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Rabbit (Oryctolagus cuniculus) — Hypoxanthine guanine phosphoribosyltransferase deficiency (hereditary; OMIA-verified species predisposition)

companion_species_health_hypoxanthine_guanine_phosphoribosyltransferase_deficiency_rabbit

companion-species-health 435 tok en 2026-08-24

Rabbit (Oryctolagus cuniculus) — Hypoxanthine guanine phosphoribosyltransferase deficiency (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: Hypoxanthine guanine phosphoribosyltransferase deficiency
  • Summary: This phene includes references to studies involving gene edited or 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: Entrez Gene ID 398298898 (no symbol in OMIA GeneSynonym) — OMIA Phene_Gene
  • OMIA molecular-genetics note: Yin et al. (2024) created a rabbit model for Lesch-Nyhan syndrome using CRISPR/Cas9 HPRT knock out.&

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. Establishment and characterization of Lesch-Nyhan syndrome rabbit model. Yi Chuan — PubMed:PMID38763775 | DOI:10.16288/j.yczz.24-012 — 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:300322 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:308000 (type: gene) — OMIA Group_OMIM (via OMIA_ID)

Sources

Rabbit (Oryctolagus cuniculus) — Hypoxanthine guanine phosphoribosyltransferase deficiency (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_hypoxanthine_guanine_phosphoribosyltransferase_deficiency_5966.txt

Machine access

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