Intraflagellar transport proteins binding to dynein

No Pathway Network information available for Intraflagellar transport proteins binding to dynein

Pathways in the Intraflagellar transport proteins binding to dynein SuperPath

#	Name	Source	Genes
1	Intraflagellar transport proteins binding to dynein	WikiPathways	DYNC1H1 DYNC1I1 DYNC1I2 DYNC1LI1 DYNC1LI2 DYNC2H1 DYNC2I1 DYNC2I2 DYNC2LI1 DYNLL1 DYNLL2 DYNLRB1 DYNLRB2 DYNLT1 DYNLT2B DYNLT3 (see all 16) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	DYNC2I2	Dynein 2 Intermediate Chain 2	Protein Coding	1
2	DYNLL1	Dynein Light Chain LC8-Type 1	Protein Coding	1
3	DYNC2H1	Dynein Cytoplasmic 2 Heavy Chain 1	Protein Coding	1
4	DYNC2I1	Dynein 2 Intermediate Chain 1	Protein Coding	1
5	DYNC2LI1	Dynein Cytoplasmic 2 Light Intermediate Chain 1	Protein Coding	1
6	DYNLT2B	Dynein Light Chain Tctex-Type 2B	Protein Coding	1
7	DYNC1LI2	Dynein Cytoplasmic 1 Light Intermediate Chain 2	Protein Coding	1
8	DYNC1I1	Dynein Cytoplasmic 1 Intermediate Chain 1	Protein Coding	1
9	DYNC1H1	Dynein Cytoplasmic 1 Heavy Chain 1	Protein Coding	1
10	DYNC1I2	Dynein Cytoplasmic 1 Intermediate Chain 2	Protein Coding	1
11	DYNLL2	Dynein Light Chain LC8-Type 2	Protein Coding	1
12	DYNLRB1	Dynein Light Chain Roadblock-Type 1	Protein Coding	1
13	DYNLRB2	Dynein Light Chain Roadblock-Type 2	Protein Coding	1
14	DYNLT1	Dynein Light Chain Tctex-Type 1	Protein Coding	1
15	DYNLT3	Dynein Light Chain Tctex-Type 3	Protein Coding	1
16	DYNC1LI1	Dynein Cytoplasmic 1 Light Intermediate Chain 1	Protein Coding	1

Disorders associated with Intraflagellar transport proteins binding to dynein SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Short-rib thoracic dysplasia 3 with or without polydactyly	Enrichment	DYNC1H1, DYNC2H1, DYNC2I1, DYNC2I2, DYNLT2B	10.61
2	Short rib-polydactyly syndrome, verma-naumoff type	Enrichment	DYNC2H1, DYNC2I1, DYNC2I2	7.87
3	Short-rib thoracic dysplasia 1 with or without polydactyly	Enrichment	DYNC2H1, DYNC2I1, DYNC2I2, DYNC2LI1	7.29
4	Jeune thoracic dystrophy	Enrichment	DYNC2H1, DYNC2I1, DYNC2I2	5.52
5	Asphyxiating thoracic dystrophy	Enrichment	DYNC2H1, DYNC2I1, DYNC2I2	5.36
6	Short-rib thoracic dysplasia 8 with or without polydactyly	Enrichment	DYNC2I1	2.93
7	Dync1h1-related disorders	Enrichment	DYNC1H1	2.93
8	Neurodevelopmental disorder with microcephaly and structural brain anomalies	Enrichment	DYNC1I2	2.93
9	Lung disease	Enrichment	DYNC2H1	2.93
10	Spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant	Enrichment	DYNC1H1	2.63
11	Short-rib thoracic dysplasia 17 with or without polydactyly	Enrichment	DYNLT2B	2.63
12	Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies	Enrichment	DYNC1I2	2.63
13	Cortical dysplasia, complex, with other brain malformations 13	Enrichment	DYNC1H1	2.63
14	Sitosterolemia 2	Enrichment	DYNC2LI1	2.63
15	Spinal muscular atrophy with lower extremity predominant	Enrichment	DYNC1H1	2.63
16	Short-rib thoracic dysplasia 15 with polydactyly	Enrichment	DYNC2LI1	2.63
17	Charcot-marie-tooth disease, axonal, type 2o	Enrichment	DYNC1H1	2.63
18	Sitosterolemia 1	Enrichment	DYNC2LI1	2.45
19	Short-rib thoracic dysplasia 11 with or without polydactyly	Enrichment	DYNC2I2	2.45
20	Sitosterolemia	Enrichment	DYNC2LI1	2.45
21	Newborn respiratory distress syndrome	Enrichment	DYNC2H1	2.33
22	Spinal muscular atrophy	Enrichment	DYNC1H1	2.23
23	Short rib-polydactyly syndrome	Enrichment	DYNC2H1	2.15
24	Polycystic kidney disease 4 with or without polycystic liver disease	Enrichment	DYNC2H1	2.03
25	Short-rib thoracic dysplasia 12	Enrichment	DYNC2H1	2.03
26	Ellis-van creveld syndrome	Enrichment	DYNC2LI1	1.98
27	Polymicrogyria	Enrichment	DYNC1H1	1.93
28	Primary bone dysplasia	Enrichment	DYNC2H1	1.93
29	Osteochondrodysplasia	Enrichment	DYNC2H1	1.89
30	Short-rib thoracic dysplasia 6 with or without polydactyly	Enrichment	DYNC2H1	1.85
31	Heart, malformation of	Enrichment	DYNC2H1	1.68
32	Charcot-marie-tooth disease type 4	Enrichment	DYNC1H1	1.68
33	Lissencephaly	Enrichment	DYNC1H1	1.61
34	Peripheral nervous system disease	Enrichment	DYNC1H1	1.43
35	Neuropathy	Enrichment	DYNC1H1	1.43
36	Myopathy	Enrichment	DYNC1H1	1.34
37	Charcot-marie-tooth disease	Enrichment	DYNC1H1	1.33
38	Autosomal dominant non-syndromic intellectual disability	Enrichment	DYNC1H1	1.24
39	Congenital nervous system abnormality	Enrichment	DYNC1H1	0.93
40	Nervous system disease	Enrichment	DYNC1H1	0.93
41	Autism spectrum disorder	Enrichment	DYNC1H1	0.92
42	Microcephaly	Enrichment	DYNC1H1	0.87
43	Hereditary retinal dystrophy	Enrichment	DYNC2H1	0.53
44	Fundus dystrophy	Enrichment	DYNC2H1	0.53

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

Intraflagellar transport proteins binding to dynein

Pathway Network for Intraflagellar transport proteins binding to dynein

Member Pathways for Intraflagellar transport proteins binding to dynein

Pathways in the Intraflagellar transport proteins binding to dynein SuperPath

Associated Genes for Intraflagellar transport proteins binding to dynein

Associated Disorders for Intraflagellar transport proteins binding to dynein

Disorders associated with Intraflagellar transport proteins binding to dynein SuperPath

STRING Interaction Network for Intraflagellar transport proteins binding to dynein

Sources for Intraflagellar transport proteins binding to dynein