OR12D2
| OR12D2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Alias | OR12D2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| IDs externes | MGI: 2177484 HomoloGene: 133728 GeneCards: OR12D2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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OR12D2 est un gène situé sur le chromosome 6 humain[5].
Maladies liées
- Rétinite pigmentaire type 6[6]
Notes et références
- GRCh38: Ensembl release 89: ENSG00000280236 - Ensembl, May 2017
- GRCm38: Ensembl release 89: ENSMUSG00000092077 - Ensembl, May 2017
- ↑ « Publications PubMed pour l'Homme », sur National Center for Biotechnology Information, U.S. National Library of Medicine
- ↑ « Publications PubMed pour la Souris », sur National Center for Biotechnology Information, U.S. National Library of Medicine
- ↑ « OR12D2 DepMap Gene Summary », sur depmap.org (consulté le )
- ↑ (en) GeneCards Human Gene Database, « OR12D2 Gene - GeneCards | O12D2 Protein | O12D2 Antibody » [archive du ], sur www.genecards.org (consulté le )
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