Foxc2 (forkhead box C2) - Rat Genome Database

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Gene: Foxc2 (forkhead box C2) Rattus norvegicus
Analyze
Symbol: Foxc2
Name: forkhead box C2
RGD ID: 621703
Description: Enables DNA binding activity. Predicted to be involved in several processes, including insulin receptor signaling pathway; negative regulation of cold-induced thermogenesis; and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including cell surface receptor signaling pathway; circulatory system development; and kidney development. Predicted to be located in nuclear body. Human ortholog(s) of this gene implicated in several diseases, including lymphedema; lymphedema-distichiasis syndrome; obesity; ptosis; and type 2 diabetes mellitus. Orthologous to human FOXC2 (forkhead box C2); INTERACTS WITH 6-propyl-2-thiouracil; acrylamide; alpha-Zearalanol.
Type: protein-coding
RefSeq Status: PROVISIONAL
Previously known as: BF-3; brain factor 3; Fkh14; Fkhl14; forkhead box C2 (MFH-1 mesenchyme forkhead 1); forkhead box C2 (MFH-1, mesenchyme forkhead 1); forkhead box protein C2; HFH-BF-3; Hfhbf3
RGD Orthologs
Human
Mouse
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81966,094,718 - 66,097,420 (+)NCBIGRCr8
mRatBN7.21949,186,034 - 49,188,736 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1949,185,662 - 49,188,737 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1955,977,317 - 55,980,018 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01956,661,030 - 56,663,732 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01958,875,485 - 58,878,187 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01953,044,379 - 53,047,081 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1953,044,379 - 53,047,081 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01963,788,037 - 63,790,739 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.11228,513,040 - 228,513,088 (-)NCBI
Celera1948,432,333 - 48,435,035 (+)NCBICelera
Cytogenetic Map19q12NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Original Reference(s)
Foxc2Ratcongestive heart failure  ISOFOXC2 (Homo sapiens)1582564 RGD 
Foxc2Rateyelid disease  ISOFOXC2 (Homo sapiens)1601217lymphedema-distichiasis syndrome more ...RGD 
Foxc2RatInsulin Resistance  ISOFOXC2 (Homo sapiens)1601219DNA:polymorphism:5'ut:-512C>TRGD 
Foxc2Ratlymphedema  ISOFOXC2 (Homo sapiens)1601216lymphedema and ptosis more ...RGD 
Foxc2Ratlymphedema  ISOFOXC2 (Homo sapiens)1601217lymphedema-distichiasis syndrome more ...RGD 
Foxc2Ratnephritis  ISOFOXC2 (Homo sapiens)1601217DNA:insertion:1006insARGD 
Foxc2Ratobesity  ISOFOXC2 (Homo sapiens)1601218DNA:polymorphism:5'ut:-512C>T(human)RGD 
Foxc2Ratptosis  ISOFOXC2 (Homo sapiens)1601216lymphedema and ptosis more ...RGD 
Foxc2Rattype 2 diabetes mellitus  ISOFOXC2 (Homo sapiens)1601217DNA:insertion:1006insARGD 
Foxc2Rattype 2 diabetes mellitus no_associationISOFOXC2 (Homo sapiens)1601220DNA:polymorphism:5'ut:-512C>T more ...RGD 
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Original Reference(s)
Foxc2Ratgenetic disease  ISOFOXC2 (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:12114478 more ...
Foxc2RatHydrops Fetalis  ISOFOXC2 (Homo sapiens)8554872ClinVar Annotator: match by term: Non-immune hydrops fetalisClinVarPMID:25741868
Foxc2Ratimmunodeficiency 32B  ISOFOXC2 (Homo sapiens)8554872ClinVar Annotator: match by term: Immunodeficiency 32BClinVarPMID:28492532
Foxc2Ratlymphedema-distichiasis syndrome  ISOFOXC2 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10417285 more ...
Foxc2RatLymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus  ISOFOXC2 (Homo sapiens)8554872ClinVar Annotator: match by term: Lymphedema-distichiasis syndrome with renal disease and diabetes mellitusClinVarPMID:15523639
Foxc2Ratpersistent fetal circulation syndrome  ISOFOXC2 (Homo sapiens)8554872ClinVar Annotator: match by term: Congenital alveolar capillary dysplasiaClinVar 
Object Symbol
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Original Reference(s)
Foxc2RatCardiovascular Abnormalities  ISOFOXC2 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:9409679
Foxc2Ratcongenital diaphragmatic hernia  ISOFOXC2 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:27663689
Foxc2RatCraniofacial Abnormalities  ISOFOXC2 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:9106663 and PMID:9409679
Foxc2Ratlymphedema-distichiasis syndrome  ISOFOXC2 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:11078474
Foxc2RatMusculoskeletal Abnormalities  ISOFOXC2 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:9106663
Foxc2Rattetralogy of Fallot  ISOFOXC2 (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:25093829
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Original Reference(s)
Foxc2Ratlymphedema-distichiasis syndrome  ISOFOXC2 (Homo sapiens)7240710 OMIM 

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Original Reference(s)
Foxc2Rat1,2-dimethylhydrazine increases expressionISOFoxc2 (Mus musculus)64804641 and 2-Dimethylhydrazine results in increased expression of FOXC2 mRNACTDPMID:22206623
Foxc2Rat17beta-estradiol multiple interactionsISOFOXC2 (Homo sapiens)6480464[Estradiol co-treated with TGFB1 protein] results in increased expression of FOXC2 mRNACTDPMID:30165855
Foxc2Rat2,3,7,8-tetrachlorodibenzodioxine increases expressionISOFoxc2 (Mus musculus)6480464Tetrachlorodibenzodioxin results in increased expression of FOXC2 mRNACTDPMID:24058054 and PMID:26139165
Foxc2Rat2,3,7,8-tetrachlorodibenzodioxine decreases expressionISOFoxc2 (Mus musculus)6480464Tetrachlorodibenzodioxin results in decreased expression of FOXC2 mRNACTDPMID:19933214
Foxc2Rat2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISOFoxc2 (Mus musculus)6480464Tetrachlorodibenzodioxin affects the reaction [AHR protein binds to FOXC2 promoter]CTDPMID:19654925
Foxc2Rat2,3,7,8-tetrachlorodibenzodioxine affects expressionISOFoxc2 (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of FOXC2 mRNACTDPMID:21570461
Foxc2Rat2,3,7,8-tetrachlorodibenzodioxine decreases expressionISOFOXC2 (Homo sapiens)6480464Tetrachlorodibenzodioxin results in decreased expression of FOXC2 mRNACTDPMID:21296121
Foxc2Rat2-hydroxypropanoic acid decreases expressionISOFOXC2 (Homo sapiens)6480464Lactic Acid results in decreased expression of FOXC2 mRNACTDPMID:30851411
Foxc2Rat2-palmitoylglycerol increases expressionISOFOXC2 (Homo sapiens)64804642-palmitoylglycerol results in increased expression of FOXC2 mRNACTDPMID:37199045
Foxc2Rat4,4'-sulfonyldiphenol increases expressionISOFoxc2 (Mus musculus)6480464bisphenol S results in increased expression of FOXC2 mRNACTDPMID:30951980
Foxc2Rat4,4'-sulfonyldiphenol increases methylationISOFoxc2 (Mus musculus)6480464bisphenol S results in increased methylation of FOXC2 exonCTDPMID:33297965
Foxc2Rat5-aza-2'-deoxycytidine increases expressionISOFoxc2 (Mus musculus)6480464Decitabine results in increased expression of FOXC2 mRNACTDPMID:27915011
Foxc2Rat6-propyl-2-thiouracil decreases expressionEXP 6480464Propylthiouracil results in decreased expression of FOXC2 mRNACTDPMID:24780913
Foxc2Ratabacavir decreases expressionISOFOXC2 (Homo sapiens)6480464abacavir results in decreased expression of FOXC2 mRNACTDPMID:31711903
Foxc2Ratacrylamide decreases expressionEXP 6480464Acrylamide results in decreased expression of FOXC2 mRNACTDPMID:28959563
Foxc2Rataflatoxin B1 decreases methylationISOFOXC2 (Homo sapiens)6480464Aflatoxin B1 results in decreased methylation of FOXC2 geneCTDPMID:27153756
Foxc2Rataldrin increases expressionISOFoxc2 (Mus musculus)6480464Aldrin results in increased expression of FOXC2 mRNACTDPMID:18579281
Foxc2Ratall-trans-retinoic acid increases expressionISOFOXC2 (Homo sapiens)6480464Tretinoin results in increased expression of FOXC2 mRNACTDPMID:21934132
Foxc2Ratall-trans-retinoic acid multiple interactionsISOFOXC2 (Homo sapiens)6480464Tretinoin inhibits the reaction [[Chir 99021 co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in increased expression of FOXC2 mRNA]CTDPMID:31711903
Foxc2Ratall-trans-retinoic acid decreases expressionISOFOXC2 (Homo sapiens)6480464Tretinoin results in decreased expression of FOXC2 mRNACTDPMID:31711903

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Biological Process
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Original Reference(s)
Foxc2Ratanatomical structure morphogenesis involved_inIBAFB:FBgn0000659 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
Foxc2Ratapoptotic process involved in outflow tract morphogenesis acts_upstream_ofISOFoxc2 (Mus musculus)1624291MGI:1347466 PMID:16839542RGDPMID:16839542
Foxc2Ratartery morphogenesis acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857740 more ...RGDPMID:10479458 and PMID:9409679
Foxc2Ratblood vessel development acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1347466 PMID:16678147RGDPMID:16678147
Foxc2Ratblood vessel diameter maintenance acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1347466 PMID:16678147RGDPMID:16678147
Foxc2Ratblood vessel remodeling acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1347466 PMID:11562355 and PMID:16678147RGDPMID:11562355 and PMID:16678147
Foxc2Ratbranching involved in blood vessel morphogenesis acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:105923 PMID:15664398RGDPMID:15664398
Foxc2Ratcamera-type eye development acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857865 PMID:10767326RGDPMID:10767326
Foxc2Ratcardiac muscle cell proliferation acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1347466 PMID:16839542RGDPMID:16839542
Foxc2Ratcell differentiation involved_inIBAFB:FBgn0000659 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
Foxc2Ratcell population proliferation acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857740 more ...RGDPMID:10364424 and PMID:9106663
Foxc2Ratcollagen fibril organization acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857865 PMID:10767326RGDPMID:10767326
Foxc2Ratembryonic cranial skeleton morphogenesis acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857865 PMID:9106663RGDPMID:9106663
Foxc2Ratembryonic heart tube development acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1347466 PMID:16678147RGDPMID:16678147
Foxc2Ratembryonic skeletal system morphogenesis acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857740 PMID:9409679RGDPMID:9409679
Foxc2Ratembryonic viscerocranium morphogenesis acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857740 PMID:9409679RGDPMID:9409679
Foxc2Ratglomerular endothelium development acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857740 PMID:16498405RGDPMID:16498405
Foxc2Ratglomerular mesangial cell development acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:1857740 PMID:16498405RGDPMID:16498405
Foxc2Ratheart development involved_inISOFOXC2 (Homo sapiens)1624291 PMID:21457232RGDPMID:21457232
Foxc2Ratheart development acts_upstream_of_or_withinISOFoxc2 (Mus musculus)1624291MGI:105923 more ...RGDPMID:10479458 more ...
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Cellular Component

  
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Original Reference(s)
Foxc2Ratnuclear body located_inIEAUniProtKB:Q99958 and ensembl:ENSP000004977591600115GO_REF:0000107EnsemblGO_REF:0000107
Foxc2Ratnuclear body located_inISOFOXC2 (Homo sapiens)1624291 RGDGO_REF:0000052
Foxc2Ratnucleoplasm located_inISOFOXC2 (Homo sapiens)1624291 RGDGO_REF:0000052
Foxc2Ratnucleus located_inISOFOXC2 (Homo sapiens)1624291 PMID:11562355 and PMID:16081467RGDPMID:11562355 and PMID:16081467

Molecular Function
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Foxc2Ratchromatin DNA binding enablesISOFOXC2 (Homo sapiens)1624291 PMID:16456100RGDPMID:16456100
Foxc2RatDNA binding enablesISOFoxc2 (Mus musculus)1624291 PMID:8325367RGDPMID:8325367
Foxc2RatDNA binding  IDA 632667 RGD 
Foxc2RatDNA-binding transcription activator activity enablesISOFOXC2 (Homo sapiens)1624291 PMID:9169153RGDPMID:9169153
Foxc2RatDNA-binding transcription activator activity enablesISOFoxc2 (Mus musculus)1624291 PMID:9169153RGDPMID:9169153
Foxc2RatDNA-binding transcription activator activity, RNA polymerase II-specific enablesISOFOXC2 (Homo sapiens)1624291 PMID:20956529RGDPMID:20956529
Foxc2RatDNA-binding transcription factor activity enablesISSUniProtKB:Q618501600115GO_REF:0000024UniProtGO_REF:0000024
Foxc2RatDNA-binding transcription factor activity enablesISOFoxc2 (Mus musculus)1624291 PMID:18187037 and PMID:18579532RGDPMID:18187037 and PMID:18579532
Foxc2RatDNA-binding transcription factor activity, RNA polymerase II-specific enablesIBAFB:FBgn0000659 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
Foxc2RatDNA-binding transcription factor activity, RNA polymerase II-specific enablesISOFoxc2 (Mus musculus)1624291MGI:1347466 PMID:16678147RGDPMID:16678147
Foxc2Ratidentical protein binding enablesISOFOXC2 (Homo sapiens)1624291UniProtKB:Q99958 and PMID:25609649RGDPMID:25609649
Foxc2Ratpromoter-specific chromatin binding enablesISSUniProtKB:Q618501600115GO_REF:0000024UniProtGO_REF:0000024
Foxc2Ratpromoter-specific chromatin binding enablesISOFoxc2 (Mus musculus)1624291 PMID:18187037RGDPMID:18187037
Foxc2Ratprotein binding enablesISOFOXC2 (Homo sapiens)1624291UniProtKB:P14373 more ...RGDPMID:25416956 and PMID:32296183
Foxc2RatRNA polymerase II cis-regulatory region sequence-specific DNA binding enablesISOFOXC2 (Homo sapiens)1624291 PMID:20956529RGDPMID:20956529
Foxc2RatRNA polymerase II cis-regulatory region sequence-specific DNA binding enablesIBAMGI:1096329 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
Foxc2RatRNA polymerase II transcription regulatory region sequence-specific DNA binding enablesISOFOXC2 (Homo sapiens)1624291 PMID:20956529RGDPMID:20956529
Foxc2Ratsequence-specific DNA binding enablesISOFOXC2 (Homo sapiens)1624291 PMID:16081467RGDPMID:16081467
Foxc2Ratsequence-specific double-stranded DNA binding enablesISOFOXC2 (Homo sapiens)1624291 PMID:28473536RGDPMID:28473536
Foxc2Rattranscription cis-regulatory region binding enablesISOFoxc2 (Mus musculus)1624291 PMID:18579532RGDPMID:18579532
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#
Reference Title
Reference Citation
1. The FOXC2 C-512T polymorphism is associated with obesity and dyslipidemia. Carlsson E, etal., Obes Res. 2004 Nov;12(11):1738-43.
2. FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance. Cederberg A, etal., Cell. 2001 Sep 7;106(5):563-73.
3. Identification of nine tissue-specific transcription factors of the hepatocyte nuclear factor 3/forkhead DNA-binding-domain family. Clevidence DE, etal., Proc Natl Acad Sci U S A 1993 May 1;90(9):3948-52.
4. Truncating mutations in FOXC2 cause multiple lymphedema syndromes. Finegold DN, etal., Hum Mol Genet. 2001 May 15;10(11):1185-9.
5. Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Gaudet P, etal., Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
6. Transcriptional genomics associates FOX transcription factors with human heart failure. Hannenhalli S, etal., Circulation. 2006 Sep 19;114(12):1269-76. Epub 2006 Sep 4.
7. Electronic Transfer of LocusLink and RefSeq Data NCBI rat LocusLink and RefSeq merged data July 26, 2002
8. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
9. Systematic search for single nucleotide polymorphisms in the FOXC2 gene: the absence of evidence for the association of three frequent single nucleotide polymorphisms and four common haplotypes with Japanese type 2 diabetes. Osawa H, etal., Diabetes. 2003 Feb;52(2):562-7.
10. GOA pipeline RGD automated data pipeline
11. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
12. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
13. FOXC2 mRNA Expression and a 5' untranslated region polymorphism of the gene are associated with insulin resistance. Ridderstrale M, etal., Diabetes. 2002 Dec;51(12):3554-60.
14. A novel frameshift mutation of FOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus. Yildirim-Toruner C, etal., Am J Med Genet A. 2004 Dec 15;131(3):281-6.
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PMID:8325367   PMID:9106663   PMID:9169153   PMID:9409679   PMID:10364424   PMID:10479458   PMID:10704385   PMID:10767326   PMID:11562355   PMID:11943768   PMID:12114478   PMID:15664398  
PMID:16081467   PMID:16456100   PMID:16498405   PMID:16678147   PMID:16839542   PMID:18187037   PMID:18579532   PMID:19170063   PMID:20956529   PMID:21457232   PMID:25609649   PMID:26824865  
PMID:33423166   PMID:34739190  



Foxc2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81966,094,718 - 66,097,420 (+)NCBIGRCr8
mRatBN7.21949,186,034 - 49,188,736 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1949,185,662 - 49,188,737 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1955,977,317 - 55,980,018 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01956,661,030 - 56,663,732 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01958,875,485 - 58,878,187 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01953,044,379 - 53,047,081 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1953,044,379 - 53,047,081 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01963,788,037 - 63,790,739 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.11228,513,040 - 228,513,088 (-)NCBI
Celera1948,432,333 - 48,435,035 (+)NCBICelera
Cytogenetic Map19q12NCBI
FOXC2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381686,566,829 - 86,569,728 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1686,566,829 - 86,569,728 (+)EnsemblGRCh38hg38GRCh38
GRCh371686,600,435 - 86,603,334 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361685,158,443 - 85,159,948 (+)NCBINCBI36Build 36hg18NCBI36
Build 341685,158,442 - 85,159,948NCBI
Celera1670,901,820 - 70,903,503 (+)NCBICelera
Cytogenetic Map16q24.1NCBI
HuRef1672,340,749 - 72,342,345 (+)NCBIHuRef
CHM1_11688,012,585 - 88,014,267 (+)NCBICHM1_1
T2T-CHM13v2.01692,635,146 - 92,638,044 (+)NCBIT2T-CHM13v2.0
Foxc2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398121,842,910 - 121,845,634 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl8121,842,910 - 121,845,634 (+)EnsemblGRCm39 Ensembl
GRCm388121,116,171 - 121,118,895 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8121,116,171 - 121,118,895 (+)EnsemblGRCm38mm10GRCm38
MGSCv378123,640,071 - 123,642,795 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv368124,002,560 - 124,004,872 (+)NCBIMGSCv36mm8
Celera8125,334,251 - 125,336,975 (+)NCBICelera
Cytogenetic Map8E1NCBI
cM Map870.33NCBI
FOXC2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21896,322,973 - 96,325,904 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan116102,240,170 - 102,243,107 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01667,237,476 - 67,239,545 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11686,569,509 - 86,571,878 (+)NCBIpanpan1.1PanPan1.1panPan2
FOXC2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1566,234,336 - 66,296,007 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl566,294,176 - 66,295,693 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha566,246,461 - 66,254,587 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0566,455,805 - 66,464,138 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1566,479,102 - 66,487,010 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0566,314,300 - 66,322,205 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0566,727,335 - 66,735,464 (-)NCBIUU_Cfam_GSD_1.0
Foxc2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934926,482,456 - 26,485,324 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366412,236,873 - 2,238,375 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366412,236,224 - 2,238,501 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FOXC2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl62,552,862 - 2,554,367 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.162,552,141 - 2,555,041 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.262,756,138 - 2,761,356 (-)NCBISscrofa10.2Sscrofa10.2susScr3
FOXC2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1571,951,980 - 71,955,021 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl571,952,632 - 71,954,134 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660473,750,917 - 3,753,843 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Foxc2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247462,632,619 - 2,634,085 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247462,632,547 - 2,634,867 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in Foxc2
5 total Variants

Predicted Target Of
Summary Value
Count of predictions:73
Count of miRNA genes:64
Interacting mature miRNAs:67
Transcripts:ENSRNOT00000072369
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 9 of 9 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
1578764Stresp19Stress response QTL 193.60.001blood renin amount (VT:0003349)plasma renin activity level (CMO:0000116)191563020157337602Rat
61350Bp32Blood pressure QTL 320.012arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)192048357557337602Rat
5135224Leukc1Leukocyte quantity QTL 1eosinophil quantity (VT:0002602)blood eosinophil count (CMO:0000033)194434021455283277Rat
724546Kidm3Kidney mass QTL 33.1kidney mass (VT:0002707)calculated kidney weight (CMO:0000160)192932249057337602Rat
7411549Bw130Body weight QTL 13050.001body mass (VT:0001259)body weight gain (CMO:0000420)191545586057337602Rat
1358200Insglur2Insulin/glucose ratio QTL 24.1blood glucose amount (VT:0000188)serum glucose level (CMO:0000543)193383821455283146Rat
724566Uae12Urinary albumin excretion QTL 125urine albumin amount (VT:0002871)urine albumin level (CMO:0000130)19218792756457239Rat
1331737Uae29Urinary albumin excretion QTL 295.5urine albumin amount (VT:0002871)urine albumin level (CMO:0000130)19409615555283277Rat
2298478Eau8Experimental allergic uveoretinitis QTL 80.0163uvea integrity trait (VT:0010551)experimental autoimmune uveitis score (CMO:0001504)191715443357337602Rat

1 to 9 of 9 rows



alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
8 8 49 113 49 48 24 10 24 6 164 81 93 45 58 24



Ensembl Acc Id: ENSRNOT00000072369   ⟹   ENSRNOP00000065254
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl1949,185,662 - 49,188,737 (+)Ensembl
Rnor_6.0 Ensembl1953,044,379 - 53,047,081 (+)Ensembl
RefSeq Acc Id: NM_001101680   ⟹   NP_001095150
RefSeq Status: PROVISIONAL
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81966,094,718 - 66,097,420 (+)NCBI
mRatBN7.21949,186,034 - 49,188,736 (+)NCBI
Rnor_6.01953,044,379 - 53,047,081 (+)NCBI
Rnor_5.01963,788,037 - 63,790,739 (+)NCBI
Celera1948,432,333 - 48,435,035 (+)RGD
Sequence:
Protein RefSeqs NP_001095150 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA41320 (Get FASTA)   NCBI Sequence Viewer  
  EDL92716 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000065254.1
GenBank Protein Q63246 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001095150   ⟸   NM_001101680
- UniProtKB: M0R736 (UniProtKB/Swiss-Prot),   Q63246 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSRNOP00000065254   ⟸   ENSRNOT00000072369

Name Modeler Protein Id AA Range Protein Structure
AF-Q63246-F1-model_v2 AlphaFold Q63246 1-494 view protein structure


eQTL   View at Phenogen
WGCNA   View at Phenogen
Tissue/Strain Expression   View at Phenogen

RGD ID:13701190
Promoter ID:EPDNEW_R11713
Type:initiation region
Name:Foxc2_1
Description:forkhead box C2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.01953,044,357 - 53,044,417EPDNEW


1 to 28 of 28 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-5453 BioCyc
Ensembl Genes ENSRNOG00000047446 Ensembl, UniProtKB/Swiss-Prot
Ensembl Transcript ENSRNOT00000072369.2 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.10.10 UniProtKB/Swiss-Prot
InterPro Fork_head_dom UniProtKB/Swiss-Prot
  FOX_domain-containing UniProtKB/Swiss-Prot
  FOXC1/C2-like_FH UniProtKB/Swiss-Prot
  TF_fork_head_CS_1 UniProtKB/Swiss-Prot
  TF_fork_head_CS_2 UniProtKB/Swiss-Prot
  WH-like_DNA-bd_sf UniProtKB/Swiss-Prot
  WH_DNA-bd_sf UniProtKB/Swiss-Prot
KEGG Report rno:171356 UniProtKB/Swiss-Prot
NCBI Gene 171356 ENTREZGENE
PANTHER FORKHEAD BOX PROTEIN UniProtKB/Swiss-Prot
  FORKHEAD BOX PROTEIN C2 UniProtKB/Swiss-Prot
Pfam Forkhead UniProtKB/Swiss-Prot
PhenoGen Foxc2 PhenoGen
PRINTS FORKHEAD UniProtKB/Swiss-Prot
PROSITE FORK_HEAD_1 UniProtKB/Swiss-Prot
  FORK_HEAD_2 UniProtKB/Swiss-Prot
  FORK_HEAD_3 UniProtKB/Swiss-Prot
RatGTEx ENSRNOG00000047446 RatGTEx
SMART SM00339 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF46785 UniProtKB/Swiss-Prot
UniProt FOXC2_RAT UniProtKB/Swiss-Prot
  M0R736 ENTREZGENE
  Q63246 ENTREZGENE
UniProt Secondary M0R736 UniProtKB/Swiss-Prot
1 to 28 of 28 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2005-01-20 Foxc2  forkhead box C2    forkhead box C2 (MFH-1, mesenchyme forkhead 1)  Name updated 1299863 APPROVED
2002-08-07 Foxc2  forkhead box C2 (MFH-1, mesenchyme forkhead 1)      Symbol and Name status set to provisional 70820 PROVISIONAL

Note Type Note Reference
gene_domains forkhead DNA-binding domain recognizes its cognate DNA binding site as a monomer 632667
gene_expression mRNA expressed in liver, brain, kidney, lung, and intestine 632667
gene_homology shares homology with Drosophila homeotic protein forkhead (fkh) 632667
gene_product member of hepatocyte nuclear transcription factor (HNF) family 632667