Transport of vitamins, nucleosides, and related molecules

Pathway network for the Transport of vitamins, nucleosides, and related molecules SuperPath

Sources:

Reactome

Pathways in the Transport of vitamins, nucleosides, and related molecules SuperPath

#	Name	Source	Genes
1	Transport of vitamins, nucleosides, and related molecules	Reactome	APOD ARL2 ARL2BP AVP LCN1 LCN12 LCN15 PDZD11 SLC16A2 SLC27A1 SLC27A4 SLC27A6 SLC28A1 SLC28A2 SLC28A3 SLC29A1 SLC29A2 SLC29A3 SLC29A4 SLC33A1 SLC35A1 SLC35A2 SLC35A3 SLC35B2 SLC35B3 SLC35B4 SLC35C1 SLC35D1 SLC35D2 SLC5A6 SLCO1A2 SLCO1B1 SLCO1B3 SLCO1C1 SLCO2A1 SLCO2B1 SLCO3A1 SLCO4A1 SLCO4C1 (see all 39) (see less)
2	Transport of organic anions	Reactome	AVP SLC16A2 SLCO1A2 SLCO1B1 SLCO1B3 SLCO1C1 SLCO2A1 SLCO2B1 SLCO3A1 SLCO4A1 SLCO4C1 (see all 11) (see less)
3	Transport of nucleotide sugars	Reactome	SLC35A1 SLC35A2 SLC35A3 SLC35B2 SLC35B3 SLC35B4 SLC35C1 SLC35D1 SLC35D2 (see all 9) (see less)
4	Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane	Reactome	ARL2 ARL2BP SLC28A1 SLC28A2 SLC28A3 SLC29A1 SLC29A2 SLC29A3 SLC29A4 (see all 9) (see less)
5	Transport of fatty acids	Reactome	APOD LCN1 LCN12 LCN15 SLC27A1 SLC27A4 SLC27A6 (see all 7) (see less)
6	Defective SLC29A3 causes histiocytosis-lymphadenopathy plus syndrome (HLAS)	Reactome	SLC29A3
7	Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS)	Reactome	SLC27A4
8	Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)	Reactome	SLCO2A1
9	Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS)	Reactome	SLC35A3
10	Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M)	Reactome	SLC35A2

Gene overlap in member pathways for Transport of vitamins, nucleosides, and related molecules SuperPath

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

#	Symbol	Description	Category	# Related Pathways
1	SLC27A4	Solute Carrier Family 27 Member 4	Protein Coding	3
2	SLC35A3	Solute Carrier Family 35 Member A3	Protein Coding	3
3	SLC29A3	Solute Carrier Family 29 Member 3	Protein Coding	3
4	SLCO2A1	Solute Carrier Organic Anion Transporter Family Member 2A1	Protein Coding	3
5	SLC35A2	Solute Carrier Family 35 Member A2	Protein Coding	3
6	SLC35A1	Solute Carrier Family 35 Member A1	Protein Coding	2
7	SLCO1B1	Solute Carrier Organic Anion Transporter Family Member 1B1	Protein Coding	2
8	SLC35D2	Solute Carrier Family 35 Member D2	Protein Coding	2
9	SLCO2B1	Solute Carrier Organic Anion Transporter Family Member 2B1	Protein Coding	2
10	SLC29A1	Solute Carrier Family 29 Member 1 (Augustine Blood Group)	Protein Coding	2
11	SLC29A4	Solute Carrier Family 29 Member 4	Protein Coding	2
12	SLC35D1	Solute Carrier Family 35 Member D1	Protein Coding	2
13	ARL2BP	ARF Like GTPase 2 Binding Protein	Protein Coding	2
14	SLCO4A1	Solute Carrier Organic Anion Transporter Family Member 4A1	Protein Coding	2
15	SLCO3A1	Solute Carrier Organic Anion Transporter Family Member 3A1	Protein Coding	2
16	SLCO1B3	Solute Carrier Organic Anion Transporter Family Member 1B3	Protein Coding	2
17	LCN12	Lipocalin 12	Protein Coding	2
18	SLC27A6	Solute Carrier Family 27 Member 6	Protein Coding	2
19	SLC29A2	Solute Carrier Family 29 Member 2	Protein Coding	2
20	APOD	Apolipoprotein D	Protein Coding	2
21	SLC35B2	Solute Carrier Family 35 Member B2	Protein Coding	2
22	SLCO4C1	Solute Carrier Organic Anion Transporter Family Member 4C1	Protein Coding	2
23	SLC27A1	Solute Carrier Family 27 Member 1	Protein Coding	2
24	LCN15	Lipocalin 15	Protein Coding	2
25	LCN1	Lipocalin 1	Protein Coding	2
26	ARL2	ARF Like GTPase 2	Protein Coding	2
27	SLC35B3	Solute Carrier Family 35 Member B3	Protein Coding	2
28	SLCO1C1	Solute Carrier Organic Anion Transporter Family Member 1C1	Protein Coding	2
29	AVP	Arginine Vasopressin	Protein Coding	2
30	SLC35C1	Solute Carrier Family 35 Member C1	Protein Coding	2
31	SLC28A3	Solute Carrier Family 28 Member 3	Protein Coding	2
32	SLC16A2	Solute Carrier Family 16 Member 2	Protein Coding	2
33	SLCO1A2	Solute Carrier Organic Anion Transporter Family Member 1A2	Protein Coding	2
34	SLC35B4	Solute Carrier Family 35 Member B4	Protein Coding	2
35	SLC28A2	Solute Carrier Family 28 Member 2	Protein Coding	2
36	SLC28A1	Solute Carrier Family 28 Member 1	Protein Coding	2
37	PDZD11	PDZ Domain Containing 11	Protein Coding	1
38	SLC5A6	Solute Carrier Family 5 Member 6	Protein Coding	1
39	SLC33A1	Solute Carrier Family 33 Member 1	Protein Coding	1

Disorders associated with Transport of vitamins, nucleosides, and related molecules SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Histiocytosis	Direct
2	Primary hypertrophic osteoarthropathy	Direct
3	Distal arthrogryposis	Direct
4	Epilepsy	Direct
5	Immunodeficiency 47	Direct
6	Early infantile epileptic encephalopathy	Direct
7	Hyperbilirubinemia, rotor type	Enrichment	SLCO1B1, SLCO1B3	5.75
8	Ichthyosis prematurity syndrome	Enrichment	SLC27A4	4.13
9	Congenital disorder of glycosylation, type iim	Enrichment	SLC35A2	3.18
10	Congenital disorder of glycosylation, type iic	Enrichment	SLC35C1	3.18
11	Leukodystrophy, hypomyelinating, 26, with chondrodysplasia	Enrichment	SLC35B2	3.18
12	Congenital disorder of glycosylation, type iif	Enrichment	SLC35A1	3.18
13	Arthrogryposis, impaired intellectual development, and seizures	Enrichment	SLC35A3	3.18
14	Isolated focal cortical dysplasia type ia	Enrichment	SLC35A2	3.18
15	Primary bone dysplasia with multiple joint dislocations	Enrichment	SLC35B2	3.18
16	Retinitis pigmentosa 82 with or without situs inversus	Enrichment	ARL2BP	3.18
17	Hemolytic disease of the fetus	Enrichment	SLC29A1	3.18
18	Uridine-cytidineuria	Enrichment	SLC28A1	3.18
19	Retinitis pigmentosa with or without situs inversus	Enrichment	ARL2BP	3.18
20	Diabetes insipidus, neurohypophyseal	Enrichment	AVP	3.09
21	Hypertrophic osteoarthropathy, primary, autosomal dominant	Enrichment	SLCO2A1	3.09
22	Allan-herndon-dudley syndrome	Enrichment	SLC16A2	3.09
23	Central diabetes insipidus	Enrichment	AVP	3.09
24	Chronic enteropathy associated with slco2a1 gene	Enrichment	SLCO2A1	3.09
25	Hereditary arginine vasopressin deficiency	Enrichment	AVP	3.09
26	Autosomal recessive congenital ichthyosis	Enrichment	SLC27A4	2.96
27	Schneckenbecken dysplasia	Enrichment	SLC35D1	2.88
28	Histiocytosis-lymphadenopathy plus syndrome	Enrichment	SLC29A3	2.88
29	Phoar2-enteropathy syndrome	Enrichment	SLCO2A1	2.79
30	Dysosteosclerosis	Enrichment	SLC29A3	2.70
31	Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1	Enrichment	ARL2	2.70
32	Hypertrophic osteoarthropathy, primary, autosomal recessive, 1	Enrichment	SLCO2A1	2.61
33	Spastic paraplegia 42, autosomal dominant	Enrichment	SLC33A1	2.54
34	Peripheral motor neuropathy, childhood-onset, biotin-responsive	Enrichment	SLC5A6	2.54
35	Huppke-brendel syndrome	Enrichment	SLC33A1	2.54
36	Sodium-dependent multivitamin transporter deficiency	Enrichment	SLC5A6	2.54
37	Diabetes insipidus	Enrichment	AVP	2.49
38	Gilbert syndrome	Enrichment	SLCO1B1	2.05
39	Congenital disorder of glycosylation, type in	Enrichment	SLC35A2	1.95
40	Hypothyroidism	Enrichment	SLC33A1	1.64
41	Hereditary spastic paraplegia	Enrichment	SLC16A2	1.47
42	Retinitis pigmentosa	Enrichment	ARL2BP	0.88
43	Hereditary retinal dystrophy	Enrichment	ARL2BP	0.75
44	Fundus dystrophy	Enrichment	ARL2BP	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

Transport of vitamins, nucleosides, and related molecules

Pathway Network for Transport of vitamins, nucleosides, and related molecules

Pathway network for the Transport of vitamins, nucleosides, and related molecules SuperPath

Member Pathways for Transport of vitamins, nucleosides, and related molecules

Pathways in the Transport of vitamins, nucleosides, and related molecules SuperPath

Gene overlap in member pathways for Transport of vitamins, nucleosides, and related molecules SuperPath

Associated Genes for Transport of vitamins, nucleosides, and related molecules

Associated Disorders for Transport of vitamins, nucleosides, and related molecules

Disorders associated with Transport of vitamins, nucleosides, and related molecules SuperPath

STRING Interaction Network for Transport of vitamins, nucleosides, and related molecules

Sources for Transport of vitamins, nucleosides, and related molecules