Reactome | FGFR2 S267P [plasma membrane]

FGFR2 S267P [plasma membrane]

Stable Identifier

R-HSA-1637920

Type

Protein [EntityWithAccessionedSequence]

Species

Homo sapiens

Compartment

plasma membrane

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Literature References

PubMed ID	Title	Journal	Year
9700203	Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand Anderson, J, Enriquez-Harris, P, Heath, JK, Burns, HD, Wilkie, AO	Hum Mol Genet	1998
11325814	Mutations in fibroblast growth factor receptor 2 and fibroblast growth factor receptor 3 genes associated with human gastric and colorectal cancers Shin, KH, Jang, JH, Park, JG	Cancer Res	2001
7655462	Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome Rutland, P, Winter, RM, Reardon, W, Pulleyn, LJ, Poole, MD, Oldridge, M, Hockley, AD, Goldin, JH, Malcolm, S, Wilkie, AO, Wake, MJ, Slaney, SF	Hum Mol Genet	1995

External Reference Information

External Reference

UniProt:P21802 FGFR2

Gene Names

FGFR2, BEK, KGFR, KSAM

Chain

signal peptide:1-21, chain:22-821

Reference Genes

BioGPS Gene:2263 FGFR2

COSMIC (genes):FGFR2 FGFR2

CTD Gene:2263 FGFR2

dbSNP Gene:2263 FGFR2

ENSEMBL:ENSG00000066468 FGFR2

HGNC:3689 FGFR2

KEGG Gene (Homo sapiens):2263 FGFR2

Monarch:2263 FGFR2

NCBI Gene:2263 FGFR2

OMIM:176943 FGFR2

UCSC:P21802 FGFR2

Reference Transcript

Other Identifiers

0000730167

0002470154

1143_s_at

1144_at

1145_g_at

11739249_a_at

11740159_x_at

11740394_a_at

11740395_a_at

11740409_a_at

11751508_a_at

11752116_a_at

11753370_s_at

11762105_at

11762745_x_at

11762987_x_at

1363_at

16719025

1970_s_at

203638_s_at

203639_s_at

208225_at

208228_s_at

208234_x_at

211401_s_at

2263

3310109

3310110

3310111

3310112

3310113

3310118

3310120

3310123

3310125

3310126

3310128

3310129

3310132

3310133

3310137

3310142

3310143

3310144

3310146

3310147

3310149

3310150

3310164

3310165

3310166

3310168

3310173

3310174

3310176

3310178

3310203

3310204

3310205

3310206

3310209

3310210

3310211

34354_at

73572_at

7936734

A_23_P303145

A_23_P303149

A_24_P206624

GE61433

GE798271

GO:0000003

GO:0000122

GO:0000165

GO:0000166

GO:0000902

GO:0001525

GO:0001657

GO:0001701

GO:0001837

GO:0002053

GO:0003148

GO:0003149

GO:0003416

GO:0003674

GO:0004672

GO:0004713

GO:0004714

GO:0005007

GO:0005515

GO:0005524

GO:0005575

GO:0005576

GO:0005622

GO:0005634

GO:0005737

GO:0005794

GO:0005886

GO:0005887

GO:0005938

GO:0006464

GO:0006468

GO:0006915

GO:0006950

GO:0007049

GO:0007165

GO:0007169

GO:0007267

GO:0007275

GO:0007409

GO:0008150

GO:0008201

GO:0008219

GO:0008283

GO:0008284

GO:0008543

GO:0008589

GO:0009058

GO:0009790

GO:0009791

GO:0009880

GO:0009887

GO:0009986

GO:0010518

GO:0010839

GO:0016020

GO:0016021

GO:0016301

GO:0016310

GO:0016331

GO:0016740

GO:0017134

GO:0018108

GO:0021769

GO:0021847

GO:0021860

GO:0022612

GO:0030154

GO:0030177

GO:0030282

GO:0030324

GO:0030855

GO:0030901

GO:0030916

GO:0031012

GO:0031069

GO:0031410

GO:0032496

GO:0032808

GO:0032991

GO:0033674

GO:0033688

GO:0034641

GO:0035265

GO:0035602

GO:0035603

GO:0035604

GO:0035607

GO:0040007

GO:0042060

GO:0042472

GO:0042476

GO:0042802

GO:0042803

GO:0043167

GO:0043226

GO:0043235

GO:0043410

GO:0044344

GO:0045165

GO:0045471

GO:0045667

GO:0045787

GO:0045944

GO:0046777

GO:0048286

GO:0048333

GO:0048557

GO:0048562

GO:0048565

GO:0048568

GO:0048608

GO:0048646

GO:0048661

GO:0048701

GO:0048705

GO:0048730

GO:0048755

GO:0048762

GO:0048856

GO:0050679

GO:0050680

GO:0051150

GO:0051301

GO:0051781

GO:0051897

GO:0055010

GO:0060045

GO:0060076

GO:0060174

GO:0060348

GO:0060349

GO:0060442

GO:0060445

GO:0060449

GO:0060463

GO:0060484

GO:0060501

GO:0060512

GO:0060523

GO:0060527

GO:0060529

GO:0060595

GO:0060601

GO:0060615

GO:0060664

GO:0060667

GO:0060670

GO:0060688

GO:0060915

GO:0060916

GO:0062023

GO:0070372

GO:0070374

GO:0071300

GO:0071560

GO:0090263

HMNXSV003001516

HMNXSV003003698

HMNXSV003045562

HMNXSV003050281

ILMN_1682270

M87770_at

PH_hs_0024624

TC10001711.hg

g13186252_3p_a_at

g13186256_3p_at

g13186266_3p_a_at

g186740_3p_a_at

g186781_3p_a_at

g6691454_3p_a_at

g6691454_3p_x_at

Participates

as a component of

FGFR2 S267P mutant dimer [plasma membrane] (Homo sapiens)

as a member of

FGFR2 ligand-independent mutants [plasma membrane] (Homo sapiens)

Other forms of this molecule

FGFR2 IIIa TM [extracellular region]

FGFR2 [plasma membrane]

FGFR2(22-767)-CCDC6(102-474) fusion [plasma membrane]

FGFR2(2-822)-CIT(927-2027) fusion [plasma membrane]

FGFR2(22-768)-BICC1(80-974) fusion [plasma membrane]

FGFR2(22-767)-AHCYL1(108-530) fusion [plasma membrane]

FGFR2(22-767)-OFD1(38-1012) fusion [plasma membrane]

FGFR2(22-767)-CASP7(1-303) fusion [plasma membrane]

FGFR2(22-767)-AFF3(292-1226) fusion [plasma membrane]

FGFR2(22-767)-CCAR(51-923) fusion [plasma membrane]

FGFR2 N549H [plasma membrane]

FGFR2 N549K [plasma membrane]

FGFR2 K660N [plasma membrane]

FGFR2 K660M [plasma membrane]

FGFR2 K660E [plasma membrane]

FGFR2 L764fs*4 [plasma membrane]

FGFR2 W290C [plasma membrane]

p-6Y FGFR2(22-767)-CCDC6(102-474) fusion [plasma membrane]

p-6Y FGFR2(22-768)-BICC1(80-974) fusion [plasma membrane]

p-6Y FGFR2(2-822)-CIT(927-2027) fusion [plasma membrane]

p-6Y FGFR2(22-767)-AHCYL1(108-530) fusion [plasma membrane]

p-6Y FGFR2(22-767)-OFD1(38-1012) fusion [plasma membrane]

p-6Y FGFR2(22-767)-AFF3(292-1226) fusion [plasma membrane]

p-6Y FGFR2(22-767)-CASP7(1-303) fusion [plasma membrane]

p-6Y FGFR2 (22-767)-CCAR(51-923) fusion [plasma membrane]

p-8Y-FGFR2 K660N [plasma membrane]

p-8Y-FGFR2 N549H [plasma membrane]

p-8Y-FGFR2 N549K [plasma membrane]

p-8Y-FGFR2 [plasma membrane]

p-8Y-FGFR2 S267P [plasma membrane]

p-8Y-FGFR2 W290C [plasma membrane]

phosphorylated FGFR2 L764fs*4 [plasma membrane]

p-8Y-FGFR2 K660E [plasma membrane]

p-8Y-FGFR2 K660M [plasma membrane]

Modified Residues

Name

L-serine 267 replaced with L-proline

Coordinate

267

PsiMod

L-serine removal [MOD:01646]

A protein modification that effectively removes or replaces an L-serine.

L-proline residue [MOD:00024]

A protein modification that effectively converts a source amino acid residue to L-proline.

Disease

Name	Identifier	Synonyms
bone development disease	DOID:0080006
Crouzon syndrome	DOID:2339	Craniofacial Dysostosis
cancer	DOID:162	malignant tumor, malignant neoplasm, primary cancer
stomach cancer	DOID:10534	malignant neoplasm of greater curvature of stomach, unspecified, malignant neoplasm of lesser curvature of stomach, NOS, malignant tumor of body of stomach (disorder), neoplasm of stomach (disorder), Ca lesser curvature - stomach (disorder), malignant neoplasm of greater curve of stomach unspecified (disorder), Ca body - stomach, ca lesser curvature of stomach, ca greater curvature of stomach, malignant neoplasm of lesser curvature of stomach, unspecified, malignant tumor of lesser curve of stomach (disorder), malignant neoplasm of body of stomach, gastric neoplasm, malignant neoplasm of greater curvature of stomach, NOS, Ca body - stomach (disorder), stomach neoplasm, Ca greater curvature - stomach (disorder), malignant neoplasm of lesser curve of stomach unspecified (disorder), malignant tumor of greater curve of stomach (disorder)

Cross References

RefSeq

NP_001138387.1, NP_075259.4, NP_075418.1, NP_001138390.1, NP_001307587.1, NP_001138388.1, NP_001138386.1, NP_001138389.1, NP_000132.3, NP_001307583.1, NP_001138391.1, NP_001138385.1

ZINC - World Drugs

FGFR2_HUMAN

Guide to Pharmacology - Targets

1809

OpenTargets

ENSG00000066468

ZINC - FDA approved

FGFR2_HUMAN

ZINC - Substances

FGFR2_HUMAN

ZINC target

P21802

ZINC - Biogenic

FGFR2_HUMAN

PRO

P21802

GlyGen

P21802

PDB

1E0O, 5UGX, 3EUU, 5UHN, 1GJO, 2PZP, 3OJ2, 1OEC, 4J97, 5UGL, 7KIA, 1DJS, 6LVK, 3CLY, 3RI1, 6AGX, 6V6Q, 1IIL, 1II4, 3CU1, 2FDB, 4J95, 4J98, 1NUN, 2PWL, 7KIE, 2PVY, 1EV2, 3OJM, 5EG3, 1WVZ, 3CAF, 2PVF, 2PSQ, 6LVL, 2PZR, 5UI0, 2PY3, 4J23, 4WV1, 3B2T, 3DAR, 2PZ5, 2Q0B, 4J99, 4J96

ZINC - Investigational

FGFR2_HUMAN

GeneCards

P21802

HPA

ENSG00000066468-FGFR2

Ensembl

ENSP00000350166, ENSP00000351276, ENSP00000353262, ENST00000369056, ENSP00000410294, ENST00000457416, ENSP00000358052, ENST00000369061, ENSP00000352309, ENSP00000358057, ENST00000360144, ENST00000356226, ENST00000369060, ENSP00000358056, ENSP00000348559, ENSP00000263451, ENST00000359354, ENST00000357555, ENSG00000066468, ENST00000358487, ENST00000346997

Pharos - Targets

P21802

Orphanet

16664

ZINC - Predictions - Purchasable

FGFR2_HUMAN

Interactors (6)

Accession	#Entities	Entities	Confidence Score	Evidence (IntAct)
ChEBI:73280 SSR			0.683	8
UniProt:P62993 GRB2	1	GRB2 [cytosol] (R-HSA-8983328)	0.655	5
UniProt:P09038 FGF2	1	FGF2(10-155) [extracellular region] (R-HSA-189898)	0.623	3
UniProt:P05230 FGF1	1	FGF1 [extracellular region] (R-HSA-189856)	0.571	2
UniProt:O15520 FGF10	1	FGF10 [extracellular region] (R-HSA-189869)	0.571	2
UniProt:Q86VI4 LAP4B			0.463	2

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