Entry - *194557 - ZINC FINGER PROTEIN 20; ZNF20 - OMIM

 
 
* 194557

ZINC FINGER PROTEIN 20; ZNF20


Alternative titles; symbols

KOX13


HGNC Approved Gene Symbol: ZNF20

Cytogenetic location: 19p13.2   Genomic coordinates (GRCh38) : 19:12,131,350-12,140,350 (from NCBI)


TEXT

▼ Mapping

Rousseau-Merck et al. (1993) mapped KOX6 (194556) and KOX13 (ZNF20) to chromosome 19p13.3-p13.2. They showed by pulsed field gel electrophoresis experiments that the pair of genes lies within a DNA segment less than 200 kb long.


▼ REFERENCES

  1. Rousseau-Merck, M.-F., Hillion, J., Jonveaux, P., Couillin, P., Seite, P., Thiesen, H.-J., Berger, R. Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19. Hum. Genet. 92: 583-587, 1993. [PubMed: 8262519, related citations] [Full Text]


Creation Date:
Victor A. McKusick : 4/21/1994
Edit History:
alopez : 07/07/2010
dkim : 6/26/1998
mark : 5/14/1996
carol : 4/21/1994

* 194557

ZINC FINGER PROTEIN 20; ZNF20


Alternative titles; symbols

KOX13


HGNC Approved Gene Symbol: ZNF20

Cytogenetic location: 19p13.2   Genomic coordinates (GRCh38) : 19:12,131,350-12,140,350 (from NCBI)


TEXT

Mapping

Rousseau-Merck et al. (1993) mapped KOX6 (194556) and KOX13 (ZNF20) to chromosome 19p13.3-p13.2. They showed by pulsed field gel electrophoresis experiments that the pair of genes lies within a DNA segment less than 200 kb long.


REFERENCES

  1. Rousseau-Merck, M.-F., Hillion, J., Jonveaux, P., Couillin, P., Seite, P., Thiesen, H.-J., Berger, R. Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19. Hum. Genet. 92: 583-587, 1993. [PubMed: 8262519] [Full Text: https://doi.org/10.1007/BF00420943]


Creation Date:
Victor A. McKusick : 4/21/1994

Edit History:
alopez : 07/07/2010
dkim : 6/26/1998
mark : 5/14/1996
carol : 4/21/1994



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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: Nov. 17, 2024