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Chromosome 7q31

Known as: 7q31 
A chromosome band present on 7q
National Institutes of Health

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8 relations
Chromosome 7qChromosomesFAM3C wt AlleleFOXP2 wt Allele

Broader (1)

Chromosomes, Human

Papers overview

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2011
2011
Association study of the CNS patterning genes and autism in Han Chinese in Taiwan
2008
2008
Expression changes of CAV1 and EZH2, located on 7q31 approximately q36, are rarely related to genomic alterations in primary prostate carcinoma.
2005
2005
Chromosome 7 deletions are associated with unfavorable prognosis in myelofibrosis with myeloid metaplasia.
Several studies suggest a poor prognosis for patients with myelofibrosis (MF) with an abnormal karyotype, but the prognostic… 
Highly Cited
2003
Highly Cited
2003
No association between the EN2 gene and autistic disorder
A utistic spectrum disorders (MIM 209850), which include autism, Asperger syndrome, and pervasive developmental disorder (PDD… 
Highly Cited
1998
Highly Cited
1998
Human N-acetylglucosamine-6-O-sulfotransferase involved in the biosynthesis of 6-sulfo sialyl Lewis X: molecular cloning, chromosomal mapping, and expression in various organs and tumor cells.
N-Acetylglucosamine-6-O-sulfotransferase catalyzes the transfer of sulfate from 3'-phosphoadenosine 5'-phosphosulfate to position… 
Highly Cited
1997
Highly Cited
1997
A molecular cytogenetic analysis of 7q31 in prostate cancer.
1996
1996
Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET.
In breast cancer, loss of heterozygosity (LOH) has been described on the long arm of chromosome 7 at band q31, suggesting the… 
1996
1996
Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31.
Congenital chloride diarrhea affects intestinal transportation of electrolytes, resulting in potentially fatal diarrhea. Linkage… 
1995
1995
452 Loss of heterozygosity on 7Q31 occurs early during breast tumorigenesis
1992
1992
Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7
Monosomy or deletion of chromosome 7 is a frequent finding in both de novo and secondary acute myeloid leukaemia (AML) and… 
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