F5 (coagulation factor V) - Rat Genome Database

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Gene: F5 (coagulation factor V) Chinchilla lanigera
Analyze
Symbol: F5
Name: coagulation factor V
RGD ID: 8725473
Description: INVOLVED IN blood circulation (ortholog); blood coagulation (ortholog); response to vitamin K (ortholog); PARTICIPATES IN acenocoumarol pharmacodynamics pathway; alteplase pharmacodynamics pathway; aminocaproic acid pharmacodynamics pathway; ASSOCIATED WITH 1q24 Deletion Syndrome (ortholog); Acute Liver Failure (ortholog); blood coagulation disease (ortholog); FOUND IN extracellular region (ortholog); extracellular space (ortholog); platelet alpha granule (ortholog)
Type: protein-coding
RefSeq Status: MODEL
Previously known as: coagulation factor V (proaccelerin, labile factor)
RGD Orthologs
Human
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: ChiLan1.0 - Chinchilla ChiLan1.0 Assembly
Position:
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554627,694,939 - 7,757,463 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554627,695,004 - 7,757,832 (+)NCBIChiLan1.0ChiLan1.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


1 to 20 of 49 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
F5ChinchillaAcute Liver Failure severityISOF5 (Homo sapiens)9068941protein:altered expression (human)RGDPMID:1740285 and REF_RGD_ID:14700653
F5ChinchillaBehcet's disease no_associationISOF5 (Homo sapiens)9068941DNA:mutation: :1691G>A (human)RGDPMID:15077257 and REF_RGD_ID:7394769
F5Chinchillabreast cancer no_associationISOF5 (Homo sapiens)9068941DNA:SNPs: :rs6025 (human)RGDPMID:25407022 and REF_RGD_ID:10449101
F5Chinchillabreast cancer  ISOF5 (Homo sapiens)9068941DNA:SNPs: :multipleRGDPMID:25407022 and REF_RGD_ID:10449101
F5ChinchillaBudd-Chiari syndrome severityISOF5 (Homo sapiens)9068941associated with hyperhomocysteinemia:DNA:missense mutation:cds: (R506Q) (human)RGDPMID:16825912 and REF_RGD_ID:14700661
F5ChinchillaBudd-Chiari syndrome susceptibilityISOF5 (Homo sapiens)9068941DNA:missense mutation:cds:R506Q (human)RGDPMID:9245936 and REF_RGD_ID:15036813
F5ChinchillaBudd-Chiari syndrome severityISOF5 (Homo sapiens)9068941Factor V Leiden and DNA:missense mutation:cds:G1691A (human)RGDPMID:29771426 and REF_RGD_ID:14700660
F5ChinchillaBudd-Chiari syndrome disease_progressionISOF5 (Homo sapiens)9068941DNA:missense mutation:cds:R506Q (human)RGDPMID:26238013 and REF_RGD_ID:11537993
F5ChinchillaColonic Neoplasms  ISOF5 (Rattus norvegicus)9068941protein:increased expression:serumRGDPMID:25200834 and REF_RGD_ID:10449102
F5Chinchillacolorectal adenoma  ISOF5 (Homo sapiens)9068941protein:increased expression:serumRGDPMID:30971492 and REF_RGD_ID:40907058
F5ChinchillaCOVID-19  ISOF5 (Homo sapiens)9068941mRNA:increased expression:peripheral blood mononuclear cell (human)RGDPMID:32228226 and REF_RGD_ID:28912744
F5ChinchillaDysarthria  ISOF5 (Homo sapiens)9068941 RGDPMID:15026880 and REF_RGD_ID:1580361
F5ChinchillaDyspnea  ISOF5 (Homo sapiens)9068941 RGDPMID:16186475 and REF_RGD_ID:4892656
F5Chinchillaend stage renal disease  ISOF5 (Homo sapiens)9068941DNA:mutation: :1691G>A(human)RGDPMID:19520684 and REF_RGD_ID:6893522
F5ChinchillaEndotoxemia  ISOF5 (Rattus norvegicus)9068941 RGDPMID:11092686 and REF_RGD_ID:7394782
F5ChinchillaExperimental Liver Cirrhosis treatmentISOF5 (Rattus norvegicus)9068941 RGDPMID:17431769 and REF_RGD_ID:7394781
F5ChinchillaFemur Head Necrosis  ISOF5 (Homo sapiens)9068941associated with kidney transplantation and 1691G>A(human)RGDPMID:16968732 and REF_RGD_ID:6902907
F5ChinchillaFetal Death no_associationISOF5 (Homo sapiens)9068941 RGDPMID:14706682 and REF_RGD_ID:1580130
F5Chinchillahepatitis severityISOF5 (Mus musculus)9068941protein:decreased expression:plasma (human)RGDPMID:15340576 and REF_RGD_ID:14700682
F5Chinchillahepatitis severityISOF5 (Homo sapiens)9068941protein:decreased expression:plasma (human)RGDPMID:15340576 and REF_RGD_ID:14700682
1 to 20 of 49 rows
1 to 20 of 20 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
F5Chinchilla1q24 Deletion Syndrome  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: 1q24q25 microdeletion syndromeClinVarPMID:25741868
F5ChinchillaBudd-Chiari syndrome  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: Budd-Chiari syndromeClinVarPMID:10328130 more ...
F5Chinchillacerebral infarction  ISOF5 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10328130 more ...
F5Chinchillacholesteatoma  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: CholesteatomaClinVar 
F5Chinchillafactor V deficiency  ISOF5 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10328130 more ...
F5Chinchillagastrointestinal stromal tumor  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: Gastrointestinal stromal tumorClinVarPMID:28492532
F5Chinchillagenetic disease  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:10328130 more ...
F5ChinchillaHabitual Abortions  ISOF5 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10328130 more ...
F5ChinchillaHemorrhage  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: HemorrhageClinVarPMID:25741868 more ...
F5Chinchillahemorrhagic disease  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: Abnormal bleedingClinVarPMID:25741868 more ...
F5ChinchillaHirschsprung's disease  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: Aganglionic megacolonClinVar 
F5Chinchillaparathyroid carcinoma  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: Parathyroid carcinomaClinVarPMID:28492532
F5Chinchillaprostate cancer  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: Malignant tumor of prostateClinVarPMID:23265383
F5ChinchillaStroke  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: CEREBROVASCULAR ACCIDENTClinVarPMID:10328130 more ...
F5Chinchillathrombocytopenia  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: ThrombocytopeniaClinVarPMID:25741868 more ...
F5ChinchillaThromboembolism  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: ThromboembolismClinVarPMID:19486170 more ...
F5Chinchillathrombophilia due to activated protein C resistance  ISOF5 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10328130 more ...
F5Chinchillathrombophilia due to thrombin defect  ISOF5 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:11950065 more ...
F5Chinchillathrombosis  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: ThrombusClinVarPMID:25741868
F5ChinchillaVenous Thrombosis  ISOF5 (Homo sapiens)8554872ClinVar Annotator: match by term: Deep venous thrombosisClinVarPMID:19486170 more ...
1 to 20 of 20 rows
1 to 11 of 11 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
F5Chinchillablood coagulation disease  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:17721328
F5Chinchillabrain ischemia  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:15534175
F5ChinchillaColonic Neoplasms  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:25200834
F5Chinchillafamilial adenomatous polyposis  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:25200834
F5ChinchillaHereditary Thrombophilia  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:9136971
F5Chinchillaliver cirrhosis  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:18485088
F5ChinchillaMesenteric Ischemia  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:24282370
F5Chinchillamyocardial infarction  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:9531249
F5Chinchillaretinal vein occlusion  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:12022286
F5Chinchillasagittal sinus thrombosis  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:18382986
F5ChinchillaVenous Thromboembolism  ISOF5 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:7500743 and PMID:9149031
1 to 11 of 11 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
F5ChinchillaBudd-Chiari syndrome  ISOF5 (Homo sapiens)7240710 OMIM 
F5Chinchillacerebral infarction  ISOF5 (Homo sapiens)7240710 OMIM 
F5Chinchillafactor V deficiency  ISOF5 (Homo sapiens)7240710 OMIM 
F5ChinchillaHabitual Abortions  ISOF5 (Homo sapiens)7240710 OMIM 
F5Chinchillathrombophilia due to activated protein C resistance  ISOF5 (Homo sapiens)7240710 OMIM 


Biological Process

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
F5Chinchillablood circulation acts_upstream_of_or_withinISOMGI:19315259068941 PMID:10669158 and PMID:8900278MGIPMID:10669158 and PMID:8900278
F5Chinchillablood coagulation acts_upstream_of_or_withinISOF5 (Mus musculus)9068941 PMID:12816857 and PMID:12855561MGIPMID:12816857 and PMID:12855561
F5Chinchillablood coagulation acts_upstream_of_or_withinISOMGI:19315259068941 PMID:8900278MGIPMID:8900278
F5Chinchillaresponse to vitamin K  ISOF5 (Rattus norvegicus)9068941 RGDPMID:658784 and REF_RGD_ID:11564341

Cellular Component

  

Molecular Function

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
F5Chinchillaprotein binding enablesISOUniProtKB:P783809068941 PMID:28514442 and PMID:33961781IntActPMID:28514442 and PMID:33961781
F5Chinchillaprotein binding enablesISOUniProtKB:P051549068941 PMID:2844223 more ...UniProtPMID:2844223 more ...

RGD Manual Annotations


  

Imported Annotations - SMPDB

1 to 15 of 15 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
F5Chinchillaacenocoumarol pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00269
F5Chinchillaalteplase pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00280
F5Chinchillaaminocaproic acid pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00286
F5Chinchillaanistreplase pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00281
F5Chinchillaaprotinin pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00288
F5Chinchillaargatroban pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00276
F5Chinchillabivalirudin pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00277
F5Chinchilladicoumarol pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00270 and SMP:00656
F5Chinchillaenoxaparin pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00272
F5Chinchillafondaparinux pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00273
F5Chinchillaheparin pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00274
F5Chinchillaphenindione pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00655
F5Chinchillareteplase pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00285
F5Chinchillatranexamic acid pharmacodynamics pathway  ISOF5 (Homo sapiens)9068941 SMPDBSMP:00287
F5Chinchillawarfarin pharmacodynamics pathway   ISOF5 (Homo sapiens)9068941 SMPDBSMP:00268
1 to 15 of 15 rows

#
Reference Title
Reference Citation
1. Transitive Annotation Pipeline Automated assignment of GO, PW and RDO ISO annotations across species
2. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
PMID:22301074  



F5
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554627,694,939 - 7,757,463 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554627,695,004 - 7,757,832 (+)NCBIChiLan1.0ChiLan1.0
F5
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381169,511,951 - 169,586,481 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1169,511,951 - 169,586,588 (-)EnsemblGRCh38hg38GRCh38
GRCh371169,481,189 - 169,555,719 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361167,747,816 - 167,822,393 (-)NCBINCBI36Build 36hg18NCBI36
Build 341166,215,066 - 166,287,379NCBI
Celera1142,590,970 - 142,665,548 (-)NCBICelera
Cytogenetic Map1q24.2NCBI
HuRef1140,703,881 - 140,778,453 (-)NCBIHuRef
CHM1_11170,903,222 - 170,977,927 (-)NCBICHM1_1
T2T-CHM13v2.01168,867,198 - 168,942,366 (-)NCBIT2T-CHM13v2.0
F5
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391163,979,396 - 164,048,539 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1163,979,407 - 164,047,846 (+)EnsemblGRCm39 Ensembl
GRCm381164,151,835 - 164,220,277 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1164,151,838 - 164,220,277 (+)EnsemblGRCm38mm10GRCm38
MGSCv371166,081,990 - 166,150,405 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361165,988,633 - 166,056,215 (+)NCBIMGSCv36mm8
Celera1166,589,960 - 166,658,650 (+)NCBICelera
Cytogenetic Map1H2.2NCBI
cM Map171.46NCBI
F5
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81379,046,657 - 79,116,247 (+)NCBIGRCr8
mRatBN7.21376,513,509 - 76,583,106 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1376,513,255 - 76,582,317 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1379,142,948 - 79,200,967 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01380,446,925 - 80,504,974 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01377,701,514 - 77,759,605 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01382,479,997 - 82,535,540 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1382,479,998 - 82,535,534 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01387,355,980 - 87,417,686 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41379,934,956 - 79,997,285 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1376,256,969 - 76,316,731 (+)NCBICelera
Cytogenetic Map13q23NCBI
F5
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2180,182,816 - 80,283,126 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1179,851,222 - 79,951,535 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01144,996,757 - 145,070,046 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11148,718,748 - 148,791,049 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1148,718,897 - 148,790,915 (-)Ensemblpanpan1.1panPan2
F5
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1728,999,481 - 29,069,603 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl728,999,512 - 29,069,296 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha728,531,164 - 28,601,084 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0728,801,509 - 28,871,406 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl728,801,237 - 28,871,399 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1728,649,506 - 28,719,863 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0728,685,240 - 28,755,563 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0728,922,027 - 28,992,360 (+)NCBIUU_Cfam_GSD_1.0
F5
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934499,267,628 - 99,332,463 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648117,114,480 - 17,178,844 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648117,114,441 - 17,178,902 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
F5
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl481,403,274 - 81,485,066 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1481,403,273 - 81,484,908 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2489,027,936 - 89,109,573 (+)NCBISscrofa10.2Sscrofa10.2susScr3
F5
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12559,465,610 - 59,539,022 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2559,466,378 - 59,538,872 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605561,142,905 - 61,215,886 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
F5
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248267,438,682 - 7,507,012 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248267,438,632 - 7,507,322 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.





RefSeq Transcripts XM_005398188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AGCD01049309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GBBH01073086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENSCLAT00000017356   ⟹   ENSCLAP00000017187
Type: CODING
Position:
Chinchilla AssemblyChrPosition (strand)Source
ChiLan1.0 EnsemblNW_0049554627,694,939 - 7,757,463 (+)Ensembl
RefSeq Acc Id: XM_005398188   ⟹   XP_005398245
Type: CODING
Position:
Chinchilla AssemblyChrPosition (strand)Source
ChiLan1.0NW_0049554627,695,004 - 7,757,832 (+)NCBI
Sequence:
Protein RefSeqs XP_005398245 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSCLAP00000017187
  ENSCLAP00000017187.1
RefSeq Acc Id: XP_005398245   ⟸   XM_005398188
- UniProtKB: A0A8C2VKV0 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSCLAP00000017187   ⟸   ENSCLAT00000017356
F5/8 type C



1 to 26 of 26 rows
Database
Acc Id
Source(s)
Ensembl Genes ENSCLAG00000011798 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENSCLAT00000017356 ENTREZGENE
  ENSCLAT00000017356.1 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.420 UniProtKB/TrEMBL
  Galactose-binding domain-like UniProtKB/TrEMBL
InterPro Cu-oxidase_N UniProtKB/TrEMBL
  Cu_oxidase_CS UniProtKB/TrEMBL
  Cupredoxin UniProtKB/TrEMBL
  FA58C UniProtKB/TrEMBL
  Factor_5/8-like UniProtKB/TrEMBL
  Galactose-bd-like_sf UniProtKB/TrEMBL
  Neuropilin_MCO_CoagFactor UniProtKB/TrEMBL
NCBI Gene F5 ENTREZGENE
PANTHER COAGULATION FACTOR V UniProtKB/TrEMBL
  F5/8 TYPE C DOMAIN-CONTAINING PROTEIN UniProtKB/TrEMBL
Pfam Cu-oxidase_3 UniProtKB/TrEMBL
  F5_F8_type_C UniProtKB/TrEMBL
PIRSF Factors_V_VIII UniProtKB/TrEMBL
PROSITE FA58C_1 UniProtKB/TrEMBL
  FA58C_2 UniProtKB/TrEMBL
  FA58C_3 UniProtKB/TrEMBL
  MULTICOPPER_OXIDASE1 UniProtKB/TrEMBL
SMART FA58C UniProtKB/TrEMBL
Superfamily-SCOP SSF49503 UniProtKB/TrEMBL
  SSF49785 UniProtKB/TrEMBL
UniProt A0A8C2VKV0 ENTREZGENE, UniProtKB/TrEMBL
1 to 26 of 26 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-08-03 F5  coagulation factor V    coagulation factor V (proaccelerin, labile factor)  Symbol and/or name change 5135510 APPROVED