Transcription_CREM signaling in testis

No Pathway Network information available for Transcription_CREM signaling in testis

Pathways in the Transcription_CREM signaling in testis SuperPath

#	Name	Source	Genes
1	Transcription_CREM signaling in testis	GeneGo (Thomson Reuters)	ACE ADCY1 CREB1 CREBBP CREM FHL5 FSHB FSHR GNAS H1-9P HK2 KIF17 LDHC ODF1 PRKACA PRKACB PRKACG PRKAR1A PRKAR1B PRKAR2A PRKAR2B TNP1 TSSK2 (see all 23) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	ADCY1	Adenylate Cyclase 1	Protein Coding	1
2	CREB1	CAMP Responsive Element Binding Protein 1	Protein Coding	1
3	CREBBP	CREB Binding Lysine Acetyltransferase	Protein Coding	1
4	CREM	CAMP Responsive Element Modulator	Protein Coding	1
5	ACE	Angiotensin I Converting Enzyme	Protein Coding	1
6	FSHB	Follicle Stimulating Hormone Subunit Beta	Protein Coding	1
7	FSHR	Follicle Stimulating Hormone Receptor	Protein Coding	1
8	GNAS	GNAS Complex Locus	Protein Coding	1
9	HK2	Hexokinase 2	Protein Coding	1
10	LDHC	Lactate Dehydrogenase C	Protein Coding	1
11	ODF1	Outer Dense Fiber Of Sperm Tails 1	Protein Coding	1
12	PRKACA	Protein Kinase CAMP-Activated Catalytic Subunit Alpha	Protein Coding	1
13	PRKACB	Protein Kinase CAMP-Activated Catalytic Subunit Beta	Protein Coding	1
14	PRKACG	Protein Kinase CAMP-Activated Catalytic Subunit Gamma	Protein Coding	1
15	PRKAR1A	Protein Kinase CAMP-Dependent Type I Regulatory Subunit Alpha	Protein Coding	1
16	PRKAR1B	Protein Kinase CAMP-Dependent Type I Regulatory Subunit Beta	Protein Coding	1
17	PRKAR2A	Protein Kinase CAMP-Dependent Type II Regulatory Subunit Alpha	Protein Coding	1
18	PRKAR2B	Protein Kinase CAMP-Dependent Type II Regulatory Subunit Beta	Protein Coding	1
19	TNP1	Transition Protein 1	Protein Coding	1
20	FHL5	Four And A Half LIM Domains 5	Protein Coding	1
21	TSSK2	Testis Specific Serine Kinase 2	Protein Coding	1
22	KIF17	Kinesin Family Member 17	Protein Coding	1
23	H1-9P	H1.9 Linker Histone, Pseudogene	Pseudogene	1

Disorders associated with Transcription_CREM signaling in testis SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Pigmented nodular adrenocortical disease, primary, 1	Enrichment	GNAS, PRKAR1A	5.56
2	Ellis-van creveld syndrome	Enrichment	PRKACA, PRKACB	4.01
3	Acrodysostosis 1 with or without hormone resistance	Enrichment	PRKAR1A	2.77
4	Pseudohypoparathyroidism, type ic	Enrichment	GNAS	2.77
5	Carney complex, type 1	Enrichment	PRKAR1A	2.77
6	Osseous heteroplasia, progressive	Enrichment	GNAS	2.77
7	Deafness, autosomal recessive 44	Enrichment	ADCY1	2.77
8	Ovarian dysgenesis 1	Enrichment	FSHR	2.77
9	Microvascular complications of diabetes 3	Enrichment	ACE	2.77
10	Acth-independent macronodular adrenal hyperplasia 1	Enrichment	GNAS	2.77
11	Twinning, dizygotic	Enrichment	FSHR	2.77
12	Pituitary adenoma 3, multiple types	Enrichment	GNAS	2.77
13	Cardioacrofacial dysplasia 2	Enrichment	PRKACB	2.77
14	Myxoma, intracardiac	Enrichment	PRKAR1A	2.77
15	Ovarian hyperstimulation syndrome	Enrichment	FSHR	2.77
16	Amenorrhea	Enrichment	FSHR	2.77
17	Pigmented nodular adrenocortical disease, primary, 4	Enrichment	PRKACA	2.77
18	Disorders of gnas inactivation	Enrichment	GNAS	2.77
19	Cardioacrofacial dysplasia 1	Enrichment	PRKACA	2.77
20	Menke-hennekam syndrome 1	Enrichment	CREBBP	2.77
21	Rubinstein-taybi syndrome due to 16p13.3 microdeletion	Enrichment	CREBBP	2.77
22	Prkar1b-related neurodegenerative dementia with intermediate filaments	Enrichment	PRKAR1B	2.77
23	Menke-hennekam syndrome	Enrichment	CREBBP	2.77
24	Monostotic fibrous dysplasia	Enrichment	GNAS	2.77
25	Mazabraud syndrome	Enrichment	GNAS	2.77
26	Pseudohypoparathyroidism, type ia	Enrichment	GNAS	2.47
27	Amelogenesis imperfecta, type ig	Enrichment	PRKAR1A	2.47
28	Thumb deformity	Enrichment	CREBBP	2.47
29	Hypogonadotropic hypogonadism 24 with or without anosmia	Enrichment	FSHB	2.47
30	Histiocytoma, angiomatoid fibrous	Enrichment	CREB1	2.47
31	Pseudopseudohypoparathyroidism	Enrichment	GNAS	2.47
32	Bleeding disorder, platelet-type, 19	Enrichment	PRKACG	2.47
33	Marbach-schaaf neurodevelopmental syndrome	Enrichment	PRKAR1B	2.47
34	Usher syndrome, type iv	Enrichment	PRKAR1A	2.47
35	Acute myeloid leukemia with kat6a-crebbp fusion	Enrichment	CREBBP	2.47
36	Acrodysostosis	Enrichment	PRKAR1A	2.47
37	Pseudohypoparathyroidism	Enrichment	GNAS	2.47
38	Fibrolamellar carcinoma	Enrichment	PRKACA	2.47
39	Ciliary dyskinesia, primary, 18	Enrichment	PRKAR1B	2.47
40	Isolated primary pigmented nodular adrenocortical disease	Enrichment	PRKAR1A	2.47
41	Acth-independent macronodular adrenal hyperplasia	Enrichment	GNAS	2.47
42	Mccune-albright syndrome	Enrichment	GNAS	2.29
43	Tethered spinal cord syndrome	Enrichment	CREBBP	2.29
44	Intraocular pressure quantitative trait locus	Enrichment	CREBBP	2.29
45	Gonadal dysgenesis	Enrichment	FSHR	2.29
46	Cushing syndrome due to bilateral macronodular adrenocortical disease	Enrichment	GNAS	2.29
47	Melanoma of soft tissue	Enrichment	CREB1	2.29
48	Pseudohypoparathyroidism, type ib	Enrichment	GNAS	2.17
49	Carney complex variant	Enrichment	PRKAR1A	2.17
50	Arrhythmogenic right ventricular dysplasia, familial, 10	Enrichment	PRKAR1A	2.17
51	Rubinstein-taybi syndrome 1	Enrichment	CREBBP	1.99
52	Renal tubular dysgenesis	Enrichment	ACE	1.99
53	Chromosome 16p13.3 deletion syndrome, proximal	Enrichment	CREBBP	1.99
54	Hemorrhage, intracerebral	Enrichment	ACE	1.99
55	Adrenocortical carcinoma	Enrichment	PRKAR1A	1.99
56	Hypertrichosis	Enrichment	CREBBP	1.99
57	Brachydactyly	Enrichment	GNAS	1.93
58	Spastic paraplegia 4, autosomal dominant	Enrichment	GNAS	1.87
59	Primary hyperaldosteronism	Enrichment	GNAS	1.82
60	Stroke, ischemic	Enrichment	ACE	1.77
61	46 xx gonadal dysgenesis	Enrichment	FSHR	1.70
62	Acute promyelocytic leukemia	Enrichment	PRKAR1A	1.66
63	Heart disease	Enrichment	CREBBP	1.63
64	Corpus callosum, agenesis of	Enrichment	CREBBP	1.60
65	Isolated corpus callosum agenesis	Enrichment	CREBBP	1.60
66	Rare genetic intellectual disability	Enrichment	CREBBP	1.60
67	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome	Enrichment	CREBBP	1.60
68	Perrault syndrome 1	Enrichment	FSHR	1.57
69	Diffuse large b-cell lymphoma	Enrichment	CREBBP	1.50
70	Myocardial infarction	Enrichment	ACE	1.44
71	Scoliosis	Enrichment	CREBBP	1.40
72	Cakut	Enrichment	ACE	1.25
73	Body mass index quantitative trait locus 11	Enrichment	GNAS	1.09
74	Myeloma, multiple	Enrichment	CREBBP	1.04
75	Autism	Enrichment	CREBBP	0.94
76	Primary ciliary dyskinesia	Enrichment	PRKAR1B	0.92
77	Rare autosomal recessive non-syndromic sensorineural deafness type dfnb	Enrichment	ADCY1	0.85
78	Congenital nervous system abnormality	Enrichment	CREBBP	0.78
79	Nervous system disease	Enrichment	CREBBP	0.78
80	Inherited cancer-predisposing syndrome	Enrichment	PRKAR1A	0.70

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁸ Cell Signaling Technology

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

Transcription_CREM signaling in testis

Pathway Network for Transcription_CREM signaling in testis

Member Pathways for Transcription_CREM signaling in testis

Pathways in the Transcription_CREM signaling in testis SuperPath

Associated Genes for Transcription_CREM signaling in testis

Associated Disorders for Transcription_CREM signaling in testis

Disorders associated with Transcription_CREM signaling in testis SuperPath

STRING Interaction Network for Transcription_CREM signaling in testis

Sources for Transcription_CREM signaling in testis