RGD Annotation Report for amelogenesis imperfecta type 1KRat Genome Database

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An association has been curated linking Sp6 and amelogenesis imperfecta type 1K in Heterocephalus glaber.

The association was inferred from sequence orthology (ISO)
The annotation was made from OMIM Disease Annotation Pipeline
The annotation has been inferred from sequence orthology with SP6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
1 RGD objects have been annotated to amelogenesis imperfecta type 1K (DOID:0060945)
0 papers in RGD have been used to annotate Sp6

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