meaney J., Gill M., Frodl T.
    Neuropsychopharmacology 37:2855-2862(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: The minor T-allele of BICC1 has a protective role against major depressive disorder and its known structural and functional brain changes.Imported.
    Source: GeneRIF:80114.
  14. 14
    "Bicc1 is a genetic determinant of osteoblastogenesis and bone mineral density."
    Mesner L.D., Ray B., Hsu Y.H., Manichaikul A., Lum E., Bryda E.C., Rich S.S., Rosen C.J., Criqui M.H., Allison M., Budoff M.J., Clemens T.L., Farber C.R.
    J. Clin. Invest. 124:2736-2749(2014) [PubMed] [Europe PMC] [Abstract]
    Annotation: identify Bicc1 as a genetic determinant of osteoblastogenesis and BMD and suggest that it does so by regulating Pkd2 transcript levels; Polymorphisms in intron 2 of BICC1 are associated with its expression and bone mineral density (BMD)Imported.
    Source: GeneRIF:80114.

    This publication is mapped to 3 other entries.

  15. 15
    "BICC1 expression is elevated in depressed subjects and contributes to depressive behavior in rodents."
    Ota K.T., Andres W., Lewis D.A., Stockmeier C.A., Duman R.S.
    Neuropsychopharmacology 40:711-718(2015) [PubMed] [Europe PMC] [Abstract]
    Annotation: findings identify a role for increased levels of BICC1 in the pathophysiology of depressive behaviorImported.
    Source: GeneRIF:80114.
  16. 16
    "GWAS-identified risk variants for major depressive disorder: Preliminary support for an association with late-life depressive symptoms and brain structural alterations."
    Ryan J., Artero S., Carriere I., Maller J.J., Meslin C., Ritchie K., Ancelin M.L.
    Eur Neuropsychopharmacol 26:113-125(2016) [PubMed] [Europe PMC] [Abstract]
    Annotation: Results provide some support for the involvement of BICC1 and PCLO in late-life depressive disorders and preliminary evidence that these genetic variants may also influence brain structural volumesImported.
    Source: GeneRIF:80114.

    This publication is mapped to 6 other entries.

  17. 17
    "Analysis of the effects of depression associated polymorphisms on the activity of the BICC1 promoter in amygdala neurones."
    Davidson S., Shanley L., Cowie P., Lear M., McGuffin P., Quinn J.P., Barrett P., MacKenzie A.
    Pharmacogenomics J. 16:366-374(2016) [PubMed] [Europe PMC] [Abstract]
    Annotation: Suggest allelic changes in the regulation of the BICC1 gene in amygdala neurones may contribute to mood disorders.Imported.
    Source: GeneRIF:80114.
  18. 18
    "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:Q9H694.

    This publication is mapped to 5387 other entries.

  19. 19
    "Evaluation of genome-wide susceptibility loci for high myopia in a Han Chinese population."
    Li F., Ye Z., Zhai Y., Gong B., Jiang L., Wu H., Lin Y., Wan L., Yang Z., Shi Y., Wu Z.
    Ophthalmic Genet. 38:330-334(2017) [PubMed] [Europe PMC] [Abstract]
    Annotation: Our findings suggested rs17648524 (intronic RBFOX1 gene) and rs7084402 (7.5kb 5' of the BICC1 gene) showed gender-specific associations with high myopia in the Han Chinese.Imported.
    Source: GeneRIF:80114.

    This publication is mapped to 9 other entries.

  20. 20
    "Assessment of BicC family RNA binding protein 1 and Ras protein specific guanine nucleotide releasing factor 1 as candidate genes for high myopia: A case-control study."
    Hepei L., Mingkun X., Li W., Jin W.
    Indian J Ophthalmol 65:926-930(2017) [PubMed] [Europe PMC] [Abstract]
    Annotation: genetic variants in BICC1 and RASGRF1 are closely associated with high myopia which appears to be a potential candidate for high myopia in Chinese Han population.Imported.
    Source: GeneRIF:80114.

    This publication is mapped to 4 other entries.

1 to 20 of 20  Show

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