Literature DB >> 3478298

Localization of the gene for the erythroid anion exchange protein, band 3 (EMPB3), to human chromosome 17.

L C Showe1, M Ballantine, K Huebner.   

Abstract

We have isolated genomic DNA clones which code for the human erythroid membrane protein band 3 (EMPB3). The identification of the gene has been confirmed by comparison of the amino acid sequence derived from the nucleotide sequence for two restriction fragments from the 5' end of the gene. Two exons have been identified. One exon encodes 20 amino acids which are identical to residues 36 to 56 of the band 3 protein, and the other encodes 44 amino acids homologous to residues 118 to 162. Southern analysis of genomic DNA derived from a panel of rodent-human somatic cell hybrids, which retain different complements of human chromosomes, with band 3 probes has allowed us to localize EMPB3 to human chromosome 17. The gene has been further localized between 17q21 and qter by analysis of DNA from somatic cell hybrids which carry derivative chromosomes from translocations involving chromosome 17 and either chromosome 15 or 21.

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Year:  1987        PMID: 3478298     DOI: 10.1016/0888-7543(87)90107-8

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  10 in total

Review 1.  Mouse chromosome 11.

Authors:  A M Buchberg; M S Buckwalter; S A Camper
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Mouse chromosome 11.

Authors:  A M Buchberg; J J Moskow; M S Buckwalter; S A Camper
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  The gene for human erythrocyte protein 4.2 maps to chromosome 15q15.

Authors:  V Najfeld; S G Ballard; J Menninger; D C Ward; E E Bouhassira; R S Schwartz; R L Nagel; A C Rybicki
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

4.  Chromosomal mapping of the rat Slc4a family of anion exchanger genes, Ae1, Ae2, and Ae3.

Authors:  J S Simon; G Deshmukh; F J Couch; S D Merajver; B L Weber; P Van Vooren; F Tissil; J Szpirer; C Szpirer; S L Alper; H J Jacob; F C Brosius
Journal:  Mamm Genome       Date:  1996-05       Impact factor: 2.957

5.  Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis.

Authors:  F E Karet; F J Gainza; A Z Györy; R J Unwin; O Wrong; M J Tanner; A Nayir; H Alpay; F Santos; S A Hulton; A Bakkaloglu; S Ozen; M J Cunningham; A di Pietro; W G Walker; R P Lifton
Journal:  Proc Natl Acad Sci U S A       Date:  1998-05-26       Impact factor: 11.205

6.  Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1).

Authors:  S E Lux; K M John; R R Kopito; H F Lodish
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

7.  Chromosomal location of the murine anion exchanger genes encoding AE2 and AE3.

Authors:  R A White; E N Geissler; L R Adkison; L L Dowler; S L Alper; S E Lux
Journal:  Mamm Genome       Date:  1994-12       Impact factor: 2.957

8.  A novel SLC4A1 variant in an autosomal dominant distal renal tubular acidosis family with a severe phenotype.

Authors:  Leping Shao; Yan Xu; Qian Dong; Yanhua Lang; Shaoheng Yue; Zhimin Miao
Journal:  Endocrine       Date:  2010-04-17       Impact factor: 3.633

9.  The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator.

Authors:  J Kere; P Sistonen; C Holmberg; A de la Chapelle
Journal:  Proc Natl Acad Sci U S A       Date:  1993-11-15       Impact factor: 11.205

Review 10.  Heteromeric Solute Carriers: Function, Structure, Pathology and Pharmacology.

Authors:  Stephen J Fairweather; Nishank Shah; Stefan Brӧer
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

  10 in total

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