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 23 of 23  Show
  1. 1
    "Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteins."
    Rupp P.A., Fouad G.T., Egelston C.A., Reifsteck C.A., Olson S.B., Knosp W.M., Glanville R.W., Thornburg K.L., Robinson S.W., Maslen C.L.
    Gene 293:47-57(2002) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), TISSUE SPECIFICITY, VARIANT VAL-13.
    Category: Expression, Sequences.
    Tissue: Fibroblast.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  2. 2
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1), VARIANT VAL-13.
    Category: Sequences.
    Tissue: Kidney.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 490 other entries.

  3. 3
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1), VARIANT VAL-13.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1015 other entries.

  4. 4
    "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] (ISOFORM 1), VARIANT VAL-13.
    Category: Sequences.
    Tissue: Amygdala.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12927 other entries.

  5. 5
    "Cloning of human full open reading frames in Gateway(TM) system entry vector (pDONR201)."
    Ebert L., Schick M., Neubert P., Schatten R., Henze S., Korn B.
    Submitted (JUN-2004) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), VARIANT VAL-13.
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  6. 6
    "The DNA sequence, annotation and analysis of human chromosome 3."
    Muzny D.M., Scherer S.E., Kaul R., Wang J., Yu J., Sudbrak R., Buhay C.J., Chen R., Cree A., Ding Y., Dugan-Rocha S., Gill R., Gunaratne P., Harris R.A., Hawes A.C., Hernandez J., Hodgson A.V., Hume J.
    Gibbs R.A.
    Nature 440:1194-1198(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3939 other entries.

  7. 7
    "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), VARIANT VAL-13.
    Category: Sequences.
    Tissue: Lung.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50448 other entries.

  8. 8
    "Hyperactivity of the Ero1alpha oxidase elicits endoplasmic reticulum stress but no broad antioxidant response."
    Hansen H.G., Schmidt J.D., Soltoft C.L., Ramming T., Geertz-Hansen H.M., Christensen B., Sorensen E.S., Juncker A.S., Appenzeller-Herzog C., Ellgaard L.
    J. Biol. Chem. 287:39513-39523(2012) [PubMed] [Europe PMC] [Abstract]
    Cited for: INDUCTION.
    Category: Expression.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 other entries.

  9. 9
    "Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects."
    Robinson S.W., Morris C.D., Goldmuntz E., Reller M.D., Jones M.A., Steiner R.D., Maslen C.L.
    Am. J. Hum. Genet. 72:1047-1052(2003) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANTS AVSD2 HIS-107; ILE-311 AND CYS-329.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 2 other entries.

  10. 10
    "Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2)."
    Zatyka M., Priestley M., Ladusans E.J., Fryer A.E., Mason J., Latif F., Maher E.R.
    Clin. Genet. 67:526-528(2005) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT AVSD2 ALA-162.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  11. 11
    Category: Interaction.
    Source: IntAct:Q96HD1.

    This publication is mapped to 1656 other entries.

  12. 12
    "Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects."
    Posch M.G., Perrot A., Schmitt K., Mittelhaus S., Esenwein E.M., Stiller B., Geier C., Dietz R., Gessner R., Ozcelik C., Berger F.
    Am. J. Med. Genet. A 146A:251-253(2008) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Mutations in CRELD1 are infrequently found in patients with congenital cardiac septal defects.
    Source: GeneRIF:78987.

    This publication is mapped to 45 other entries.

  13. 13
    "RTN3 inducing apoptosis is modulated by an adhesion protein CRELD1."
    Xiang R., Zhao S.
    Mol. Cell. Biochem. 331:225-230(2009) [PubMed] [Europe PMC] [Abstract]
    Category: Subcellular Location, Interaction.
    Annotation: CRELD1 could partly change the localization of RTN3 from the endoplasmic reticulum to the plasma membrane and modulate the apoptotic activity of RTN3 through binding with it.
    Source: GeneRIF:78987.

    This publication is mapped to 9 other entries.

  14. 14
    "Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia."
    Jugessur A., Shi M., Gjessing H.K., Lie R.T., Wilcox A.J., Weinberg C.R., Christensen K., Boyles A.L., Daack-Hirsch S., Nguyen T.T., Christiansen L., Lidral A.C., Murray J.C.
    PLoS ONE 5:e11493-e11493(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: Observational study of gene-disease association. (HuGE Navigator).
    Source: GeneRIF:78987.

    This publication is mapped to 1712 other entries.

  15. 15
    "Novel CRELD1 gene mutations in patients with atrioventricular septal defect."
    Guo Y., Shen J., Yuan L., Li F., Wang J., Sun K.
    World J Pediatr 6:348-352(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: CRELD1 is likely to be an AVSD-susceptibility gene and CRELD1 mutations may increase the risk of developing a heart defect rather than being a direct causative mutation; Observational study of gene-disease association. (HuGE Navigator).
    Source: GeneRIF:78987.

    This publication is mapped to 1 other entry.

  16. 16
    "A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India."
    Kusuma L., Dinesh S.M., Savitha M.R., Krishnamurthy B., Narayanappa D., Ramachandra N.B.
    Genet Test Mol Biomarkers 15:483-487(2011) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: SNP c.985 C>T of CRELD1 is involved in causing congenital heart disease in patients of Mysore South India.
    Source: GeneRIF:78987.

    This publication is mapped to 1 other entry.

  17. 17
    "Specific association of missense mutations in CRELD1 with cardiac atrioventricular septal defects in heterotaxy syndrome."
    Zhian S., Belmont J., Maslen C.L.
    Am. J. Med. Genet. A 158A:2047-2049(2012) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: study indicates that deleterious CRELD1 missense mutations are specifically associated with AVSD and are not correlated with other aspects of the heterotaxy phenotype.
    Source: GeneRIF:78987.

    This publication is mapped to 1 other entry.

  18. 18
    "Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect."
    Ghosh P., Bhaumik P., Ghosh S., Ozbek U., Feingold E., Maslen C., Sarkar B., Pramanik V., Biswas P., Bandyopadhyay B., Dey S.K.
    Am. J. Med. Genet. A 158A:2843-2848(2012) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech, Sequences.
    Annotation: we identified two CRELD1 haplotypes associated with AVSD phenotype among DS and euploid individuals.
    Source: GeneRIF:78987.

    This publication is mapped to 1 other entry.

  19. 19
    "[Potential role of CRELD1 gene in the pathogenesis of atrioventricular septal defect]."
    Guo Y., Shen J., Li F., Wang J., Wang X., Guo A., Sun K.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 31:263-267(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: Mutation of the CRELD1 gene increased the risk for atrioventricular septal defect.
    Source: GeneRIF:78987.

    This publication is mapped to 1 other entry.

  20. 20
    "The MEKK1 PHD ubiquitinates TAB1 to activate MAPKs in response to cytokines."
    Charlaftis N., Suddason T., Wu X., Anwar S., Karin M., Gallagher E.
    EMBO J. 33:2581-2596(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q96HD1.

    This publication is mapped to 174 other entries.

  21. 21
    Category: Sequences.
    Annotation: Germline mutations in the NKX2-5 GATA4 and CRELD1 genes do not appear to be associated with CHD in Mexican DS patients.
    Source: GeneRIF:78987.

    This publication is mapped to 36 other entries.

  22. 22
    "Protein interactome mining defines melatonin MT1 receptors as integral component of presynaptic protein complexes of neurons."
    Benleulmi-Chaachoua A., Chen L., Sokolina K., Wong V., Jurisica I., Emerit M.B., Darmon M., Espin A., Stagljar I., Tafelmeyer P., Zamponi G.W., Delagrange P., Maurice P., Jockers R.
    J. Pineal Res. 60:95-108(2016) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:Q96HD1.

    This publication is mapped to 361 other entries.

  23. 23
    "CRELD1 gene variants and atrioventricular septal defects in Down syndrome."
    Asim A., Agarwal S., Panigrahi I., Sarangi A.N., Muthuswamy S., Kapoor A.
    Gene 641:180-185(2018) [PubMed] [Europe PMC] [Abstract]
    Category: Sequences.
    Annotation: The CRELD1 gene is likely to have a major role in causation of AVSD phenotype in selected DS patients.
    Source: GeneRIF:78987.

    This publication is mapped to 1 other entry.

1 to 23 of 23  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