Entry - *400034 - CHONDROITIN SULFATE PROTEOGLYCAN 4 PSEUDOGENE 1, Y-LINKED; CSPG4P1Y - OMIM

 
 
* 400034

CHONDROITIN SULFATE PROTEOGLYCAN 4 PSEUDOGENE 1, Y-LINKED; CSPG4P1Y


Alternative titles; symbols

CHONDROITIN SULFATE PROTEOGLYCAN 4-LIKE, Y-LINKED; CSPG4LY
CSPG4-LIKE, Y-LINKED


HGNC Approved Gene Symbol: CSPG4P1Y

Cytogenetic location: Yq11.23     Genomic coordinates (GRCh38): Y:25,482,908-25,486,705 (from NCBI)


TEXT

▼ Cloning and Expression

Skaletsky et al. (2003) stated that CSPG4LY is transcribed, but it does not appear to encode a protein.


▼ Mapping

Skaletsky et al. (2003) identified 2 copies of the CSPG4LY gene on chromosome Yq. The genes are in opposite orientation and are located within the male-specific region of chromosome Y (MSY).


▼ Molecular Genetics

Repping et al. (2004) identified the b2/b3 deletion within the AZFc region (415000) of the Y chromosome, in which 1 of the 2 copies of the CSPG4LY gene is deleted. The b2/b3 deletion has no obvious effect on fitness.


▼ REFERENCES

  1. Repping, S., van Daalen, S. K. M., Korver, C. M., Brown, L. G., Marszalek, J. D., Gianotten, J., Oates, R. D., Silber, S., van der Veen, F., Page, D. C., Rozen, S. A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region. Genomics 83: 1046-1052, 2004. [PubMed: 15177557, related citations] [Full Text]

  2. Skaletsky, H., Kuroda-Kawaguchi, T., Minx, P. J., Cordum, H. S., Hillier, L., Brown, L. G., Repping, S., Pyntikova, T., Ali, J., Bieri, T., Chinwalla, A., Delehaunty, A., and 28 others. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature 423: 825-837, 2003. [PubMed: 12815422, related citations] [Full Text]


Creation Date:
Patricia A. Hartz : 7/7/2004
Edit History:
carol : 10/20/2017
mgross : 07/07/2004

* 400034

CHONDROITIN SULFATE PROTEOGLYCAN 4 PSEUDOGENE 1, Y-LINKED; CSPG4P1Y


Alternative titles; symbols

CHONDROITIN SULFATE PROTEOGLYCAN 4-LIKE, Y-LINKED; CSPG4LY
CSPG4-LIKE, Y-LINKED


HGNC Approved Gene Symbol: CSPG4P1Y

Cytogenetic location: Yq11.23     Genomic coordinates (GRCh38): Y:25,482,908-25,486,705 (from NCBI)


TEXT

Cloning and Expression

Skaletsky et al. (2003) stated that CSPG4LY is transcribed, but it does not appear to encode a protein.


Mapping

Skaletsky et al. (2003) identified 2 copies of the CSPG4LY gene on chromosome Yq. The genes are in opposite orientation and are located within the male-specific region of chromosome Y (MSY).


Molecular Genetics

Repping et al. (2004) identified the b2/b3 deletion within the AZFc region (415000) of the Y chromosome, in which 1 of the 2 copies of the CSPG4LY gene is deleted. The b2/b3 deletion has no obvious effect on fitness.


REFERENCES

  1. Repping, S., van Daalen, S. K. M., Korver, C. M., Brown, L. G., Marszalek, J. D., Gianotten, J., Oates, R. D., Silber, S., van der Veen, F., Page, D. C., Rozen, S. A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region. Genomics 83: 1046-1052, 2004. [PubMed: 15177557] [Full Text: https://doi.org/10.1016/j.ygeno.2003.12.018]

  2. Skaletsky, H., Kuroda-Kawaguchi, T., Minx, P. J., Cordum, H. S., Hillier, L., Brown, L. G., Repping, S., Pyntikova, T., Ali, J., Bieri, T., Chinwalla, A., Delehaunty, A., and 28 others. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature 423: 825-837, 2003. [PubMed: 12815422] [Full Text: https://doi.org/10.1038/nature01722]


Creation Date:
Patricia A. Hartz : 7/7/2004

Edit History:
carol : 10/20/2017
mgross : 07/07/2004



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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