Details Of Published TSH Receptor Mutation

Phe 631 Ile

c.1891T>A

Constitutively Activating TSH Receptor Mutation

Type
gain
Manifestation
carcinoma
Exon
10
Molecular Characteristics:
default 
Clinical Features:
follicular carcinoma with clinical phenotype of "hot nodule"

*based on 2 hot nodules investigated by Sancak et al. 2011 and 1 hot thyroid carcinoma investigated by Führer et al. 2003 
Treatment:
default
Functional Characteristics:
cAMP
(basal)
cAMP
(TSH)
IP
(basal)
IP
(TSH)
TSH-Binding
Cell Surface Expression
Prevalence
LRA
Ref
3.7
0.8
1.1
0.2
0.4
1
8.6 ± 0.7
1
Legend:
cAMP (basal): basal in vitro cAMP production of mutant over wild-type TSHR
cAMP (TSH): maximal in vitro cAMP production of mutant over wild-type TSHR
IP (basal): basal in vitro IP production of mutant over wild-type TSHR
IP (TSH): maximal in vitro IP production of mutant over wild-type TSHR
TSH-binding: maximal TSH-binding compared to the wild-type TSHR
Cell surface expression: cell surface expression of mutant compared to WT-TSHR
LRA: linear regression analysis (LRA) of constitutive activity as a function of TSHR expression determined by 125I-bTSH binding or FACS analysis compared to the wild-type TSHR
Prevalence: Prevalence of (somatic and germline) activating mutations*
Ref: Reference for functional characterization
Child: Found in children.
Reference 1:
Jäschke et al.
Clin Endocrinol (Oxf) 73:815-20
Lack of in vitro constitutive activity for four previously reported TSH receptor mutations identified in patients with nonautoimmune hyperthyroidism and hot thyroid carcinomas
2010
Reference 2:
Führer et al.
Endocr Relat Cancer. 10:591-600
Two somatic TSH receptor mutations in a patient with toxic metastasising follicular thyroid carcinoma and non-functional lung metastases.
2003