Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisation

H J Eyre; P A Akkari; C Meredith; S D Wilton; D C Callen; L Kedes; N G Laing

doi:10.1159/000133467

Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisation

Cytogenet Cell Genet. 1993;62(2-3):181-2. doi: 10.1159/000133467.

Authors

H J Eyre¹, P A Akkari, C Meredith, S D Wilton, D C Callen, L Kedes, N G Laing

Affiliation

¹ Department of Cytogenetics and Molecular Genetics, Adelaide Children's Hospital, Australia.

PMID: 8428521
DOI: 10.1159/000133467

Abstract

The human gene for slow-twitch skeletal muscle troponin I (TNNI1) has previously been mapped to 1q12-->qter using somatic cell hybrids. The TNNI1 locus has now been further localised to 1q32 using fluorescence in situ hybridization. This result confirms the previous assignment of this locus and maps the gene to a single chromosome band.

Publication types

Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.

MeSH terms

Chromosome Mapping
Chromosomes, Human, Pair 1*
Genomic Library
Humans
In Situ Hybridization, Fluorescence
Male
Terminator Regions, Genetic
Troponin / genetics*

Substances

Troponin