Entry - *147566 - INTERFERON, ALPHA-6; IFNA6 - OMIM

 
 
* 147566

INTERFERON, ALPHA-6; IFNA6


HGNC Approved Gene Symbol: IFNA6

Cytogenetic location: 9p21.3     Genomic coordinates (GRCh38): 9:21,350,318-21,350,887 (from NCBI)


TEXT

▼ Mapping

The IFNA6 gene was positioned in the cluster of interferon genes on 9p22 by deletion mapping (Olopade et al., 1992).


▼ REFERENCES

  1. Olopade, O. I., Bohlander, S. K., Pomykala, H., Maltepe, E., Van Melle, E., Le Beau, M. M., Diaz, M. O. Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia. Genomics 14: 437-443, 1992. [PubMed: 1385305, related citations] [Full Text]


Creation Date:
Victor A. McKusick : 6/8/1994
Edit History:
alopez : 02/21/2014
jason : 6/8/1994

* 147566

INTERFERON, ALPHA-6; IFNA6


HGNC Approved Gene Symbol: IFNA6

Cytogenetic location: 9p21.3     Genomic coordinates (GRCh38): 9:21,350,318-21,350,887 (from NCBI)


TEXT

Mapping

The IFNA6 gene was positioned in the cluster of interferon genes on 9p22 by deletion mapping (Olopade et al., 1992).


REFERENCES

  1. Olopade, O. I., Bohlander, S. K., Pomykala, H., Maltepe, E., Van Melle, E., Le Beau, M. M., Diaz, M. O. Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia. Genomics 14: 437-443, 1992. [PubMed: 1385305] [Full Text: https://doi.org/10.1016/s0888-7543(05)80238-1]


Creation Date:
Victor A. McKusick : 6/8/1994

Edit History:
alopez : 02/21/2014
jason : 6/8/1994



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.

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 30, 2024