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New Zealand White (Rabbit) — Cerebral palsy, RHOB-related (hereditary; OMIA-verified breed predisposition)

companion_breed_health_new_zealand_white_rabbit_omia6041_rabbit

Other Compilations derived_from_dataset companion-breed-health

New Zealand White (Rabbit) — Cerebral palsy, RHOB-related (hereditary; OMIA-verified breed predisposition)

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

Claims

  • Breed: New Zealand White (Rabbit)
  • Disorder:
  • Summary: Wu et al. (2024) created a rabbit model using the SpG-BE4max system to mimic a de novo RhoB p.S73F mutation associated with cerebral palsy in humans. This study involves genetically modified organisms (GMO).brbr
  • Defect: yes

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: Entrez Gene ID 398298915 (no symbol in OMIA GeneSynonym) — OMIA Phene_Gene

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.

  • 2024. The RhoB p.S73F mutation leads to cerebral palsy through dysregulation of lipid homeostasis. EMBO Mol Med — PubMed:PMID39080495 | DOI:10.1038/s44321-024-00113-2 — OMIA Phene_Article / Article

Machine access

AI agents: this compilation is also available as GET /api/v1/llm_context?topic=companion_breed_health_new_zealand_white_rabbit_omia6041_rabbit (max 500 tokens, whitelisted).

Raw JSON ↗ llm.txt OpenAPI