Literature DB >> 8929944

Five novel mutations in the L1CAM gene in families with X linked hydrocephalus.

S M Gu1, U Orth, A Veske, H Enders, K Klunder, M Schlosser, W Engel, E Schwinger, A Gal.   

Abstract

Five novel mutations have been identified in the gene encoding L1CAM, a neural cell adhesion protein, in families with X linked hydrocephalus (XHC). Interestingly, all five mutations are in the evolutionarily highly conserved Ig-like domains of the protein. The two frameshift mutations (52insC and 955delG) and the nonsense mutation (Trp276Ter) most probably result in functional null alleles and complete absence of L1CAM at the cell surface. The two missense mutations (Tyr194Cys and Pro240Leu) may considerably alter the structure of the L1CAM protein. These data provide convincing evidence that XHC is genetically extremely heterogeneous.

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Year:  1996        PMID: 8929944      PMCID: PMC1051833          DOI: 10.1136/jmg.33.2.103

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  12 in total

1.  Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

Authors:  P J Willems; L Vits; P Raeymaekers; J Beuten; P Coucke; J J Holden; C Van Broeckhoven; S T Warren; M Sagi; D Robinson
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

2.  Molecular structure and functional testing of human L1CAM: an interspecies comparison.

Authors:  M L Hlavin; V Lemmon
Journal:  Genomics       Date:  1991-10       Impact factor: 5.736

3.  Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus.

Authors:  A Rosenthal; M Jouet; S Kenwrick
Journal:  Nat Genet       Date:  1992-10       Impact factor: 38.330

4.  Several extracellular domains of the neural cell adhesion molecule L1 are involved in neurite outgrowth and cell body adhesion.

Authors:  F Appel; J Holm; J F Conscience; M Schachner
Journal:  J Neurosci       Date:  1993-11       Impact factor: 6.167

5.  A duplication in the L1CAM gene associated with X-linked hydrocephalus.

Authors:  G Van Camp; L Vits; P Coucke; S Lyonnet; C Schrander-Stumpel; J Darby; J Holden; A Munnich; P J Willems
Journal:  Nat Genet       Date:  1993-08       Impact factor: 38.330

6.  Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family.

Authors:  P Coucke; L Vits; G Van Camp; F Serville; S Lyonnet; S Kenwrick; A Rosenthal; M Wehnert; A Munnich; P J Willems
Journal:  Hum Mol Genet       Date:  1994-04       Impact factor: 6.150

7.  Neural adhesion molecule L1 as a member of the immunoglobulin superfamily with binding domains similar to fibronectin.

Authors:  M Moos; R Tacke; H Scherer; D Teplow; K Früh; M Schachner
Journal:  Nature       Date:  1988-08-25       Impact factor: 49.962

8.  X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene.

Authors:  M Jouet; A Rosenthal; G Armstrong; J MacFarlane; R Stevenson; J Paterson; A Metzenberg; V Ionasescu; K Temple; S Kenwrick
Journal:  Nat Genet       Date:  1994-07       Impact factor: 38.330

9.  The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52.

Authors:  S Lyonnet; A Pelet; G Royer; O Delrieu; F Serville; B le Marec; A Gruensteudel; R A Pfeiffer; M L Briard; C Dubay
Journal:  Genomics       Date:  1992-10       Impact factor: 5.736

10.  Structure of the chicken neuron-glia cell adhesion molecule, Ng-CAM: origin of the polypeptides and relation to the Ig superfamily.

Authors:  M P Burgoon; M Grumet; V Mauro; G M Edelman; B A Cunningham
Journal:  J Cell Biol       Date:  1991-03       Impact factor: 10.539

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  7 in total

1.  Outline structure of the human L1 cell adhesion molecule and the sites where mutations cause neurological disorders.

Authors:  A Bateman; M Jouet; J MacFarlane; J S Du; S Kenwrick; C Chothia
Journal:  EMBO J       Date:  1996-11-15       Impact factor: 11.598

2.  CRASH syndrome: mutations in L1CAM correlate with severity of the disease.

Authors:  M Yamasaki; P Thompson; V Lemmon
Journal:  Neuropediatrics       Date:  1997-06       Impact factor: 1.947

3.  The site of a missense mutation in the extracellular Ig or FN domains of L1CAM influences infant mortality and the severity of X linked hydrocephalus.

Authors:  R C Michaelis; Y Z Du; C E Schwartz
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

4.  Genotype-phenotype correlation in L1 associated diseases.

Authors:  E Fransen; G Van Camp; R D'Hooge; L Vits; P J Willems
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

5.  Relationships between gene expression and brain wiring in the adult rodent brain.

Authors:  Leon French; Paul Pavlidis
Journal:  PLoS Comput Biol       Date:  2011-01-06       Impact factor: 4.475

6.  Cloning and expression of a zebrafish SCN1B ortholog and identification of a species-specific splice variant.

Authors:  Amanda J Fein; Laurence S Meadows; Chunling Chen; Emily A Slat; Lori L Isom
Journal:  BMC Genomics       Date:  2007-07-10       Impact factor: 3.969

7.  NOG-Derived Peptides Can Restore Neuritogenesis on a CRASH Syndrome Cell Model.

Authors:  Matteo Gasparotto; Yuriko Suemi Hernandez Gomez; Daniele Peterle; Alessandro Grinzato; Federica Zen; Giulia Pontarollo; Laura Acquasaliente; Giorgia Scapin; Elisabetta Bergantino; Vincenzo De Filippis; Francesco Filippini
Journal:  Biomedicines       Date:  2022-01-04
  7 in total

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