R38K_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.R38K Arg38Lys c.113G>A (p.R19K Arg19Lys without 19-aminoacid signal peptide) exon 2 heterozygote

References (3)

Title : Thyroglobulin gene mutations in Chinese patients with congenital hypothyroidism - Hu_2016_Mol.Cell.Endocrinol_423_60
Author(s) : Hu X , Chen R , Fu C , Fan X , Wang J , Qian J , Yi S , Li C , Luo J , Su J , Zhang S , Xie B , Zheng H , Lai Y , Chen Y , Li H , Gu X , Chen S , Shen Y
Ref : Mol Cell Endocrinol , 423 :60 , 2016
Abstract : Hu_2016_Mol.Cell.Endocrinol_423_60
ESTHER : Hu_2016_Mol.Cell.Endocrinol_423_60
PubMedSearch : Hu_2016_Mol.Cell.Endocrinol_423_60
PubMedID: 26777470
Gene_locus related to this paper: human-TG

Title : Defective protein folding and intracellular retention of thyroglobulin-R19K mutant as a cause of human congenital goiter - Kim_2008_Mol.Endocrinol_22_477
Author(s) : Kim PS , Lee J , Jongsamak P , Menon S , Li B , Hossain SA , Bae JH , Panijpan B , Arvan P
Ref : Mol Endocrinol , 22 :477 , 2008
Abstract : Kim_2008_Mol.Endocrinol_22_477
ESTHER : Kim_2008_Mol.Endocrinol_22_477
PubMedSearch : Kim_2008_Mol.Endocrinol_22_477
PubMedID: 17916655
Gene_locus related to this paper: human-TG

Title : Thyroglobulin gene mutations and other genetic defects associated with congenital hypothyroidism - Vono-Toniolo_2004_Arq.Bras.Endocrinol.Metabol_48_70
Author(s) : Vono-Toniolo J , Kopp P
Ref : Arq Bras Endocrinol Metabol , 48 :70 , 2004
Abstract : Vono-Toniolo_2004_Arq.Bras.Endocrinol.Metabol_48_70
ESTHER : Vono-Toniolo_2004_Arq.Bras.Endocrinol.Metabol_48_70
PubMedSearch : Vono-Toniolo_2004_Arq.Bras.Endocrinol.Metabol_48_70
PubMedID: 15611820
Gene_locus related to this paper: human-TG