Entry - *194525 - ZINC FINGER PROTEIN 19; ZNF19 - OMIM

 
 
* 194525

ZINC FINGER PROTEIN 19; ZNF19


Alternative titles; symbols

KOX12


HGNC Approved Gene Symbol: ZNF19

Cytogenetic location: 16q22.2     Genomic coordinates (GRCh38): 16:71,473,583-71,489,324 (from NCBI)


TEXT

▼ Cloning and Expression

Bray et al. (1991) screened a placental genomic library at moderate stringency with a degenerate oligodeoxynucleotide probe designed to hybridize to the his/cys (H/C) link region between adjoining zinc fingers. Genomic clones were cross-hybridized with a set of 30 zinc finger-encoding cDNAs (KOX1-KOX30) isolated from a human T-cell cDNA library. KOX12 matched one of the genomic clones.


▼ Mapping

Bray et al. (1991) mapped the ZNF19 gene (KOX12) to 16q22 by chromosomal in situ suppression hybridization with fluorescent probe detection.


▼ History

Rousseau-Merck et al. (1991) concluded from in situ hybridization experiments that ZNF19 shows 'a double localization on chromosome 19q13 and chromosome 16q23.'

▼ REFERENCES

  1. Bray, P., Lichter, P., Thiesen, H.-J., Ward, D. C., Dawid, I. B. Characterization and mapping of human genes encoding zinc finger proteins. Proc. Nat. Acad. Sci. 88: 9563-9567, 1991. [PubMed: 1946370, related citations] [Full Text]

  2. Rousseau-Merck, M.-F., Berger, R., Thiesen, H.-J. Chromosomal localization of ZNF19, ZNF22 and ZNF25, three members of the Kox genes family. (Abstract) Cytogenet. Cell Genet. 58: 1953, 1991.


Creation Date:
Victor A. McKusick : 12/4/1991
Edit History:
alopez : 07/06/2010
dkim : 6/26/1998
mark : 5/14/1996
supermim : 3/16/1992
carol : 2/23/1992
carol : 12/17/1991
carol : 12/4/1991

* 194525

ZINC FINGER PROTEIN 19; ZNF19


Alternative titles; symbols

KOX12


HGNC Approved Gene Symbol: ZNF19

Cytogenetic location: 16q22.2     Genomic coordinates (GRCh38): 16:71,473,583-71,489,324 (from NCBI)


TEXT

Cloning and Expression

Bray et al. (1991) screened a placental genomic library at moderate stringency with a degenerate oligodeoxynucleotide probe designed to hybridize to the his/cys (H/C) link region between adjoining zinc fingers. Genomic clones were cross-hybridized with a set of 30 zinc finger-encoding cDNAs (KOX1-KOX30) isolated from a human T-cell cDNA library. KOX12 matched one of the genomic clones.


Mapping

Bray et al. (1991) mapped the ZNF19 gene (KOX12) to 16q22 by chromosomal in situ suppression hybridization with fluorescent probe detection.


History

Rousseau-Merck et al. (1991) concluded from in situ hybridization experiments that ZNF19 shows 'a double localization on chromosome 19q13 and chromosome 16q23.'

REFERENCES

  1. Bray, P., Lichter, P., Thiesen, H.-J., Ward, D. C., Dawid, I. B. Characterization and mapping of human genes encoding zinc finger proteins. Proc. Nat. Acad. Sci. 88: 9563-9567, 1991. [PubMed: 1946370] [Full Text: https://doi.org/10.1073/pnas.88.21.9563]

  2. Rousseau-Merck, M.-F., Berger, R., Thiesen, H.-J. Chromosomal localization of ZNF19, ZNF22 and ZNF25, three members of the Kox genes family. (Abstract) Cytogenet. Cell Genet. 58: 1953, 1991.


Creation Date:
Victor A. McKusick : 12/4/1991

Edit History:
alopez : 07/06/2010
dkim : 6/26/1998
mark : 5/14/1996
supermim : 3/16/1992
carol : 2/23/1992
carol : 12/17/1991
carol : 12/4/1991



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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 4, 2024