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1p13.2

A chromosome band present on 1p
National Institutes of Health

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Chromosome 1 Short ArmChromosomesDCLRE1B wt AlleleEPS8L3 wt Allele

Papers overview

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2019
2019
Region 1p13.2 including the RSBN1, PTPN22, AP4B1 and long non‐coding RNA genes does not bear risk factors for endemic pemphigus foliaceus (fogo selvagem)
Pemphigus foliaceus (PF) is an autoimmune skin disease characterized by autoantibodies directed mainly against desmoglein‐1. The… 
2016
2016
Abstract LB-370: Fine mapping of 32 breast cancer risk loci in women of East Asian ancestry
Background: Genome-wide association studies (GWAS) have identified multiple genetic susceptibility loci for breast cancer risk… 
2011
2011
Evidence for PTPN22 R620W Polymorphism As the Sole Common Risk Variant for Rheumatoid Arthritis in the 1p13.2 Region
Objective. The PTPN22 rs2476601 genetic variant has been associated with rheumatoid arthritis (RA) and other autoimmune diseases… 
2011
2011
A new locus (SPG47) maps to 1p13.2–1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum
2011
2011
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses.
We report molecular cytogenetic characterization of mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy… 
2009
2009
Haploinsufficiency of the nerve growth factor beta gene in a 1p13 deleted female child with an insensitivity to pain
Pain insensitivity is mediated at the genetic level by the disruption of specific genes associated with neuronal development… 
2004
2004
Putative gene loci associated with carcinogenesis and metastasis of endocervical adenocarcinomas of uterus determined by conventional and array-based CGH.
2001
2001
Refined localization of twenty-one genes in subregion p13.1 of human chromosome 1
In this report, we describe a refinement of the human transcript map of chromosome 1p13.1, a subregion undergoing many… 
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