Peptide hormone metabolism

Pathway network for the Peptide hormone metabolism SuperPath

Sources:

Reactome
WikiPathways
PubChem

Pathways in the Peptide hormone metabolism SuperPath

#	Name	Source	Genes
1	Peptide hormone metabolism	Reactome	ACE ACE2 ACHE AGT ANPEP ATP6AP2 BCHE CDX2 CES1 CGA CGB3 CGB5 CGB8 CLTRN CMA1 CPA3 CPB1 CPB2 CPE CRHR2 CTNNB1 CTSD CTSG CTSZ DPP4 ENPEP ERO1B EXOC1 EXOC2 EXOC3 EXOC4 EXOC5 EXOC6 EXOC7 EXOC8 FFAR1 FFAR4 FSHB GATA4 GCG GH1 GHRL GIP GNAT3 GNB1 GNB3 GNG13 GPR119 GRP GZMH IGF1 INHA INHBA INHBB INHBC INHBE INS ISL1 KIF5A KIF5B KIF5C KLF4 LEP LHB MBOAT4 MME MYO5A MYRIP P4HB PAX6 PCSK1 PCSK2 PLA2G7 POMC RAB27A REN SEC11A SEC11C SLC30A5 SLC30A8 SPCS1 SPCS2 SPCS3 STX1A TCF7L2 TSHB UCN VAMP2 (see all 88) (see less)
2	Synthesis, secretion, and deacylation of Ghrelin	Reactome	ACHE BCHE CRHR2 GCG GH1 GHRL IGF1 INS KLF4 LEP MBOAT4 PCSK1 PLA2G7 SEC11A SEC11C SPCS1 SPCS2 SPCS3 UCN (see all 19) (see less)
3	Metabolism of Angiotensinogen to Angiotensins	WikiPathways	ACE ACE2 AGT ANPEP AOPEP ATP6AP2 CMA1 CPA3 CPB1 CPB2 CTSD CTSG CTSZ ENPEP GZMH MME REN (see all 17) (see less)
4	Metabolism of Angiotensinogen to Angiotensins	Reactome	ACE ACE2 AGT ANPEP ATP6AP2 CES1 CMA1 CPA3 CPB1 CPB2 CTSD CTSG CTSZ ENPEP GZMH MME REN (see all 17) (see less)
5	Peptide hormone biosynthesis	Reactome	CGA CGB3 CGB5 CGB8 FSHB INHA INHBA INHBB INHBC INHBE LHB PCSK1 POMC TSHB (see all 14) (see less)
6	Glycoprotein hormones	Reactome	CGA CGB3 CGB5 CGB8 FSHB INHA INHBA INHBB INHBC INHBE LHB TSHB (see all 12) (see less)
7	thyroid hormone biosynthesis	PubChem	CTSD

Gene overlap in member pathways for Peptide hormone metabolism SuperPath

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

#	Symbol	Description	Category	# Related Pathways
1	CTSD	Cathepsin D	Protein Coding	4
2	ATP6AP2	ATPase H+ Transporting Accessory Protein 2	Protein Coding	3
3	CGA	Glycoprotein Hormones, Alpha Polypeptide	Protein Coding	3
4	CGB3	Chorionic Gonadotropin Subunit Beta 3	Protein Coding	3
5	CMA1	Chymase 1	Protein Coding	3
6	CPA3	Carboxypeptidase A3	Protein Coding	3
7	CPB1	Carboxypeptidase B1	Protein Coding	3
8	CPB2	Carboxypeptidase B2	Protein Coding	3
9	CTSG	Cathepsin G	Protein Coding	3
10	CTSZ	Cathepsin Z	Protein Coding	3
11	ACE	Angiotensin I Converting Enzyme	Protein Coding	3
12	AGT	Angiotensinogen	Protein Coding	3
13	ENPEP	Glutamyl Aminopeptidase	Protein Coding	3
14	FSHB	Follicle Stimulating Hormone Subunit Beta	Protein Coding	3
15	ANPEP	Alanyl Aminopeptidase, Membrane	Protein Coding	3
16	GZMH	Granzyme H	Protein Coding	3
17	INHA	Inhibin Subunit Alpha	Protein Coding	3
18	INHBA	Inhibin Subunit Beta A	Protein Coding	3
19	INHBB	Inhibin Subunit Beta B	Protein Coding	3
20	INHBC	Inhibin Subunit Beta C	Protein Coding	3
21	LHB	Luteinizing Hormone Subunit Beta	Protein Coding	3
22	MME	Membrane Metalloendopeptidase	Protein Coding	3
23	PCSK1	Proprotein Convertase Subtilisin/Kexin Type 1	Protein Coding	3
24	ACE2	Angiotensin Converting Enzyme 2	Protein Coding	3
25	REN	Renin	Protein Coding	3
26	TSHB	Thyroid Stimulating Hormone Subunit Beta	Protein Coding	3
27	INHBE	Inhibin Subunit Beta E	Protein Coding	3
28	CGB5	Chorionic Gonadotropin Subunit Beta 5	Protein Coding	3
29	CGB8	Chorionic Gonadotropin Subunit Beta 8	Protein Coding	3
30	CES1	Carboxylesterase 1	Protein Coding	2
31	CRHR2	Corticotropin Releasing Hormone Receptor 2	Protein Coding	2
32	SEC11A	SEC11 Homolog A, Signal Peptidase Complex Subunit	Protein Coding	2
33	GCG	Glucagon	Protein Coding	2
34	GH1	Growth Hormone 1	Protein Coding	2
35	SPCS1	Signal Peptidase Complex Subunit 1	Protein Coding	2
36	IGF1	Insulin Like Growth Factor 1	Protein Coding	2
37	INS	Insulin	Protein Coding	2
38	LEP	Leptin	Protein Coding	2
39	ACHE	Acetylcholinesterase (Yt Blood Group)	Protein Coding	2
40	GHRL	Ghrelin And Obestatin Prepropeptide	Protein Coding	2
41	POMC	Proopiomelanocortin	Protein Coding	2
42	BCHE	Butyrylcholinesterase	Protein Coding	2
43	SPCS3	Signal Peptidase Complex Subunit 3	Protein Coding	2
44	MBOAT4	Membrane Bound Ghrelin O-Acyltransferase MBOAT4	Protein Coding	2
45	UCN	Urocortin	Protein Coding	2
46	PLA2G7	Phospholipase A2 Group VII	Protein Coding	2
47	SEC11C	SEC11 Homolog C, Signal Peptidase Complex Subunit	Protein Coding	2
48	KLF4	KLF Transcription Factor 4	Protein Coding	2
49	SPCS2	Signal Peptidase Complex Subunit 2	Protein Coding	2
50	CDX2	Caudal Type Homeobox 2	Protein Coding	1
51	EXOC5	Exocyst Complex Component 5	Protein Coding	1
52	EXOC3	Exocyst Complex Component 3	Protein Coding	1
53	CPE	Carboxypeptidase E	Protein Coding	1
54	GPR119	G Protein-Coupled Receptor 119	Protein Coding	1
55	EXOC8	Exocyst Complex Component 8	Protein Coding	1
56	CTNNB1	Catenin Beta 1	Protein Coding	1
57	SLC30A8	Solute Carrier Family 30 Member 8	Protein Coding	1
58	DPP4	Dipeptidyl Peptidase 4	Protein Coding	1
59	EXOC7	Exocyst Complex Component 7	Protein Coding	1
60	MYRIP	Myosin VIIA And Rab Interacting Protein	Protein Coding	1
61	GATA4	GATA Binding Protein 4	Protein Coding	1
62	GIP	Gastric Inhibitory Polypeptide	Protein Coding	1
63	GNB1	G Protein Subunit Beta 1	Protein Coding	1
64	GNB3	G Protein Subunit Beta 3	Protein Coding	1
65	FFAR1	Free Fatty Acid Receptor 1	Protein Coding	1
66	GRP	Gastrin Releasing Peptide	Protein Coding	1
67	FFAR4	Free Fatty Acid Receptor 4	Protein Coding	1
68	GNAT3	G Protein Subunit Alpha Transducin 3	Protein Coding	1
69	ISL1	ISL LIM Homeobox 1	Protein Coding	1
70	KIF5A	Kinesin Family Member 5A	Protein Coding	1
71	KIF5B	Kinesin Family Member 5B	Protein Coding	1
72	KIF5C	Kinesin Family Member 5C	Protein Coding	1
73	MYO5A	Myosin VA	Protein Coding	1
74	P4HB	Prolyl 4-Hydroxylase Subunit Beta	Protein Coding	1
75	PAX6	Paired Box 6	Protein Coding	1
76	PCSK2	Proprotein Convertase Subtilisin/Kexin Type 2	Protein Coding	1
77	GNG13	G Protein Subunit Gamma 13	Protein Coding	1
78	EXOC6	Exocyst Complex Component 6	Protein Coding	1
79	EXOC1	Exocyst Complex Component 1	Protein Coding	1
80	EXOC2	Exocyst Complex Component 2	Protein Coding	1
81	ERO1B	Endoplasmic Reticulum Oxidoreductase 1 Beta	Protein Coding	1
82	CLTRN	Collectrin, Amino Acid Transport Regulator	Protein Coding	1
83	RAB27A	RAB27A, Member RAS Oncogene Family	Protein Coding	1
84	EXOC4	Exocyst Complex Component 4	Protein Coding	1
85	SLC30A5	Solute Carrier Family 30 Member 5	Protein Coding	1
86	STX1A	Syntaxin 1A	Protein Coding	1
87	VAMP2	Vesicle Associated Membrane Protein 2	Protein Coding	1
88	TCF7L2	Transcription Factor 7 Like 2	Protein Coding	1
89	AOPEP	Aminopeptidase O (Putative)	Protein Coding	1

Disorders associated with Peptide hormone metabolism SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Renal tubular dysgenesis	Enrichment	ACE, AGT, REN	7.49
2	Ceroid lipofuscinosis, neuronal, 10	Enrichment	CTSD	4.13
3	Hypogonadotropic hypogonadism 23 with or without anosmia	Enrichment	LHB	3.05
4	Hypothyroidism, congenital, nongoitrous, 4	Enrichment	TSHB	3.05
5	Ovary adenocarcinoma	Enrichment	INHBA	3.05
6	Neuronal ceroid lipofuscinosis	Enrichment	CTSD	2.96
7	Body mass index quantitative trait locus 11	Enrichment	PCSK1, POMC	2.93
8	Congenital disorder of glycosylation, type iir	Enrichment	ATP6AP2	2.90
9	Spinocerebellar ataxia 43	Enrichment	MME	2.90
10	Microvascular complications of diabetes 3	Enrichment	ACE	2.90
11	Dystonia 31	Enrichment	AOPEP	2.90
12	Parkinsonism with spasticity, x-linked	Enrichment	ATP6AP2	2.90
13	Intellectual developmental disorder, x-linked, syndromic, hedera type	Enrichment	ATP6AP2	2.90
14	Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization	Enrichment	MME	2.90
15	Charcot-marie-tooth disease type 2t	Enrichment	MME	2.90
16	Mme-related autosomal dominant charcot marie tooth disease type 2	Enrichment	MME	2.90
17	Syndromic x-linked intellectual disability hedera type	Enrichment	ATP6AP2	2.90
18	Drug metabolism, altered, ces1-related	Enrichment	CES1	2.90
19	Yt blood group antigen	Enrichment	ACHE	2.85
20	Platelet-activating factor acetylhydrolase deficiency	Enrichment	PLA2G7	2.85
21	Butyrylcholinesterase deficiency	Enrichment	BCHE	2.85
22	Hypogonadotropic hypogonadism 24 with or without anosmia	Enrichment	FSHB	2.75
23	Tubulointerstitial kidney disease, autosomal dominant 4	Enrichment	REN	2.60
24	Charcot-marie-tooth disease, axonal, type 2t	Enrichment	MME	2.60
25	Maturity-onset diabetes of the young, type 10	Enrichment	INS	2.55
26	Hyperproinsulinemia	Enrichment	INS	2.55
27	Kowarski syndrome	Enrichment	GH1	2.55
28	Diabetes mellitus, permanent neonatal, 4	Enrichment	INS	2.55
29	Short stature due to growth hormone qualitative anomaly	Enrichment	GH1	2.55
30	Growth delay due to insulin-like growth factor type 1 deficiency	Enrichment	IGF1	2.55
31	Obesity, early-onset, with adrenal insufficiency and red hair	Enrichment	POMC	2.51
32	Body mass index quantitative trait locus 12	Enrichment	PCSK1	2.51
33	Proprotein convertase 1/3 deficiency	Enrichment	PCSK1	2.51
34	Obesity due to pro-opiomelanocortin deficiency	Enrichment	POMC	2.51
35	Type 1 diabetes mellitus 2	Enrichment	INS	2.38
36	Isolated growth hormone deficiency, type ib	Enrichment	GH1	2.38
37	Mpv17-related mitochondrial dna maintenance defect	Enrichment	UCN	2.38
38	Hypertension, essential	Enrichment	AGT, GNB3	2.27
39	Isolated growth hormone deficiency, type ii	Enrichment	GH1	2.25
40	Mitochondrial dna depletion syndrome 6	Enrichment	UCN	2.25
41	Leptin deficiency or dysfunction	Enrichment	LEP	2.25
42	Neonatal diabetes mellitus	Enrichment	INS	2.25
43	Charcot-marie-tooth disease, axonal, type 2ee	Enrichment	UCN	2.25
44	Cole-carpenter syndrome 1	Enrichment	P4HB	2.19
45	Griscelli syndrome, type 2	Enrichment	RAB27A	2.19
46	Spastic paraplegia 10, autosomal dominant	Enrichment	KIF5A	2.19
47	Griscelli syndrome, type 1	Enrichment	MYO5A	2.19
48	Elejalde neuroectodermal melanolysosomal syndrome	Enrichment	MYO5A	2.19
49	Atrioventricular septal defect 4	Enrichment	GATA4	2.19
50	Bdv syndrome	Enrichment	CPE	2.19
51	Myoclonus, intractable, neonatal	Enrichment	KIF5A	2.19
52	Amyotrophic lateral sclerosis 25	Enrichment	KIF5A	2.19
53	Body mass index quantitative trait locus 10	Enrichment	FFAR4	2.19
54	Atrial septal defect 2	Enrichment	GATA4	2.19
55	Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements	Enrichment	VAMP2	2.19
56	Cortical dysplasia, complex, with other brain malformations 2	Enrichment	KIF5C	2.19
57	Testicular anomalies with or without congenital heart disease	Enrichment	GATA4	2.19
58	8p23.1 microdeletion syndrome	Enrichment	GATA4	2.19
59	Intellectual developmental disorder, autosomal dominant 42	Enrichment	GNB1	2.19
60	Neurodevelopmental disorder with seizures and brain atrophy	Enrichment	EXOC7	2.19
61	Neurodevelopmental disorder with microcephaly, seizures, and brain atrophy	Enrichment	EXOC8	2.19
62	Griscelli syndrome	Enrichment	RAB27A	2.19
63	Adenoid ameloblastoma	Enrichment	CTNNB1	2.19
64	Sirenomelia	Enrichment	CDX2	2.19
65	Cpe-related prader-willi-like syndrome	Enrichment	CPE	2.19
66	Partial atrioventricular septal defect with ventricular hypoplasia	Enrichment	GATA4	2.19
67	Anorectal malformation	Enrichment	CDX2	2.19
68	Autosomal dominant charcot-marie-tooth disease type 2 due to kif5a mutation	Enrichment	KIF5A	2.19
69	Microcystic stromal tumor	Enrichment	CTNNB1	2.19
70	Neuropathy, hereditary motor and sensory, okinawa type	Enrichment	KIF5A, MME	2.18
71	Insulin-like growth factor i	Enrichment	IGF1	2.16
72	Hemorrhage, intracerebral	Enrichment	ACE	2.13
73	Hepatoblastoma	Enrichment	CTNNB1, REN	2.09
74	Type 1 diabetes mellitus	Enrichment	INS	2.08
75	Fanconi anemia, complementation group c	Enrichment	AOPEP	2.00
76	Isolated growth hormone deficiency, type ia	Enrichment	GH1	1.95
77	Permanent neonatal diabetes mellitus	Enrichment	INS	1.95
78	Stroke, ischemic	Enrichment	ACE	1.90
79	Keratitis, hereditary	Enrichment	PAX6	1.89
80	Foveal hypoplasia 1	Enrichment	PAX6	1.89
81	Osteopathia striata with cranial sclerosis	Enrichment	CTNNB1	1.89
82	Griscelli syndrome, type 3	Enrichment	MYO5A	1.89
83	Optic nerve hypoplasia, bilateral	Enrichment	PAX6	1.89
84	Hartnup disorder	Enrichment	CLTRN	1.89
85	Night blindness, congenital stationary, type 1h	Enrichment	GNB3	1.89
86	Retinal dystrophy, iris coloboma, and comedogenic acne syndrome	Enrichment	FFAR4	1.89
87	Childhood hepatocellular carcinoma	Enrichment	CTNNB1	1.89
88	Bladder exstrophy	Enrichment	ISL1	1.89
89	Frontotemporal dementia and/or amyotrophic lateral sclerosis 4	Enrichment	KIF5A	1.89
90	46,xy sex reversal 3	Enrichment	GATA4	1.89
91	Juvenile nasopharyngeal angiofibroma	Enrichment	CTNNB1	1.89
92	Neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia	Enrichment	EXOC2	1.89
93	Demyelinating polyneuropathy	Enrichment	KIF5A	1.89
94	Progressive retinal dystrophy due to retinol transport defect	Enrichment	FFAR4	1.89
95	Teratoma	Enrichment	CTNNB1	1.89
96	Skeletal muscle disease	Enrichment	KIF5B	1.89
97	Cerebral visual impairment	Enrichment	GNB1	1.89
98	Diabetes mellitus	Enrichment	INS	1.82
99	Peripheral nervous system disease	Enrichment	KIF5A, MME	1.74
100	Neuropathy	Enrichment	KIF5A, MME	1.74
101	Desmoid disease, hereditary	Enrichment	CTNNB1	1.71
102	Gillespie syndrome	Enrichment	PAX6	1.71
103	Neurodevelopmental disorder with spastic diplegia and visual defects	Enrichment	CTNNB1	1.71
104	Anus, imperforate	Enrichment	CTNNB1	1.71
105	Exudative vitreoretinopathy 7	Enrichment	CTNNB1	1.71
106	Desmoid tumor	Enrichment	CTNNB1	1.71
107	Cole-carpenter syndrome	Enrichment	P4HB	1.71
108	Dystonia	Enrichment	GNB1, MYO5A	1.67
109	Aniridia 1	Enrichment	PAX6	1.59
110	Pilomatrixoma	Enrichment	CTNNB1	1.59
111	Alazami syndrome	Enrichment	CTNNB1	1.59
112	Craniopharyngioma	Enrichment	CTNNB1	1.59
113	Eyelid coloboma	Enrichment	PAX6	1.59
114	Transposition of the great arteries	Enrichment	GATA4	1.59
115	Lens coloboma	Enrichment	PAX6	1.59
116	Myocardial infarction	Enrichment	ACE	1.56
117	Maturity-onset diabetes of the young	Enrichment	INS	1.56
118	Type 2 diabetes mellitus	Enrichment	SLC30A8, TCF7L2	1.52
119	Hypertrophic cardiomyopathy	Enrichment	KIF5B, SLC30A5	1.50
120	Exudative vitreoretinopathy 1	Enrichment	CTNNB1	1.49
121	Kearns-sayre syndrome	Enrichment	KIF5B	1.49
122	Ventricular septal defect 1	Enrichment	GATA4	1.49
123	Congenital heart defects, multiple types, 4	Enrichment	GATA4	1.49
124	2q23.1 microduplication syndrome	Enrichment	KIF5C	1.49
125	Aniridia	Enrichment	PAX6	1.49
126	Coloboma of choroid and retina	Enrichment	PAX6	1.49
127	Coloboma of optic nerve	Enrichment	PAX6	1.42
128	Osteogenesis imperfecta, type i	Enrichment	P4HB	1.42
129	Weyers acrofacial dysostosis	Enrichment	CTNNB1	1.42
130	Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndrome	Enrichment	PAX6	1.42
131	Anterior segment dysgenesis 5	Enrichment	PAX6	1.42
132	Adrenocortical carcinoma	Enrichment	CTNNB1	1.42
133	Cakut	Enrichment	ACE	1.38
134	Fanconi anemia, complementation group a	Enrichment	AOPEP	1.37
135	Gallbladder cancer	Enrichment	CTNNB1	1.35
136	Exudative vitreoretinopathy	Enrichment	CTNNB1	1.29
137	Hypothyroidism	Enrichment	GNB1	1.29
138	Adult hepatocellular carcinoma	Enrichment	CTNNB1	1.24
139	Hydrops fetalis	Enrichment	SLC30A5	1.24
140	Cat eye syndrome	Enrichment	PAX6	1.20
141	Peters-plus syndrome	Enrichment	PAX6	1.20
142	Leukemia, acute lymphoblastic	Enrichment	GNB1	1.16
143	Myelodysplastic syndrome	Enrichment	GNB1	1.16
144	Autism	Enrichment	STX1A, TCF7L2	1.10
145	Microphthalmia/coloboma 12	Enrichment	PAX6	1.09
146	Medulloblastoma	Enrichment	CTNNB1	1.06
147	Aortic aneurysm, familial thoracic 1	Enrichment	GATA4	1.06
148	Heart disease	Enrichment	GATA4	1.06
149	46,xy partial gonadal dysgenesis	Enrichment	GATA4	1.06
150	Breast cancer	Enrichment	AOPEP	1.05
151	Coloboma of macula	Enrichment	PAX6	1.03
152	Anterior segment dysgenesis	Enrichment	PAX6	1.03
153	Colorectal cancer	Enrichment	AOPEP	0.98
154	Cleft palate, isolated	Enrichment	GNB1	0.98
155	Polycystic liver disease	Enrichment	CTNNB1	0.98
156	Autosomal dominant polycystic liver disease	Enrichment	CTNNB1	0.98
157	Heart, malformation of	Enrichment	GATA4	0.96
158	Patent foramen ovale	Enrichment	GATA4	0.96
159	Ovarian cancer	Enrichment	AOPEP	0.92
160	Williams-beuren syndrome	Enrichment	STX1A	0.91
161	Macs syndrome	Enrichment	PAX6	0.91
162	Hepatocellular carcinoma	Enrichment	CTNNB1	0.87
163	Attention deficit-hyperactivity disorder	Enrichment	KIF5B	0.87
164	Microphthalmia	Enrichment	PAX6	0.87
165	Multisystem inflammatory syndrome in children	Enrichment	RAB27A	0.87
166	Congenital stationary night blindness	Enrichment	GNB3	0.86
167	Familial atrial fibrillation	Enrichment	GATA4	0.84
168	Autoinflammatory disease	Enrichment	RAB27A	0.84
169	Inherited cancer-predisposing syndrome	Enrichment	AOPEP	0.81
170	Tetralogy of fallot	Enrichment	GATA4	0.81
171	Auditory neuropathy	Enrichment	KIF5A	0.81
172	Strabismus	Enrichment	GNB1	0.79
173	Bladder cancer	Enrichment	CTNNB1	0.76
174	Meckel syndrome, type 1	Enrichment	EXOC4	0.76
175	Cystic fibrosis	Enrichment	STX1A	0.73
176	Microcephaly	Enrichment	CTNNB1, GNB1	0.72
177	Left ventricular noncompaction	Enrichment	SLC30A5	0.69
178	Cerebral palsy	Enrichment	GNB1	0.65
179	Hereditary spastic paraplegia	Enrichment	KIF5A	0.62
180	Autosomal dominant non-syndromic intellectual disability	Enrichment	GNB1	0.56
181	Hypertelorism	Enrichment	PAX6	0.54
182	Male infertility with azoospermia or oligozoospermia due to single gene mutation	Enrichment	GATA4	0.51
183	Dilated cardiomyopathy	Enrichment	KIF5B	0.39
184	Congenital nervous system abnormality	Enrichment	CTNNB1	0.30
185	Nervous system disease	Enrichment	CTNNB1	0.30
186	Autism spectrum disorder	Enrichment	GNB1	0.29
187	Complex neurodevelopmental disorder	Enrichment	TCF7L2	0.26

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

Peptide hormone metabolism

Pathway Network for Peptide hormone metabolism

Pathway network for the Peptide hormone metabolism SuperPath

Member Pathways for Peptide hormone metabolism

Pathways in the Peptide hormone metabolism SuperPath

Gene overlap in member pathways for Peptide hormone metabolism SuperPath

Associated Genes for Peptide hormone metabolism

Associated Disorders for Peptide hormone metabolism

Disorders associated with Peptide hormone metabolism SuperPath

STRING Interaction Network for Peptide hormone metabolism

Sources for Peptide hormone metabolism