โ† Other Compilations

Rabbit (Oryctolagus cuniculus) โ€” XY sex reversal, SRY-related (hereditary; OMIA-verified species predisposition)

companion_species_health_xy_sex_reversal_sry_related_rabbit

Other Compilations derived_from_dataset companion-species-health

Rabbit (Oryctolagus cuniculus) โ€” XY sex reversal, SRY-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: XY sex reversal, SRY-related
  • Summary: Song et al. (2017) "mutated Sp1-binding sites in the 5โ€ฒ flanking region of the rabbit SRY gene using the CRISPR/Cas9 system. As expected, the [resultant] SRY-Sp1 knockout rabbits had female external and internal genitalia and exhibited normal female copulatory behaviors, but they were infertile, and the adults displayed reduced follicles." Thus, these animals are 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 389099481 (no symbol in OMIA GeneSynonym) โ€” 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.

  • 2017. Mutation of the Sp1 binding site in the 5' flanking region of SRY causes sex reversal in rabbits. Oncotarget โ€” PubMed:PMID28445127 | DOI:10.18632/oncotarget.16979 โ€” 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:400044 (type: trait) โ€” OMIA Group_OMIM (via OMIA_ID)
  • OMIM:480000 (type: gene) โ€” OMIA Group_OMIM (via OMIA_ID)