Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
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Enzyme
Compound
Query: UMLS:C0011854 (
type 1 diabetes
)
20,749
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The IDDM5 gene, which is identified by whole-genome searches, is located on chromosome 6q25.
TAB2
(MAP3K7IP2 [mitogen-activating protein kinase kinase kinase 7 interacting protein 2]) is a potential candidate gene for
type 1 diabetes
because it is located on chromosome 6q25 and is involved in nuclear factor (NF)-kappaB regulation. We have conducted familial association studies using 478 families and demonstrate that a
type 1 diabetes
susceptibility gene resides within a 212-kb region containing the
TAB2
gene (Tsp = 1.0 x 10(-2) to 4.0 x 10(-4)). No amino acid polymorphisms were detected in
TAB2
; however, multiple single nucleotide polymorphisms (SNPs) found within 5' untranslated, 3' untranslated, and intron regions were associated with
type 1 diabetes
susceptibility. Two additional genes, LOC340152, a predicted gene with currently unknown function, and SMT3, which has homology to SUMO (small ubiquitin-related modifier) were found within the 212-kb region and were associated with
type 1 diabetes
susceptibility. Functional studies of the three genes will be required to determine their biological relevance to
type 1 diabetes
. However, both
TAB2
and SUMO are involved in NF-kappaB activation and may thus be involved in
type 1 diabetes
through apoptosis in pancreatic beta-cells.
...
PMID:A 212-kb region on chromosome 6q25 containing the TAB2 gene is associated with susceptibility to type 1 diabetes. 1522 Feb 15
Several functional genetic variants that can potentially modulate the activity of NFkappaB have been recently described. As reduced NFkappaB activity has been implicated in risk for autoimmune diabetes in the NOD mouse, these variants were tested for allelic association with
type 1 diabetes
(T1D) in a family based study. Alleles at markers in the
TAB2
/SUMO4 locus on chromosome 6q had been previously reported to be associated with T1D in two separate studies, but these studies disagreed on the identity of the risk allele. The current study failed to confirm either of these results. No significant evidence of association with T1D was obtained for three SNP markers in the
TAB2
/SUMO4 region. An additional functional variant in the promoter of the NFKB1 gene that has been shown to directly affect the expression of NFkappaB was also tested.
...
PMID:Functional variants in SUMO4, TAB2, and NFkappaB and the risk of type 1 diabetes. 1572 64