Other interleukin signaling

No Pathway Network information available for Other interleukin signaling

Pathways in the Other interleukin signaling SuperPath

#	Name	Source	Genes
1	Other interleukin signaling	Reactome	CD4 CSF1 CSF1R CSF3 CSF3R IFNL1 IFNLR1 IL10RB IL16 IL32 IL34 JAK1 PRTN3 PTPRZ1 SDC1 SNAP25 STX1A STX3 STX4 STXBP2 TXLNA TYK2 VAMP2 (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	CSF1	Colony Stimulating Factor 1	Protein Coding	1
2	CSF1R	Colony Stimulating Factor 1 Receptor	Protein Coding	1
3	CSF3	Colony Stimulating Factor 3	Protein Coding	1
4	CSF3R	Colony Stimulating Factor 3 Receptor	Protein Coding	1
5	IL34	Interleukin 34	Protein Coding	1
6	IFNLR1	Interferon Lambda Receptor 1	Protein Coding	1
7	TXLNA	Taxilin Alpha	Protein Coding	1
8	IFNL1	Interferon Lambda 1	Protein Coding	1
9	IL10RB	Interleukin 10 Receptor Subunit Beta	Protein Coding	1
10	IL16	Interleukin 16	Protein Coding	1
11	JAK1	Janus Kinase 1	Protein Coding	1
12	PRTN3	Proteinase 3	Protein Coding	1
13	PTPRZ1	Protein Tyrosine Phosphatase Receptor Type Z1	Protein Coding	1
14	SDC1	Syndecan 1	Protein Coding	1
15	SNAP25	Synaptosome Associated Protein 25	Protein Coding	1
16	STX1A	Syntaxin 1A	Protein Coding	1
17	STX3	Syntaxin 3	Protein Coding	1
18	STX4	Syntaxin 4	Protein Coding	1
19	STXBP2	Syntaxin Binding Protein 2	Protein Coding	1
20	VAMP2	Vesicle Associated Membrane Protein 2	Protein Coding	1
21	TYK2	Tyrosine Kinase 2	Protein Coding	1
22	CD4	CD4 Molecule	Protein Coding	1
23	IL32	Interleukin 32	Protein Coding	1

Disorders associated with Other interleukin signaling SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Immunodeficiency 35	Enrichment	TYK2	2.77
2	Diarrhea 12, with microvillus atrophy	Enrichment	STX3	2.77
3	Developmental and epileptic encephalopathy 117	Enrichment	SNAP25	2.77
4	Okt4 epitope deficiency	Enrichment	CD4	2.77
5	Familial hemophagocytic lymphohistiocytosis 5	Enrichment	STXBP2	2.77
6	Hemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease	Enrichment	STXBP2	2.77
7	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements	Enrichment	VAMP2	2.77
8	Deafness, autosomal recessive 123	Enrichment	STX4	2.77
9	Epilepsy with generalized tonic-clonic seizures	Enrichment	SNAP25	2.77
10	Brain abnormalities, neurodegeneration, and dysosteosclerosis	Enrichment	CSF1R	2.77
11	Immunodeficiency 79	Enrichment	CD4	2.77
12	Retinal dystrophy and microvillus inclusion disease	Enrichment	STX3	2.77
13	Csf1r-related disorder	Enrichment	CSF1R	2.77
14	Chronic neutrophilic leukemia	Enrichment	CSF3R	2.77
15	Early-onset calcifying leukoencephalopathy-skeletal dysplasia	Enrichment	CSF1R	2.77
16	Mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiency	Enrichment	JAK1	2.77
17	Neutrophilia, hereditary	Enrichment	CSF3R	2.47
18	Neutropenia, severe congenital, 7, autosomal recessive	Enrichment	CSF3R	2.47
19	Severe congenital neutropenia 7	Enrichment	CSF3R	2.47
20	Autoinflammation, immune dysregulation, and eosinophilia	Enrichment	JAK1	2.47
21	Mitochondrial complex iv deficiency, nuclear type 12	Enrichment	STXBP2	2.47
22	Lymphomatoid papulosis	Enrichment	TYK2	2.47
23	Primary cutaneous anaplastic large cell lymphoma	Enrichment	TYK2	2.47
24	Leukoencephalopathy, hereditary diffuse, with spheroids 1	Enrichment	CSF1R	2.29
25	Microvillus inclusion disease	Enrichment	STX3	2.29
26	Breast implant-associated anaplastic large cell lymphoma	Enrichment	JAK1	2.29
27	Inflammatory bowel disease 25	Enrichment	IL10RB	2.29
28	Developmental and epileptic encephalopathy 2	Enrichment	SNAP25	2.17
29	Hepatitis b	Enrichment	IL10RB	2.17
30	Hemophagocytic lymphohistiocytosis, familial, 1	Enrichment	STXBP2	2.07
31	Inflammatory bowel disease 25, autosomal recessive	Enrichment	IL10RB	1.99
32	Granulomatosis with polyangiitis	Enrichment	PRTN3	1.99
33	Il10-related early-onset inflammatory bowel disease	Enrichment	IL10RB	1.99
34	Focal epilepsy	Enrichment	SNAP25	1.93
35	Severe congenital neutropenia	Enrichment	CSF3R	1.87
36	Atypical chronic myeloid leukemia, bcr-abl1 negative	Enrichment	CSF3R	1.82
37	Frontotemporal dementia 1	Enrichment	CSF1R	1.73
38	Presynaptic congenital myasthenic syndromes	Enrichment	SNAP25	1.73
39	Alzheimer's disease	Enrichment	CSF1R	1.66
40	Stereotypic movement disorder	Enrichment	SNAP25	1.66
41	Alzheimer disease, familial, 1	Enrichment	CSF1R	1.55
42	Williams-beuren syndrome	Enrichment	STX1A	1.48
43	Mitochondrial complex iv deficiency, nuclear type 1	Enrichment	STXBP2	1.44
44	Autoinflammatory disease	Enrichment	STXBP2	1.40
45	Severe covid-19	Enrichment	IL10RB	1.32
46	Cystic fibrosis	Enrichment	STX1A	1.28
47	Developmental and epileptic encephalopathy	Enrichment	SNAP25	1.23
48	Optic atrophy plus syndrome	Enrichment	SNAP25	1.14
49	Sensorineural hearing loss	Enrichment	STX4	1.11
50	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	Enrichment	CSF1R	1.03
51	Autism	Enrichment	STX1A	0.94
52	Microcephaly	Enrichment	SNAP25	0.72

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

Other interleukin signaling

Pathway Network for Other interleukin signaling

Member Pathways for Other interleukin signaling

Pathways in the Other interleukin signaling SuperPath

Associated Genes for Other interleukin signaling

Associated Disorders for Other interleukin signaling

Disorders associated with Other interleukin signaling SuperPath

STRING Interaction Network for Other interleukin signaling

Sources for Other interleukin signaling