abnormal thyroid gland development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure or abnormality in the formation of the thyroid gland during organogenesis (Mammalian Phenotype Ontology, MP_0003421)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003421
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13 gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
EYA1 EYA transcriptional coactivator and phosphatase 1
FOXE1 forkhead box E1
HHEX hematopoietically expressed homeobox
HOXA3 homeobox A3
HOXA5 homeobox A5
NKX2-1 NK2 homeobox 1
PAX3 paired box 3
PAX8 paired box 8
PAX9 paired box 9
RIPPLY3 ripply transcriptional repressor 3
TBX1 T-box 1
TPO thyroid peroxidase