Skip Header

You are using a version of browser that may not display all the features of this website. Please consider upgrading your browser.
1 to 24 of 24  Show
  1. 1
    "Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro."
    Ishikawa K., Nagase T., Suyama M., Miyajima N., Tanaka A., Kotani H., Nomura N., Ohara O.
    DNA Res. 5:169-176(1998) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2).
    Category: Sequences.
    Tissue: Brain.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 99 other entries.

  2. 2
    "DNA sequence and analysis of human chromosome 9."
    Humphray S.J., Oliver K., Hunt A.R., Plumb R.W., Loveland J.E., Howe K.L., Andrews T.D., Searle S., Hunt S.E., Scott C.E., Jones M.C., Ainscough R., Almeida J.P., Ambrose K.D., Ashwell R.I.S., Babbage A.K., Babbage S., Bagguley C.L.
    Dunham I.
    Nature 429:369-374(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 2219 other entries.

  3. 3
    "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 2; 4 AND 6), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 532-1339 (ISOFORM 3).
    Category: Sequences.
    Tissue: Brain, Cervix and Eye.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50459 other entries.

  4. 4
    "Molecular cloning of human astrotactin-2."
    Tomoda T.
    Submitted (DEC-1998) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 227-1339 (ISOFORM 2).
    Category: Sequences.
    Tissue: Uterus.
    Source: UniProtKB/Swiss-Prot (reviewed).
  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] OF 274-470 (ISOFORM 1).
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12928 other entries.

  6. 6
    "Structure of astrotactin-2: a conserved vertebrate-specific and perforin-like membrane protein involved in neuronal development."
    Ni T., Harlos K., Gilbert R.
    Open Biol. 0:0-0(2016)
    Cited for: X-RAY CRYSTALLOGRAPHY (3.16 ANGSTROMS) OF 768-1339, DISULFIDE BONDS, GLYCOSYLATION AT ASN-770 AND ASN-783, CALCIUM-BINDING, FUNCTION, MUTAGENESIS OF ARG-1175, DOMAIN.
    Category: Function, Pathology & Biotech, PTM / Processing, Structure, Family & Domains.
    Source: UniProtKB/Swiss-Prot (reviewed).
  7. 7
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 974 and mapped to 2 other entries.

  8. 8
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 72 other entries.

  9. 9
    "Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies."
    Lesch K.P., Timmesfeld N., Renner T.J., Halperin R., Roser C., Nguyen T.T., Craig D.W., Romanos J., Heine M., Meyer J., Freitag C., Warnke A., Romanos M., Schafer H., Walitza S., Reif A., Stephan D.A., Jacob C.
    J Neural Transm (Vienna) 115:1573-1585(2008) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Observational study and genome-wide association study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 22 other entries.

  10. 10
    Category: Pathology & Biotech, Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 38 other entries.

  11. 11
    "Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment."
    Gratacos M., Costas J., de Cid R., Bayes M., Gonzalez J.R., Baca-Garcia E., de Diego Y., Fernandez-Aranda F., Fernandez-Piqueras J., Guitart M., Martin-Santos R., Martorell L., Menchon J.M., Roca M., Saiz-Ruiz J., Sanjuan J., Torrens M., Urretavizcaya M.
    Carracedo A.
    Am. J. Med. Genet. B Neuropsychiatr. Genet. 150B:808-816(2009) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 1427 other entries.

  12. 12
    "Confirmation of genomewide association signals in Chinese Han population reveals risk loci for ischemic stroke."
    Ding H., Xu Y., Bao X., Wang X., Cui G., Wang W., Hui R., Wang D.W.
    Stroke 41:177-180(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 46 other entries.

  13. 13
    "Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs."
    Adkins D.E., Aberg K., McClay J.L., Bukszar J., Zhao Z., Jia P., Stroup T.S., Perkins D., McEvoy J.P., Lieberman J.A., Sullivan P.F., van den Oord E.J.
    Mol. Psychiatry 16:321-332(2011) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Clinical trial and genome-wide association study of gene-disease association. (HuGE Navigator)Imported, Associated with PHARMACOGENOMIC: response to antipsychotic treatment.Imported.
    Source: GAD:600163, GeneRIF:23245.

    This publication is mapped to 64 other entries.

  14. 14
    "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]
    Category: Function.
    Annotation: Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 11747 other entries.

  15. 15
    "A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder."
    Wang K.S., Liu X.F., Aragam N.
    Schizophr. Res. 124:192-199(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Meta-analysis and genome-wide association study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 48 other entries.

  16. 16
    "Common variants at 12q14 and 12q24 are associated with hippocampal volume."
    Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium
    Bis J.C., DeCarli C., Smith A.V., van der Lijn F., Crivello F., Fornage M., Debette S., Shulman J.M., Schmidt H., Srikanth V., Schuur M., Yu L., Choi S.H., Sigurdsson S., Verhaaren B.F., DeStefano A.L., Lambert J.C., Jack C.R. Jr.
    Thompson P.M.
    Nat. Genet. 44:545-551(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: Single nucleotide polymorphism in ASTN2 gene is associated with cognition disorders.Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 7 other entries.

  17. 17
    Category: Pathology & Biotech.
    Annotation: 3' terminal ASTN2 deletions are significantly enriched in males with neurodevelopmental disorders but not in females.Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 9 other entries.

  18. 18
    "Polymorphisms within ASTN2 gene are associated with age at onset of Alzheimer's disease."
    Wang K.S., Tonarelli S., Luo X., Wang L., Su B., Zuo L., Mao C., Rubin L., Briones D., Xu C.
    J Neural Transm (Vienna) 122:701-708(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Study found a significant association of ASTN2 genetic variants with age at onset in Alzheimer's disease in two independent samples together with in silico analysis that demonstrated potential role of ASTN2 in the pathogenesis of the diseaseImported.
    Source: GeneRIF:23245.

    This publication is mapped to 7 other entries.

  19. 19
    "Investigation of association between hip osteoarthritis susceptibility loci and radiographic proximal femur shape."
    arcOGEN Consortium
    Lindner C., Thiagarajah S., Wilkinson J.M., Panoutsopoulou K., Day-Williams A.G., Cootes T.F., Wallis G.A., Loughlin J., Arden N., Birrell F., Carr A., Chapman K., Deloukas P., Doherty M., McCaskie A., Ollier W.E., Rai A., Ralston S.H.
    Zeggini E.
    Arthritis Rheumatol 67:2076-2084(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: rs4836732 may contribute to hip OA susceptibility by altering proximal femur shape.Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 16 other entries.

  20. 20
    "iCLIP identifies novel roles for SAFB1 in regulating RNA processing and neuronal function."
    Rivers C., Idris J., Scott H., Rogers M., Lee Y.B., Gaunt J., Phylactou L., Curk T., Campbell C., Ule J., Norman M., Uney J.B.
    BMC Biol. 13:111-111(2015) [PubMed] [Europe PMC] [Abstract]
    Annotation: The expression of coding and non-coding genes with SAFB1 cross-link sites was altered by SAFB1 knockdown. The isoform-specific expression of neural cell adhesion molecule (NCAM1) and ASTN2 was influenced by SAFB1.Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 23 other entries.

  21. 21
    "The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits."
    Freitag C.M., Lempp T., Nguyen T.T., Jacob C.P., Weissflog L., Romanos M., Renner T.J., Walitza S., Warnke A., Rujescu D., Lesch K.P., Reif A.
    J Neural Transm (Vienna) 123:849-858(2016) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: The findings of this study do not support a major role of ASTN2 variants in ADHD or its comorbid disorders respective aADHD associated personality traits.Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 7 other entries.

  22. 22
    "Structure of astrotactin-2: a conserved vertebrate-specific and perforin-like membrane protein involved in neuronal development."
    Ni T., Harlos K., Gilbert R.
    Open Biol 6:0-0(2016) [PubMed] [Europe PMC] [Abstract]
    Category: Structure.
    Annotation: Results present the structure of ASTN-2 consisting of a combination of polypeptide folds: a perforin-like domain a minimal epidermal growth factor-like module a unique form of fibronectin type III domain and an annexin-like domain. Structural and biophysical data show that ASTN-2 binds inositol triphosphates suggesting a mechanism for membrane recognition or secondary messenger regulation of its activity.Imported.
    Source: PDB:5J67, PDB:5J68, PDB:5J69, GeneRIF:23245.

    This publication is mapped to 7 other entries.

  23. 23
    "Multilocus analysis reveals three candidate genes for Chinese migraine susceptibility."
    An X.K., Fang J., Yu Z.Z., Lin Q., Lu C.X., Qu H.L., Ma Q.L.
    Clin. Genet. 92:143-149(2017) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Our study suggests that the MEF2D PRDM16 and ASTN2 genes from GWAS are associated with migraine susceptibility especially migraine without aura among Chinese patients. It appears that there is no association with serotonin receptor related genes.Imported.
    Source: GeneRIF:23245.

    This publication is mapped to 13 other entries.

  24. 24
    "ASTN2 modulates synaptic strength by trafficking and degradation of surface proteins."
    Behesti H., Fore T.R., Wu P., Horn Z., Leppert M., Hull C., Hatten M.E.
    Proc. Natl. Acad. Sci. U.S.A. 115:E9717-E9726(2018) [PubMed] [Europe PMC] [Abstract]
    Annotation: ASTN2 localizes primarily to endocytic and autophagocytic vesicles in the cell soma and in subsets of dendritic spinesImported.
    Source: GeneRIF:23245.

    This publication is mapped to 7 other entries.

1 to 24 of 24  Show
UniProt is an ELIXIR core data resource
Main funding by: National Institutes of Health

We'd like to inform you that we have updated our Privacy Notice to comply with Europe’s new General Data Protection Regulation (GDPR) that applies since 25 May 2018.

Do not show this banner again