← All Topics / companion-species-health

Rabbit (Oryctolagus cuniculus) — Short QT syndrome, KCNH2-related (hereditary; OMIA-verified species predisposition)

companion_species_health_short_qt_syndrome_kcnh2_related_rabbit

companion-species-health 564 tok en 2026-08-24

Rabbit (Oryctolagus cuniculus) — Short QT syndrome, KCNH2-related (hereditary; OMIA-verified species predisposition)

Source: first-hand OMIA (University of Sydney) species-specific hereditary-disorder record, saved verbatim to source_file; every claim below is a C1 byte-substring of it.

Claims

  • Species: Rabbit (Oryctolagus cuniculus)
  • Disorder: Short QT syndrome, KCNH2-related
  • Summary: This phene includes references to studies involving genetically modified organisms (GMO).

Associated gene(s)

Derived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.

  • Gene: ERG (Entrez Gene ID 388912484) — OMIA Phene_Gene / GeneSynonym

Evidence (references)

Derived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.

  • 2022. Transgenic rabbit models for cardiac disease research. Br J Pharmacol — PubMed:PMID33822374 | DOI:10.1111/bph.15484 — OMIA Phene_Article / Article
  • 2019. Transgenic short-QT syndrome 1 rabbits mimic the human disease phenotype with QT/action potential duration shortening in the atria and ventricles and increased ventricular tachycardia/ventricular fibrillation inducibility. Eur Heart J — PubMed:PMID30496390 | DOI:10.1093/eurheartj/ehy761 — OMIA Phene_Article / Article
  • 2024. Beneficial normalization of cardiac repolarization by carnitine in transgenic SQT1 rabbit models. Cardiovasc Res — PubMed:PMID39018021 | DOI:10.1093/cvr/cvae149 — OMIA Phene_Article / Article
  • 2025. AAV9-mediated KCNH2 suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndrome. Eur Heart J — PubMed:PMID40884219 | DOI:10.1093/eurheartj/ehaf660 — OMIA Phene_Article / Article

Comparative medicine (human OMIM)

Derived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.

  • OMIM:609620 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:152427 (type: gene) — OMIA Group_OMIM (via OMIA_ID)

Sources

Rabbit (Oryctolagus cuniculus) — Short QT syndrome, KCNH2-related (hereditary; OMIA-verified species predisposition)
Source document: OMIA — Online Mendelian Inheritance in Animals (University of Sydney)
OMIA — Online Mendelian Inheritance in Animals (University of Sydney)OMIA species-specific hereditary-disorder records (omia.org), derived from local OMIA database dump; dataset: https://doi.org/10.25910/2AMR-PV70retrieved 2026-08-24

Verification file: pdf-raw/species-health/rabbit_short_qt_syndrome_kcnh2_related_4727.txt

Machine access

AI agents: this page mirrors GET /api/v1/llm_context?topic=companion_species_health_short_qt_syndrome_kcnh2_related_rabbit (max 500 tokens, whitelisted). Rate limit 120 req/min for recognized AI crawlers.

Raw JSON ↗ llm.txt OpenAPI