S450fsX477_human-TG

General

Gene Locus : human-TG

Mode of mutation : Natural mutant

Disease : Goiter, familial with hypothyroidism, autosomal recessive

Summary :

AAA Change :

Allelic Variant :

Risk Factor :

Inhibitor :

Structure :

Disease by interaction :

Interact Gene Locus :

Xenobiotic sensitivity :

Modification :

Torpedo_number : No torpedo number

Kinetic Parameter : No kinetic parameter

News : No news

Comment : p.S450fsX477 Ser450fsTer477 c.1348delT (p.S431fsX459 Ser431fsTer459 without 19-aminoacid signal peptide), located in exon 9, which caused a frameshift at codon 450(431) and ran into a stop codon after 27 altered amino acid residues (457 truncated polypeptide).

References (1)

Title : Six new mutations of the thyroglobulin gene discovered in taiwanese children presenting with thyroid dyshormonogenesis - Niu_2009_J.Clin.Endocrinol.Metab_94_5045
Author(s) : Niu DM , Hsu JH , Chong KW , Huang CH , Lu YH , Kao CH , Yu HC , Lo MY , Jap TS
Ref : J Clinical Endocrinology Metab , 94 :5045 , 2009
Abstract : Niu_2009_J.Clin.Endocrinol.Metab_94_5045
ESTHER : Niu_2009_J.Clin.Endocrinol.Metab_94_5045
PubMedSearch : Niu_2009_J.Clin.Endocrinol.Metab_94_5045
PubMedID: 19837936
Gene_locus related to this paper: human-TG