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Rabbit (Oryctolagus cuniculus) — Premature aging syndrome (hereditary; OMIA-verified species predisposition)

companion_species_health_premature_aging_syndrome_rabbit

companion-species-health 644 tok en 2026-08-24

Rabbit (Oryctolagus cuniculus) — Premature aging syndrome (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: Premature aging syndrome
  • Summary: The affected rabbits produced by Sui et al. (2019) are the result of "precise LMNA targeting in rabbits via co-injection of Cas9/sgRNA mRNA into zygotes", i.e. it is a knock-out model of human premature aging inherited disorders.

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 389109936 (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.

  • 1960. Hereditary premature sensescence of the rabbit. I. Chronic form; general features. J Exp Med — PubMed:PMID13733754 | DOI:10.1084/jem.111.4.485 — OMIA Phene_Article / Article
  • 1960. Hereditary premature senescence of the rabbit. II. Acute form; general features. J Exp Med — PubMed:PMID13733753 | DOI:10.1084/jem.111.4.505 — OMIA Phene_Article / Article
  • 2019. LMNA-mutated rabbits: A model of premature aging syndrome with muscular dystrophy and dilated cardiomyopathy. Aging Dis — PubMed:PMID30705772 | DOI:10.14336/AD.2018.0209 — OMIA Phene_Article / Article
  • 2018. Highly efficient RNA-guided base editing in rabbit. Nat Commun — PubMed:PMID30006570 | DOI:10.1038/s41467-018-05232-2 — OMIA Phene_Article / Article
  • 2020. Efficient base editing with high precision in rabbits using YFE-BE4max. Cell Death Dis — PubMed:PMID31959743 | DOI:10.1038/s41419-020-2244-3 — OMIA Phene_Article / Article
  • 2022. Highly efficient A-to-G base editing by ABE8.17 in rabbits. Mol Ther Nucleic Acids — PubMed:PMID35282412 | DOI:10.1016/j.omtn.2022.01.019 — 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:150330 (type: gene) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:176670 (type: trait) — OMIA Group_OMIM (via OMIA_ID)

Sources

Rabbit (Oryctolagus cuniculus) — Premature aging syndrome (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_premature_aging_syndrome_2091.txt