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Rabbit (Oryctolagus cuniculus) — Hypercholesterolaemia, PCSK9-related (hereditary; OMIA-verified species predisposition)

companion_species_health_hypercholesterolaemia_pcsk9_related_rabbit

Other Compilations derived_from_dataset companion-species-health

Rabbit (Oryctolagus cuniculus) — Hypercholesterolaemia, PCSK9-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: Hypercholesterolaemia, PCSK9-related
  • Summary: Genetically-modified organism; 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: Entrez Gene ID 389105140 (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.

  • 2021. Construction of point mutation rabbits using CRISPR/Cas9. Zhejiang Da Xue Xue Bao Yi Xue Ban — PubMed:PMID34137224 | DOI:10.3724/zdxbyxb-2021-0133 — 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:603776 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:607786 (type: gene) — OMIA Group_OMIM (via OMIA_ID)

Machine access

AI agents: this compilation is also available as GET /api/v1/llm_context?topic=companion_species_health_hypercholesterolaemia_pcsk9_related_rabbit (max 500 tokens, whitelisted).

Raw JSON ↗ llm.txt OpenAPI