Literature DB >> 1639415

Sequence of the human factor VIII-associated gene is conserved in mouse.

B Levinson1, J R Bermingham, A Metzenberg, S Kenwrick, V Chapman, J Gitschier.   

Abstract

cDNA and genomic clones corresponding to the human factor VIII-associated gene (F8A) were isolated from mouse cDNA and F8A-enriched genomic libraries. The sequences of these clones revealed an intronless gene coding for 380 amino acids, with 85% identity to the predicted human sequence. The single murine gene copy is genetically linked to factor VIII, but appears to lie outside the factor VIII gene by physical mapping. Like the human gene, the mouse F8A gene is highly expressed in a wide variety of tissues. This evolutionary comparison has helped to clarify the derived amino acid sequence in the human and strongly supports the hypothesis that the F8A gene encodes a protein.

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Year:  1992        PMID: 1639415     DOI: 10.1016/0888-7543(92)90170-w

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  9 in total

1.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-10-11       Impact factor: 16.971

2.  Aerosol gene delivery in vivo.

Authors:  R Stribling; E Brunette; D Liggitt; K Gaensler; R Debs
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

3.  Comparative genome sequence analysis of the Bpa/Str region in mouse and Man.

Authors:  A M Mallon; M Platzer; R Bate; G Gloeckner; M R Botcherby; G Nordsiek; M A Strivens; P Kioschis; A Dangel; D Cunningham; R N Straw; P Weston; M Gilbert; S Fernando; K Goodall; G Hunter; J S Greystrong; D Clarke; C Kimberley; M Goerdes; K Blechschmidt; A Rump; B Hinzmann; C R Mundy; W Miller; A Poustka; G E Herman; M Rhodes; P Denny; A Rosenthal; S D Brown
Journal:  Genome Res       Date:  2000-06       Impact factor: 9.043

4.  Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.

Authors:  T A Angel; C J Faust; J C Gonzales; S Kenwrick; R A Lewis; G E Herman
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

Review 5.  Animal models of hemophilia and related bleeding disorders.

Authors:  Jay N Lozier; Timothy C Nichols
Journal:  Semin Hematol       Date:  2013-04       Impact factor: 3.851

6.  Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A.

Authors:  Richard D Bagnall; Karen L Ayres; Peter M Green; Francesco Giannelli
Journal:  Genome Res       Date:  2005-02       Impact factor: 9.043

Review 7.  Haemophilia A and haemophilia B: molecular insights.

Authors:  D J Bowen
Journal:  Mol Pathol       Date:  2002-04

Review 8.  Haemophilia A and haemophilia B: molecular insights.

Authors:  D J Bowen
Journal:  Mol Pathol       Date:  2002-02

9.  Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

Authors:  M D'Esposito; N A Quaderi; A Ciccodicola; P Bruni; T Esposito; M D'Urso; S D Brown
Journal:  Mamm Genome       Date:  1996-07       Impact factor: 2.957

  9 in total

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