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Article

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis.

Nature genetics - 1 Dec 2003

Helms Cynthia, Cao Li, Krueger James G, Wijsman Ellen M, Chamian Francesca, Gordon Derek, Heffernan Michael, Daw Jil A Wright, Robarge Jason, Ott Jurg, Kwok Pui-Yan, Menter Alan, Bowcock Anne M

Abstract excerpt

Psoriasis (OMIM 177900) is a chronic inflammatory skin disorder of unknown pathogenesis affecting approximately 2% of the Western population. It occurs more frequently in individuals with human immunodeficiency virus, and 20-30% of individuals with psoriasis have psoriatic arthritis. Psoriasis is associated with HLA class I alleles, and previous linkage analysis by our group identified a second psoriasis locus at...

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Share to Arylamine N-Acetyltransferase
Share to Chromosomes, Human, Pair 17

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Core Binding Factor Alpha 2 Subunit

Share to Electrophoretic Mobility Shift Assay

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Source

Identifiers

PMID: 14608357
DOI: 10.1038/ng1268

Genes

NAT9
RUNX1
NHERF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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