Insulin receptor recycling

Pathway network for the Insulin receptor recycling SuperPath

Sources:

Reactome
PubChem

Pathways in the Insulin receptor recycling SuperPath

#	Name	Source	Genes
1	Insulin receptor recycling	Reactome	ATP6AP1 ATP6V0A1 ATP6V0A2 ATP6V0A4 ATP6V0B ATP6V0C ATP6V0D1 ATP6V0D2 ATP6V0E1 ATP6V0E2 ATP6V1A ATP6V1B1 ATP6V1B2 ATP6V1C1 ATP6V1C2 ATP6V1D ATP6V1E1 ATP6V1E2 ATP6V1F ATP6V1G1 ATP6V1G2 ATP6V1G3 ATP6V1H CTSD IDE INS INSR PTPN1 PTPRF TCIRG1 (see all 30) (see less)
2	Iron uptake and transport	Reactome	ABCG2 ACO1 ATP6AP1 ATP6V0A1 ATP6V0A2 ATP6V0A4 ATP6V0B ATP6V0C ATP6V0D1 ATP6V0D2 ATP6V0E1 ATP6V0E2 ATP6V1A ATP6V1B1 ATP6V1B2 ATP6V1C1 ATP6V1C2 ATP6V1D ATP6V1E1 ATP6V1E2 ATP6V1F ATP6V1G1 ATP6V1G2 ATP6V1G3 ATP6V1H CAND1 CP CUL1 CYBRD1 FBXL5 FLVCR1 FTH1 FTL FTMT GLRX3 HEPH HFE HMOX1 HMOX2 IREB2 LCN2 MCOLN1 NEDD8 RPS27A SKP1 SLC11A2 SLC22A17 SLC40A1 SLC46A1 STEAP3 STEAP4 TCIRG1 TF TFR2 TFRC UBA52 UBB UBC (see all 58) (see less)
3	ROS and RNS production in phagocytes	Reactome	ATP6V0A1 ATP6V0A2 ATP6V0A4 ATP6V0B ATP6V0C ATP6V0D1 ATP6V0D2 ATP6V0E1 ATP6V0E2 ATP6V1A ATP6V1B1 ATP6V1B2 ATP6V1C1 ATP6V1C2 ATP6V1D ATP6V1E1 ATP6V1E2 ATP6V1F ATP6V1G1 ATP6V1G2 ATP6V1G3 ATP6V1H CYBA CYBB HVCN1 LPO MPO NCF1 NCF2 NCF4 NOS1 NOS2 NOS3 RAC2 SLC11A1 TCIRG1 (see all 36) (see less)
4	Transferrin endocytosis and recycling	Reactome	ATP6AP1 ATP6V0A1 ATP6V0A2 ATP6V0A4 ATP6V0B ATP6V0C ATP6V0D1 ATP6V0D2 ATP6V0E1 ATP6V0E2 ATP6V1A ATP6V1B1 ATP6V1B2 ATP6V1C1 ATP6V1C2 ATP6V1D ATP6V1E1 ATP6V1E2 ATP6V1F ATP6V1G1 ATP6V1G2 ATP6V1G3 ATP6V1H HFE MCOLN1 STEAP3 STEAP4 TCIRG1 TF TFR2 TFRC (see all 31) (see less)
5	ATP biosynthesis	PubChem	ATP6V0A1 ATP6V0B ATP6V0C ATP6V0D1 ATP6V0E1 ATP6V1A ATP6V1B2 ATP6V1C1 ATP6V1D ATP6V1E1 ATP6V1F ATP6V1G1 ATP6V1H (see all 13) (see less)
6	Events associated with phagocytolytic activity of PMN cells	Reactome	LPO MPO
7	melatonin degradation III	PubChem	MPO

Gene overlap in member pathways for Insulin receptor recycling SuperPath

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

#	Symbol	Description	Category	# Related Pathways
1	ATP6V1D	ATPase H+ Transporting V1 Subunit D	Protein Coding	5
2	ATP6V1H	ATPase H+ Transporting V1 Subunit H	Protein Coding	5
3	ATP6V1A	ATPase H+ Transporting V1 Subunit A	Protein Coding	5
4	ATP6V1B2	ATPase H+ Transporting V1 Subunit B2	Protein Coding	5
5	ATP6V0C	ATPase H+ Transporting V0 Subunit C	Protein Coding	5
6	ATP6V1C1	ATPase H+ Transporting V1 Subunit C1	Protein Coding	5
7	ATP6V1E1	ATPase H+ Transporting V1 Subunit E1	Protein Coding	5
8	ATP6V0B	ATPase H+ Transporting V0 Subunit B	Protein Coding	5
9	ATP6V0A1	ATPase H+ Transporting V0 Subunit A1	Protein Coding	5
10	ATP6V0E1	ATPase H+ Transporting V0 Subunit E1	Protein Coding	5
11	ATP6V0D1	ATPase H+ Transporting V0 Subunit D1	Protein Coding	5
12	ATP6V1F	ATPase H+ Transporting V1 Subunit F	Protein Coding	5
13	ATP6V1G1	ATPase H+ Transporting V1 Subunit G1	Protein Coding	5
14	TCIRG1	T Cell Immune Regulator 1, ATPase H+ Transporting V0 Subunit A3	Protein Coding	4
15	ATP6V1G3	ATPase H+ Transporting V1 Subunit G3	Protein Coding	4
16	ATP6V0E2	ATPase H+ Transporting V0 Subunit E2	Protein Coding	4
17	ATP6V0A2	ATPase H+ Transporting V0 Subunit A2	Protein Coding	4
18	ATP6V0D2	ATPase H+ Transporting V0 Subunit D2	Protein Coding	4
19	ATP6V1C2	ATPase H+ Transporting V1 Subunit C2	Protein Coding	4
20	ATP6V0A4	ATPase H+ Transporting V0 Subunit A4	Protein Coding	4
21	ATP6V1B1	ATPase H+ Transporting V1 Subunit B1	Protein Coding	4
22	ATP6V1G2	ATPase H+ Transporting V1 Subunit G2	Protein Coding	4
23	ATP6V1E2	ATPase H+ Transporting V1 Subunit E2	Protein Coding	4
24	ATP6AP1	ATPase H+ Transporting Accessory Protein 1	Protein Coding	3
25	MPO	Myeloperoxidase	Protein Coding	3
26	HFE	Homeostatic Iron Regulator	Protein Coding	2
27	STEAP3	STEAP3 Metalloreductase	Protein Coding	2
28	MCOLN1	Mucolipin TRP Cation Channel 1	Protein Coding	2
29	TF	Transferrin	Protein Coding	2
30	TFR2	Transferrin Receptor 2	Protein Coding	2
31	TFRC	Transferrin Receptor	Protein Coding	2
32	STEAP4	STEAP4 Metalloreductase	Protein Coding	2
33	LPO	Lactoperoxidase	Protein Coding	2
34	CTSD	Cathepsin D	Protein Coding	1
35	IDE	Insulin Degrading Enzyme	Protein Coding	1
36	INS	Insulin	Protein Coding	1
37	INSR	Insulin Receptor	Protein Coding	1
38	PTPN1	Protein Tyrosine Phosphatase Non-Receptor Type 1	Protein Coding	1
39	PTPRF	Protein Tyrosine Phosphatase Receptor Type F	Protein Coding	1
40	GLRX3	Glutaredoxin 3	Protein Coding	1
41	SLC46A1	Solute Carrier Family 46 Member 1	Protein Coding	1
42	CP	Ceruloplasmin	Protein Coding	1
43	FTH1	Ferritin Heavy Chain 1	Protein Coding	1
44	FTL	Ferritin Light Chain	Protein Coding	1
45	FBXL5	F-Box And Leucine Rich Repeat Protein 5	Protein Coding	1
46	FLVCR1	FLVCR Choline And Heme Transporter 1	Protein Coding	1
47	SLC40A1	Solute Carrier Family 40 Member 1	Protein Coding	1
48	HMOX1	Heme Oxygenase 1	Protein Coding	1
49	HMOX2	Heme Oxygenase 2	Protein Coding	1
50	IREB2	Iron Responsive Element Binding Protein 2	Protein Coding	1
51	LCN2	Lipocalin 2	Protein Coding	1
52	NEDD8	NEDD8 Ubiquitin Like Modifier	Protein Coding	1
53	ACO1	Aconitase 1	Protein Coding	1
54	SLC11A2	Solute Carrier Family 11 Member 2	Protein Coding	1
55	SLC22A17	Solute Carrier Family 22 Member 17	Protein Coding	1
56	CAND1	Cullin Associated And Neddylation Dissociated 1	Protein Coding	1
57	RPS27A	Ribosomal Protein S27a	Protein Coding	1
58	SKP1	S-Phase Kinase Associated Protein 1	Protein Coding	1
59	UBA52	Ubiquitin A-52 Residue Ribosomal Protein Fusion Product 1	Protein Coding	1
60	UBB	Ubiquitin B	Protein Coding	1
61	UBC	Ubiquitin C	Protein Coding	1
62	CYBRD1	Cytochrome B Reductase 1	Protein Coding	1
63	CUL1	Cullin 1	Protein Coding	1
64	FTMT	Ferritin Mitochondrial	Protein Coding	1
65	ABCG2	ATP Binding Cassette Subfamily G Member 2 (JR Blood Group)	Protein Coding	1
66	HEPH	Hephaestin	Protein Coding	1
67	CYBA	Cytochrome B-245 Alpha Chain	Protein Coding	1
68	CYBB	Cytochrome B-245 Beta Chain	Protein Coding	1
69	NCF2	Neutrophil Cytosolic Factor 2	Protein Coding	1
70	NCF4	Neutrophil Cytosolic Factor 4	Protein Coding	1
71	NOS1	Nitric Oxide Synthase 1	Protein Coding	1
72	NOS2	Nitric Oxide Synthase 2	Protein Coding	1
73	NOS3	Nitric Oxide Synthase 3	Protein Coding	1
74	RAC2	Rac Family Small GTPase 2	Protein Coding	1
75	NCF1	Neutrophil Cytosolic Factor 1	Protein Coding	1
76	SLC11A1	Solute Carrier Family 11 Member 1	Protein Coding	1
77	HVCN1	Hydrogen Voltage Gated Channel 1	Protein Coding	1

Disorders associated with Insulin receptor recycling SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Chronic granulomatous disease	Enrichment	CYBA, CYBB, NCF1, NCF2, NCF4	10.49
2	Autosomal recessive cutis laxa type ii classic type	Enrichment	ATP6V0A2, ATP6V1A, ATP6V1E1	8.01
3	Myeloperoxidase deficiency	Enrichment	LPO, MPO	7.19
4	Renal tubular acidosis, distal, 1	Enrichment	ATP6V0A4, ATP6V1B1, ATP6V1C2	6.71
5	Distal renal tubular acidosis	Enrichment	ATP6V0A4, ATP6V1B1, ATP6V1C2	6.71
6	Alzheimer's disease 1	Enrichment	LPO, MPO	6.64
7	Alzheimer disease, familial, 1	Enrichment	LPO, MPO	5.83
8	Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome	Enrichment	ATP6V1B2, ATP6V1C1	5.59
9	Renal tubular acidosis, distal, 3, with or without sensorineural hearing loss	Enrichment	ATP6V0A4, ATP6V1B1	4.85
10	Granulomatous disease, chronic, autosomal recessive, 2	Enrichment	NCF1, NCF2	4.69
11	Digenic hemochromatosis	Enrichment	HFE, TFR2	4.52
12	Granulomatous disease, chronic, x-linked	Enrichment	CYBB, NCF1	4.39
13	Autosomal recessive distal renal tubular acidosis	Enrichment	ATP6V0A4, ATP6V1B1	4.15
14	Hemochromatosis, type 1	Enrichment	HFE, TFR2	3.85
15	Cutis laxa	Enrichment	ATP6V0A2, ATP6V1E1	3.51
16	Deafness, congenital, with onychodystrophy, autosomal dominant	Enrichment	ATP6V1B2	3.02
17	Cutis laxa, autosomal recessive, type iid	Enrichment	ATP6V1A	3.02
18	Zimmermann-laband syndrome 2	Enrichment	ATP6V1B2	3.02
19	Cutis laxa, autosomal recessive, type iic	Enrichment	ATP6V1E1	3.02
20	Developmental and epileptic encephalopathy 104	Enrichment	ATP6V0A1	3.02
21	Neurodevelopmental disorder with epilepsy and brain atrophy	Enrichment	ATP6V0A1	3.02
22	Epilepsy, early-onset, 3, with or without developmental delay	Enrichment	ATP6V0C	3.02
23	Autosomal dominant deafness - onychodystrophy syndrome	Enrichment	ATP6V1B2	3.02
24	Alzheimer's disease	Enrichment	MPO	3.02
25	Developmental and epileptic encephalopathy 93	Enrichment	ATP6V1A	2.72
26	Childhood-onset epilepsy syndrome	Enrichment	ATP6V0C	2.72
27	Donohue syndrome	Enrichment	INSR	2.66
28	Hyperinsulinemic hypoglycemia, familial, 5	Enrichment	INSR	2.66
29	Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities	Enrichment	INSR	2.66
30	Diabetes mellitus, insulin-resistant, with acanthosis nigricans	Enrichment	INSR	2.66
31	Breasts and/or nipples, aplasia or hypoplasia of, 1	Enrichment	PTPRF	2.66
32	Ceroid lipofuscinosis, neuronal, 10	Enrichment	CTSD	2.66
33	Breasts and/or nipples, aplasia or hypoplasia of, 2	Enrichment	PTPRF	2.66
34	Atransferrinemia	Enrichment	TF	2.64
35	Immunodeficiency 46	Enrichment	TFRC	2.64
36	Pyloric stenosis, infantile hypertrophic, 1	Enrichment	NOS1	2.58
37	Granulomatous disease, chronic, autosomal recessive, 4	Enrichment	CYBA	2.58
38	Buruli ulcer	Enrichment	SLC11A1	2.58
39	Immunodeficiency 34	Enrichment	CYBB	2.58
40	Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis	Enrichment	RAC2	2.58
41	Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia	Enrichment	RAC2	2.58
42	Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia	Enrichment	RAC2	2.58
43	Infantile lad-like disease due to rac2 deficiency	Enrichment	RAC2	2.58
44	Reticular dysgenesis-like severe combined immunodeficiency	Enrichment	RAC2	2.58
45	Rac2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome	Enrichment	RAC2	2.58
46	Zimmermann-laband syndrome 1	Enrichment	ATP6V1B2	2.54
47	Type 2 diabetes mellitus	Enrichment	INSR, PTPN1	2.41
48	Retinopathy-sensory neuropathy syndrome	Enrichment	FLVCR1	2.37
49	Aceruloplasminemia	Enrichment	CP	2.37
50	Neurodegeneration with brain iron accumulation 3	Enrichment	FTL	2.37
51	Uric acid concentration, serum, quantitative trait locus 1	Enrichment	ABCG2	2.37
52	Anemia, hypochromic microcytic, with iron overload 1	Enrichment	SLC11A2	2.37
53	Hereditary sensory neuropathy	Enrichment	FLVCR1	2.37
54	Hemochromatosis, type 4	Enrichment	SLC40A1	2.37
55	L-ferritin deficiency	Enrichment	FTL	2.37
56	Neurodevelopmental disorder with microcephaly, absent speech, and hypotonia	Enrichment	FLVCR1	2.37
57	Blood group, junior system	Enrichment	ABCG2	2.37
58	Heme oxygenase 1 deficiency	Enrichment	HMOX1	2.37
59	Neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia	Enrichment	IREB2	2.37
60	Genetic hyperferritinemia without iron overload	Enrichment	FTL	2.37
61	Renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss	Enrichment	ATP6V1B1	2.35
62	Hyperinsulinemic hypoglycemia, familial, 4	Enrichment	INSR	2.35
63	Maturity-onset diabetes of the young, type 10	Enrichment	INS	2.35
64	Wrinkly skin syndrome	Enrichment	ATP6V0A2	2.35
65	Hyperproinsulinemia	Enrichment	INS	2.35
66	Osteopetrosis, autosomal recessive 1	Enrichment	TCIRG1	2.35
67	Renal tubular acidosis	Enrichment	ATP6V1B1	2.35
68	Diabetes mellitus, permanent neonatal, 4	Enrichment	INS	2.35
69	Porphyria cutanea tarda, type i	Enrichment	HFE	2.34
70	Anemia, hypochromic microcytic, with iron overload 2	Enrichment	STEAP3	2.34
71	Mucolipidosis iv	Enrichment	MCOLN1	2.34
72	Corneal dystrophy, lisch epithelial	Enrichment	MCOLN1	2.34
73	Hemochromatosis type 2	Enrichment	HFE	2.34
74	Granulomatous disease, chronic, autosomal recessive, 1	Enrichment	NCF1	2.28
75	Granulomatous disease, chronic, autosomal recessive, 3	Enrichment	NCF4	2.28
76	Type 1 diabetes mellitus 2	Enrichment	INS	2.18
77	Choreoacanthocytosis	Enrichment	TCIRG1	2.18
78	Cutis laxa, autosomal recessive, type iia	Enrichment	ATP6V0A2	2.18
79	Neutropenia, severe congenital, 1, autosomal dominant	Enrichment	TCIRG1	2.18
80	Dysosteosclerosis	Enrichment	TCIRG1	2.18
81	Osteopetrosis, autosomal recessive 6	Enrichment	TCIRG1	2.18
82	Atp6v0a2-related cutis laxa	Enrichment	ATP6V0A2	2.18
83	Hemochromatosis, type 3	Enrichment	TFR2	2.16
84	Microvascular complications of diabetes 7	Enrichment	HFE	2.16
85	Transferrin serum level quantitative trait locus 2	Enrichment	HFE	2.16
86	Mucolipidosis	Enrichment	MCOLN1	2.16
87	Periventricular leukomalacia	Enrichment	MCOLN1	2.16
88	Familial porphyria cutanea tarda	Enrichment	HFE	2.16
89	Autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia	Enrichment	CYBA	2.10
90	Autoimmune polyendocrine syndrome type 1	Enrichment	CYBA	2.10
91	Cystic fibrosis	Enrichment	HFE, HMOX1	2.09
92	Vitreoretinochoroidopathy	Enrichment	FTH1	2.07
93	Retinitis pigmentosa 50	Enrichment	FTH1	2.07
94	Hermansky-pudlak syndrome 3	Enrichment	CP	2.07
95	Hyperferritinemia with or without cataract	Enrichment	FTL	2.07
96	Hemochromatosis, type 5	Enrichment	FTH1	2.07
97	Neurodegeneration with brain iron accumulation 9	Enrichment	FTH1	2.07
98	Submucosal cleft palate	Enrichment	UBB	2.07
99	Cleft hard palate	Enrichment	UBB	2.07
100	Neonatal diabetes mellitus	Enrichment	INS	2.05
101	Autosomal recessive osteopetrosis	Enrichment	TCIRG1	2.05
102	Porphyria cutanea tarda	Enrichment	HFE	2.04
103	Tuberculosis	Enrichment	SLC11A1	1.98
104	Idiopathic achalasia	Enrichment	NOS1	1.98
105	Congenital disorder of glycosylation, type il	Enrichment	ATP6V0A2	1.96
106	Osteopetrosis	Enrichment	TCIRG1	1.96
107	Alg9-congenital disorder of glycosylation	Enrichment	ATP6V0A2	1.96
108	Autosomal dominant severe congenital neutropenia	Enrichment	TCIRG1	1.96
109	Variegate porphyria	Enrichment	HFE	1.94
110	Uvula, bifid	Enrichment	UBB	1.89
111	Cleft soft palate	Enrichment	UBB	1.89
112	Folate malabsorption, hereditary	Enrichment	SLC46A1	1.89
113	Type 1 diabetes mellitus	Enrichment	INS	1.88
114	46,xy disorder of sex development	Enrichment	INSR	1.88
115	Alzheimer disease 2	Enrichment	NOS3	1.88
116	Pre-eclampsia	Enrichment	NOS3	1.88
117	Pain disorder	Enrichment	HFE	1.87
118	Bestrophinopathy, autosomal recessive	Enrichment	FTH1	1.77
119	Immunodeficiency 47	Enrichment	ATP6AP1	1.76
120	Severe congenital neutropenia	Enrichment	TCIRG1	1.76
121	Permanent neonatal diabetes mellitus	Enrichment	INS	1.76
122	Macular dystrophy, vitelliform, 2	Enrichment	FTH1	1.67
123	Nephrocalcinosis	Enrichment	ATP6V1B1	1.66
124	Nephrolithiasis	Enrichment	ATP6V1B1	1.66
125	Cardiomyopathy, familial hypertrophic, 4	Enrichment	NCF1	1.63
126	Diabetes mellitus	Enrichment	INS	1.62
127	Congenital nervous system abnormality	Enrichment	HFE, MCOLN1	1.61
128	Nervous system disease	Enrichment	HFE, MCOLN1	1.61
129	Rasopathy	Enrichment	ATP6V1E1	1.61
130	Combined immunodeficiency	Enrichment	TFRC	1.60
131	Combined t cell and b cell immunodeficiency	Enrichment	TFRC	1.60
132	Combined t and b cell immunodeficiency	Enrichment	TFRC	1.60
133	Stroke, ischemic	Enrichment	NOS3	1.58
134	Polydactyly, postaxial, type a1	Enrichment	ATP6V1B1	1.49
135	Neuronal ceroid lipofuscinosis	Enrichment	CTSD	1.49
136	Neurodegeneration with brain iron accumulation	Enrichment	CP	1.38
137	Maturity-onset diabetes of the young	Enrichment	INS	1.36
138	Hypertension, essential	Enrichment	NOS3	1.35
139	Williams-beuren syndrome	Enrichment	NCF1	1.29
140	Undetermined early-onset epileptic encephalopathy	Enrichment	ATP6V1A	1.28
141	Pulmonary disease, chronic obstructive	Enrichment	HMOX1	1.27
142	Malaria	Enrichment	NOS2	1.23
143	Hermansky-pudlak syndrome	Enrichment	CP	1.21
144	Hermansky-pudlak syndrome 1	Enrichment	CP	1.18
145	Autism	Enrichment	ATP6V0A1	1.17
146	Peripheral nervous system disease	Enrichment	HFE	1.15
147	Neuropathy	Enrichment	HFE	1.15
148	Non-syndromic x-linked intellectual disability	Enrichment	ATP6AP1	1.12
149	Sensorineural hearing loss	Enrichment	ATP6V0A4	1.00
150	Jeune thoracic dystrophy	Enrichment	FLVCR1	0.99
151	Microcephaly	Enrichment	ATP6V0A1	0.95
152	Complex neurodevelopmental disorder	Enrichment	ATP6V0A1	0.95
153	Asphyxiating thoracic dystrophy	Enrichment	FLVCR1	0.95
154	Stargardt disease 1	Enrichment	FLVCR1	0.92
155	Short-rib thoracic dysplasia 1 with or without polydactyly	Enrichment	FLVCR1	0.88
156	Primary ovarian insufficiency	Enrichment	NOS3	0.84
157	Rare genetic deafness	Enrichment	ATP6V1B1	0.79
158	Inherited cancer-predisposing syndrome	Enrichment	HFE	0.58
159	Hereditary retinal dystrophy	Enrichment	FLVCR1, FTH1	0.45
160	Fundus dystrophy	Enrichment	FLVCR1, FTH1	0.45
161	Retinitis pigmentosa	Enrichment	FLVCR1	0.22

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

Insulin receptor recycling

Pathway Network for Insulin receptor recycling

Pathway network for the Insulin receptor recycling SuperPath

Member Pathways for Insulin receptor recycling

Pathways in the Insulin receptor recycling SuperPath

Gene overlap in member pathways for Insulin receptor recycling SuperPath

Associated Genes for Insulin receptor recycling

Associated Disorders for Insulin receptor recycling

Disorders associated with Insulin receptor recycling SuperPath

STRING Interaction Network for Insulin receptor recycling

Sources for Insulin receptor recycling