Entry - *489500 - XG REGULATOR; XGR - OMIM

 
 
* 489500

XG REGULATOR; XGR


Alternative titles; symbols

XG AND MIC2 EXPRESSION ON ERYTHROCYTES


Cytogenetic location: Yp11     Genomic coordinates (GRCh38): Y:1-10,400,000


▼ TEXT

Goodfellow et al. (1987) presented evidence suggesting the existence of a pseudoautosomal locus that regulates the expression of MIC2 (313470) and XG (300879). This would place the postulated locus at Xp22.32 (Goodfellow, 1990) and at Yp11.


▼ REFERENCES

  1. Goodfellow, P. J. Personal Communication. London, England 9/9/1990.

  2. Goodfellow, P. J., Pritchard, C., Tippett, P., Goodfellow, P. N. Recombination between the X and Y chromosomes: implications for the relationship between MIC2, XG and YG. Ann. Hum. Genet. 51: 161-167, 1987. [PubMed: 3502698, related citations] [Full Text]


Creation Date:
Victor A. McKusick : 5/25/1993
Edit History:
mgross : 09/11/2012
davew : 7/25/1994
mimadm : 3/11/1994
carol : 5/25/1993

* 489500

XG REGULATOR; XGR


Alternative titles; symbols

XG AND MIC2 EXPRESSION ON ERYTHROCYTES


Cytogenetic location: Yp11     Genomic coordinates (GRCh38): Y:1-10,400,000


TEXT

Goodfellow et al. (1987) presented evidence suggesting the existence of a pseudoautosomal locus that regulates the expression of MIC2 (313470) and XG (300879). This would place the postulated locus at Xp22.32 (Goodfellow, 1990) and at Yp11.


REFERENCES

  1. Goodfellow, P. J. Personal Communication. London, England 9/9/1990.

  2. Goodfellow, P. J., Pritchard, C., Tippett, P., Goodfellow, P. N. Recombination between the X and Y chromosomes: implications for the relationship between MIC2, XG and YG. Ann. Hum. Genet. 51: 161-167, 1987. [PubMed: 3502698] [Full Text: https://doi.org/10.1111/j.1469-1809.1987.tb01058.x]


Creation Date:
Victor A. McKusick : 5/25/1993

Edit History:
mgross : 09/11/2012
davew : 7/25/1994
mimadm : 3/11/1994
carol : 5/25/1993



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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: May 3, 2024