Miscellaneous transport and binding events

No Pathway Network information available for Miscellaneous transport and binding events

Pathways in the Miscellaneous transport and binding events SuperPath

#	Name	Source	Genes
1	Miscellaneous transport and binding events	Reactome	ADD2 ADD3 ANKH AZGP1 CSN1S1 CSN3 CTNS DMTN LRRC8A LRRC8B LRRC8C LRRC8D LRRC8E MAGT1 MMGT1 MRS2 NIPA1 NIPA2 NIPAL1 NIPAL2 NIPAL3 NIPAL4 PIP SLC66A1 TUSC3 (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	ADD2	Adducin 2	Protein Coding	1
2	ADD3	Adducin 3	Protein Coding	1
3	NIPA1	NIPA Magnesium Transporter 1	Protein Coding	1
4	CSN1S1	Casein Alpha S1	Protein Coding	1
5	CSN3	Casein Kappa	Protein Coding	1
6	CTNS	Cystinosin, Lysosomal Cystine Transporter	Protein Coding	1
7	NIPAL1	NIPA Like Domain Containing 1	Protein Coding	1
8	DMTN	Dematin Actin Binding Protein	Protein Coding	1
9	LRRC8B	Leucine Rich Repeat Containing 8 VRAC Subunit B	Protein Coding	1
10	NIPAL4	NIPA Like Domain Containing 4	Protein Coding	1
11	PIP	Prolactin Induced Protein	Protein Coding	1
12	SLC66A1	Solute Carrier Family 66 Member 1	Protein Coding	1
13	LRRC8D	Leucine Rich Repeat Containing 8 VRAC Subunit D	Protein Coding	1
14	ANKH	ANKH Inorganic Pyrophosphate Transport Regulator	Protein Coding	1
15	LRRC8A	Leucine Rich Repeat Containing 8 VRAC Subunit A	Protein Coding	1
16	AZGP1	Alpha-2-Glycoprotein 1, Zinc-Binding	Protein Coding	1
17	NIPAL3	NIPA Like Domain Containing 3	Protein Coding	1
18	MRS2	Magnesium Transporter MRS2	Protein Coding	1
19	NIPAL2	NIPA Like Domain Containing 2	Protein Coding	1
20	TUSC3	Tumor Suppressor Candidate 3	Protein Coding	1
21	LRRC8E	Leucine Rich Repeat Containing 8 VRAC Subunit E	Protein Coding	1
22	NIPA2	NIPA Magnesium Transporter 2	Protein Coding	1
23	MAGT1	Magnesium Transporter 1	Protein Coding	1
24	LRRC8C	Leucine Rich Repeat Containing 8 VRAC Subunit C	Protein Coding	1
25	MMGT1	Membrane Magnesium Transporter 1	Protein Coding	1

Disorders associated with Miscellaneous transport and binding events SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Chromosome 15q11.2 deletion syndrome	Enrichment	NIPA1, NIPA2	4.49
2	Intellectual developmental disorder, autosomal recessive 7	Enrichment	TUSC3	2.73
3	Congenital disorder of glycosylation, type icc	Enrichment	MAGT1	2.73
4	Cerebral palsy, spastic quadriplegic, 3	Enrichment	ADD3	2.73
5	Agammaglobulinemia 5, autosomal dominant	Enrichment	LRRC8A	2.73
6	Telangiectasia, impaired intellectual development, microcephaly, metaphyseal dysplasia, eye abnormalities, and short stature	Enrichment	LRRC8C	2.73
7	Cystinosis, adult nonnephropathic	Enrichment	CTNS	2.43
8	Cystinosis, late-onset juvenile or adolescent nephropathic type	Enrichment	CTNS	2.43
9	Cystinosis, nephropathic	Enrichment	CTNS	2.43
10	Spastic paraplegia 6, autosomal dominant	Enrichment	NIPA1	2.43
11	Immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection, and neoplasia	Enrichment	MAGT1	2.43
12	Cystinosis	Enrichment	CTNS	2.43
13	Craniometaphyseal dysplasia	Enrichment	ANKH	2.43
14	Ichthyosis, congenital, autosomal recessive 6	Enrichment	NIPAL4	2.43
15	Intellectual developmental disorder, autosomal recessive 24	Enrichment	TUSC3	2.43
16	Craniometaphyseal dysplasia, autosomal dominant	Enrichment	ANKH	2.26
17	Fanconi syndrome	Enrichment	CTNS	2.26
18	Chondrocalcinosis 2	Enrichment	ANKH	2.13
19	Spastic quadriplegic cerebral palsy	Enrichment	ADD3	2.13
20	Erythrokeratodermia variabilis et progressiva 1	Enrichment	NIPAL4	1.83
21	Congenital nonbullous ichthyosiform erythroderma	Enrichment	NIPAL4	1.74
22	Autosomal non-syndromic agammaglobulinemia	Enrichment	LRRC8A	1.74
23	Autosomal recessive congenital ichthyosis	Enrichment	NIPAL4	1.56
24	Congenital disorder of glycosylation, type in	Enrichment	MAGT1	1.51
25	Cerebral palsy	Enrichment	ADD3	1.16
26	Hereditary spastic paraplegia	Enrichment	NIPA1	1.13
27	Nephrotic syndrome	Enrichment	CTNS	1.12
28	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	Enrichment	NIPA1	0.99
29	Autosomal recessive non-syndromic intellectual disability	Enrichment	TUSC3	0.99
30	Congenital nervous system abnormality	Enrichment	TUSC3	0.75
31	Nervous system disease	Enrichment	TUSC3	0.75

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

Miscellaneous transport and binding events

Pathway Network for Miscellaneous transport and binding events

Member Pathways for Miscellaneous transport and binding events

Pathways in the Miscellaneous transport and binding events SuperPath

Associated Genes for Miscellaneous transport and binding events

Associated Disorders for Miscellaneous transport and binding events

Disorders associated with Miscellaneous transport and binding events SuperPath

STRING Interaction Network for Miscellaneous transport and binding events

Sources for Miscellaneous transport and binding events