| A |
| Unique sequences: | upper case letters |
| Repeat sequences: | lower case letters |
| Sequence gaps: | N |
| Transcriptional units: | red |
| Exons: | dark red |
| Repeats outside transcriptional units: | green |
|
The software RepeatMasker has been used
to define repeat sequences. Where possible, gene names are used
according to the HUGO nomenclature committee.
In other cases genes were named according to accession numbers
or clone names. Sequence coordinates are given for each transcriptional
unit and denote start and end of longest available transcripts.
X chromosome sequence generated by:
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK
Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA
Institute of Molecular Biotechnology, Jena, Germany
Genome Sequencing Center, Washington University, St. Louis, MO, USA
Max Planck Institute for Molecular Genetics, Berlin, Germany
Gene structures annotated by:
Wellcome Trust Sanger Institute, HAVANA Group, Cambridge, UK
Institute of Molecular Biotechnology, Jena, Germany
Formatted sequence files generated by:
Howe K. Sanger Institute
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| B |
X chromosome after GTG-banding. |
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| C |
FISH-hybridisation pattern of the X chromosome.
Cross-hybridisation of the Y chromosome to the X chromosome
is visible as bands representing the PAR1 (Xp22.3) and the
XY-HR (Xp21.3). PAR2 (Xq28) is not detected with the probe
set used. (Azofeifa et al. Am J Hum Genet 66:1684-88, 2000)
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