Genes targeted by miRNAs in adipocytes

No Pathway Network information available for Genes targeted by miRNAs in adipocytes

Pathways in the Genes targeted by miRNAs in adipocytes SuperPath

#	Name	Source	Genes
1	Genes targeted by miRNAs in adipocytes	WikiPathways	ERG GJA1 HAND2 HCN2 HCN4 HDAC4 IGF1 KCNE1 KCNJ2 KCNQ1 PTBP2 SRF TMSB4X (see all 13) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	HDAC4	Histone Deacetylase 4	Protein Coding	1
2	HAND2	Heart And Neural Crest Derivatives Expressed 2	Protein Coding	1
3	TMSB4X	Thymosin Beta 4 X-Linked	Protein Coding	1
4	SRF	Serum Response Factor	Protein Coding	1
5	HCN2	Hyperpolarization Activated Cyclic Nucleotide Gated Potassium And Sodium Channel 2	Protein Coding	1
6	KCNQ1	Potassium Voltage-Gated Channel Subfamily Q Member 1	Protein Coding	1
7	KCNJ2	Potassium Inwardly Rectifying Channel Subfamily J Member 2	Protein Coding	1
8	KCNE1	Potassium Voltage-Gated Channel Subfamily E Regulatory Subunit 1	Protein Coding	1
9	IGF1	Insulin Like Growth Factor 1	Protein Coding	1
10	GJA1	Gap Junction Protein Alpha 1	Protein Coding	1
11	ERG	ETS Transcription Factor ERG	Protein Coding	1
12	HCN4	Hyperpolarization Activated Cyclic Nucleotide Gated Potassium Channel 4	Protein Coding	1
13	PTBP2	Polypyrimidine Tract Binding Protein 2	Protein Coding	1

Disorders associated with Genes targeted by miRNAs in adipocytes SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Jervell-lange nielsen syndrome	Enrichment	KCNE1, KCNQ1	6.07
2	Familial atrial fibrillation	Enrichment	KCNE1, KCNJ2, KCNQ1	5.86
3	Jervell and lange-nielsen syndrome 1	Enrichment	KCNE1, KCNQ1	5.29
4	Congenital short qt syndrome	Enrichment	KCNJ2, KCNQ1	5.07
5	Congenital long qt syndrome	Enrichment	KCNE1, KCNQ1	4.25
6	Long qt syndrome 1	Enrichment	KCNE1, KCNQ1	3.44
7	Long qt syndrome	Enrichment	KCNE1, KCNQ1	3.41
8	Palmoplantar keratoderma and congenital alopecia 1	Enrichment	GJA1	3.02
9	Sick sinus syndrome 2	Enrichment	HCN4	3.02
10	Hypoplastic left heart syndrome 1	Enrichment	GJA1	3.02
11	Jervell and lange-nielsen syndrome 2	Enrichment	KCNE1	3.02
12	Short qt syndrome 3	Enrichment	KCNJ2	3.02
13	Oculodentodigital dysplasia	Enrichment	GJA1	3.02
14	Long qt syndrome 5	Enrichment	KCNE1	3.02
15	Craniometaphyseal dysplasia, autosomal recessive	Enrichment	GJA1	3.02
16	Epilepsy, idiopathic generalized 17	Enrichment	HCN2	3.02
17	Epilepsy, idiopathic generalized 18	Enrichment	HCN4	3.02
18	Chromosome 2q37 deletion syndrome	Enrichment	HDAC4	3.02
19	Familial febrile seizures 2	Enrichment	HCN2	3.02
20	Oculodentodigital dysplasia, autosomal recessive	Enrichment	GJA1	3.02
21	Atrial fibrillation, familial, 9	Enrichment	KCNJ2	3.02
22	Erythrokeratodermia variabilis et progressiva 3	Enrichment	GJA1	3.02
23	Neurodevelopmental disorder with central hypotonia and dysmorphic facies	Enrichment	HDAC4	3.02
24	Lymphatic malformation 14	Enrichment	ERG	3.02
25	Andersen cardiodysrhythmic periodic paralysis	Enrichment	KCNJ2	2.72
26	Hallermann-streiff syndrome	Enrichment	GJA1	2.72
27	Syndactyly, type iii	Enrichment	GJA1	2.72
28	Syndactyly, type v	Enrichment	GJA1	2.72
29	Craniometaphyseal dysplasia	Enrichment	GJA1	2.72
30	Cardiovascular system disease	Enrichment	KCNQ1	2.72
31	Growth delay due to insulin-like growth factor type 1 deficiency	Enrichment	IGF1	2.72
32	Rare genetic deafness	Enrichment	KCNE1, KCNQ1	2.60
33	Atrial fibrillation, familial, 3	Enrichment	KCNQ1	2.54
34	Short qt syndrome 2	Enrichment	KCNQ1	2.54
35	Brugada syndrome 8	Enrichment	HCN4	2.54
36	Long qt syndrome 2	Enrichment	KCNQ1	2.42
37	Atrial fibrillation	Enrichment	KCNQ1	2.42
38	Pregnancy loss, recurrent 1	Enrichment	KCNQ1	2.42
39	Familial sick sinus syndrome	Enrichment	HCN4	2.42
40	Insulin-like growth factor i	Enrichment	IGF1	2.32
41	Cleft upper lip	Enrichment	GJA1	2.32
42	Silver-russell syndrome 1	Enrichment	KCNQ1	2.17
43	Erythrokeratodermia variabilis et progressiva 1	Enrichment	GJA1	2.12
44	Ewing sarcoma	Enrichment	ERG	2.12
45	Hypoplastic left heart syndrome	Enrichment	GJA1	2.12
46	Neurofibromatosis, type i	Enrichment	ERG	2.07
47	Wolff-parkinson-white syndrome	Enrichment	KCNQ1	1.82
48	Sudden infant death syndrome	Enrichment	KCNQ1	1.79
49	Beckwith-wiedemann syndrome	Enrichment	KCNQ1	1.77
50	Cardiomyopathy, dilated, 1a	Enrichment	HAND2	1.70
51	Ear malformation	Enrichment	KCNQ1	1.64
52	Brugada syndrome	Enrichment	HCN4	1.61
53	Left ventricular noncompaction	Enrichment	HCN4	1.48
54	Sensorineural hearing loss	Enrichment	KCNE1	1.35
55	Familial isolated dilated cardiomyopathy	Enrichment	HAND2	1.30
56	Myeloma, multiple	Enrichment	HDAC4	1.28
57	Dilated cardiomyopathy	Enrichment	KCNE1	1.13
58	Rare autosomal recessive non-syndromic sensorineural deafness type dfnb	Enrichment	GJA1	1.09

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

Genes targeted by miRNAs in adipocytes

Pathway Network for Genes targeted by miRNAs in adipocytes

Member Pathways for Genes targeted by miRNAs in adipocytes

Pathways in the Genes targeted by miRNAs in adipocytes SuperPath

Associated Genes for Genes targeted by miRNAs in adipocytes

Associated Disorders for Genes targeted by miRNAs in adipocytes

Disorders associated with Genes targeted by miRNAs in adipocytes SuperPath

STRING Interaction Network for Genes targeted by miRNAs in adipocytes

Sources for Genes targeted by miRNAs in adipocytes