absent thyroid gland Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description lack of the endocrine gland that is normally located in the front and to the sides of the upper part of the trachea and which secretes thyroid hormone and calcitonin (Mammalian Phenotype Ontology, MP_0005314)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005314
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Genes

7 gene mutations causing the absent thyroid gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA5 ATP-binding cassette, sub-family A (ABC1), member 5
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FOXE1 forkhead box E1
NKX2-1 NK2 homeobox 1
PAX3 paired box 3
PAX8 paired box 8