Glucocorticoid Pathway (Peripheral Tissue), Pharmacodynamics

No Pathway Network information available for Glucocorticoid Pathway (Peripheral Tissue), Pharmacodynamics

#	Name	Source	Genes
1	Glucocorticoid Pathway (Peripheral Tissue), Pharmacodynamics	PharmGKB	CREBBP FKBP4 HSP90AA1 HSPA4 NCOA3 NR3C1 SERPINA6 ST13 TBP (see all 9) (see less)

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

#	Symbol	Description	Category	# Related Pathways
1	HSP90AA1	Heat Shock Protein 90 Alpha Family Class A Member 1	Protein Coding	1
2	NR3C1	Nuclear Receptor Subfamily 3 Group C Member 1	Protein Coding	1
3	ST13	ST13 Hsp70 Interacting Protein	Protein Coding	1
4	TBP	TATA-Box Binding Protein	Protein Coding	1
5	NCOA3	Nuclear Receptor Coactivator 3	Protein Coding	1
6	SERPINA6	Serpin Family A Member 6	Protein Coding	1
7	HSPA4	Heat Shock Protein Family A (Hsp70) Member 4	Protein Coding	1
8	FKBP4	FKBP Prolyl Isomerase 4	Protein Coding	1
9	CREBBP	CREB Binding Lysine Acetyltransferase	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Corticosteroid-binding globulin deficiency	Enrichment	SERPINA6	3.18
2	Glucocorticoid resistance, generalized	Enrichment	NR3C1	3.18
3	Menke-hennekam syndrome 1	Enrichment	CREBBP	3.18
4	Rubinstein-taybi syndrome due to 16p13.3 microdeletion	Enrichment	CREBBP	3.18
5	Menke-hennekam syndrome	Enrichment	CREBBP	3.18
6	Galactosemia ii	Enrichment	NR3C1	2.88
7	Thumb deformity	Enrichment	CREBBP	2.88
8	Spinocerebellar ataxia 17	Enrichment	TBP	2.88
9	Acute myeloid leukemia with kat6a-crebbp fusion	Enrichment	CREBBP	2.88
10	Tethered spinal cord syndrome	Enrichment	CREBBP	2.70
11	Intraocular pressure quantitative trait locus	Enrichment	CREBBP	2.70
12	Rubinstein-taybi syndrome 1	Enrichment	CREBBP	2.40
13	Chromosome 16p13.3 deletion syndrome, proximal	Enrichment	CREBBP	2.40
14	Hypertrichosis	Enrichment	CREBBP	2.40
15	Primary hyperaldosteronism	Enrichment	NR3C1	2.22
16	Heart disease	Enrichment	CREBBP	2.03
17	Corpus callosum, agenesis of	Enrichment	CREBBP	2.00
18	Isolated corpus callosum agenesis	Enrichment	CREBBP	2.00
19	Rare genetic intellectual disability	Enrichment	CREBBP	2.00
20	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome	Enrichment	CREBBP	2.00
21	Diffuse large b-cell lymphoma	Enrichment	CREBBP	1.90
22	Parkinson's disease	Enrichment	TBP	1.90
23	Parkinson disease, late-onset	Enrichment	TBP	1.80
24	Scoliosis	Enrichment	CREBBP	1.80
25	Myeloma, multiple	Enrichment	CREBBP	1.44
26	Autism	Enrichment	CREBBP	1.33
27	Congenital nervous system abnormality	Enrichment	CREBBP	1.17
28	Nervous system disease	Enrichment	CREBBP	1.17

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

Pathway Network for Glucocorticoid Pathway (Peripheral Tissue), Pharmacodynamics