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

Evolutionary diversification of DYX1C1 transcripts via an HERV-H LTR integration event.

Genes & genetic systems - 1 Jan 2011

Kim Yun-Ji, Huh Jae-Won, Kim Dae-Soo, Han Kyudong, Kim Hwan-Mook, Kim Heui-Soo

Abstract excerpt

DYX1C1 is a candidate gene for developmental dyslexia and has three alternative pre-mRNA spliced forms in the human genome. One of the transcripts contains an HERV-H LTR that could affect the expression level of DYX1C1. We speculate that the HERV-H LTR integrated into the DYX1C1 locus in the catarrhine lineage after its divergence from the platyrrhine lineage. Reverse transcription-PCR of the HERV-H LTR-related...

Read the complete abstract on PubMed

Topics

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

Share to Genome, Human
Share to Chromosomes, Mammalian
Share to Cytoskeletal Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Endogenous Retroviruses

Share to Gene Duplication

Share to Macaca mulatta

Share to Terminal Repeat Sequences

Share to Virus Integration

Source

Identifiers

PMID: 22214596
DOI: 10.1266/ggs.86.277

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Evolutionary diversification of DYX1C1 transcripts via an HERV-H LTR integration event.PMID 22214596Read ↗

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.Semantic proximity Read ↗

Molecular characterization of the DYX1C1 gene and its application as a cancer biomarker.Semantic proximity Read ↗

Identification and expression analysis of human endogenous retrovirus Y (HERV-Y) in various human tissues.Semantic proximity Read ↗

Human endogenous retrovirus K14C drove genomic diversification of the Y chromosome during primate evolution.Semantic proximity Read ↗

The birth of a human-specific neural gene by incomplete duplication and gene fusion.Semantic proximity Read ↗

Functional evolutionary convergence of long noncoding RNAs involved in embryonic developmentSemantic proximity Read ↗

Recurrent 8q13.2-13.3 microdeletions associated with branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks.Semantic proximity Read ↗

Birth of two chimeric genes in the Hominidae lineage.Semantic proximity Read ↗

The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.Semantic proximity Read ↗

Sequence, "subtle" alternative splicing and expression of the CYYR1 (cysteine/tyrosine-rich 1) mRNA in human neuroendocrine tumors.Semantic proximity Read ↗

Functional consequences of new exon acquisition in mammalian chromodomain Y-like (CDYL) genes.Semantic proximity Read ↗

Identification of a novel human doublecortin-domain-containing gene (DCDC1) expressed mainly in testis.Semantic proximity Read ↗

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