abnormal thyroid follicle morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the small spherical vesicular components of the thyroid gland that are lined with epithelium and contain a colloid substance that both serves as a reservoir of materials for thyroid hormone production and stores thyroid hormones (Mammalian Phenotype Ontology, MP_0004696)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004696
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Genes

18 gene mutations causing the abnormal thyroid follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA5 ATP-binding cassette, sub-family A (ABC1), member 5
ATCAY ataxia, cerebellar, Cayman type
CAV1 caveolin 1, caveolae protein, 22kDa
CGA glycoprotein hormones, alpha polypeptide
DUOX2 dual oxidase 2
FAS Fas cell surface death receptor
LHX3 LIM homeobox 3
MANBA mannosidase, beta A, lysosomal
MARVELD2 MARVEL domain containing 2
NKX2-1 NK2 homeobox 1
PAX8 paired box 8
PTEN phosphatase and tensin homolog
RUNX2 runt-related transcription factor 2
TG thyroglobulin
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta
TPO thyroid peroxidase
TSHR thyroid stimulating hormone receptor