pale spleen Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description spleen lacks normal reddish coloration; often occurs with a bloodless or reduced vasculature condition (Mammalian Phenotype Ontology, MP_0009246)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009246
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Genes

5 gene mutations causing the pale spleen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
FEN1 flap structure-specific endonuclease 1
GATA1 GATA binding protein 1 (globin transcription factor 1)
IFNG interferon, gamma
RASA3 RAS p21 protein activator 3