Cellular response to heat stress

Pathway network for the Cellular response to heat stress SuperPath

Sources:

Reactome

Pathways in the Cellular response to heat stress SuperPath

#	Name	Source	Genes
1	Cellular response to heat stress	Reactome	AAAS AKT1S1 ATM ATR BAG1 BAG2 BAG3 BAG5 CAMK2A CAMK2B CAMK2D CAMK2G CCAR2 CREBBP CRYAB DNAJB1 DNAJB6 DNAJC2 DNAJC7 EEF1A1 EP300 FKBP4 GSK3B HDAC6 HIKESHI HSBP1 HSF1 HSP90AA1 HSP90AB1 HSPA12A HSPA12B HSPA13 HSPA14 HSPA1A HSPA1B HSPA1L HSPA2 HSPA4 HSPA4L HSPA5 HSPA6 HSPA8 HSPA9 HSPB8 HSPH1 MAPK1 MAPK3 MAPKAPK2 MLST8 MTOR NDC1 NUP107 NUP133 NUP153 NUP155 NUP160 NUP188 NUP205 NUP210 NUP214 NUP35 NUP37 NUP42 NUP43 NUP50 NUP54 NUP58 NUP62 NUP85 NUP88 NUP93 NUP98 POM121 PTGES3 RAE1 RANBP2 RPA1 RPA2 RPA3 RPS19BP1 RPTOR SEC13 SEH1L SIRT1 ST13 TPR VCP YWHAE (see all 88) (see less)
2	Regulation of HSF1-mediated heat shock response	Reactome	AAAS ATM ATR BAG1 BAG2 BAG3 BAG5 CCAR2 DNAJB1 DNAJB6 DNAJC2 DNAJC7 GSK3B HIKESHI HSF1 HSPA12A HSPA12B HSPA13 HSPA14 HSPA1A HSPA1B HSPA1L HSPA2 HSPA4 HSPA4L HSPA5 HSPA6 HSPA8 HSPA9 HSPH1 MAPK1 MAPK3 MAPKAPK2 NDC1 NUP107 NUP133 NUP153 NUP155 NUP160 NUP188 NUP205 NUP210 NUP214 NUP35 NUP37 NUP42 NUP43 NUP50 NUP54 NUP58 NUP62 NUP85 NUP88 NUP93 NUP98 POM121 RAE1 RANBP2 RPA1 RPA2 RPA3 RPS19BP1 SEC13 SEH1L SIRT1 ST13 TPR YWHAE (see all 68) (see less)
3	HSF1 activation	Reactome	EEF1A1 HDAC6 HSBP1 HSF1 HSP90AA1 HSP90AB1 PTGES3 RPA1 RPA2 RPA3 VCP YWHAE (see all 12) (see less)

Gene overlap in member pathways for Cellular response to heat stress SuperPath

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

#	Symbol	Description	Category	# Related Pathways
1	HSF1	Heat Shock Transcription Factor 1	Protein Coding	3
2	RPA1	Replication Protein A1	Protein Coding	3
3	RPA2	Replication Protein A2	Protein Coding	3
4	RPA3	Replication Protein A3	Protein Coding	3
5	YWHAE	Tyrosine 3-Monooxygenase/Tryptophan 5-Monooxygenase Activation Protein Epsilon	Protein Coding	3
6	HDAC6	Histone Deacetylase 6	Protein Coding	2
7	DNAJB6	DnaJ Heat Shock Protein Family (Hsp40) Member B6	Protein Coding	2
8	PTGES3	Prostaglandin E Synthase 3	Protein Coding	2
9	NUP50	Nucleoporin 50	Protein Coding	2
10	HSPH1	Heat Shock Protein Family H (Hsp110) Member 1	Protein Coding	2
11	NUP42	Nucleoporin 42	Protein Coding	2
12	HSPA12B	Heat Shock Protein Family A (Hsp70) Member 12B	Protein Coding	2
13	NUP35	Nucleoporin 35	Protein Coding	2
14	EEF1A1	Eukaryotic Translation Elongation Factor 1 Alpha 1	Protein Coding	2
15	HSPA4L	Heat Shock Protein Family A (Hsp70) Member 4 Like	Protein Coding	2
16	NUP205	Nucleoporin 205	Protein Coding	2
17	NUP210	Nucleoporin 210	Protein Coding	2
18	NUP160	Nucleoporin 160	Protein Coding	2
19	SIRT1	Sirtuin 1	Protein Coding	2
20	NUP188	Nucleoporin 188	Protein Coding	2
21	NUP62	Nucleoporin 62	Protein Coding	2
22	HSPA12A	Heat Shock Protein Family A (Hsp70) Member 12A	Protein Coding	2
23	DNAJC2	DnaJ Heat Shock Protein Family (Hsp40) Member C2	Protein Coding	2
24	GSK3B	Glycogen Synthase Kinase 3 Beta	Protein Coding	2
25	HSBP1	Heat Shock Factor Binding Protein 1	Protein Coding	2
26	HSPA1A	Heat Shock Protein Family A (Hsp70) Member 1A	Protein Coding	2
27	HSPA1B	Heat Shock Protein Family A (Hsp70) Member 1B	Protein Coding	2
28	HSPA1L	Heat Shock Protein Family A (Hsp70) Member 1 Like	Protein Coding	2
29	HSPA2	Heat Shock Protein Family A (Hsp70) Member 2	Protein Coding	2
30	HSPA4	Heat Shock Protein Family A (Hsp70) Member 4	Protein Coding	2
31	HSPA5	Heat Shock Protein Family A (Hsp70) Member 5	Protein Coding	2
32	HSPA6	Heat Shock Protein Family A (Hsp70) Member 6	Protein Coding	2
33	HSPA8	Heat Shock Protein Family A (Hsp70) Member 8	Protein Coding	2
34	HSPA9	Heat Shock Protein Family A (Hsp70) Member 9	Protein Coding	2
35	HSP90AA1	Heat Shock Protein 90 Alpha Family Class A Member 1	Protein Coding	2
36	HSP90AB1	Heat Shock Protein 90 Alpha Family Class B Member 1	Protein Coding	2
37	DNAJB1	DnaJ Heat Shock Protein Family (Hsp40) Member B1	Protein Coding	2
38	NUP43	Nucleoporin 43	Protein Coding	2
39	ATM	ATM Serine/Threonine Kinase	Protein Coding	2
40	NUP88	Nucleoporin 88	Protein Coding	2
41	NUP98	Nucleoporin 98 And 96 Precursor	Protein Coding	2
42	HSPA14	Heat Shock Protein Family A (Hsp70) Member 14	Protein Coding	2
43	HIKESHI	Heat Shock Protein Nuclear Import Factor Hikeshi	Protein Coding	2
44	NUP54	Nucleoporin 54	Protein Coding	2
45	ATR	ATR Checkpoint Kinase	Protein Coding	2
46	NDC1	NDC1 Transmembrane Nucleoporin	Protein Coding	2
47	NUP133	Nucleoporin 133	Protein Coding	2
48	MAPK1	Mitogen-Activated Protein Kinase 1	Protein Coding	2
49	MAPK3	Mitogen-Activated Protein Kinase 3	Protein Coding	2
50	NUP107	Nucleoporin 107	Protein Coding	2
51	BAG1	BAG Cochaperone 1	Protein Coding	2
52	CCAR2	Cell Cycle And Apoptosis Regulator 2	Protein Coding	2
53	RANBP2	RAN Binding Protein 2	Protein Coding	2
54	SEC13	SEC13 Homolog, Nuclear Pore And COPII Component	Protein Coding	2
55	ST13	ST13 Hsp70 Interacting Protein	Protein Coding	2
56	HSPA13	Heat Shock Protein Family A (Hsp70) Member 13	Protein Coding	2
57	TPR	Translocated Promoter Region, Nuclear Basket Protein	Protein Coding	2
58	DNAJC7	DnaJ Heat Shock Protein Family (Hsp40) Member C7	Protein Coding	2
59	VCP	Valosin Containing Protein	Protein Coding	2
60	NUP37	Nucleoporin 37	Protein Coding	2
61	NUP85	Nucleoporin 85	Protein Coding	2
62	NUP214	Nucleoporin 214	Protein Coding	2
63	AAAS	Aladin WD Repeat Nucleoporin	Protein Coding	2
64	SEH1L	SEH1 Like Nucleoporin	Protein Coding	2
65	RAE1	Ribonucleic Acid Export 1	Protein Coding	2
66	RPS19BP1	Ribosomal Protein S19 Binding Protein 1	Protein Coding	2
67	MAPKAPK2	MAPK Activated Protein Kinase 2	Protein Coding	2
68	BAG5	BAG Cochaperone 5	Protein Coding	2
69	BAG3	BAG Cochaperone 3	Protein Coding	2
70	BAG2	BAG Cochaperone 2	Protein Coding	2
71	NUP155	Nucleoporin 155	Protein Coding	2
72	NUP93	Nucleoporin 93	Protein Coding	2
73	NUP58	Nucleoporin 58	Protein Coding	2
74	POM121	POM121 Transmembrane Nucleoporin	Protein Coding	2
75	NUP153	Nucleoporin 153	Protein Coding	2
76	CREBBP	CREB Binding Lysine Acetyltransferase	Protein Coding	1
77	CRYAB	Crystallin Alpha B	Protein Coding	1
78	EP300	EP300 Lysine Acetyltransferase	Protein Coding	1
79	FKBP4	FKBP Prolyl Isomerase 4	Protein Coding	1
80	MTOR	Mechanistic Target Of Rapamycin Kinase	Protein Coding	1
81	HSPB8	Heat Shock Protein Family B (Small) Member 8	Protein Coding	1
82	RPTOR	Regulatory Associated Protein Of MTOR Complex 1	Protein Coding	1
83	MLST8	MTOR Associated Protein MLST8	Protein Coding	1
84	CAMK2A	Calcium/Calmodulin Dependent Protein Kinase II Alpha	Protein Coding	1
85	CAMK2B	Calcium/Calmodulin Dependent Protein Kinase II Beta	Protein Coding	1
86	CAMK2D	Calcium/Calmodulin Dependent Protein Kinase II Delta	Protein Coding	1
87	CAMK2G	Calcium/Calmodulin Dependent Protein Kinase II Gamma	Protein Coding	1
88	AKT1S1	AKT1 Substrate 1	Protein Coding	1

Disorders associated with Cellular response to heat stress SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Genetic steroid-resistant nephrotic syndrome	Enrichment	NUP107, NUP133, NUP160, NUP205, NUP37, NUP85, NUP93	9.55
2	Rare genetic intellectual disability	Enrichment	CREBBP, EP300, MTOR	3.95
3	Familial infantile bilateral striatal necrosis	Enrichment	NUP54, NUP62	3.83
4	Rubinstein-taybi syndrome 1	Enrichment	CREBBP, EP300	3.21
5	Chromosome 16p13.3 deletion syndrome, proximal	Enrichment	CREBBP, EP300	3.21
6	Renal cell carcinoma, papillary, 1	Enrichment	ATM, MTOR	3.07
7	Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia	Enrichment	HDAC6	3.05
8	Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1	Enrichment	VCP	3.05
9	Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 6	Enrichment	RPA1	3.05
10	Frontotemporal dementia and/or amyotrophic lateral sclerosis 6	Enrichment	VCP	3.05
11	Multisystem proteinopathy	Enrichment	VCP	3.05
12	Adult-onset distal myopathy due to vcp mutation	Enrichment	VCP	3.05
13	Distal 17p13.3 microdeletion syndrome	Enrichment	YWHAE	3.05
14	Galloway-mowat syndrome	Enrichment	NUP107, NUP133	2.96
15	Amyotrophic lateral sclerosis 6 with or without frontotemporal dementia	Enrichment	VCP	2.75
16	Spastic paraplegia-paget disease of bone syndrome	Enrichment	VCP	2.75
17	Seckel syndrome	Enrichment	ATR, NUP85	2.66
18	Miller-dieker lissencephaly syndrome	Enrichment	YWHAE	2.58
19	Chromosome 17p13.3, centromeric, duplication syndrome	Enrichment	YWHAE	2.58
20	Inclusion body myopathy with paget disease of bone and frontotemporal dementia	Enrichment	VCP	2.58
21	Renal cell carcinoma, nonpapillary	Enrichment	ATM, MTOR	2.38
22	Dementia, lewy body	Enrichment	VCP	2.35
23	Charcot-marie-tooth disease, axonal, type 2e	Enrichment	VCP	2.35
24	Endometrial stromal sarcoma	Enrichment	YWHAE	2.35
25	Familial isolated dilated cardiomyopathy	Enrichment	BAG3, BAG5, CRYAB	2.31
26	Muscular dystrophy, limb-girdle, autosomal dominant 1	Enrichment	DNAJB6	2.30
27	Seckel syndrome 1	Enrichment	ATR	2.30
28	Even-plus syndrome	Enrichment	HSPA9	2.30
29	Leukodystrophy, hypomyelinating, 13	Enrichment	HIKESHI	2.30
30	Cardiomyopathy, dilated, 1hh	Enrichment	BAG3	2.30
31	Anemia, sideroblastic, 4	Enrichment	HSPA9	2.30
32	Fetal akinesia deformation sequence 4	Enrichment	NUP88	2.30
33	Neurodevelopmental disorder with achalasia, polyneuropathy, and alacrima	Enrichment	NDC1	2.30
34	Atrial fibrillation, familial, 15	Enrichment	NUP155	2.30
35	Noonan syndrome 13	Enrichment	MAPK1	2.30
36	Dystonia 37, early-onset, with striatal lesions	Enrichment	NUP54	2.30
37	Cardiomyopathy, dilated, 2f	Enrichment	BAG5	2.30
38	Nephrotic syndrome, type 19	Enrichment	NUP160	2.30
39	Galloway-mowat syndrome 8	Enrichment	NUP133	2.30
40	Nephrotic syndrome, type 13	Enrichment	NUP205	2.30
41	Myopathy, myofibrillar, 6	Enrichment	BAG3	2.30
42	Microcephaly 24, primary, autosomal recessive	Enrichment	NUP37	2.30
43	Galloway-mowat syndrome 7	Enrichment	NUP107	2.30
44	Cutaneous telangiectasia and cancer syndrome, familial	Enrichment	ATR	2.30
45	Nephrotic syndrome, type 12	Enrichment	NUP93	2.30
46	Endometrial serous adenocarcinoma	Enrichment	ATM	2.30
47	Nephrotic syndrome, type 11	Enrichment	NUP107	2.30
48	Encephalopathy, acute, infection-induced 9	Enrichment	NUP214	2.30
49	Sandestig-stefanova syndrome	Enrichment	NUP188	2.30
50	Ovarian dysgenesis 6	Enrichment	NUP107	2.30
51	Intellectual developmental disorder, autosomal recessive 79	Enrichment	TPR	2.30
52	Nephrotic syndrome, type 18	Enrichment	NUP133	2.30
53	Charcot-marie-tooth disease, axonal, type 2jj	Enrichment	BAG3	2.30
54	B-cell non-hodgkin lymphoma	Enrichment	ATM	2.30
55	Neuronopathy, distal hereditary motor, autosomal dominant 15	Enrichment	BAG3	2.30
56	C11orf73-related autosomal recessive hypomyelinating leukodystrophy	Enrichment	HIKESHI	2.30
57	Familial acute necrotizing encephalopathy	Enrichment	RANBP2	2.30
58	Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome	Enrichment	ATR	2.30
59	Kidney clear cell sarcoma	Enrichment	YWHAE	2.28
60	Cardiomyopathy, dilated, 1ii	Enrichment	CRYAB	2.19
61	Intellectual developmental disorder, autosomal recessive 63	Enrichment	CAMK2A	2.19
62	Intellectual developmental disorder, autosomal dominant 54	Enrichment	CAMK2B	2.19
63	Myopathy, myofibrillar, 2b, infantile-onset	Enrichment	CRYAB	2.19
64	Charcot-marie-tooth disease, axonal, type 2l	Enrichment	HSPB8	2.19
65	Myopathy, myofibrillar, 2a, adult-onset	Enrichment	CRYAB	2.19
66	Myopathy, myofibrillar, 13, with rimmed vacuoles	Enrichment	HSPB8	2.19
67	Menke-hennekam syndrome 1	Enrichment	CREBBP	2.19
68	Intellectual developmental disorder, autosomal dominant 53	Enrichment	CAMK2A	2.19
69	Intellectual developmental disorder, autosomal dominant 59	Enrichment	CAMK2G	2.19
70	Rubinstein-taybi syndrome due to 16p13.3 microdeletion	Enrichment	CREBBP	2.19
71	Menke-hennekam syndrome	Enrichment	CREBBP	2.19
72	Autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome	Enrichment	HSPB8	2.19
73	Progressive non-fluent aphasia	Enrichment	VCP	2.10
74	Behavioral variant of frontotemporal dementia	Enrichment	VCP	2.10
75	Microcephaly	Enrichment	CAMK2B, EP300, MAPK1, NUP188	2.08
76	Frontotemporal dementia and/or amyotrophic lateral sclerosis 1	Enrichment	VCP	2.05
77	Camptodactyly-arthropathy-coxa vara-pericarditis syndrome	Enrichment	TPR	2.00
78	Striatonigral degeneration, infantile	Enrichment	NUP62	2.00
79	Cardiac valvular dysplasia, x-linked	Enrichment	ATM	2.00
80	Nephrotic syndrome, type 17	Enrichment	NUP85	2.00
81	High grade glioma	Enrichment	ATM	2.00
82	Fibrolamellar carcinoma	Enrichment	DNAJB1	2.00
83	T-cell prolymphocytic leukemia	Enrichment	ATM	2.00
84	Autosomal recessive sideroblastic anemia	Enrichment	HSPA9	2.00
85	Acute myeloid leukemia with t(6;9) (p23;q34.1)	Enrichment	NUP214	2.00
86	Acute necrotizing encephalopathy of childhood	Enrichment	RANBP2	2.00
87	Alzheimer's disease	Enrichment	VCP	1.94
88	Cardiomyopathy, familial restrictive, 1	Enrichment	CRYAB	1.89
89	Thumb deformity	Enrichment	CREBBP	1.89
90	Cebalid syndrome	Enrichment	MTOR	1.89
91	Menke-hennekam syndrome 2	Enrichment	EP300	1.89
92	Acute myeloid leukemia with kat6a-crebbp fusion	Enrichment	CREBBP	1.89
93	Cataract 16, multiple types	Enrichment	CRYAB	1.89
94	Smith-kingsmore syndrome	Enrichment	MTOR	1.89
95	Alzheimer disease, familial, 1	Enrichment	VCP	1.83
96	Ataxia-telangiectasia	Enrichment	ATM	1.82
97	Polycythemia vera	Enrichment	ATM	1.82
98	Ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive	Enrichment	RANBP2	1.82
99	Koolen-de vries syndrome	Enrichment	ATM	1.82
100	Adenocarcinoma	Enrichment	ATM	1.82
101	Neuropathy, hereditary motor and sensory, okinawa type	Enrichment	VCP	1.78
102	Tethered spinal cord syndrome	Enrichment	CREBBP	1.71
103	Distal myopathy	Enrichment	HSPB8	1.71
104	Intraocular pressure quantitative trait locus	Enrichment	CREBBP	1.71
105	Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive	Enrichment	RANBP2	1.70
106	Achalasia-addisonianism-alacrima syndrome	Enrichment	AAAS	1.70
107	Chromosome 22q11.2 deletion syndrome, distal	Enrichment	MAPK1	1.70
108	Mantle cell lymphoma	Enrichment	ATM	1.70
109	Ectodermal dysplasia	Enrichment	RANBP2	1.70
110	Oculomotor apraxia	Enrichment	ATM	1.70
111	Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant	Enrichment	RANBP2	1.61
112	Glioblastoma	Enrichment	ATM	1.61
113	Autosomal recessive hypohidrotic ectodermal dysplasia syndrome	Enrichment	RANBP2	1.61
114	Focal cortical dysplasia, type ii	Enrichment	MTOR	1.59
115	Myopathy, autophagic vacuolar, infantile-onset	Enrichment	HSPB8	1.59
116	Isolated focal cortical dysplasia type ii	Enrichment	MTOR	1.59
117	Inflammatory myofibroblastic tumor	Enrichment	RANBP2	1.53
118	Clear cell renal cell carcinoma	Enrichment	ATM	1.53
119	Congenital nervous system abnormality	Enrichment	AAAS, CAMK2B, CREBBP	1.50
120	Nervous system disease	Enrichment	AAAS, CAMK2B, CREBBP	1.50
121	Neuronopathy, distal hereditary motor, autosomal dominant 2	Enrichment	HSPB8	1.49
122	Rubinstein-taybi syndrome 2	Enrichment	EP300	1.49
123	Hemimegalencephaly	Enrichment	MTOR	1.49
124	Mitochondrial dna depletion syndrome 4a	Enrichment	RANBP2	1.46
125	Hypertrichosis	Enrichment	CREBBP	1.42
126	Mitochondrial dna depletion syndrome 4b	Enrichment	RANBP2	1.40
127	Myocarditis	Enrichment	BAG3	1.40
128	Autosomal dominant non-syndromic intellectual disability	Enrichment	CAMK2A, CAMK2B	1.38
129	Colonic benign neoplasm	Enrichment	ATM	1.35
130	Overgrowth syndrome	Enrichment	MTOR	1.35
131	Lynch syndrome 1	Enrichment	ATM	1.31
132	Leukemia, chronic lymphocytic	Enrichment	ATM	1.31
133	Frontotemporal dementia and/or amyotrophic lateral sclerosis 7	Enrichment	VCP	1.30
134	Early-onset posterior polar cataract	Enrichment	CRYAB	1.29
135	Myeloma, multiple	Enrichment	ATM, CREBBP	1.29
136	Immune deficiency disease	Enrichment	ATM	1.27
137	Uterine corpus cancer	Enrichment	ATM	1.27
138	Familial colorectal cancer type x	Enrichment	ATM	1.27
139	Specific learning disability	Enrichment	MAPK1	1.27
140	Charge syndrome	Enrichment	EP300	1.24
141	46 xx gonadal dysgenesis	Enrichment	NUP107	1.23
142	Breast-ovarian cancer, familial 1	Enrichment	ATM	1.20
143	Early-onset lamellar cataract	Enrichment	CRYAB	1.16
144	Gliosarcoma	Enrichment	ATM	1.11
145	Autism	Enrichment	CAMK2G, CREBBP	1.10
146	Giant cell glioblastoma	Enrichment	ATM	1.09
147	Heart, malformation of	Enrichment	MAPK1	1.06
148	Heart disease	Enrichment	CREBBP	1.06
149	Parkinson's disease	Enrichment	DNAJB6	1.04
150	Polydactyly, postaxial, type a1	Enrichment	EP300	1.03
151	Corpus callosum, agenesis of	Enrichment	CREBBP	1.03
152	Isolated corpus callosum agenesis	Enrichment	CREBBP	1.03
153	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome	Enrichment	CREBBP	1.03
154	Focal segmental glomerulosclerosis	Enrichment	NUP93	1.02
155	Cardiomyopathy, dilated, 1a	Enrichment	BAG3	1.00
156	Endometrial cancer	Enrichment	ATM	1.00
157	Tooth agenesis	Enrichment	RANBP2	0.98
158	Precursor t-cell acute lymphoblastic leukemia	Enrichment	NUP214	0.96
159	Colorectal cancer	Enrichment	ATM, EP300	0.96
160	Early-onset nuclear cataract	Enrichment	CRYAB	0.96
161	Parkinson disease, late-onset	Enrichment	DNAJB6	0.94
162	Familial atrial fibrillation	Enrichment	NUP155	0.94
163	Diffuse large b-cell lymphoma	Enrichment	CREBBP	0.93
164	Pancreatic cancer	Enrichment	ATM	0.93
165	Bladder cancer	Enrichment	ATM	0.87
166	Hirschsprung disease 1	Enrichment	NUP98	0.87
167	Prostate cancer	Enrichment	ATM	0.87
168	Differentiated thyroid carcinoma	Enrichment	TPR	0.87
169	Scoliosis	Enrichment	CREBBP	0.84
170	Primary autosomal recessive microcephaly	Enrichment	NUP37	0.83
171	Peripheral nervous system disease	Enrichment	BAG3	0.83
172	Neuropathy	Enrichment	BAG3	0.83
173	Fetal akinesia deformation sequence 1	Enrichment	NUP88	0.77
174	Leukemia, acute myeloid	Enrichment	NUP214	0.74
175	Gastric cancer	Enrichment	ATM	0.71
176	Nephrotic syndrome	Enrichment	NUP93	0.71
177	Hereditary breast carcinoma	Enrichment	ATM	0.70
178	Dystonia	Enrichment	CAMK2B	0.69
179	Hereditary breast ovarian cancer syndrome	Enrichment	ATM	0.62
180	Autosomal recessive non-syndromic intellectual disability	Enrichment	TPR	0.60
181	Breast cancer	Enrichment	ATM	0.50
182	Dilated cardiomyopathy	Enrichment	BAG3	0.48
183	Ovarian cancer	Enrichment	ATM	0.40
184	Inherited cancer-predisposing syndrome	Enrichment	ATM	0.31

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

Cellular response to heat stress

Pathway Network for Cellular response to heat stress

Pathway network for the Cellular response to heat stress SuperPath

Member Pathways for Cellular response to heat stress

Pathways in the Cellular response to heat stress SuperPath

Gene overlap in member pathways for Cellular response to heat stress SuperPath

Associated Genes for Cellular response to heat stress

Associated Disorders for Cellular response to heat stress

Disorders associated with Cellular response to heat stress SuperPath

STRING Interaction Network for Cellular response to heat stress

Sources for Cellular response to heat stress