RGD Annotation Report for congenital nystagmusRat Genome Database

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An association has been curated linking MYO7A and congenital nystagmus in Canis lupus familiaris.

The association was inferred from sequence orthology (ISO)
The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
The annotation has been inferred from sequence orthology with MYO7A (Homo sapiens)
22 RGD objects have been annotated to congenital nystagmus (DOID:9649)
0 papers in RGD have been used to annotate MYO7A
Curation Notes: associated with Leber Congenital Amaurosis;DNA:missense mutation:cds:c.578C>T (p.T193I)(human)
Original References(s): PMID:21901789 REF_RGD_ID:11537385

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.