Human Disease Genes and Their Cloned Mouse Orthologs: Exploration of the FANTOM2 cDNA Sequence Data Set
Author(s) -
Lynn M. Schriml,
David P. Hill,
Judith A. Blake,
Hidemasa Bono,
Anthony WynshawBoris,
William J. Pavan,
Brian Z. Ring,
Kirk W. Beisel,
Mitsutoshi Setou,
Yasushi Okazaki
Publication year - 2003
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.979503
Subject(s) - biology , complementary dna , gene , genetics , human genome , genome , sequence (biology) , computational biology , expressed sequence tag , human disease , sequence analysis
The FANTOM2 cDNA sequence data set is an excellent model to demonstrate the power of large-scale cDNA sequencing, with the goal of providing a full-length transcript sequence for each mouse gene. This data set enhances the use of the mouse as a model for human disease. Here we identify mouse cDNA sequences in the FANTOM2 data set for a set of 67 human disease genes that as of May 2002 had no corresponding mouse cDNA annotated in the Mouse Genome Informatics (MGI) database. These 67 human disease genes include genes related to neurological and eye disorders and cancer. We also present a list of the human disease genes and their cloned mouse orthologs found in two public databases, LocusLink and MGI. Allelic variant and gene functional information available in MGI provides additional information relative to these mouse models, whereas computed sequence-based connections at NCBI support facile navigation through multiple genomes.
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