IVS3-3C>G_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 : IVS3-3C>G skipping of exon4

References (2)

Title : A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism - Ieiri_1991_J.Clin.Invest_88_1901
Author(s) : Ieiri T , Cochaux P , Targovnik HM , Suzuki M , Shimoda S , Perret J , Vassart G
Ref : J Clinical Investigation , 88 :1901 , 1991
Abstract : Ieiri_1991_J.Clin.Invest_88_1901
ESTHER : Ieiri_1991_J.Clin.Invest_88_1901
PubMedSearch : Ieiri_1991_J.Clin.Invest_88_1901
PubMedID: 1752952

Title : Identification of a splicing mutation responsible for a human hereditary goiter with hypothyroidism. (Abstract) -
Author(s) : Cochaux P , Ieiri T , Targovnik H , Suzuki M , Shimoda SI , Perret J , Vassart G
Ref : American Journal of Human Genetics , 49 (suppl.) :131 , 1991
PubMedID: