Entry - *300783 - CANCER/TESTIS ANTIGEN FAMILY 47, MEMBER A4; CT47A4 - OMIM

 
 
* 300783

CANCER/TESTIS ANTIGEN FAMILY 47, MEMBER A4; CT47A4


Alternative titles; symbols

CT47.4


HGNC Approved Gene Symbol: CT47A4

Cytogenetic location: Xq24     Genomic coordinates (GRCh38): X:120,967,886-120,971,208 (from NCBI)


TEXT

▼ Cloning and Expression

Chen et al. (2006) identified 13 tandem copies of the CT47 gene, including CT47A4, on chromosome Xq24.

Using an accession number provided by Strausberg et al. (2002) and assigned to CT47A11 (300592), (GenBank BC029540), Hartz (2009) identified 12 copies of the CT47 gene on chromosome Xq24 (build 36.1). Of these copies, 9 share 100% nucleotide identity, and 3 share over 90.0% nucleotide identity. All contain 3 exons.

See 300592 for further information.

▼ Mapping

Hartz (2009) mapped the duplications of the CT47 gene to chromosome Xq24 based on alignment of a sequence containing CT47A11 (GenBank AB097024) with the genomic sequence (build 36.1).

▼ REFERENCES

  1. Chen, Y.-T., Iseli, C., Venditti, C. A., Old, L. J., Simpson, A. J. G., Jongeneel, C. V. Identification of a new cancer/testis gene family, CT47, among expressed multicopy genes on the human X chromosome. Genes Chromosomes Cancer 45: 392-400, 2006. [PubMed: 16382448, related citations] [Full Text]

  2. Hartz, P. A. Personal Communication. Baltimore, Md. 6/26/2009.

  3. Strausberg, R. L., Feingold, E. A., Grouse, L. H., Derge, J. G., Klausner, R. D., Collins, F. S., Wagner, L., Shenmen, C. M., Schuler, G. D., Altschul, S. F., Zeeberg, B., Buetow, K. H., and 71 others. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc. Nat. Acad. Sci. 99: 16899-16903, 2002. [PubMed: 12477932, images, related citations] [Full Text]


Creation Date:
Patricia A. Hartz : 6/29/2009
Edit History:
wwang : 09/25/2009
wwang : 6/29/2009

* 300783

CANCER/TESTIS ANTIGEN FAMILY 47, MEMBER A4; CT47A4


Alternative titles; symbols

CT47.4


HGNC Approved Gene Symbol: CT47A4

Cytogenetic location: Xq24     Genomic coordinates (GRCh38): X:120,967,886-120,971,208 (from NCBI)


TEXT

Cloning and Expression

Chen et al. (2006) identified 13 tandem copies of the CT47 gene, including CT47A4, on chromosome Xq24.

Using an accession number provided by Strausberg et al. (2002) and assigned to CT47A11 (300592), (GenBank BC029540), Hartz (2009) identified 12 copies of the CT47 gene on chromosome Xq24 (build 36.1). Of these copies, 9 share 100% nucleotide identity, and 3 share over 90.0% nucleotide identity. All contain 3 exons.

See 300592 for further information.

Mapping

Hartz (2009) mapped the duplications of the CT47 gene to chromosome Xq24 based on alignment of a sequence containing CT47A11 (GenBank AB097024) with the genomic sequence (build 36.1).

REFERENCES

  1. Chen, Y.-T., Iseli, C., Venditti, C. A., Old, L. J., Simpson, A. J. G., Jongeneel, C. V. Identification of a new cancer/testis gene family, CT47, among expressed multicopy genes on the human X chromosome. Genes Chromosomes Cancer 45: 392-400, 2006. [PubMed: 16382448] [Full Text: https://doi.org/10.1002/gcc.20298]

  2. Hartz, P. A. Personal Communication. Baltimore, Md. 6/26/2009.

  3. Strausberg, R. L., Feingold, E. A., Grouse, L. H., Derge, J. G., Klausner, R. D., Collins, F. S., Wagner, L., Shenmen, C. M., Schuler, G. D., Altschul, S. F., Zeeberg, B., Buetow, K. H., and 71 others. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc. Nat. Acad. Sci. 99: 16899-16903, 2002. [PubMed: 12477932] [Full Text: https://doi.org/10.1073/pnas.242603899]


Creation Date:
Patricia A. Hartz : 6/29/2009

Edit History:
wwang : 09/25/2009
wwang : 6/29/2009



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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: April 19, 2024