Fgd1 (FYVE, RhoGEF and PH domain containing 1) - Rat Genome Database

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Gene: Fgd1 (FYVE, RhoGEF and PH domain containing 1) Mus musculus
Analyze
Symbol: Fgd1
Name: FYVE, RhoGEF and PH domain containing 1
RGD ID: 1558012
MGI Page MGI
Description: Predicted to enable guanyl-nucleotide exchange factor activity and small GTPase binding activity. Involved in regulation of cell shape. Acts upstream of or within cytoskeleton organization. Located in Golgi apparatus; lamellipodium; and ruffle. Is expressed in several structures, including alimentary system; brain; genitourinary system; hemolymphoid system gland; and limb. Human ortholog(s) of this gene implicated in X-linked Aarskog syndrome and non-syndromic X-linked intellectual disability. Orthologous to human FGD1 (FYVE, RhoGEF and PH domain containing 1).
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: faciogenital dysplasia 1 protein homolog; faciogenital dysplasia homolog; FYVE, RhoGEF and PH domain-containing protein 1; rho/Rac GEF; rho/Rac guanine nucleotide exchange factor FGD1; ZFYVE; ZFYVE3; zinc finger FYVE domain-containing protein 3
RGD Orthologs
Human
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCm39 - Mouse Genome Assembly GRCm39
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X149,829,141 - 149,872,682 (+)NCBIGRCm39GRCm39mm39
GRCm39 EnsemblX149,829,146 - 149,872,517 (+)EnsemblGRCm39 Ensembl
GRCm38X151,046,141 - 151,089,686 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX151,046,150 - 151,089,521 (+)EnsemblGRCm38mm10GRCm38
MGSCv37X147,481,776 - 147,523,642 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36X146,387,949 - 146,429,815 (+)NCBIMGSCv36mm8
MGSCv36X128,052,708 - 128,094,514 (+)NCBIMGSCv36mm8
CeleraX133,315,143 - 133,357,665 (-)NCBICelera
Cytogenetic MapXF3NCBI
cM MapX68.46NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model



  
Object Symbol
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Original Reference(s)
Fgd1Mouseinvasive ductal carcinoma  ISORGD:135122811554027protein:increased expression:breast (human)RGD 
Fgd1Mousenon-syndromic X-linked intellectual disability  ISORGD:135122811554032DNA:missense mutation:cds:p.P312L (human)RGD 
Fgd1Mouseprostate cancer  ISORGD:135122811554027protein:increased expression:prostate gland (human)RGD 
Fgd1MouseX-linked Aarskog syndrome  ISORGD:135122811554024DNA:insertion:cds:c.2121_2122insG (human)RGD 
Fgd1MouseX-linked Aarskog syndrome  ISORGD:135122811554031DNA:deletion:cds:c.2189delA (human)RGD 
Fgd1MouseX-linked Aarskog syndrome  ISORGD:135122811554030DNA:nonsense mutation:cds:p.W447X (human)RGD 
Fgd1MouseX-linked Aarskog syndrome  ISORGD:135122811554029DNA:mutations:multiple (human)RGD 
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Original Reference(s)
Fgd1MouseAarskog syndrome  ISORGD:13512288554872ClinVar Annotator: match by term: Aarskog disease | ClinVar Annotator: match by term: Aarskog syndromeClinVarPMID:000740980|PMID:10930571|PMID:11093277|PMID:11940089|PMID:14560308|PMID:15809997|PMID:16353258|PMID:16688726|PMID:17152066|PMID:17847065|PMID:20082460|PMID:21739585|PMID:21965325|PMID:23211637|PMID:25046119|PMID:25741868|PMID:26029706|PMID:27959697|PMID:28492532|PMID:29276006|PMID:39033378|PMID:4146757|PMID:7954831
Fgd1MouseAtkin Syndrome  ISORGD:13512288554872ClinVar Annotator: match by term: Atkin Flaitz Patil Smith syndromeClinVarPMID:26059843|PMID:28492532
Fgd1Mouseautistic disorder  ISORGD:13512288554872ClinVar Annotator: match by term: AutismClinVarPMID:21681106|PMID:30208311
Fgd1MouseCornelia de Lange syndrome 2  ISORGD:13512288554872ClinVar Annotator: match by term: Congenital muscular hypertrophy-cerebral syndromeClinVarPMID:26386245|PMID:27334371|PMID:28166369|PMID:28492532|PMID:28548707|PMID:31334757|PMID:31602316
Fgd1MouseDiamond-Blackfan anemia 14 with mandibulofacial dysostosis  ISORGD:13512288554872ClinVar Annotator: match by term: TSR2-related conditionClinVarPMID:24033266|PMID:28492532
Fgd1Mousegenetic disease  ISORGD:13512288554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:000740980|PMID:11093277|PMID:11940089|PMID:14560308|PMID:17576681|PMID:17847065|PMID:19261807|PMID:19344873|PMID:20082460|PMID:21739585|PMID:21965325|PMID:23211637|PMID:23375260|PMID:24033266|PMID:25046119|PMID:25741868|PMID:26029706|PMID:26467025|PMID:27535533|PMID:27959697|PMID:28492532|PMID:7954831|PMID:8969170|PMID:9536098
Fgd1Mouseintellectual disability  ISORGD:13512288554872ClinVar Annotator: match by term: Intellectual disabilityClinVarPMID:11940089|PMID:21739585|PMID:23211637|PMID:25046119|PMID:25741868|PMID:26029706|PMID:28492532
Fgd1Mousenon-syndromic X-linked intellectual disability 1  ISORGD:13512288554872ClinVar Annotator: match by term: INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 1ClinVarPMID:26059843|PMID:28492532
Fgd1Mousesyndromic X-linked intellectual disability Claes-Jensen type  ISORGD:13512288554872ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked, syndromic 16ClinVarPMID:25741868|PMID:28492532
Fgd1Mousesyndromic X-linked intellectual disability Lubs type  ISORGD:13512288554872ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs typeClinVarPMID:25741868
Fgd1MouseX-linked Aarskog syndrome  ISORGD:13512288554872ClinVar Annotator: match by term: FGD1-Related DisordersClinVarPMID:000740980|PMID:11940089|PMID:14560308|PMID:21739585|PMID:23211637|PMID:25046119|PMID:25741868|PMID:26029706|PMID:26467025|PMID:28492532|PMID:29276006|PMID:39033378|PMID:7954831
Fgd1MouseX-linked intellectual disability-psychosis-macroorchidism syndrome  ISORGD:13512288554872ClinVar Annotator: match by term: Intellectual developmental disorder, X-linked, syndromic 16ClinVarPMID:25741868|PMID:28492532
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Original Reference(s)
Fgd1MouseAarskog syndrome  ISORGD:135122811554173CTD Direct Evidence: marker/mechanismCTDPMID:7954831|PMID:10930571|PMID:11093277|PMID:14560308|PMID:15327482|PMID:17152066
Fgd1Mouseattention deficit hyperactivity disorder  ISORGD:135122811554173CTD Direct Evidence: marker/mechanismCTDPMID:15809997
Fgd1MouseCongenital Foot Deformities  ISORGD:135122811554173CTD Direct Evidence: marker/mechanismCTDPMID:11940089
Fgd1MouseCraniofacial Abnormalities  ISORGD:135122811554173CTD Direct Evidence: marker/mechanismCTDPMID:7954831
Fgd1MouseGrowth Disorders  ISORGD:135122811554173CTD Direct Evidence: marker/mechanismCTDPMID:7954831|PMID:10930571|PMID:11093277|PMID:11940089
Fgd1MouseNervous System Malformations  ISORGD:135122811554173CTD Direct Evidence: marker/mechanismCTDPMID:11093277
Fgd1MouseUrogenital Abnormalities  ISORGD:135122811554173CTD Direct Evidence: marker/mechanismCTDPMID:7954831|PMID:10930571|PMID:11093277
Fgd1MouseX-Linked Intellectual Developmental Disorders  ISORGD:135122811554173CTD Direct Evidence: marker/mechanismCTDPMID:11940089
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Original Reference(s)
Fgd1MouseX-linked Aarskog syndrome  ISORGD:13512287240710 OMIM 

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Fgd1Mouse(1->4)-beta-D-glucan multiple interactionsEXP 6480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in increased expression of FGD1 mRNACTDPMID:36331819
Fgd1Mouse1,2,4-trichloro-5-(2,5-dichlorophenyl)benzene multiple interactionsEXP 6480464[2,4,4'-trichlorobiphenyl co-treated with 2,5,2',5'-tetrachlorobiphenyl co-treated with 2,4,5,2',5'-pentachlorobiphenyl co-treated with 2,2',3',4,4',5-hexachlorobiphenyl co-treated with 2,4,5,2',4',5'-hexachlorobiphenyl co-treated with more ...CTDPMID:25510870
Fgd1Mouse17alpha-ethynylestradiol increases expressionEXP 6480464Ethinyl Estradiol results in increased expression of FGD1 mRNACTDPMID:17942748
Fgd1Mouse17alpha-ethynylestradiol multiple interactionsEXP 6480464[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of FGD1 mRNACTDPMID:17942748
Fgd1Mouse17beta-estradiol multiple interactionsISORGD:13512286480464[Estradiol co-treated with Bucladesine co-treated with Medroxyprogesterone Acetate] results in decreased expression of FGD1 mRNACTDPMID:20823114
Fgd1Mouse2,2',4,4',5,5'-hexachlorobiphenyl multiple interactionsEXP 6480464[2,4,4'-trichlorobiphenyl co-treated with 2,5,2',5'-tetrachlorobiphenyl co-treated with 2,4,5,2',5'-pentachlorobiphenyl co-treated with 2,2',3',4,4',5-hexachlorobiphenyl co-treated with 2,4,5,2',4',5'-hexachlorobiphenyl co-treated with more ...CTDPMID:25510870
Fgd1Mouse2,2',5,5'-tetrachlorobiphenyl multiple interactionsEXP 6480464[2,4,4'-trichlorobiphenyl co-treated with 2,5,2',5'-tetrachlorobiphenyl co-treated with 2,4,5,2',5'-pentachlorobiphenyl co-treated with 2,2',3',4,4',5-hexachlorobiphenyl co-treated with 2,4,5,2',4',5'-hexachlorobiphenyl co-treated with more ...CTDPMID:25510870
Fgd1Mouse2,3,7,8-tetrachlorodibenzodioxine multiple interactionsEXP 6480464[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of FGD1 mRNACTDPMID:17942748
Fgd1Mouse2,3,7,8-tetrachlorodibenzodioxine decreases expressionISORGD:15651886480464Tetrachlorodibenzodioxin results in decreased expression of FGD1 mRNACTDPMID:21215274
Fgd1Mouse2,4,4'-trichlorobiphenyl multiple interactionsEXP 6480464[2,4,4'-trichlorobiphenyl co-treated with 2,5,2',5'-tetrachlorobiphenyl co-treated with 2,4,5,2',5'-pentachlorobiphenyl co-treated with 2,2',3',4,4',5-hexachlorobiphenyl co-treated with 2,4,5,2',4',5'-hexachlorobiphenyl co-treated with more ...CTDPMID:25510870
Fgd1Mouse3,4-methylenedioxymethamphetamine increases expressionEXP 6480464N-Methyl-3,4-methylenedioxyamphetamine results in increased expression of FGD1 mRNACTDPMID:20188158
Fgd1Mousearistolochic acid A increases expressionISORGD:13512286480464aristolochic acid I results in increased expression of FGD1 mRNACTDPMID:33212167
Fgd1Mousebenzo[a]pyrene affects methylationISORGD:13512286480464Benzo(a)pyrene affects the methylation of FGD1 3' UTR; Benzo(a)pyrene affects the methylation of FGD1 exon; more ...CTDPMID:27901495|PMID:30157460
Fgd1Mousebisphenol A decreases methylationEXP 6480464bisphenol A results in decreased methylation of FGD1 promoterCTDPMID:27312807
Fgd1Mousebucladesine multiple interactionsISORGD:13512286480464[Estradiol co-treated with Bucladesine co-treated with Medroxyprogesterone Acetate] results in decreased expression of FGD1 mRNACTDPMID:20823114
Fgd1Mousecadmium atom multiple interactionsISORGD:13512286480464[Cadmium Chloride results in increased abundance of Cadmium] which results in decreased expression of FGD1 more ...CTDPMID:35301059
Fgd1Mousecadmium dichloride multiple interactionsISORGD:13512286480464[Cadmium Chloride results in increased abundance of Cadmium] which results in decreased expression of FGD1 more ...CTDPMID:35301059
Fgd1Mousecaffeine decreases phosphorylationISORGD:13512286480464Caffeine results in decreased phosphorylation of FGD1 proteinCTDPMID:35688186
Fgd1Mousecholine multiple interactionsEXP 6480464[Methionine deficiency co-treated with Choline deficiency co-treated with Folic Acid deficiency] results in increased expression more ...CTDPMID:20938992
Fgd1Mousecoumarin decreases phosphorylationISORGD:13512286480464coumarin results in decreased phosphorylation of FGD1 proteinCTDPMID:35688186

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Biological Process

  
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Original Reference(s)
Fgd1Mouseactin cytoskeleton organization involved_inIEAUniProtKB:P98174|ensembl:ENSP000003642772290270 EnsemblGO_REF:0000107
Fgd1Mouseactin cytoskeleton organization involved_inISOUniProtKB:P981742290270 GO_CentralGO_REF:0000119
Fgd1Mousecytoskeleton organization involved_inIBAPANTHER:PTN000292819|UniProtKB:P98174|MGI:1045662290270 GO_CentralGO_REF:0000033
Fgd1Mousecytoskeleton organization acts_upstream_of_or_withinIDA 2290270 PMID:12913069MGIPMID:12913069
Fgd1Mousefilopodium assembly involved_inIBAPANTHER:PTN000292819|UniProtKB:P98174|MGI:13536572290270 GO_CentralGO_REF:0000033
Fgd1Mousefilopodium assembly involved_inIEAUniProtKB:P98174|ensembl:ENSP000003642772290270 EnsemblGO_REF:0000107
Fgd1Mousefilopodium assembly involved_inISOUniProtKB:P981742290270 GO_CentralGO_REF:0000119
Fgd1Mouseregulation of cell shape involved_inIDA 2290270 PMID:12913069UniProtPMID:12913069

Cellular Component

  
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Fgd1Mousecytoplasm is_active_inIBAPANTHER:PTN000292731|dictyBase:DDB_G0269610|FB:FBgn0035761|PomBase:SPAC31A2.16|dictyBase:DDB_G0284845|WB:WBGene00001366|MGI:104566|dictyBase:DDB_G0277987|dictyBase:DDB_G0291978|dictyBase:DDB_G0279733|MGI:13470842290270 GO_CentralGO_REF:0000033
Fgd1Mousecytoplasm located_inIDA 2290270 PMID:12913069MGIPMID:12913069
Fgd1Mousecytoskeleton located_inIEAUniProtKB-SubCell:SL-00902290270 UniProtGO_REF:0000044
Fgd1Mousecytosol located_inIEAUniProtKB:P98174|ensembl:ENSP000003642772290270 EnsemblGO_REF:0000107
Fgd1MouseGolgi apparatus located_inIDA 2290270 PMID:12913069MGIPMID:12913069
Fgd1Mouselamellipodium located_inIDA 2290270 PMID:12913069MGIPMID:12913069
Fgd1Mouseplasma membrane located_inIEAUniProtKB:P98174|ensembl:ENSP000003642772290270 EnsemblGO_REF:0000107
Fgd1Mouseruffle located_inIDA 2290270 PMID:12913069MGIPMID:12913069

Molecular Function
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Fgd1Mouseguanyl-nucleotide exchange factor activity enablesIBAPANTHER:PTN000292731|UniProtKB:P98174|PomBase:SPAC31A2.16|FB:FBgn0035761|MGI:1347084|dictyBase:DDB_G0291978|dictyBase:DDB_G02779872290270 GO_CentralGO_REF:0000033
Fgd1Mouseguanyl-nucleotide exchange factor activity enablesIEAUniProtKB:P98174|ensembl:ENSP000003642772290270 EnsemblGO_REF:0000107
Fgd1Mouseguanyl-nucleotide exchange factor activity enablesISOUniProtKB:P981742290270 GO_CentralGO_REF:0000119
Fgd1Mouseprotein binding enablesIPIUniProtKB:Q60598|UniProtKB:Q624182290270 PMID:12913069UniProtPMID:12913069
Fgd1Mouseprotein binding enablesIPIPR:Q640L32290270 PMID:17000758MGIPMID:17000758
Fgd1Mouseprotein binding enablesIPIPR:Q60598|PR:Q624182290270 PMID:12913069MGIPMID:12913069
Fgd1Mousesmall GTPase binding enablesISOUniProtKB:P981742290270 GO_CentralGO_REF:0000119
Fgd1Mousesmall GTPase binding enablesIEAUniProtKB:P98174|ensembl:ENSP000003642772290270 EnsemblGO_REF:0000107
Fgd1Mousezinc ion binding enablesIEAUniProtKB-KW:KW-08632290270 UniProtGO_REF:0000043
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Fgd1Mouseabnormal craniofacial morphology  IEA 5509061 MGI 
Fgd1Mouseabnormal embryo size  IEA 5509061 MGI 
Fgd1Mouseedema  IEA 5509061 MGI 
Fgd1Mouseembryonic growth retardation  IEA 5509061 MGI 
Fgd1Mouseenlarged thymus  IEA 5509061 MGI 
Fgd1Mousemicrophthalmia  IEA 5509061 MGI 

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Reference Title
Reference Citation
1. Novel FGD1 mutation underlying Aarskog-Scott syndrome with myopathy and distal arthropathy. Al-Semari A, etal., Clin Dysmorphol. 2013 Jan;22(1):13-7. doi: 10.1097/MCD.0b013e32835b6dc4.
2. Faciogenital dysplasia protein Fgd1 regulates invadopodia biogenesis and extracellular matrix degradation and is up-regulated in prostate and breast cancer. Ayala I, etal., Cancer Res. 2009 Feb 1;69(3):747-52. doi: 10.1158/0008-5472.CAN-08-1980. Epub 2009 Jan 13.
3. Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene. Lebel RR, etal., Clin Genet. 2002 Feb;61(2):139-45.
4. MGDs mouse GO annotations MGD data from the GO Consortium
5. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
6. Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene. Orrico A, etal., Am J Med Genet A. 2010 Feb;152A(2):313-8. doi: 10.1002/ajmg.a.33199.
7. Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor. Pasteris NG, etal., Cell. 1994 Nov 18;79(4):669-78.
8. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
9. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
10. Clinical variation of Aarskog syndrome in a large family with 2189delA in the FGD1 gene. Shalev SA, etal., Am J Med Genet A. 2006 Jan 15;140(2):162-5.
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PMID:8535076   PMID:8889548   PMID:8889551   PMID:8969170   PMID:8994827   PMID:9624130   PMID:9671479   PMID:10349636   PMID:10721717   PMID:10906777   PMID:11042159   PMID:11076861  
PMID:11181572   PMID:11217851   PMID:12466851   PMID:12477932   PMID:12904583   PMID:12913069   PMID:14610273   PMID:14691545   PMID:14992579   PMID:15782199   PMID:16141072   PMID:16141073  
PMID:16602821   PMID:17000758   PMID:17967808   PMID:18363964   PMID:18799693   PMID:19261807   PMID:21267068   PMID:21873635   PMID:21965325   PMID:38355793  



Fgd1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X149,829,141 - 149,872,682 (+)NCBIGRCm39GRCm39mm39
GRCm39 EnsemblX149,829,146 - 149,872,517 (+)EnsemblGRCm39 Ensembl
GRCm38X151,046,141 - 151,089,686 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX151,046,150 - 151,089,521 (+)EnsemblGRCm38mm10GRCm38
MGSCv37X147,481,776 - 147,523,642 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36X146,387,949 - 146,429,815 (+)NCBIMGSCv36mm8
MGSCv36X128,052,708 - 128,094,514 (+)NCBIMGSCv36mm8
CeleraX133,315,143 - 133,357,665 (-)NCBICelera
Cytogenetic MapXF3NCBI
cM MapX68.46NCBI
FGD1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X54,445,454 - 54,496,234 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 EnsemblX54,445,454 - 54,496,234 (-)EnsemblGRCh38hg38GRCh38
GRCh37X54,471,887 - 54,522,667 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X54,488,612 - 54,539,324 (-)NCBINCBI36Build 36hg18NCBI36
Build 34X54,354,909 - 54,405,620NCBI
CeleraX58,304,448 - 58,355,160 (-)NCBICelera
Cytogenetic MapXp11.22NCBI
HuRefX51,522,464 - 51,572,796 (-)NCBIHuRef
CHM1_1X54,462,541 - 54,513,238 (-)NCBICHM1_1
T2T-CHM13v2.0X53,736,310 - 53,787,092 (-)NCBIT2T-CHM13v2.0
Fgd1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8X23,466,791 - 23,509,773 (+)NCBIGRCr8
mRatBN7.2X20,023,746 - 20,066,734 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 EnsemblX20,023,746 - 20,066,566 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_UtxX17,462,039 - 17,504,869 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0X22,618,713 - 22,661,545 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0X20,552,995 - 20,595,814 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0X20,100,942 - 20,143,871 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 EnsemblX20,100,942 - 20,143,871 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 EnsemblX20,216,587 - 20,225,955 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0X20,846,380 - 20,888,661 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4X40,364,211 - 40,407,213 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
CeleraX20,281,249 - 20,323,819 (+)NCBICelera
Cytogenetic MapXq12NCBI
Fgd1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554751,703,374 - 1,752,710 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554751,703,374 - 1,752,710 (-)NCBIChiLan1.0ChiLan1.0
FGD1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2X55,834,119 - 55,884,005 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1X55,837,723 - 55,887,601 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0X46,648,765 - 46,699,444 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1X54,880,751 - 54,930,672 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 EnsemblX54,880,513 - 54,930,672 (-)Ensemblpanpan1.1panPan2
FGD1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1X46,194,950 - 46,239,291 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 EnsemblX46,194,735 - 46,270,701 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_TashaX37,583,900 - 37,627,968 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0X46,516,320 - 46,560,389 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 EnsemblX46,516,275 - 46,560,769 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1X46,014,132 - 46,058,399 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0X46,464,507 - 46,508,560 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0X46,531,810 - 46,575,872 (-)NCBIUU_Cfam_GSD_1.0
Fgd1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X39,012,340 - 39,057,557 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367511,351,795 - 1,397,288 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367511,355,606 - 1,397,282 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
FGD1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 EnsemblX47,192,427 - 47,231,342 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1X47,191,838 - 47,231,656 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2X53,049,149 - 53,088,229 (-)NCBISscrofa10.2Sscrofa10.2susScr3
FGD1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X50,554,648 - 50,609,437 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 EnsemblX50,556,168 - 50,583,010 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660864,520,644 - 4,572,317 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Fgd1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249092,316,431 - 2,370,179 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249092,316,749 - 2,370,097 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

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Variants in Fgd1
315 total Variants

Predicted Target Of
Summary Value
Count of predictions:1172
Count of miRNA genes:478
Interacting mature miRNAs:557
Transcripts:ENSMUST00000026296, ENSMUST00000112685, ENSMUST00000124882, ENSMUST00000125620
Prediction methods:Miranda, Pita, Pita,Targetscan, Rnahybrid, Targetscan
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 10 of 11 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
10401118Pgia39_mproteoglycan induced arthritis 39 (mouse)Not determinedX144474380169476592Mouse
1558900Bw3_mbody weight QTL 3 (mouse)Not determinedX133540040165298595Mouse
1302000Pgia25_mproteoglycan induced arthritis 2 (mouse)Not determinedX144474380169476592Mouse
25314309Syncl5_msynaptonemal complex length 5 (mouse)X121909697152582996Mouse
13824981Svwq2_mseminal vesicle weight QTL 2 (mouse)X128900749153782996Mouse
12738421Lfibq17_mliver fibrosis QTL 17 (mouse)X148148453164945064Mouse
1301209Cia19_mcollagen induced arthritis 19 (mouse)Not determinedX120993165160213038Mouse
10412164Cmv2_mcytomegalovirus resistance 2 (mouse)Not determinedX125685149159685269Mouse
1357823Spha3_msperm head anomaly 3 (mouse)Not determinedX102055848162758941Mouse
1357433Dbts2_mdiabetes 2 (mouse)Not determinedX7226295150107038Mouse

1 to 10 of 11 rows
DXMit153  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X151,055,859 - 151,056,001UniSTSGRCm38
MGSCv37X147,490,402 - 147,490,544UniSTSGRCm37
Cytogenetic MapXF3UniSTS
cM MapX62.2UniSTS
Whitehead GeneticX50.3UniSTS
Whitehead_YACX UniSTS
px-2c2  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X151,076,357 - 151,076,709UniSTSGRCm38
MGSCv37X147,510,900 - 147,511,252UniSTSGRCm37
CeleraX133,327,490 - 133,327,836UniSTS
Cytogenetic MapXF3UniSTS
cM MapX64.0UniSTS
Fgd1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X151,088,714 - 151,088,880UniSTSGRCm38
MGSCv37X147,523,257 - 147,523,423UniSTSGRCm37
CeleraX133,315,360 - 133,315,526UniSTS
Cytogenetic MapXF3UniSTS
cM MapX64.0UniSTS






1 to 17 of 17 rows
RefSeq Transcripts NM_008001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006528699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_004940326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AI195396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK148151 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK162865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK190384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK219664 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL805937 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AV367660 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC004838 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC011462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA328503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH466641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN531569 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN702035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U22325 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 17 of 17 rows

Ensembl Acc Id: ENSMUST00000026296   ⟹   ENSMUSP00000026296
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX149,830,166 - 149,872,517 (+)Ensembl
GRCm38.p6 EnsemblX151,047,170 - 151,089,521 (+)Ensembl
Ensembl Acc Id: ENSMUST00000112685   ⟹   ENSMUSP00000108305
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX149,829,146 - 149,872,517 (+)Ensembl
GRCm38.p6 EnsemblX151,046,150 - 151,089,521 (+)Ensembl
Ensembl Acc Id: ENSMUST00000124882
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX149,850,379 - 149,852,664 (+)Ensembl
GRCm38.p6 EnsemblX151,067,383 - 151,069,668 (+)Ensembl
Ensembl Acc Id: ENSMUST00000125620
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX149,869,106 - 149,870,177 (+)Ensembl
GRCm38.p6 EnsemblX151,086,110 - 151,087,181 (+)Ensembl
RefSeq Acc Id: NM_008001   ⟹   NP_032027
RefSeq Status: REVIEWED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39X149,830,166 - 149,872,682 (+)NCBI
GRCm38X151,047,170 - 151,089,686 (+)NCBI
MGSCv37X147,481,776 - 147,523,642 (+)RGD
CeleraX133,314,554 - 133,357,728 (-)NCBI
cM MapX ENTREZGENE
Sequence:
RefSeq Acc Id: XM_006528699   ⟹   XP_006528762
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39X149,829,141 - 149,872,528 (+)NCBI
GRCm38X151,046,141 - 151,089,685 (+)NCBI
Sequence:
RefSeq Acc Id: XR_004940326
Type: NON-CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39X149,829,735 - 149,872,517 (+)NCBI
Sequence:
1 to 12 of 12 rows
Protein RefSeqs NP_032027 (Get FASTA)   NCBI Sequence Viewer  
  XP_006528762 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA96001 (Get FASTA)   NCBI Sequence Viewer  
  AAH04838 (Get FASTA)   NCBI Sequence Viewer  
  AAH11462 (Get FASTA)   NCBI Sequence Viewer  
  BAE28377 (Get FASTA)   NCBI Sequence Viewer  
  BAE37091 (Get FASTA)   NCBI Sequence Viewer  
  EDL07497 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSMUSP00000026296
  ENSMUSP00000026296.8
  ENSMUSP00000108305
GenBank Protein P52734 (Get FASTA)   NCBI Sequence Viewer  
1 to 12 of 12 rows
RefSeq Acc Id: NP_032027   ⟸   NM_008001
- UniProtKB: Q921L2 (UniProtKB/Swiss-Prot),   P52734 (UniProtKB/Swiss-Prot),   Q3UG32 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006528762   ⟸   XM_006528699
- Peptide Label: isoform X1
- UniProtKB: A2ALP5 (UniProtKB/TrEMBL),   Q3UG32 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSMUSP00000026296   ⟸   ENSMUST00000026296
Ensembl Acc Id: ENSMUSP00000108305   ⟸   ENSMUST00000112685
DH   FYVE-type   PH

Name Modeler Protein Id AA Range Protein Structure
AF-P52734-F1-model_v2 AlphaFold P52734 1-960 view protein structure

RGD ID:6845697
Promoter ID:MM_KWN:62326
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day0,   3T3L1_Day1,   3T3L1_Day2,   3T3L1_Day3,   3T3L1_Day6,   Brain,   ES_Cell,   Liver,   Lung,   MEF_B4,   MEF_B6
Transcripts:ENSMUST00000101166,   OTTMUST00000046115
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X147,481,201 - 147,482,422 (+)MPROMDB
RGD ID:6845700
Promoter ID:MM_KWN:62327
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Brain
Transcripts:OTTMUST00000046117
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X147,500,951 - 147,501,451 (+)MPROMDB
RGD ID:6845701
Promoter ID:MM_KWN:62328
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Brain,   Kidney,   MEF_B6
Transcripts:OTTMUST00000046118
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X147,520,061 - 147,521,002 (+)MPROMDB
RGD ID:13681618
Promoter ID:EPDNEW_M24958
Type:initiation region
Name:Fgd1_1
Description:Mus musculus FYVE, RhoGEF and PH domain containing 1 , mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm38X151,047,201 - 151,047,261EPDNEW


1 to 40 of 41 rows
Database
Acc Id
Source(s)
Ensembl Genes ENSMUSG00000025265 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENSMUST00000026296 ENTREZGENE
  ENSMUST00000026296.8 UniProtKB/Swiss-Prot
  ENSMUST00000112685 ENTREZGENE
Gene3D-CATH 1.20.900.10 UniProtKB/Swiss-Prot
  2.30.29.30 UniProtKB/Swiss-Prot
  3.30.40.10 UniProtKB/Swiss-Prot
InterPro DBL_dom_sf UniProtKB/Swiss-Prot
  DH-domain UniProtKB/Swiss-Prot
  FGD1-4_PH2 UniProtKB/Swiss-Prot
  FGD1_PH1 UniProtKB/Swiss-Prot
  FYVE_RhoGEF_PH UniProtKB/Swiss-Prot
  PH-like_dom_sf UniProtKB/Swiss-Prot
  PH_domain UniProtKB/Swiss-Prot
  Znf_FYVE UniProtKB/Swiss-Prot
  Znf_FYVE-rel UniProtKB/Swiss-Prot
  Znf_RING/FYVE/PHD UniProtKB/Swiss-Prot
KEGG Report mmu:14163 UniProtKB/Swiss-Prot
MGD MGI:104566 ENTREZGENE
NCBI Gene 14163 ENTREZGENE
PANTHER FACIOGENITAL DYSPLASIA PROTEIN UniProtKB/Swiss-Prot
  FYVE, RHOGEF AND PH DOMAIN-CONTAINING PROTEIN 1 UniProtKB/Swiss-Prot
Pfam FYVE UniProtKB/Swiss-Prot
  PF00169 UniProtKB/Swiss-Prot
  RhoGEF UniProtKB/Swiss-Prot
PhenoGen Fgd1 PhenoGen
PROSITE DH_2 UniProtKB/Swiss-Prot
  PH_DOMAIN UniProtKB/Swiss-Prot
  ZF_FYVE UniProtKB/Swiss-Prot
SMART FYVE UniProtKB/Swiss-Prot
  RhoGEF UniProtKB/Swiss-Prot
  SM00233 UniProtKB/Swiss-Prot
Superfamily-SCOP PH domain-like UniProtKB/Swiss-Prot
  SSF48065 UniProtKB/Swiss-Prot
UniProt A2ALP5 ENTREZGENE, UniProtKB/TrEMBL
  FGD1_MOUSE UniProtKB/Swiss-Prot, ENTREZGENE
  Q3TRD9_MOUSE UniProtKB/TrEMBL
  Q3UG32 ENTREZGENE, UniProtKB/TrEMBL
  Q921L2 ENTREZGENE
  Q99K79_MOUSE UniProtKB/TrEMBL
1 to 40 of 41 rows