Introduction to Data on Imprinted Genes

The data on Genomic Imprinting held within MouseBook comprise information on mouse chromosome regions associated with imprinted phenotypes, imprinted genes within these regions, and imprinted genes in other regions of the genome. The Composite Imprinting Map shows all chromosomes with imprinted genes and/or regions or phenotypes. The individual imprinting maps show greater detail of the position of imprinted regions and imprinted phenotypes. Regions of human homology for mouse imprinted regions are shown on the left of the individual maps, and are linked to references for human imprinted genes on http://igc.otago.ac.nz/. More information on the imprinted genes shown on the maps can be obtained from the tables of imprinted genes and their functions. The genes in the table are listed in Chromosome order. The order of the genes on each Chromosome, as shown on the map, is based on nucleotide position from MGI. Some imprinted genes are not listed in MGI; they are in order on the map and are at the end of the entries for each chromosome in the table.

The maps were formerly published in Mouse Genome and are based on mouse genetic studies in which Robertsonian (Rb) and reciprocal (T) translocations have been used to generate uniparental disomies and uniparental duplications of whole or selected chromosome regions, respectively. The approved Nomenclature Rules applicable to these genetic studies are also given. Chromosome regions exhibiting imprinting effects (phenotypes) with 2 maternal (M) and no paternal, or 2 paternal (P) and no maternal copies are illustrated on both the ideogram, Evans (1996), Beechey & Evans (2004) and genetic maps. These maps are not exhaustive as some imprinting effects may be subtle. Imprinted genes within domains are not necessarily shown in the correct order relative to each other or to chromosomal orientation (centromere to telomere).

Other areas of the genome where imprinted genes have been identified are also shown, (chromosome 1, 5, 10, 13, 14, 15 and 19), despite no obvious abnormal phenotype being associated with maternal or paternal duplication.

All currently known imprinted genes, imprinted small nucleolar RNAs (snoRNAs), microRNAs, (miRNAs) and their expressed parental allele are identified on the individual maps, along with the chromosome anomalies used to define each imprinting region. Gene symbols written in red are expressed from the maternal allele and those in blue from the paternal allele. MGI gene smbols are used. Each imprinted gene has links to the appropriate reference(s). Symbols for Robertsonian (Rb) translocations used to identify imprinting phenotypes are shown above each chromosome. The positions of reciprocal translocations (T) which currently define the regions with imprinting phenotypes are shown in bold with their positions, if known, on both the linkage and physical maps. Other reciprocal translocations, insertions (Is) and deletions (Del) that have been used to define or investigate imprinting regions are also identified.

Evans EP (1996) Standard Idiogram. In Lyon MF, Rastan S & Brown SDM (eds.) Genetic Variants and Strains of the Laboratory Mouse , 3rd ed. Oxford University Press: pp 1446-1448

Beechey CV & Evans EP (2004), MRC Harwell, Harwell, Oxfordshire. Standard Ideogram/Anomaly Breakpoints of the Mouse (URL:http://www.har.mrc.ac.uk/).

Lyon MF, Cocking Y & Gao XQ (1997) Mouse Genome 94 :29-77

E-mail Contact and Citation Information

Send comments and new information to : Christine Williamson, Jo Peters & Andrew Blake .

When citing information retreived from the MRC Harwell Imprinting Web pages please use the following format:

Williamson CM, Blake A, Thomas S, Beechey CV, Hancock J, Cattanach BM, and Peters J (2010), MRC Harwell, Oxfordshire. World Wide Web Site - Mouse Imprinting Data and References - http://www.har.mrc.ac.uk/research/genomic_imprinting/

Chr 1	Chr 2	Chr 5	Chr 6	Chr 7
Chr 9	Chr 10	Chr 11	Chr 12	Chr 13
Chr 14	Chr 15	Chr 17	Chr 18	Chr 19
Composite Map
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