Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

ZNF41 gene

Known as: MGC8941, MRX89, ZINC FINGER PROTEIN 41 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Verification of ZNF41 as a serum candidate biomarker for ventricular septal defect
Objective To validate zinc finger protein 41( ZNF41) as a serum candidate biomarker in patients with ventricular septal defect… Expand
Is this relevant?
2013
2013
Whole Genome Sequencing Analysis of an Idiopathic Intellectual Disability Syndrome
We present a new idiopathic intellectual disability syndrome accompanied with distinctive facial dysmorphology. X-chromosome… Expand
  • figure 1
Is this relevant?
2012
2012
335.4 kb microduplication in chromosome band Xp11.2p11.3 associated with developmental delay, growth retardation, autistic disorder and dysmorphic features.
About 10% of causative mutations for mental retardation in male patients involve X chromosome (X-linked mental retardation, XLMR… Expand
Is this relevant?
2010
2010
Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation.
ZNF630 is a member of the primate-specific Xp11 zinc finger gene cluster that consists of six closely related genes, of which… Expand
  • table I
  • figure 1
  • figure 2
  • table II
Is this relevant?
Review
2005
Review
2005
X linked mental retardation: a clinical guide.
Mental retardation is more common in males than females in the population, assumed to be due to mutations on the X chromosome… Expand
  • table 1
  • table 2
  • figure 1
  • table 3
Is this relevant?
2004
2004
Loss of functional ZNF41 in a female patient with a balanced translocation t(X;7)(p11.3;q11.21) and severe mental retardation: evidence for a role for ZNF41 in cognitive development
 
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation.
Nonsyndromic X-linked mental retardation (MRX) is defined by an X-linked inheritance pattern of low IQ, problems with adaptive… Expand
  • figure 4
Is this relevant?
1999
1999
Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41
ZNF41 belongs to a cluster of human zinc finger genes residing within a gene-rich region at Xp11.23. ZNF41 encodes a KRAB/FPB (Kr… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
1994
1994
Clustered organization of Krüppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: a physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1.
The ZNF21, ZNF41, and ZNF81 genes encode Krüppel-type zinc-finger proteins (ZFPs) and have previously been mapped to chromosome… Expand
Is this relevant?
1991
1991
Isolation and expression analysis of a human zinc finger gene (ZNF41) located on the short arm of the X chromosome.
We have isolated a novel human zinc finger gene, ZNF41, from a human X-chromosome-specific library. Nucleotide sequence analysis… Expand
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE