RGD Annotation Report for congenital bilateral absence of vas deferensRat Genome Database

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An association has been curated linking Cftr^em1Sage and congenital bilateral absence of vas deferens in Rattus norvegicus.

The association was inferred from mutant phenotype (IMP)
The annotation was made from Tuggle KL, etal., PLoS One. 2014 Mar 7;9(3):e91253. doi: 10.1371/journal.pone.0091253. eCollection 2014.
42 additional annotations were made from Tuggle KL, etal., PLoS One. 2014 Mar 7;9(3):e91253. doi: 10.1371/journal.pone.0091253. eCollection 2014.
4 RGD objects have been annotated to congenital bilateral absence of vas deferens (DOID:0111862)
2 papers in RGD have been used to annotate Cftr^em1Sage

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