Entry - *148022 - KERATIN-ASSOCIATED PROTEIN 5-1; KRTAP5-1 - OMIM

 
 
* 148022

KERATIN-ASSOCIATED PROTEIN 5-1; KRTAP5-1


Alternative titles; symbols

KERATIN, CUTICLE, ULTRAHIGH-SULFUR, 1-LIKE; KRN1L


HGNC Approved Gene Symbol: KRTAP5-1

Cytogenetic location: 11p15.5     Genomic coordinates (GRCh38): 11:1,584,342-1,585,283 (from NCBI)


TEXT

▼ Mapping

MacKinnon et al. (1991) found by in situ hybridization that a gene with similarities to the KRN1 gene (148021), which maps to chromosome 11q13.5, is located on 11p15.5.


▼ REFERENCES

  1. MacKinnon, P. J., Powell, B. C., Rogers, G. E., Baker, E. G., MacKinnon, R. N., Hyland, V. J., Callen, D. F., Sutherland, G. R. An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15. Mammalian Genome 1: 53-56, 1991. [PubMed: 1724400, related citations] [Full Text]


Creation Date:
Victor A. McKusick : 12/14/1990
Edit History:
alopez : 10/23/2014
carol : 3/26/2008
carol : 7/20/1998
supermim : 3/16/1992
carol : 12/14/1990

* 148022

KERATIN-ASSOCIATED PROTEIN 5-1; KRTAP5-1


Alternative titles; symbols

KERATIN, CUTICLE, ULTRAHIGH-SULFUR, 1-LIKE; KRN1L


HGNC Approved Gene Symbol: KRTAP5-1

Cytogenetic location: 11p15.5     Genomic coordinates (GRCh38): 11:1,584,342-1,585,283 (from NCBI)


TEXT

Mapping

MacKinnon et al. (1991) found by in situ hybridization that a gene with similarities to the KRN1 gene (148021), which maps to chromosome 11q13.5, is located on 11p15.5.


REFERENCES

  1. MacKinnon, P. J., Powell, B. C., Rogers, G. E., Baker, E. G., MacKinnon, R. N., Hyland, V. J., Callen, D. F., Sutherland, G. R. An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15. Mammalian Genome 1: 53-56, 1991. [PubMed: 1724400] [Full Text: https://doi.org/10.1007/BF00350846]


Creation Date:
Victor A. McKusick : 12/14/1990

Edit History:
alopez : 10/23/2014
carol : 3/26/2008
carol : 7/20/1998
supermim : 3/16/1992
carol : 12/14/1990



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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 6, 2024