Rabbit (Oryctolagus cuniculus) — Usher syndrome, USH2A-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: Usher syndrome, USH2A-relatedSummary: 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 389122258 (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.
- 2023. USH2A gene mutations in rabbits lead to progressive retinal degeneration and hearing loss. Transl Vis Sci Technol — PubMed:PMID36795064 | DOI:10.1167/tvst.12.2.26 — OMIA Phene_Article / Article
- 2023. Multimodal photoacoustic microscopy, optical coherence tomography, and fluorescence imaging of USH2A knockout rabbits. Sci Rep — PubMed:PMID38086867 | DOI:10.1038/s41598-023-48872-1 — 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:276901 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:608400 (type: gene) — OMIA Group_OMIM (via OMIA_ID)