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SLX4 wt Allele

Known as: KIAA1784, FANCP, BTB (POZ) Domain Containing 12 Gene 
Human SLX4 wild-type allele is located in the vicinity of 16p13.3 and is approximately 30 kb in length. This allele, which encodes structure-specific… 
National Institutes of Health

Related topics

Related topics

3 relations
16p13.3DNA RepairEnzyme Induction

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Chapter 3 Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX 4 / FANCP
2012
2012
The nuclease hSNM 1 B / Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP / SLX 4
The recessive genetic disorder Fanconi anemia (FA) is clinically characterized by congenital defects, bone marrow failure and an… 
2011
2011
Cancel all Hollidays for SLX4 mutations: identification of a new Fanconi anemia subtype, FANCP
SLX4, a coordinator of structure‐specific endo‐nucleases, is mutated in a new Fanconi anemia subtype 
2011
2011
HotSpots Cancel all Hollidays for SLX 4 mutations : identification of a new Fanconi anemia subtype , FANCP
For the clinician, the two major challenges in correctly diagnosing Fanconi anemia (FA; OMIM# 227650) are its clinical… 
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