Entry - *194624 - ZINC FINGER PROTEIN 117; ZNF117 - OMIM

 
 
* 194624

ZINC FINGER PROTEIN 117; ZNF117


HGNC Approved Gene Symbol: ZNF117

Cytogenetic location: 7q11.21     Genomic coordinates (GRCh38): 7:64,971,772-64,991,036 (from NCBI)


TEXT

▼ Mapping

A cluster of Kruppel-type zinc finger genes of the KRAB subclass is located on human chromosome 19p13.1-p12. Bellefroid et al. (1992) reported that ZNF117 (HPF9), a closely related zinc finger gene of that KRAB subfamily, was located on 7q11.2 by in situ hybridization.


▼ REFERENCES

  1. Bellefroid, E. J., Ried, T., Riviere, M., Marine, J.-C., Levan, G., Szpirer, J., Szpirer, C., Ward, D. C., Martial, J. A. Localization of the human KRAB finger gene ZNF117 (HPF9) to chromosome 7q11.2. Genomics 14: 780-781, 1992. [PubMed: 1427907, related citations] [Full Text]


Creation Date:
Victor A. McKusick : 9/8/1993
Edit History:
alopez : 07/07/2010
dkim : 6/26/1998
carol : 9/8/1993

* 194624

ZINC FINGER PROTEIN 117; ZNF117


HGNC Approved Gene Symbol: ZNF117

Cytogenetic location: 7q11.21     Genomic coordinates (GRCh38): 7:64,971,772-64,991,036 (from NCBI)


TEXT

Mapping

A cluster of Kruppel-type zinc finger genes of the KRAB subclass is located on human chromosome 19p13.1-p12. Bellefroid et al. (1992) reported that ZNF117 (HPF9), a closely related zinc finger gene of that KRAB subfamily, was located on 7q11.2 by in situ hybridization.


REFERENCES

  1. Bellefroid, E. J., Ried, T., Riviere, M., Marine, J.-C., Levan, G., Szpirer, J., Szpirer, C., Ward, D. C., Martial, J. A. Localization of the human KRAB finger gene ZNF117 (HPF9) to chromosome 7q11.2. Genomics 14: 780-781, 1992. [PubMed: 1427907] [Full Text: https://doi.org/10.1016/s0888-7543(05)80185-5]


Creation Date:
Victor A. McKusick : 9/8/1993

Edit History:
alopez : 07/07/2010
dkim : 6/26/1998
carol : 9/8/1993



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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 5, 2024