abnormal parotid gland morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of either of the largest of the major salivary glands situated below and in front of each ear (Mammalian Phenotype Ontology, MP_0003452)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003452
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Genes

6 gene mutations causing the abnormal parotid gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BHLHA15 basic helix-loop-helix family, member a15
CCR7 chemokine (C-C motif) receptor 7
E2F1 E2F transcription factor 1
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
KCNN4 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4
SIX1 SIX homeobox 1