Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	2160
Gene name Gene Name - the full gene name approved by the HGNC.	Coagulation factor XI
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	F11
Synonyms (NCBI Gene) Gene synonyms aliases	FXI, PTA
Chromosome Chromosome number	4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	4q35.2
Summary Summary of gene provided in NCBI Entrez Gene.	This gene encodes coagulation factor XI of the blood coagulation cascade. This protein is present in plasma as a zymogen, which is a unique plasma coagulation enzyme because it exists as a homodimer consisting of two identical polypeptide chains linked by

Show/Hide all(64)

SNP ID	Visualize variation	Clinical significance	Consequence
rs28934608	C>T	Likely-pathogenic	Non coding transcript variant, missense variant, coding sequence variant, genic downstream transcript variant
rs121965063	G>T	Pathogenic	Stop gained, coding sequence variant, non coding transcript variant
rs121965064	T>C	Pathogenic, pathogenic-likely-pathogenic	Coding sequence variant, genic downstream transcript variant, missense variant, non coding transcript variant, intron variant
rs121965066	C>A	Likely-pathogenic	Stop gained, coding sequence variant, non coding transcript variant
rs121965067	C>A	Pathogenic	Coding sequence variant, genic downstream transcript variant, missense variant, 3 prime UTR variant, downstream transcript variant, non coding transcript variant
rs121965068	C>T	Pathogenic	Coding sequence variant, genic downstream transcript variant, missense variant, downstream transcript variant, non coding transcript variant
rs121965069	T>C	Likely-pathogenic	Missense variant, coding sequence variant, non coding transcript variant
rs121965070	A>T	Conflicting-interpretations-of-pathogenicity, uncertain-significance	Missense variant, coding sequence variant, genic downstream transcript variant, non coding transcript variant
rs121965071	G>A,C,T	Likely-pathogenic	Coding sequence variant, genic downstream transcript variant, missense variant, downstream transcript variant, non coding transcript variant
rs143648758	C>A	Likely-pathogenic, pathogenic	Stop gained, non coding transcript variant, coding sequence variant
rs281875244	C>A,G,T	Not-provided, likely-pathogenic, uncertain-significance	Coding sequence variant, non coding transcript variant, missense variant
rs281875245	G>A,T	Not-provided, likely-pathogenic	Genic downstream transcript variant, intron variant, non coding transcript variant, coding sequence variant, missense variant
rs281875257	G>A	Not-provided, likely-pathogenic	Coding sequence variant, genic downstream transcript variant, non coding transcript variant, missense variant
rs281875266	G>A,T	Not-provided, likely-pathogenic	3 prime UTR variant, genic downstream transcript variant, non coding transcript variant, coding sequence variant, missense variant
rs281875272	A>G	Conflicting-interpretations-of-pathogenicity, not-provided	Coding sequence variant, non coding transcript variant, missense variant
rs369650561	G>A	Pathogenic	Coding sequence variant, non coding transcript variant, missense variant
rs375440170	T>C	Likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant, genic downstream transcript variant
rs533335580	C>T	Likely-pathogenic	Coding sequence variant, non coding transcript variant, 3 prime UTR variant, genic downstream transcript variant, missense variant
rs538083600	C>T	Pathogenic-likely-pathogenic	Coding sequence variant, downstream transcript variant, non coding transcript variant, stop gained, genic downstream transcript variant
rs747702749	C>T	Likely-pathogenic	Genic downstream transcript variant, coding sequence variant, stop gained, non coding transcript variant, intron variant
rs752907087	C>T	Likely-pathogenic	Genic downstream transcript variant, coding sequence variant, stop gained, non coding transcript variant, intron variant
rs753909969	G>A	Pathogenic	Missense variant, genic downstream transcript variant, downstream transcript variant, coding sequence variant, non coding transcript variant
rs754087775	C>T	Likely-pathogenic	Genic downstream transcript variant, coding sequence variant, stop gained, non coding transcript variant, intron variant
rs755700350	G>T	Likely-pathogenic	Missense variant, non coding transcript variant, initiator codon variant
rs756908183	C>T	Pathogenic-likely-pathogenic, pathogenic, conflicting-interpretations-of-pathogenicity	Non coding transcript variant, coding sequence variant, stop gained
rs757817254	G>A	Conflicting-interpretations-of-pathogenicity	Intron variant, genic downstream transcript variant, missense variant, coding sequence variant, non coding transcript variant
rs762013077	G>A,T	Likely-pathogenic	Coding sequence variant, missense variant, stop gained, non coding transcript variant
rs763496524	C>T	Pathogenic	Coding sequence variant, missense variant, non coding transcript variant, genic downstream transcript variant
rs767727775	T>C	Likely-pathogenic	Coding sequence variant, non coding transcript variant, missense variant
rs768409400	C>T	Pathogenic, likely-pathogenic	Coding sequence variant, non coding transcript variant, stop gained
rs768474112	G>A	Likely-pathogenic	Coding sequence variant, non coding transcript variant, missense variant
rs770505620	C>T	Pathogenic	Coding sequence variant, genic downstream transcript variant, stop gained, non coding transcript variant
rs771896253	C>T	Likely-pathogenic	Genic downstream transcript variant, coding sequence variant, missense variant, non coding transcript variant, 3 prime UTR variant
rs773905328	C>A,T	Pathogenic-likely-pathogenic	Genic downstream transcript variant, stop gained, coding sequence variant, synonymous variant, non coding transcript variant
rs779802284	G>A	Pathogenic-likely-pathogenic	Non coding transcript variant, genic downstream transcript variant, coding sequence variant, downstream transcript variant, missense variant
rs786204429	A>-	Likely-pathogenic	Genic downstream transcript variant, frameshift variant, coding sequence variant, non coding transcript variant
rs786204449	TG>-	Likely-pathogenic	Genic downstream transcript variant, frameshift variant, coding sequence variant, non coding transcript variant
rs786204722	G>-	Likely-pathogenic	Non coding transcript variant, intron variant, genic downstream transcript variant, coding sequence variant, frameshift variant
rs933333847	A>G	Likely-pathogenic	Genic downstream transcript variant, intron variant
rs1024865708	A>C,G	Pathogenic	Missense variant, coding sequence variant, non coding transcript variant, splice acceptor variant, synonymous variant, genic downstream transcript variant
rs1057516431	AC>-	Likely-pathogenic	Genic downstream transcript variant, coding sequence variant, non coding transcript variant, frameshift variant
rs1057516616	CATT>-	Likely-pathogenic	Coding sequence variant, non coding transcript variant, frameshift variant
rs1057516695	A>G	Likely-pathogenic	Genic downstream transcript variant, splice acceptor variant, intron variant
rs1057516738	G>A	Likely-pathogenic	Splice donor variant
rs1057517116	CGCGCAGCTTGT>-	Likely-pathogenic	Coding sequence variant, splice acceptor variant, non coding transcript variant, intron variant, genic downstream transcript variant
rs1057517151	G>-	Likely-pathogenic	Coding sequence variant, non coding transcript variant, frameshift variant
rs1057517364	G>A	Pathogenic	Splice acceptor variant
rs1057517446	CTCA>-	Likely-pathogenic	Coding sequence variant, non coding transcript variant, downstream transcript variant, frameshift variant, genic downstream transcript variant
rs1173748968	G>A,C	Pathogenic	Intron variant, 3 prime UTR variant
rs1220869989	T>C	Pathogenic-likely-pathogenic	Splice donor variant, intron variant, genic downstream transcript variant
rs1262002209	C>T	Likely-pathogenic	Missense variant, non coding transcript variant, coding sequence variant, genic downstream transcript variant, intron variant
rs1316806485	G>A,C	Likely-pathogenic	Non coding transcript variant, genic downstream transcript variant, splice donor variant
rs1340928778	C>A,T	Conflicting-interpretations-of-pathogenicity	Missense variant, coding sequence variant, non coding transcript variant
rs1349655563	G>C	Likely-pathogenic	Genic downstream transcript variant, splice donor variant
rs1439195599	GTTG>-	Likely-pathogenic, pathogenic	Intron variant, genic downstream transcript variant, 3 prime UTR variant
rs1459304265	TCGACA>-	Likely-pathogenic	Inframe deletion, non coding transcript variant, intron variant, genic downstream transcript variant, coding sequence variant
rs1554081281	T>A	Likely-pathogenic	Non coding transcript variant, missense variant, initiator codon variant
rs1554081288	C>T	Likely-pathogenic	Non coding transcript variant, stop gained, coding sequence variant
rs1554081886	->A	Likely-pathogenic	Non coding transcript variant, stop gained, coding sequence variant
rs1554082832	C>-	Likely-pathogenic	Frameshift variant, non coding transcript variant, coding sequence variant, genic downstream transcript variant
rs1554082938	T>-,TT	Likely-pathogenic	Frameshift variant, non coding transcript variant, coding sequence variant, genic downstream transcript variant
rs1580075457	T>-	Likely-pathogenic	Non coding transcript variant, coding sequence variant, frameshift variant
rs1580090765	T>C	Likely-pathogenic	Genic downstream transcript variant, non coding transcript variant, coding sequence variant, missense variant
rs1580098946	->GATATTA	Pathogenic	Downstream transcript variant, non coding transcript variant, frameshift variant, genic downstream transcript variant, coding sequence variant

Show/Hide all(38)

miRTarBase ID	miRNA	Experiments
MIRT974028	hsa-miR-15a	CLIP-seq
MIRT974029	hsa-miR-15b	CLIP-seq
MIRT974030	hsa-miR-16	CLIP-seq
MIRT974031	hsa-miR-195	CLIP-seq
MIRT974032	hsa-miR-424	CLIP-seq
MIRT974033	hsa-miR-4327	CLIP-seq
MIRT974034	hsa-miR-4514	CLIP-seq
MIRT974035	hsa-miR-4692	CLIP-seq
MIRT974036	hsa-miR-497	CLIP-seq
MIRT974037	hsa-miR-507	CLIP-seq
MIRT974038	hsa-miR-511	CLIP-seq
MIRT974039	hsa-miR-557	CLIP-seq
MIRT974040	hsa-miR-577	CLIP-seq
MIRT974041	hsa-miR-628-5p	CLIP-seq
MIRT974042	hsa-miR-646	CLIP-seq
MIRT1988582	hsa-miR-128	CLIP-seq
MIRT1988583	hsa-miR-2117	CLIP-seq
MIRT1988584	hsa-miR-375	CLIP-seq
MIRT1988585	hsa-miR-4273	CLIP-seq
MIRT1988586	hsa-miR-4279	CLIP-seq
MIRT1988587	hsa-miR-4659a-3p	CLIP-seq
MIRT1988588	hsa-miR-4659b-3p	CLIP-seq
MIRT1988589	hsa-miR-4677-5p	CLIP-seq
MIRT974038	hsa-miR-511	CLIP-seq
MIRT2223027	hsa-miR-299-3p	CLIP-seq
MIRT2223028	hsa-miR-3671	CLIP-seq
MIRT2223029	hsa-miR-4491	CLIP-seq
MIRT2223030	hsa-miR-4504	CLIP-seq
MIRT2223031	hsa-miR-4657	CLIP-seq
MIRT2223032	hsa-miR-607	CLIP-seq
MIRT1988583	hsa-miR-2117	CLIP-seq
MIRT1988584	hsa-miR-375	CLIP-seq
MIRT1988585	hsa-miR-4273	CLIP-seq
MIRT1988586	hsa-miR-4279	CLIP-seq
MIRT1988587	hsa-miR-4659a-3p	CLIP-seq
MIRT1988588	hsa-miR-4659b-3p	CLIP-seq
MIRT1988589	hsa-miR-4677-5p	CLIP-seq
MIRT974038	hsa-miR-511	CLIP-seq

Show/Hide all(15)

GO ID	Ontology	Definition	Evidence	Reference
GO:0004252	Function	Serine-type endopeptidase activity	NAS	9593722
GO:0005515	Function	Protein binding	IPI	2844223, 15545266
GO:0005576	Component	Extracellular region	NAS	9593722
GO:0005576	Component	Extracellular region	TAS
GO:0005615	Component	Extracellular space	IDA	89876
GO:0005886	Component	Plasma membrane	TAS
GO:0007596	Process	Blood coagulation	IDA	9169594
GO:0007596	Process	Blood coagulation	NAS	9593722
GO:0007597	Process	Blood coagulation, intrinsic pathway	TAS
GO:0008201	Function	Heparin binding	IEA
GO:0016020	Component	Membrane	NAS	9593722
GO:0031639	Process	Plasminogen activation	IDA	89876
GO:0051919	Process	Positive regulation of fibrinolysis	IDA	89876
GO:0070009	Function	Serine-type aminopeptidase activity	IEA
GO:0070062	Component	Extracellular exosome	HDA	19056867

MIM	HGNC	e!Ensembl
264900	3529	ENSG00000088926

Protein

UniProt ID

P03951

Protein name

Coagulation factor XI (FXI) (EC 3.4.21.27) (Plasma thromboplastin antecedent) (PTA) [Cleaved into: Coagulation factor XIa heavy chain; Coagulation factor XIa light chain]

Protein function

Factor XI triggers the middle phase of the intrinsic pathway of blood coagulation by activating factor IX.

PDB

1XX9 , 1XXD , 1XXF , 1ZHM , 1ZHP , 1ZHR , 1ZJD , 1ZLR , 1ZMJ , 1ZML , 1ZMN , 1ZOM , 1ZPB , 1ZPC , 1ZPZ , 1ZRK , 1ZSJ , 1ZSK , 1ZSL , 1ZTJ , 1ZTK , 1ZTL , 2FDA , 2J8J , 2J8L , 3BG8 , 3SOR , 3SOS , 4CR5 , 4CR9 , 4CRA , 4CRB , 4CRC , 4CRD , 4CRE , 4CRF , 4CRG , 4D76 , 4D7F , 4D7G , 4NA7 , 4NA8 , 4TY6 , 4TY7 , 4WXI , 4X6M , 4X6N , 4X6O , 4X6P , 4Y8X , 4Y8Y

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF00024	PAN_1	20 → 103	PAN domain	Domain
PF00024	PAN_1	110 → 193	PAN domain	Domain
PF00024	PAN_1	200 → 283	PAN domain	Domain
PF00024	PAN_1	291 → 374	PAN domain	Domain
PF00089	Trypsin	388 → 618	Trypsin	Domain

Tissue specificity

TISSUE SPECIFICITY: Isoform 2 is produced by platelets and megakaryocytes but absent from other blood cells.

Sequence

MIFLYQVVHFILFTSVSGECVTQLLKDTCFEGGDITTVFTPSAKYCQVVCTYHPRCLLFT
FTAESPSEDPTRWFTCVLKDSVTETLPRVNRTAAISGYSFKQCSHQISACNKDIYVDLDM
KGINYNSSVAKSAQECQERCTDDVHCHFFTYATRQFPSLEHRNICLLKHTQTGTPTRITK
LDKVVSGFSLKSCALSNLACIRDIFPNTVFADSNIDSVMAPDAFVCGRICTHHPGCLFFT
FFSQEWPKESQRNLCLLKTSESGLPSTRIKKSKALSGFSLQSCRHSIPVFCHSSFYHDTD
FLGEELDIVAAKSHEACQKLCTNAVRCQFFTYTPAQASCNEGKGKCYLKLSSNGSPTKIL
HGRGGISGYTLRLCKMDNECTTKIKPRIVGGTASVRGEWPWQVTLHTTSPTQRHLCGGSI
IGNQWILTAAHCFYGVESPKILRVYSGILNQSEIKEDTSFFGVQEIIIHDQYKMAESGYD
IALLKLETTVNYTDSQRPICLPSKGDRNVIYTDCWVTGWGYRKLRDKIQNTLQKAKIPLV
TNEECQKRYRGHKITHKMICAGYREGGKDACKGDSGGPLSCKHNEVWHLVGITSWGEGCA
QRERPGVYTNVVEYVDWILEKTQAV

Sequence length

625

Interactions

View interactions

	KEGG		Reactome
	Complement and coagulation cascades		Intrinsic Pathway of Fibrin Clot Formation

Show/Hide Causal Diseases (2)

Disease term	Disease name	dbSNP ID	References
Causal
Hereditary factor xi deficiency	Hereditary Factor XI Deficiency	rs373297713, rs121965063, rs121965064, rs1024865708, rs1173748968, rs121965065, rs121965066, rs28934608, rs28934609, rs121965069, rs121965071, rs121965072, rs281875266, rs281875250, rs281875255 View all (68 more)	25074526, 10027710, 11127865, 14508802, 23332144, 16835901, 27067486, 18515884, 15953011, 9401068, 12879434, 21457405, 23305485, 19652879, 17549289 View all (56 more)
Hypertension	Hypertensive disease	rs13306026	6383834

Show/Hide Unknown Diseases (1)

Disease term	Disease name	Evidence	References	Source
Unknown
Cardioembolic Stroke	Cardioembolic Stroke			GWAS

Show/Hide Text Mining Associations (43)

Disease Name	Relationship Type	References
Associations from Text Mining
Abortion Spontaneous	Associate	25517908
Antiphospholipid Syndrome	Associate	38003459
Atrial Fibrillation	Associate	31558144, 39864423, 40304040
Blood Coagulation Disorders	Associate	15456480, 19552680, 30801944, 37751848
Brain Infarction	Associate	37364690
Carcinoma Hepatocellular	Associate	39207047
Cardiovascular Diseases	Associate	31558144
Cerebral Infarction	Associate	24086496, 28053049, 30355187, 37364690, 40304040
Cerebral Infarction	Inhibit	31558144
Coagulation Protein Disorders	Associate	10090892
Coma Post Head Injury	Associate	27627722
Cushing's symphalangism	Associate	24086496
Death	Associate	37364690
Diabetes Mellitus Type 2	Associate	40304040
Diabetic Nephropathies	Associate	39838413
Embolic Stroke	Associate	30355187, 40596960
Factor XI Deficiency	Associate	12879434, 14717969, 15140127, 15456480, 15456490, 18029554, 22016685, 27723456, 32118380, 33421272
Fractures Bone	Associate	27627722
Genetic Diseases Inborn	Associate	34200207
Hemorrhage	Associate	15456480, 27723456, 28053049
Hemostatic Disorders	Associate	37364690
Hepatitis B	Associate	39207047
Hypertension Pregnancy Induced	Associate	16613788
Immunologic Deficiency Syndromes	Associate	14717969
Inflammation	Associate	29378352, 30801944, 37364690
Intrahepatic Cholestasis of Pregnancy	Associate	22533697
Kidney Failure Chronic	Associate	34085768
Liver Cirrhosis	Associate	39207047
Myocardial Infarction	Associate	30355187
Neoplasms	Associate	32671915, 37751848
Obesity	Associate	21959347
Rufous oculocutaneous albinism	Associate	15140127
Sepsis	Inhibit	30600428
Skin Manifestations	Associate	23332144
Stroke	Associate	30355187
Thrombophilia	Associate	14521595
Thrombophilia hereditary	Associate	14521595
Thrombosis	Associate	24086496, 28053049, 28445521, 30355187, 30600428, 30801944, 31558144
Venous Thromboembolism	Associate	23150947, 23650146, 25472531, 26260105, 28053049, 29094466, 30773804, 32671915, 34200207, 37364690
Venous Thromboembolism	Inhibit	37751848
Venous Thrombosis	Associate	10706899, 18349091, 19583818, 22533697, 27627722, 28444748, 34200207
Venous Thrombosis	Inhibit	31558144
von Willebrand Diseases	Associate	34059196

F11 (coagulation factor XI)