Literature DB >> 6282177

Assignment of phosphoglycerate mutase (PGAMA) to human chromosome 10. Regional mapping of GOT1 and PGAMA to subbands 10q26.1 (or q25.3).

C Junien, S Despoisse, C Turleau, J de Grouchy, T Bucher, R Fundele.   

Abstract

Human phosphoglycerate mutase (PGAM, EC 2.7.5.3) is under the control of two structural loci that code for subunits A and B. By means of gene-dosage studies, Bücher et al. (1980) have assigned the loci for GOT1 and PGAMA to chromosome 19 of Mus musculus. Because of the known homologies between human and murine chromosomes, gene dosage studies were carried out in erythrocytes from one patient trisomic for the entire band 10q26 and from another patient monosomic for 10q26.2 and q26.3. Results were compatible with the assignment of PGAMA and GOT1 to 10q26.1 (or 10q25.3).

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Year:  1982        PMID： 6282177

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  9 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34----7q22.

Authors:  F Barichard; V Joulin; I Henry; M C Garel; C Valentin; R Rosa; M Cohen-Solal; C Junien
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

Review 3.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

4.  A precise localization of a mouse gene encoding increased phosphoglycerate mutase activity (Pgam1e1) on chromosome 19.

Authors:  W Pretsch; J Favor
Journal:  Mamm Genome       Date:  1996-08       Impact factor: 2.957

5.  A second locus encoding elevated phosphoglycerate mutase activity (Pgam2e) maps to mouse chromosome 4.

Authors:  W Pretsch; J Favor
Journal:  Mamm Genome       Date:  1997-04       Impact factor: 2.957

Review 6.  Eleven new cases of del(9p) and features from 80 cases.

Authors:  J L Huret; C Leonard; B Forestier; M O Rethoré; J Lejeune
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

7.  Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

Authors:  J Brusnický; K M van Heerden; G de Jong; A S Cronjé; A E Retief
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

8.  A case of interstitial deletion of 10q25.2----q26.1.

Authors:  D E Rooney; K Williams; D V Coleman; A Habel
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

9.  In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13.

Authors:  J Castella-Escola; M G Mattei; D M Ojcius; E Passage; C Valentin; M Cohen-Solal
Journal:  Hum Genet       Date:  1990-01       Impact factor: 4.132
  9 in total

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