Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic screening of the canine zinc finger protein multitype 2 (cZFPM2) gene in dogs with tetralogy of Fallot (TOF).

Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie - 1 Aug 2009

Lee J-S, Hyun C

Abstract excerpt

A recent genetic study in humans where the ZFPM2 gene was screened for mutations revealed a heterozygous mutation that was found to contribute to several sporadic cases of tetralogy of Fallot (TOF). We hypothesized that this would also hold true for a study group of dogs with TOF. We isolated the full-length cDNA of the canine ZFPM2 and aligned the deduced amino acid sequence against sequences from other species....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Conserved Sequence
Share to Dogs

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Protein Structure, Tertiary

Share to RNA Splice Sites

Share to Sequence Alignment

Share to Tetralogy of Fallot

Share to Zinc Fingers

Source

Identifiers

PMID: 19630881
DOI: 10.1111/j.1439-0388.2008.00776.x

Genes

ZFPM2

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic screening of the canine zinc finger protein multitype 2 (cZFPM2) gene in dogs with tetralogy of Fallot (TOF).PMID 19630881Read ↗

A novel mitofusin 2 mutation causes canine fetal-onset neuroaxonal dystrophy.Semantic proximity Read ↗

New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle.Semantic proximity Read ↗

Prevalence and penetrance of ZFPM2 mutations and deletions causing congenital diaphragmatic hernia.Semantic proximity Read ↗

Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations.Semantic proximity Read ↗

Mutations ofZFPM2/FOG2 gene in sporadic cases of tetralogy of FallotSemantic proximity Read ↗

A mutation in the canine gene encoding folliculin-interacting protein 2 (FNIP2) associated with a unique disruption in spinal cord myelination.Semantic proximity Read ↗

Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic Tetralogy of Fallot and double outlet right ventricle in a Chinese Han population.Semantic proximity Read ↗

Evaluation of tafazzin as candidate for dilated cardiomyopathy in Irish wolfhounds.Semantic proximity Read ↗

Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients.Semantic proximity Read ↗

PITX2 loss-of-function mutation contributes to tetralogy of FallotSemantic proximity Read ↗

Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types.Semantic proximity Read ↗

ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.