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10q25.3

A chromosome band present on 10q
National Institutes of Health

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10qChromosomesKCNK18 wt AlleleSHTN1 wt Allele

Papers overview

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2020
2020
Research of the Genotype Association by Locus Rs7903146 of the Tcf7l2 Gene and the Risk of Abdominal Obesity Development among Young Residents of the North
Currently, interest in studying obesity as a chronic inflammatory disease continues to grow. Despite numerous recommendations for… 
2017
2017
Association of GWAS-Reported Variant rs11196288 near HABP2 with Ischemic Stroke in Chinese Han Population
A recent genome-wide association analysis identified a novel single nucleotide polymorphism locus on chromosome 10q25.3… 
2005
2005
Down-regulation of DMBT1 gene expression in human oral squamous cell carcinoma.
Deleted in malignant brain tumors 1 (DMBT1) gene was recently isolated on chromosome 10q25.3-26.1 and has been proposed as a… 
2005
2005
Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter)
2000
2000
Cloning, chromosomal sublocalization of the human soluble aminopeptidase P gene (XPNPEP1) to 10q25.3 and conservation of the putative proton shuttle and metal ligand binding sites with XPNPEP2.
Human soluble ("cytosolic") aminopeptidase P (hsAmP) is an aminoacylprolyl hydrolase (EC 3.4.11.9) present in all tissues yet… 
2000
2000
A gene-anchored map position of the rat warfarin-resistance locus, Rw, and its orthologs in mice and humans.
The locus underlying hereditary resistance to the anticoagulant warfarin (symbol in the rat, Rw) was placed in relation to 8… 
1997
1997
Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologies
Female pseudohermaphroditism with caudal dysplasia is a clinical entity in which normal‐appearing male genitalia may occur in the… 
1983
1983
Clinical features of monosomy 10qter.
The authors report a 10qter deletion in a 16-month-old boy. The patient's phenotype includes: low birth weight, mental and growth… 
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