Differentiation of white and brown adipocyte

No Pathway Network information available for Differentiation of white and brown adipocyte

Pathways in the Differentiation of white and brown adipocyte SuperPath

#	Name	Source	Genes
1	Differentiation of white and brown adipocyte	WikiPathways	ADIPOQ BMP2 BMP4 BMP7 CEBPA CEBPB CEBPG CIDEA EBF3 HOXC8 HOXC9 HSPB7 LEP MPZL2 PLAC8 PPARG PPARGC1A PPARGC1B PRDM16 SLC7A10 SMAD1 SMAD5 SMAD9 ZIC1 ZNF423 (see all 25) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	ADIPOQ	Adiponectin, C1Q And Collagen Domain Containing	Protein Coding	1
2	ZIC1	Zic Family Zinc Finger 1	Protein Coding	1
3	BMP7	Bone Morphogenetic Protein 7	Protein Coding	1
4	BMP4	Bone Morphogenetic Protein 4	Protein Coding	1
5	BMP2	Bone Morphogenetic Protein 2	Protein Coding	1
6	PRDM16	PR/SET Domain 16	Protein Coding	1
7	PPARG	Peroxisome Proliferator Activated Receptor Gamma	Protein Coding	1
8	PLAC8	Placenta Associated 8	Protein Coding	1
9	SMAD9	SMAD Family Member 9	Protein Coding	1
10	SMAD5	SMAD Family Member 5	Protein Coding	1
11	SMAD1	SMAD Family Member 1	Protein Coding	1
12	LEP	Leptin	Protein Coding	1
13	EBF3	EBF Transcription Factor 3	Protein Coding	1
14	ZNF423	Zinc Finger Protein 423	Protein Coding	1
15	PPARGC1B	PPARG Coactivator 1 Beta	Protein Coding	1
16	CIDEA	Cell Death Inducing DFFA Like Effector A	Protein Coding	1
17	PPARGC1A	PPARG Coactivator 1 Alpha	Protein Coding	1
18	CEBPB	CCAAT Enhancer Binding Protein Beta	Protein Coding	1
19	CEBPA	CCAAT Enhancer Binding Protein Alpha	Protein Coding	1
20	CEBPG	CCAAT Enhancer Binding Protein Gamma	Protein Coding	1
21	MPZL2	Myelin Protein Zero Like 2	Protein Coding	1
22	SLC7A10	Solute Carrier Family 7 Member 10	Protein Coding	1
23	HOXC9	Homeobox C9	Protein Coding	1
24	HOXC8	Homeobox C8	Protein Coding	1
25	HSPB7	Heat Shock Protein Family B (Small) Member 7	Protein Coding	1

Disorders associated with Differentiation of white and brown adipocyte SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Leptin deficiency or dysfunction	Enrichment	LEP, PPARG	4.71
2	Ventricular septal defect 1	Enrichment	BMP2, BMP7	4.49
3	Craniosynostosis 6	Enrichment	ZIC1	2.73
4	Urinary tract infections, recurrent	Enrichment	EBF3	2.73
5	Microphthalmia, syndromic 6	Enrichment	BMP4	2.73
6	Left ventricular noncompaction 8	Enrichment	PRDM16	2.73
7	Orofacial cleft 11	Enrichment	BMP4	2.73
8	Nephronophthisis 14	Enrichment	ZNF423	2.73
9	Pulmonary hypertension, primary, 2	Enrichment	SMAD9	2.73
10	Structural brain anomalies with impaired intellectual development and craniosynostosis	Enrichment	ZIC1	2.73
11	Hypotonia, ataxia, and delayed development syndrome	Enrichment	EBF3	2.73
12	20p12.3 microdeletion syndrome	Enrichment	BMP2	2.73
13	Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1	Enrichment	BMP2	2.73
14	Pparg-associated congenital generalized lipodystrophy	Enrichment	PPARG	2.73
15	Acute myeloid leukemia with mutated cebpa	Enrichment	CEBPA	2.73
16	Carotid intimal medial thickness 1	Enrichment	PPARG	2.43
17	Chromosome 10q26 deletion syndrome	Enrichment	EBF3	2.43
18	Deafness, autosomal recessive 111	Enrichment	MPZL2	2.43
19	Neurogenic bladder	Enrichment	EBF3	2.43
20	Craniosynostosis 7	Enrichment	BMP2	2.43
21	Isolated dandy-walker malformation with hydrocephalus	Enrichment	ZIC1	2.43
22	Familial partial lipodystrophy	Enrichment	PPARG	2.43
23	Transposition of the great arteries, dextro-looped	Enrichment	BMP2	2.26
24	Adiponectin deficiency	Enrichment	ADIPOQ	2.26
25	Pulmonary arterial hypertension associated with congenital heart disease	Enrichment	SMAD9	2.26
26	Isolated dandy-walker malformation without hydrocephalus	Enrichment	ZIC1	2.26
27	Brachydactyly, type a2	Enrichment	BMP2	2.13
28	Lipodystrophy, familial partial, type 3	Enrichment	PPARG	2.13
29	Congenital generalized lipodystrophy	Enrichment	PPARG	2.13
30	Non-syndromic bicoronal craniosynostosis	Enrichment	ZIC1	2.13
31	Moebius syndrome	Enrichment	EBF3	2.04
32	Congenital heart defects, multiple types, 4	Enrichment	BMP7	2.04
33	Inherited acute myeloid leukemia	Enrichment	CEBPA	2.04
34	Acute myeloid leukemia with t(8;21)(q22;q22) translocation	Enrichment	CEBPA	2.04
35	Atrial septal defect 1	Enrichment	BMP2	1.96
36	Pierre robin syndrome	Enrichment	EBF3	1.96
37	Renal tubular dysgenesis	Enrichment	EBF3	1.96
38	Anterior segment dysgenesis 5	Enrichment	BMP4	1.96
39	Arima syndrome	Enrichment	ZNF423	1.89
40	Vesicoureteral reflux	Enrichment	EBF3	1.89
41	Hemochromatosis, type 1	Enrichment	BMP2	1.83
42	Infantile nephronophthisis	Enrichment	ZNF423	1.83
43	Peters-plus syndrome	Enrichment	BMP4	1.74
44	Stickler syndrome	Enrichment	BMP4	1.74
45	Heritable pulmonary arterial hypertension	Enrichment	SMAD9	1.70
46	Renal hypodysplasia/aplasia 3	Enrichment	BMP4	1.66
47	Chromosome 1p36 deletion syndrome	Enrichment	PRDM16	1.63
48	Cleft lip/palate	Enrichment	BMP4	1.59
49	Gliosarcoma	Enrichment	PPARG	1.54
50	Giant cell glioblastoma	Enrichment	PPARG	1.51
51	Differentiated thyroid carcinoma	Enrichment	PPARG	1.28
52	Left ventricular noncompaction	Enrichment	PRDM16	1.20
53	Leukemia, acute myeloid	Enrichment	CEBPA	1.15
54	Type 2 diabetes mellitus	Enrichment	PPARG	1.13
55	Body mass index quantitative trait locus 11	Enrichment	PPARG	1.05
56	Familial isolated dilated cardiomyopathy	Enrichment	PRDM16	1.03
57	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	Enrichment	PPARGC1A	0.99
58	Deafness, autosomal recessive	Enrichment	MPZL2	0.96
59	Autosomal recessive nonsyndromic deafness	Enrichment	MPZL2	0.95
60	Colorectal cancer	Enrichment	PPARG	0.83
61	Rare autosomal recessive non-syndromic sensorineural deafness type dfnb	Enrichment	MPZL2	0.82
62	Autism spectrum disorder	Enrichment	EBF3	0.74
63	Inherited cancer-predisposing syndrome	Enrichment	CEBPA	0.66

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

Differentiation of white and brown adipocyte

Pathway Network for Differentiation of white and brown adipocyte

Member Pathways for Differentiation of white and brown adipocyte

Pathways in the Differentiation of white and brown adipocyte SuperPath

Associated Genes for Differentiation of white and brown adipocyte

Associated Disorders for Differentiation of white and brown adipocyte

Disorders associated with Differentiation of white and brown adipocyte SuperPath

STRING Interaction Network for Differentiation of white and brown adipocyte

Sources for Differentiation of white and brown adipocyte