Mitotic Telophase/Cytokinesis

No Pathway Network information available for Mitotic Telophase/Cytokinesis

Pathways in the Mitotic Telophase/Cytokinesis SuperPath

#	Name	Source	Genes
1	Mitotic Telophase/Cytokinesis	Reactome	KIF20A KIF23 MAU2 NIPBL PDS5A PDS5B PLK1 RAD21 SMC1A SMC3 STAG1 STAG2 WAPL (see all 13) (see less)
2	Cohesin Loading onto Chromatin	Reactome	MAU2 NIPBL PDS5A PDS5B RAD21 SMC1A SMC3 STAG1 STAG2 WAPL (see all 10) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	STAG1	STAG1 Cohesin Complex Component	Protein Coding	2
2	STAG2	STAG2 Cohesin Complex Component	Protein Coding	2
3	PDS5B	PDS5 Cohesin Associated Factor B	Protein Coding	2
4	WAPL	WAPL Cohesin Release Factor	Protein Coding	2
5	PDS5A	PDS5 Cohesin Associated Factor A	Protein Coding	2
6	MAU2	MAU2 Sister Chromatid Cohesion Factor	Protein Coding	2
7	NIPBL	NIPBL Cohesin Loading Factor	Protein Coding	2
8	RAD21	RAD21 Cohesin Complex Component	Protein Coding	2
9	SMC1A	Structural Maintenance Of Chromosomes 1A	Protein Coding	2
10	SMC3	Structural Maintenance Of Chromosomes 3	Protein Coding	2
11	KIF20A	Kinesin Family Member 20A	Protein Coding	1
12	PLK1	Polo Like Kinase 1	Protein Coding	1
13	KIF23	Kinesin Family Member 23	Protein Coding	1

Disorders associated with Mitotic Telophase/Cytokinesis SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Cornelia de lange syndrome 1	Enrichment	NIPBL, RAD21, SMC1A, SMC3	10.80
2	Cornelia de lange syndrome	Enrichment	NIPBL, RAD21, SMC1A, SMC3	10.80
3	Wiedemann-steiner syndrome	Enrichment	SMC1A, SMC3	5.14
4	Semilobar holoprosencephaly	Enrichment	SMC1A, STAG2	4.13
5	Microcephaly	Enrichment	KIF23, NIPBL, SMC1A	3.71
6	Developmental and epileptic encephalopathy 85 with or without midline brain defects	Enrichment	SMC1A	3.13
7	Holoprosencephaly 13, x-linked	Enrichment	STAG2	3.13
8	Cornelia de lange syndrome 3 with or without midline brain defects	Enrichment	SMC3	3.13
9	Cornelia de lange syndrome 4 with or without midline brain defects	Enrichment	RAD21	3.13
10	Mullegama-klein-martinez syndrome	Enrichment	STAG2	3.13
11	Intellectual developmental disorder, autosomal dominant 47	Enrichment	STAG1	3.13
12	Mungan syndrome	Enrichment	RAD21	3.13
13	Xq25 microduplication syndrome	Enrichment	STAG2	3.13
14	Cardiomyopathy, familial restrictive, 6	Enrichment	KIF20A	3.02
15	Cornelia de lange syndrome 2	Enrichment	SMC1A	2.83
16	Chromosome 5p13 duplication syndrome	Enrichment	NIPBL	2.83
17	Anemia, congenital dyserythropoietic, type iiia	Enrichment	KIF23	2.72
18	Trichorhinophalangeal syndrome, type ii	Enrichment	RAD21	2.53
19	Brachydactyly	Enrichment	NIPBL	2.29
20	Vesicoureteral reflux	Enrichment	NIPBL	2.29
21	Rett syndrome, congenital variant	Enrichment	SMC1A	2.23
22	Cryptorchidism	Enrichment	NIPBL	2.23
23	Cryptorchidism, unilateral or bilateral	Enrichment	NIPBL	2.18
24	Familial isolated restrictive cardiomyopathy	Enrichment	KIF20A	2.17
25	Diaphragmatic hernia, congenital	Enrichment	NIPBL	2.02
26	Cleft palate, isolated	Enrichment	NIPBL	1.90
27	Alobar holoprosencephaly	Enrichment	STAG2	1.90
28	Tetralogy of fallot	Enrichment	NIPBL	1.72
29	Congenital nervous system abnormality	Enrichment	SMC1A	1.12
30	Nervous system disease	Enrichment	SMC1A	1.12
31	Autism spectrum disorder	Enrichment	SMC3	1.11

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

Mitotic Telophase/Cytokinesis

Pathway Network for Mitotic Telophase/Cytokinesis

Member Pathways for Mitotic Telophase/Cytokinesis

Pathways in the Mitotic Telophase/Cytokinesis SuperPath

Associated Genes for Mitotic Telophase/Cytokinesis

Associated Disorders for Mitotic Telophase/Cytokinesis

Disorders associated with Mitotic Telophase/Cytokinesis SuperPath

STRING Interaction Network for Mitotic Telophase/Cytokinesis

Sources for Mitotic Telophase/Cytokinesis