Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10673
Gene Symbol: TNFSF13B
TNFSF13B
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.220 Biomarker MGD

Entrez Id: 6768
Gene Symbol: ST14
ST14
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD

Entrez Id: 6097
Gene Symbol: RORC
RORC
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD

Entrez Id: 3399
Gene Symbol: ID3
ID3
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.210 Biomarker MGD A T cell intrinsic role of Id3 in a mouse model for primary Sjogren's syndrome. 15485632

2004

Entrez Id: 9020
Gene Symbol: MAP3K14
MAP3K14
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD aly/aly mice: a unique model of biliary disease. 9620319

1998

Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD An age-related ovarian phenotype in mice with targeted disruption of the Cyp 19 (aromatase) gene. 10875266

2000

Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Another cell death induction system: TNF-alpha acts as a ligand for Fas in vaginal cells. 10453074

1999

Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Anti-DNA B cells in MRL/lpr mice show altered differentiation and editing pattern. 12486097

2002

Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Aromatase controls Sjögren syndrome-like lesions through monocyte chemotactic protein-1 in target organ and adipose tissue-associated macrophages. 25447050

2015

Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Aromatase-deficient (ArKO) mice have reduced blood pressure and baroreflex sensitivity. 15178650

2004

Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Aromatase-deficient mice spontaneously develop a lymphoproliferative autoimmune disease resembling Sjogren's syndrome. 15314222

2004

Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Beta-amyloid induces neuronal apoptosis via a mechanism that involves the c-Jun N-terminal kinase pathway and the induction of Fas ligand. 11567045

2001

Entrez Id: 1236
Gene Symbol: CCR7
CCR7
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD CCR7 signals are essential for cortex-medulla migration of developing thymocytes. 15302902

2004

Entrez Id: 1236
Gene Symbol: CCR7
CCR7
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD CCR7-dependent cortex-to-medulla migration of positively selected thymocytes is essential for establishing central tolerance. 16473829

2006

Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD CD4 regulatory T cells prevent lethal autoimmunity in IL-2Rbeta-deficient mice. Implications for the nonredundant function of IL-2. 12196288

2002

Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Characterization of mice deficient in aromatase (ArKO) because of targeted disruption of the cyp19 gene. 9618522

1998

Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Cognitive and neurologic deficits in the MRL/lpr mouse: a clinicopathologic study. 8496852

1993

Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Comparative influence of steroid hormones and immunosuppressive agents on autoimmune expression in lacrimal glands of a female mouse model of Sjögren's syndrome. 8163351

1994

Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Complement C4 inhibits systemic autoimmunity through a mechanism independent of complement receptors CR1 and CR2. 11067882

2000

Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Conditional ablation of MHC-II suggests an indirect role for MHC-II in regulatory CD4 T cell maintenance. 16709807

2006

Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Conditional IL-2 Gene Deletion: Consequences for T Cell Proliferation. 22590468

2012

Entrez Id: 4792
Gene Symbol: NFKBIA
NFKBIA
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Defective feedback regulation of NF-kappaB underlies Sjogren's syndrome in mice with mutated kappaB enhancers of the IkappaBalpha promoter. 20696914

2010

Entrez Id: 10758
Gene Symbol: TRAF3IP2
TRAF3IP2
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Deficiency of Act1, a critical modulator of B cell function, leads to development of Sjögren's syndrome. 18624351

2008

Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Deficiency of P-selectin or P-selectin glycoprotein ligand-1 leads to accelerated development of glomerulonephritis and increased expression of CC chemokine ligand 2 in lupus-prone mice. 17142777

2006

Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
0.200 Biomarker MGD Deficient interleukin 2 activity in MRL/Mp and C57BL/6J mice bearing the lpr gene. 6975351

1981