abnormal harderian gland pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the coloring of the sebaceous gland located behind the eyeball in the orbit that excretes fluid that facilitates movement of the third eyelid, due to changes in the amount, shape, or distribution of cells producing pigment (Mammalian Phenotype Ontology, MP_0003798)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003798
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Genes

1 gene mutations causing the abnormal harderian gland pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
RAB27A RAB27A, member RAS oncogene family