Zika, Hungary (Rabbit) — Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related (hereditary; OMIA-verified breed predisposition)

--- license: permission_granted topic_id: companion_breed_health_zika_hungary_rabbit_omia423_rabbit category: companion-breed-health title: "Zika, Hungary (Rabbit) — Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related (hereditary; OMIA-verified breed predisposition)" lang: en source: "OMIA (Online Mendelian Inheritance in Animals, University of Sydney) breed-specific hereditary-disorder record, saved verbatim to source_file; C1 substring-verified. Pulled 2026-08-23 from local OMIA database dump." source_file: pdf-raw/breed-health/zika_hungary_rabbit_omia423_423.txt date_parsed: 2026-08-23 tokens_estimated: 80 verification: method: substring_match claims: 5 passed: 5 date: 2026-08-23 recovered: false path: companion-breed-health/companion_breed_health_zika_hungary_rabbit_omia423_rabbit/01_companion_breed_health_zika_hungary_rabbit_omia423_rabbit.md source_document: "OMIA — Online Mendelian Inheritance in Animals (University of Sydney)" citation: authority: "OMIA — Online Mendelian Inheritance in Animals (University of Sydney)" title: "Zika, Hungary (Rabbit) — Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related (hereditary; OMIA-verified breed predisposition)" url: "https://omia.org/OMIA000202/9986/" retrieved: "2026-08-23" ref: "OMIA breed-specific hereditary-disorder records (omia.org), derived from local OMIA database dump; dataset: https://doi.org/10.25910/2AMR-PV70" doc_type: "academic animal-genetics database (breed-specific disorder entries)" needs_review: false

verification_derived: method: derived_from_dataset source: "OMIA database dump (omia.xml, local); fields Gene/Variant/Article/OMIM" note: "Structured fields (gene, variant rsID/protein change, PubMed/DOI references, OMIM cross-link) extracted from OMIA dump and presented with first-hand values; not verbatim prose."---

Zika, Hungary (Rabbit) — Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-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: Zika, Hungary (Rabbit)
• Disorder:
• Mode of inheritance: Autosomal recessive
• Summary: See Robinson (1958, pp. 338-340)
• 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 4118478 (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.

• 1987. Linkage of albino and hemoglobin beta-chain loci in the rabbit. Journal of Heredity — PubMed:PMID3584936 — OMIA Phene_Article / Article
• 1993. Drug-Induced Retinal Toxicity in Albino Rabbits - The Effects of Imipenem and Aztreonam. Investigative Ophthalmology & Visual Science — PubMed:PMID8225881 — OMIA Phene_Article / Article
• 1994. Blue-Light-Induced Dysfunction of the Blood-Retinal Barrier at the Pigment Epithelium in Albino Versus Pigmented Rabbits. Experimental Eye Research — PubMed:PMID8157099 | DOI:10.1006/exer.1994.1192 — OMIA Phene_Article / Article
• 1995. Comparative ocular pharmacokinetics of brimonidine after a single dose application to the eyes of albino and pigmented rabbits. Drug Metabolism and Disposition — PubMed:PMID7587958 — OMIA Phene_Article / Article
• 2000. Tyrosinase gene variants in different rabbit strains. Mamm Genome — PubMed:PMID10920244 | DOI:10.1007/s003350010120 — OMIA Phene_Article / Article
• 1996. Expression of the murine wild-type tyrosinase gene in transgenic rabbits. Transgenic Res — PubMed:PMID8840523 | DOI:10.1007/BF01980205 — OMIA Phene_Article / Article
• 1996. YAC transgenesis in farm animals: rescue of albinism in rabbits. Mol Reprod Dev — PubMed:PMID8722692 | DOI:10.1002/(SICI)1098-2795(199605)44:1<56::AID-MRD6>3.0.CO;2-S — OMIA Phene_Article / Article
• 1964. Catechol-O-methyl transferase and monamine oxidase activity in the ocular tissue of albino rabbits. Invest Ophthalmol — PubMed:PMID14238873 — OMIA Phene_Article / Article
• 1905. Mendelism. Macmillan and Bowes, Cambridge — OMIA Phene_Article / Article
• 2006. A first-generation microsatellite-based integrated genetic and cytogenetic map for the European rabbit (Oryctolagus cuniculus) and localization of angora and albino. Anim Genet — PubMed:PMID16879342 | DOI:10.1111/j.1365-2052.2006.01462.x — OMIA Phene_Article / Article
• 1958. Genetic studies of the rabbit. Bibliographia Genetica — OMIA Phene_Article / Article
• 1973. Recombination between buphthalmos and albino loci in the rabbit. J Hered — PubMed:PMID4782848 | DOI:10.1093/oxfordjournals.jhered.a108442 — OMIA Phene_Article / Article
• (9 additional references in OMIA)

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:203100 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
• OMIM:606952 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
• OMIM:606933 (type: gene) — OMIA Group_OMIM (via OMIA_ID)