FGF10 - fibroblast growth factor 10 Gene

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 2255

About FGF10

Cytogenetic location: 5p12 Genomic coordinates (GRCh38): 5:44,300,247-44,389,420 (from NCBI)

This gene has 2 transcripts (splice variants), 275 orthologues, 21 paralogues and is associated with 6 phenotypes. Broad expression in ovary (RPKM 9.2), fat (RPKM 4.7) and 15 other tissues.

Summary

The protein encoded by this gene is a member of the Fibroblast Growth Factor (FGF) family. FGF Family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein exhibits mitogenic activity for keratinizing epidermal cells, but essentially no activity for fibroblasts, which is similar to the biological activity of FGF7. Studies of the mouse homolog of suggested that this gene is required for embryonic epidermal morphogenesis including brain development, lung morphogenesis, and initiation of lim bud formation. This gene is also implicated to be a primary factor in the process of wound healing. [provided by RefSeq, Jul 2008]

FGF10 Products (1)

mRNA	Protein	Name
NM_004465.2	NP_004456.1	fibroblast growth factor 10 precursor

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	References	Source
enables chemoattractant activity	IDA IDA: Inferred from direct assay	9740653	GOA
enables fibroblast growth factor receptor binding	IDA IDA: Inferred from direct assay	11923311	GOA
enables growth factor activity	IDA IDA: Inferred from direct assay	11923311	GOA
enables heparin binding	IDA IDA: Inferred from direct assay	11923311	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	12591959	GOA
enables type 2 fibroblast growth factor receptor binding	IPI IPI: Inferred from physical interaction	19224135	GOA

Biological Process GO Annotation	Evidence	References	Source
involved in ERK1 and ERK2 cascade	IDA IDA: Inferred from direct assay	17959718	GOA
involved in actin cytoskeleton organization	IDA IDA: Inferred from direct assay	17449030	GOA
involved in branching morphogenesis of an epithelial tube	IDA IDA: Inferred from direct assay	17959718	GOA
acts upstream of or within bud outgrowth involved in lung branching	IDA IDA: Inferred from direct assay	9740653	GOA
involved in epithelial cell proliferation	IDA IDA: Inferred from direct assay	19224135	GOA
acts upstream of or within fibroblast growth factor receptor signaling pathway	IDA IDA: Inferred from direct assay	11923311	GOA
involved in lacrimal gland development	IMP IMP: Inferred from mutant phenotype	17213838	GOA
acts upstream of or within lung epithelium development	IDA IDA: Inferred from direct assay	9740653	GOA
involved in lung saccule development	IMP IMP: Inferred from mutant phenotype	17071719	GOA
involved in mesonephros development	IEP IEP: Inferred from expression pattern	18437684	GOA
involved in metanephros development	IEP IEP: Inferred from expression pattern	18437684	GOA
acts upstream of or within positive chemotaxis	IDA IDA: Inferred from direct assay	9740653	GOA
involved in positive chemotaxis	IDA IDA: Inferred from direct assay	17449030	GOA
involved in positive regulation of ATP-dependent activity	IDA IDA: Inferred from direct assay	12804770	GOA
involved in positive regulation of DNA repair	IDA IDA: Inferred from direct assay	14975937	GOA
involved in positive regulation of G1/S transition of mitotic cell cycle	IDA IDA: Inferred from direct assay	17188682	GOA
involved in positive regulation of MAPK cascade	IDA IDA: Inferred from direct assay	12804770	GOA
involved in positive regulation of Ras protein signal transduction	IDA IDA: Inferred from direct assay	12804770	GOA
involved in positive regulation of epithelial cell migration	IDA IDA: Inferred from direct assay	17500053	GOA
involved in positive regulation of epithelial cell proliferation	IDA IDA: Inferred from direct assay	15690149	GOA
involved in positive regulation of hair follicle cell proliferation	IDA IDA: Inferred from direct assay	16086254	GOA
involved in positive regulation of keratinocyte migration	IDA IDA: Inferred from direct assay	17449030	GOA
involved in positive regulation of keratinocyte proliferation	IDA IDA: Inferred from direct assay	17449030	GOA
involved in positive regulation of lymphocyte proliferation	IDA IDA: Inferred from direct assay	19152659	GOA
involved in positive regulation of peptidyl-tyrosine phosphorylation	IDA IDA: Inferred from direct assay	17449030	GOA
acts upstream of or within positive regulation of urothelial cell proliferation	IDA IDA: Inferred from direct assay	11923311	GOA
involved in positive regulation of urothelial cell proliferation	IDA IDA: Inferred from direct assay	11923311	GOA
involved in protein localization to cell surface	IDA IDA: Inferred from direct assay	17449030	GOA
involved in regulation of saliva secretion	IMP IMP: Inferred from mutant phenotype	19102732	GOA
involved in salivary gland development	IMP IMP: Inferred from mutant phenotype	17213838	GOA
involved in secretion by lung epithelial cell involved in lung growth	IDA IDA: Inferred from direct assay	10541313	GOA
involved in tear secretion	IMP IMP: Inferred from mutant phenotype	19102732	GOA
involved in thymus development	IDA IDA: Inferred from direct assay	17969154	GOA
involved in urothelial cell proliferation	IDA IDA: Inferred from direct assay	11923311	GOA
involved in wound healing	IDA IDA: Inferred from direct assay	11896977	GOA

Cellular Component GO Annotation	Evidence	References	Source
located in cell surface	IDA IDA: Inferred from direct assay	16597614	GOA
colocalizes with collagen-containing extracellular matrix	IDA IDA: Inferred from direct assay	17959718	GOA
located in extracellular space	IDA IDA: Inferred from direct assay	16597614	GOA
located in nucleus	IDA IDA: Inferred from direct assay	11923311	GOA
located in plasma membrane	IDA IDA: Inferred from direct assay	16597614	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

FGF10 Protein Structure

FGF

0
100
208 a.a.

Protein Preferred Names	Protein Names
fibroblast growth factor 10	FGF-10

FGF10 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	FGF10	O15520	SREK1IP1	Homo sapiens	Q8N9Q2	Validated Y2H	32296183
Intra	FGF10	O15520	FGFR2	Homo sapiens	P21802	PLA	25241761
Intra	FGF10	O15520	FGFR2	Homo sapiens	P21802	X-Ray Diffraction	12591959
Intra	FGF10	O15520	THAP1	Homo sapiens	Q9NVV9	Y2H Array	32296183
Intra	FGF10	O15520	THAP1	Homo sapiens	Q9NVV9	Y2H Prey Pooling	32296183
Intra	FGF10	O15520	THAP1	Homo sapiens	Q9NVV9	Validated Y2H	32296183

Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant FGF10 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P7048	KGF-2/FGF-10 Protein, Human (169a.a)	O15520 (L40-S208)	≥ 95%, as determined by reducing SDS-PAGE.
HY-P78123	KGF-2/FGF-10 Protein, Human (Biotinylated)	O15520 (Q38-S208)	≥ 95%, as determined by Bis-Tris PAGE.
HY-P78878	KGF-2/FGF-10 Protein, Human (Biotinylated, His-Avi)	O15520 (Q38-S208)	≥ 95%, as determined by reducing SDS-PAGE.
HY-P7342AF	Animal-Free KGF-2/FGF-10 Protein, Human (His)	O15520 (L40-S208)	≥ 95%, as determined by reducing SDS-PAGE.
HY-P700279	KGF-2/FGF-10 Protein, Human (N-His)	O15520 (L40-S208)	≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases	Alias
Lacrimoauriculodentodigital Syndrome	Ladd Syndrome Levy-Hollister Syndrome Lacrimo-Auriculo-Dento-Digital Syndrome LADD Lacrimoauriculodento-Digital Syndrome Levy Hollister Syndrome Lard Syndrome Lacrimoauriculoradiodental Syndrome LADDS Congenital Duodenal Obstruction Due To Malrotation Of Intestine
Aplasia Of Lacrimal And Salivary Glands	ALSG Congenital Absence Of Lacrimal Puncta And Salivary Glands Xerostomia Absence Of Salivary Glands Parotid Aplasia Or Hypoplasia Congenital Absence Of Lacrimal Puncta Or Salivary Glands Alsg - [Aplasia Of Lacrimal Or Salivary Glands]
Pulmonary Hypoplasia, Primary	Pulmonary Agenesis Lung Agenesis Primary Pulmonary Hypoplasia Congenital Absence Of Lung Congenital Lung Agenesis Unilateral Lobar Pulmonary Agenesis Unilateral Lung Agenesis Absence Of Lung Aplasia Of Lung Apulmonism Congenital Aplasia Of Lung Agenesis Of Lobe Of Lung Absence Of Lobe Of Lung Congenital Absence Of Lobe Of Lung
Pulmonary Hypoplasia, Familial Primary	Familial Primary Pulmonary Hypoplasia
Apert Syndrome	Acrocephalosyndactyly Type I Acs1 Acrocephalosyndactylia Acrocephalosyndactyly Acs I Apert-Crouzon Disease Acrocephalosyndactyly Type 1 Acrocephalosyndactyly, Type I Acs 1 Acrocephalo-Syndactyly Type 1 Syndactylic Oxycephaly Apert'S Syndrome Type I Acrocephalosyndactyly APRS
Craniosynostosis	Premature Closure Of Cranial Sutures Craniostenosis Craniosynostosis Syndrome Cso Craniosynostoses Congenital Ossification Of Cranial Sutures Congenital Ossification Of Sutures Of Skull Craniostosis Imperfect Fusion Of Skull Congenital Imperfect Closure Skull Imperfect Closure Skull Premature Closure Cranium Sutures Deficiency Of Craniofacial Axis
Acanthoma
Pfeiffer Syndrome	Infectious Mononucleosis Acs5 Craniofacial-Skeletal-Dermatologic Dysplasia Acs V Noack Syndrome Gammaherpesviral Mononucleosis Acrocephalosyndactyly Type 5 Pfeiffer Syndrome Type 3 Acrocephalosyndactyly, Type V Glandular Fever Pfeiffer Type Acrocephalosyndactyly Pfeiffer Syndrome Type 2 Acrocephalosyndactylia Type V Filatov'S Disease Monocytic Angina Mononucleosis Pfeiffer'S Disease Acsv Acrocephalosyndactyly, Type 5 Craniofacial-Skeletal-Dermatologic Syndrome Pfeiffer Syndrome Type 1 Classic Pfeiffer Syndrome PS Pfeiffer Syndrome Variant Dysplasia, Craniofacial-Skeletal-Dermatologic Pfeiffer Kissing Disease Infectious Adenitis Pfeiffer Disease
Blastoma	Embryoma
Hypospadias	Hypospadias Familial Familial Hypospadias
Bronchopulmonary Dysplasia	Bpd
Cleft Lip	Cheiloschisis Labium Leporinum Cleft Lip, Unilateral, Complete Complete Unilateral Cleft Lip Hare Lip Congenital Fissure Of Lip Isolated Cleft Lip Cleft Lip Without Cleft Palate Cleft Lip Without Cleft Palate, Unilateral Isolated Cleft Lip, Unilateral Cleft Lip Without Cleft Palate, Bilateral Isolated Cleft Lip, Bilateral
Tracheomalacia	Congenital Tracheomalacia Congenital Major Airway Collapse Tracheomalacia, Congenital Type 1 Tracheomalacia
Duodenal Atresia	Duodenal Stenosis Familial Duodenal Atresia
Ischiocoxopodopatellar Syndrome With Or Without Pulmonary Arterial Hypertension	Small Patella Syndrome Ischiopatellar Dysplasia Coxopodopatellar Syndrome Scott-Taor Syndrome Sps Ischiocoxopodopatellar Syndrome Patella Aplasia, Coxa Vara, And Tarsal Synostosis ICPPS Congenital Coxa Vara, Patella Aplasia And Tarsal Synostosis Coxo-Podo-Patellar Syndrome Patella Aplasia, Coxa Vara, Tarsal Synostosis Coxopodipatellar Syndrome
Exudative Vitreoretinopathy 7	EVR7 Vitreoretinopathy, Exudative 7 Vitreoretinopathy Exudative, Type 7
Cataract 23, Multiple Types	Cataract 23 CTRCT23 Lamellar Cataract 23 Cataract 23, Multiple Types, With Or Without Microcornea Isolated Microphthalmia With Cataract 4 Mcopct4 Cataract, Type 23 Microphthalmia, Isolated, With Cataract 4
Chronic Inflammation Of Lacrimal Passage
Dacryocystocele	Lacrimal Mucocele
Muenke Syndrome	Muenke Nonsyndromic Coronal Craniosynostosis Fgfr3-Related Craniosynostosis Fgfr3-Associated Coronal Synostosis Coronal Craniosynostosis MNKES Syndrome Of Coronal Craniosynostosis MNKS Fgfr3-Related Isolated Coronal Synostosis Muenke Non-Syndromic Coronal Craniosynostosis
Mucositis	Inflammatory Disease Of Mucous Membrane Gastrointestinal Mucositis
Mesenteric Vascular Occlusion
Tracheal Stenosis	Stenosis Of Trachea
Cleft Palate, Isolated	Cleft Palate Isolated Cleft Palate CPI Cp Palatoschisis Cleft Palate Isolated Uranostaphyloschisis Congenital Fissure Of Palate Cleft Of Secondary Palate
Intestinal Atresia
Ectodermal Dysplasia	Congenital Ectodermal Defect Congenital Ectodermal Dysplasia Ectodermal Dysplasia Syndrome Dysplasia, Ectodermal
Diaphragm Disease	Abnormality Of The Diaphragm Disease Of Diaphragm Diaphragmatic Disorder Disorder Of Diaphragm
Crouzon Syndrome	Crouzon Craniofacial Dysostosis Craniofacial Dysostosis Cfd1 Craniofacial Dysostosis Type 1 Crouzon Disease Crouzon'S Disease Craniofacial Dysostosis, Type I Craniofacial Dysarthrosis Craniofacial Dysostosis Syndrome CS Craniofacial Dysostosis Type I Vogt Cephalosyndactyly
Neonatal Respiratory Failure	Respiratory Failure Of Newborn Inadequate Pulmonary Ventilation Of Newborn Newborn Lung Insufficiency Newborn Pulmonary Function Inadequate Newborn Pulmonary Insufficiency Newborn Respiration Failure Newborn Respiratory Insufficiency Respiratory Insufficiency Syndrome Of Newborn
Tracheal Disease	Tracheal Diseases Tracheal Anomaly Tracheal Disorders
Granulomatous Endometritis
Ectopic Thymus
Holt-Oram Syndrome	HOS Atriodigital Dysplasia Heart-Hand Syndrome Atrio-Digital Syndrome Cardiac-Limb Syndrome Heart-Hand Syndrome, Type 1 Ventriculo-Radial Syndrome Hos1 Heart Hand Syndrome Atrio Digital Syndrome Hos 1 Atriodigital Dysplasia Type 1 Heart-Hand Syndrome Type 1 Holt Oram Syndrome
Jackson-Weiss Syndrome	JWS Craniosynostosis, Midfacial Hypoplasia, And Foot Abnormalities Craniosynostosis-Midfacial Hypoplasia-Foot Abnormalities Syndrome Craniosynostosis-Midfacial Hypoplasia-Foot Abnormalities
Renal Hypodysplasia/Aplasia 1	Renal Agenesis Renal Adysplasia Renal Aplasia RHDA1 Hereditary Renal Aplasia Hra Hereditary Urogenital Adysplasia Hypodysplasia/Aplasia, Renal, Type 1 Congenital Absence Of Kidneys Syndrome Congenital Absence Of Kidney Aplastic Kidney
Orofacial Cleft	Cleft, Orofacial
Diaphragmatic Hernia, Congenital	Congenital Diaphragmatic Hernia Diaphragmatic Hernia Cdh Congenital Diaphragmatic Defect Hernia, Diaphragmatic Dih Hernia, Congenital Diaphragmatic Hcd Diaphragmatic Defect, Congenital Diaphragm, Unilateral Agenesis Of Hemidiaphragm, Agenesis Of Diaphragmatic Hernia 1 Agenesis Of Hemidiaphragm Unilateral Agenesis Of Diaphragm Hernia Diaphragmatic Hernia Diaphragmatic Congenital Hernia, Diaphragmatic, Type 1 Hiatus Hernia Oesophageal Hiatus Hernia Paraoesophageal Hernia Sliding Hiatus Hernia Congenital Diaphragm Hernia Congenital Diaphragm Defect With Hernia Gross Congenital Diaphragm Defect
Developmental And Epileptic Encephalopathy 24	DEE24 Epileptic Encephalopathy, Early Infantile, 24 Eiee24 Developmental And Epileptic Encephalopathy, 24 Early Infantile Epileptic Encephalopathy 24 Encephalopathy, Epileptic, Early Infantile, Type 24
Myopia	Near-Sightedness Short-Sightedness Nearsightedness Nearsighted Near Vision Close Sighted Myopic Short-Sighted Near Sighted
Breast Cancer	Breast Carcinoma Male Breast Cancer Breast Cancer, Familial Malignant Neoplasm Of Breast Breast Cancer, Susceptibility To Breast Cancer, Early-Onset Malignant Tumor Of Breast Carcinoma Of Male Breast Breast Cancer, Invasive Ductal Breast Cancer, Protection Against Breast Cancer, Somatic Breast Cancer, Male Breast Cancer, Lobular, Somatic Breast Tumor Mammary Cancer Mammary Tumor Malignant Neoplasm Of Male Breast Mammary Carcinoma Male Breast Carcinoma Familial Cancer Of Breast Invasive Ductal Breast Carcinoma Breast Cancer Susceptibility Breast Cancer, Male, Susceptibility To Breast Cancer, Early-Onset, Susceptibility To Malignant Tumor Of The Breast Mammary Neoplasm Primary Breast Cancer Neoplasm Of Male Breast Carcinoma Of Breast Breast Cancer In Men Familial Breast Cancer Cancer Of Breast BC Breast Cancer Familial Breast Cancer Familial Male Breast Cancer, Familial Male Breast Male Carcinoma Breast Neoplasms Breast Neoplasms, Male Mammary Tumors Mammary Carcinomas Cancer, Breast Cancer, Breast, Susceptibility Invasive Breast Ductal Carcinoma Breast Neoplasm Susceptibility To Breast Cancer Mammary Neoplasms Animal Mammary Neoplasms Primary Malignant Neoplasm Of Breast Infiltrating Ductal Carcinoma Of Breast Infiltrating Duct Carcinoma Of Unspecified Site Infiltrating Ductular Carcinoma Of Unspecified Site Invasive Breast Carcinoma Of No Special Type Microinvasive Carcinoma Of Breast Carcinoma With Apocrine Differentiation
Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive	Hypohidrotic Ectodermal Dysplasia Hed Anhidrotic Ectodermal Dysplasia Ectodermal Dysplasia, Hypohidrotic Eda Christ-Siemens-Touraine Syndrome ECTD10B Ectodermal Dysplasia Anhidrotic Ectodermal Dysplasia, Anhidrotic Cst Syndrome Ectodermal Dysplasia Hypohidrotic Autosomal Recessive Dysplasia, Ectodermal, Type 10b, Hypohidrotic/Hair/Tooth, Autosomal Recessive Dysplasia, Ectodermal, Hypohidrotic Ectodermal Dysplasia 11b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive Ectodermal Dysplasia 3, Anhidrotic Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Double Outlet Right Ventricle	Double Outlet Right Ventricle With Subpulmonary Ventricular Septal Defect Taussig-Bing Syndrome Dextrotransposition Of Aorta Taussig-Bing Syndrome Or Defect Dorv Dorv With Subpulmonary Vsd Dorv-Tga Double Outlet Right Ventricle With Transposition Of The Great Arteries Double Outlet Right Ventricle With Subpulmonary Interventricular Communication, Transposition Type Taussig-Bing Heart Taussig-Bing Malformation Taussig-Bing Complex Taussig-Bing Defect Taussig-Bing Double Outlet Right Ventricle With Remote Ventricular Septal Defect Double Outlet Right Ventricle With Uncommitted Ventricular Septal Defect Double Outlet Right Ventricle With Non-Committed Interventricular Communication Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication Without Pulmonary Stenosis Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication And Pulmonary Stenosis
Branchiooculofacial Syndrome	Branchio-Oculo-Facial Syndrome BOFS Bof Syndrome Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome Branchial Clefts With Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, And Premature Aging Branchial Clefts With Characteristic Facies Growth Retardation Imperforate Nasolacrimal Duct And Premature Aging Bofs Syndrome Lip Pseudocleft-Hemagiomatous Branchial Cyst Syndrome
Tooth Agenesis	Oligodontia Hypodontia Selective Tooth Agenesis Tooth Agenesis, Selective Familial Tooth Agenesis Anodontia Congenital Absence Of One Tooth
Esophageal Atresia	Tracheoesophageal Fistula Congenital Atresia Of Esophagus Congenital Imperforate Esophagus Imperforate Esophagus Oesophageal Atresia Te Fistula Tef Tracheoesophageal Fistula With Or Without Esophageal Atresia
Tetralogy Of Fallot	TOF Fallot Tetralogy Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle Tetrad Of Fallot Fallot Tetrad Fallot Disease Fallot Complex Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle Interventricular Septal Defect, In Tetralogy Of Fallot Ventricular Septal Defect With Obstructed Right Ventricular Outflow Tof - [Tetralogy Of Fallot] Pulmonary Atresia With Ventricular Septal Defect [Fallot Type] Pulmonary Atresia, Ventricular Septal Defect And Mapcas Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
Interstitial Lung Disease 2	Idiopathic Pulmonary Fibrosis Ipf Fibrocystic Pulmonary Dysplasia Pulmonary Fibrosis, Idiopathic Pulmonary Fibrosis, Idiopathic, Susceptibility To Cryptogenic Fibrosing Alveolitis ILD2 Idiopathic Pulmonary Fibrosis, Familial Fibrosing Alveolitis, Cryptogenic Uip Fibrosing Alveolitis Interstitial Pneumonitis, Usual Familial Idiopathic Pulmonary Fibrosis Idiopathic Fibrosing Alveolitis, Chronic Form Usual Interstitial Pneumonia Fibrosing Alveolitis Cryptogenic Hamman-Rich Disease Idiopathic Pulmonary Fibrosis Familial Interstitial Pneumonitis Usual Fibrosis Idiopathic Pulmonary Fibrosis, Pulmonary, Idiopathic Hamman-Rich Syndrome Chronic Idiopathic Pulmonary Fibrosis Acute Interstitial Pneumonia Interstitial Pulmonary Fibrosis Ipf - [Idiopathic Pulmonary Fibrosis] Idiopathic Lung Fibrosis Fibrosing Lung Disease Pulmonary Fibrosis Nos Fibrosing Pneumonitis

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (4)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS04887	FGF10 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-174711	Human FGF10 mRNA		/	Unkown
HY-RS16590	Fgf10 Mouse Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS23025	Fgf10 Rat Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Inhibitory Antibodies (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-P991584	HuGAL-FR21	Inhibitor	97.80%	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	FGF10	RGD	RGD:2606
Macaca mulatta	FGF10	VGNC	VGNC:84378
Mus musculus	FGF10	MGD	MGI:1099809
Felis catus	FGF10	VGNC	VGNC:102207
Canis familiaris	FGF10	VGNC	VGNC:40839
Bos taurus	FGF10	VGNC	VGNC:106742
Others	FGF10	NCBI