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Publication : Chromosomal localization of the human and mouse hyaluronan synthase genes.

First Author  Spicer AP Year  1997
Journal  Genomics Volume  41
Issue  3 Pages  493-7
PubMed ID  9169154 Mgi Jnum  J:40157
Mgi Id  MGI:87501 Doi  10.1006/geno.1997.4696
Citation  Spicer AP, et al. (1997) Chromosomal localization of the human and mouse hyaluronan synthase genes. Genomics 41(3):493-7
abstractText  We have recently identified a new vertebrate gene family encoding putative hyaluronan (HA) synthases. Three highly conserved related genes have been identified, designated HAS1, HAS2, and HAS3 in humans and Has1, Has2, and Has3 in the mouse, All three genes encode predicted plasma membrane proteins with multiple transmembrane domains and approximately 25% amino acid sequence identity to the Streptococcus pyogenes HA synthase, HasA. Furthermore, expression of any one AAS gene in transfected mammalian cells leads to high levels of HA biosynthesis. We now report the chromosomal localization of the three HAS genes in human and in mouse. The genes localized to three different positions within both the human and the mouse genomes. HAS1 was localized to the human chromosome 19q13.3-q13.4 boundary and Has1 to mouse Chr 17. HAS2 was localized to human chromosome 8q24.12 and Has2 to mouse Chr 15. HAS3 was localized to human chromosome 16q22.1 and Has3 to mouse Chr 8, The map position for HAS1 reinforces the recently reported relationship between a small region of human chromosome 19q and proximal mouse chromosome 17, HAS2 mapped outside the predicted critical region delineated for the Langer-Giedion syndrome and can thus be excluded as a candidate gene for this genetic syndrome. (C) 1997 Academic Press.
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