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5q33.1

A chromosome band present on 5q.
National Institutes of Health

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7 relations
ANXA6 wt AlleleChromosomesGPX3 wt AlleleIRGM wt Allele

Papers overview

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2011
2011
A 10 Mb duplication in chromosome band 5q31.3-5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis.
2010
2010
An unusual case of granulomatous cutaneous T‐cell lymphoma showing subcutaneous/muscular involvement and a 5q33.1 deletion
1 Bieber T. Atopic dermatitis. N Engl J Med 2008; 358:1483–94. 2 Leung DY, Boguniewicz M, Howell MD et al. New insights into… 
2006
2006
Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia.
2006
2006
Identification of the microdeletion breakpoint in a GLRA1null allele of Turkish hyperekplexia patients
Hyperekplexia (startle disease) is a hereditary motor disease caused by mutations within the GLRA1 gene (Chr. 5q33.1), which… 
2004
2004
Molecular and Functional Characterisation of a new Mammalian Family of Proton-coupled Amino Acid Transporters
Proton-coupled amino acid transport (PAT) systems in the apical membrane of epithelial cells of the small intestine and the renal… 
Highly Cited
2003
Highly Cited
2003
A cluster of proton/amino acid transporter genes in the human and mouse genomes.
1992
1992
The human macrophage colony-stimulating factor gene is localized at chromosome 1 band p21 and not at 5q33.1
Macrophage colony-stimulating factor (M-CSF) is a homodimeric glycoprotein that supports the growth and differentiation of… 
1991
1991
Characterization of the 5q- breakpoint in an acute nonlymphocytic leukemia patient using pulsed-field gel electrophoresis.
Multiple genes of hematopoietic importance have been localized to the long arm of chromosome 5 including granulocytemacrophage… 
1990
1990
Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).
Here we report on a de novo apparently balanced reciprocal 5q;7p translocation in a 15-year-old girl with apparent Cohen syndrome… 
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