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Center for Computational Systems Medicine
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Gene summary

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Gene structures and expression levels

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Exon skipping events with PSIs in TCGA

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Exon skipping events with PSIs in GTEx

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Open reading frame (ORF) annotation in the exon skipping event

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Exon skipping events in the canonical protein sequence

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SNVs in the skipped exons with depth of coverage

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Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon

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Related drugs with this gene

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Related diseases with this gene

Gene summary for FMN2

check button Gene summary
Gene informationGene symbol

FMN2

Gene ID

56776

Gene nameformin 2
Synonyms-
Cytomap

1q43

Type of geneprotein-coding
Descriptionformin-2
Modification date20180519
UniProtAcc

Q9NZ56

ContextPubMed: FMN2 [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract]
- Title (PMID)

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID

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Exon skipping events across known transcript of Ensembl for FMN2 from UCSC genome browser

check buttonSkipped exons in TCGA and GTEx based on Ensembl gene isoform structure.
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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Gene isoform structures and expression levels for FMN2

check button Expression levels of gene isoforms across TCGA.
gencode gene structure

check button Expression levels of gene isoforms across GTEx.
gencode gene structure


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Exon skipping events with PSIs in TCGA for FMN2

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_196921240341220:240341368:240343468:240343480:240351506:240351562240343468:240343480ENSG00000155816.15ENST00000447095.1
exon_skip_196941240351506:240351562:240370098:240372032:240374390:240374535240370098:240372032ENSG00000155816.15ENST00000319653.9
exon_skip_197061240421244:240421332:240458121:240458183:240492375:240492467240458121:240458183ENSG00000155816.15ENST00000463398.1,ENST00000319653.9,ENST00000441342.1
exon_skip_197081240493902:240494049:240497186:240497246:240497408:240497529240497186:240497246ENSG00000155816.15ENST00000319653.9,ENST00000545751.1
exon_skip_197111240497408:240497529:240519115:240519208:240555810:240555862240519115:240519208ENSG00000155816.15ENST00000319653.9,ENST00000545751.1
exon_skip_197121240519115:240519208:240555810:240555862:240601360:240601510240555810:240555862ENSG00000155816.15ENST00000319653.9,ENST00000545751.1

check button PSI values of skipped exons in TCGA.
psi tcga

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Exon skipping events with PSIs in GTEx for FMN2

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_196921240341220:240341368:240343468:240343480:240351506:240351562240343468:240343480ENSG00000155816.15ENST00000447095.1
exon_skip_196941240351506:240351562:240370098:240372032:240374390:240374535240370098:240372032ENSG00000155816.15ENST00000319653.9
exon_skip_197061240421244:240421332:240458121:240458183:240492375:240492467240458121:240458183ENSG00000155816.15ENST00000319653.9,ENST00000463398.1,ENST00000441342.1
exon_skip_197081240493902:240494049:240497186:240497246:240497408:240497529240497186:240497246ENSG00000155816.15ENST00000319653.9,ENST00000545751.1
exon_skip_197111240497408:240497529:240519115:240519208:240555810:240555862240519115:240519208ENSG00000155816.15ENST00000319653.9,ENST00000545751.1
exon_skip_197121240519115:240519208:240555810:240555862:240601360:240601510240555810:240555862ENSG00000155816.15ENST00000319653.9,ENST00000545751.1

check button PSI values of skipped exons in GTEx.
psi gtex

* Skipped exon sequences.

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Open reading frame (ORF) annotation in the exon skipping event for FMN2

check button Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST00000319653240370098240372032Frame-shift
ENST00000319653240458121240458183Frame-shift
ENST00000319653240555810240555862Frame-shift
ENST00000319653240497186240497246In-frame
ENST00000319653240519115240519208In-frame

check button Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST00000319653240370098240372032Frame-shift
ENST00000319653240458121240458183Frame-shift
ENST00000319653240555810240555862Frame-shift
ENST00000319653240497186240497246In-frame
ENST00000319653240519115240519208In-frame

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Infer the effects of exon skipping event on protein functional features for FMN2

check button Exon skipping at the protein sequence level and followed lost functional features.
* Click on the image to enlarge it in a new window.
prot feature distribution

check button Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST00000319653645117222404971862404972464815487415281548
ENST00000319653645117222405191152405192084996508815881619

check button Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST00000319653645117222404971862404972464815487415281548
ENST00000319653645117222405191152405192084996508815881619

check button Lost protein functional features of individual exon skipping events in TCGA.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature
Q9NZ561528154811722ChainID=PRO_0000194888;Note=Formin-2
Q9NZ561528154812831698DomainNote=FH2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00774
Q9NZ561588161911722ChainID=PRO_0000194888;Note=Formin-2
Q9NZ561588161915671597Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q9NZ561588161912831698DomainNote=FH2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00774


check button Lost protein functional features of individual exon skipping events in GTEx.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature
Q9NZ561528154811722ChainID=PRO_0000194888;Note=Formin-2
Q9NZ561528154812831698DomainNote=FH2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00774
Q9NZ561588161911722ChainID=PRO_0000194888;Note=Formin-2
Q9NZ561588161915671597Coiled coilOntology_term=ECO:0000255;evidence=ECO:0000255
Q9NZ561588161912831698DomainNote=FH2;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00774


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SNVs in the skipped exons for FMN2

check button - Lollipop plot for presenting exon skipping associated SNVs.
* Click on the image to enlarge it in a new window.
lollipop

check button - Differential PSIs between mutated versus non-mutated samples.

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
ACCTCGA-OR-A5LJ-01exon_skip_19694
240370099240372032240370291240370295Frame_Shift_DelAGGTT-p.726_728del
LIHCTCGA-DD-A3A0-01exon_skip_19694
240370099240372032240370325240370325Frame_Shift_DelT-p.I738fs
ESCATCGA-JY-A938-01exon_skip_19694
240370099240372032240370345240370345Frame_Shift_DelC-p.Q745fs
COADTCGA-AA-3713-01exon_skip_19694
240370099240372032240370419240370419Frame_Shift_DelC-p.C769fs
LIHCTCGA-DD-A1EG-01exon_skip_19694
240370099240372032240370419240370419Frame_Shift_DelC-p.C769fs
LIHCTCGA-DD-A39Y-01exon_skip_19694
240370099240372032240370419240370419Frame_Shift_DelC-p.C769fs
LIHCTCGA-DD-A1EG-01exon_skip_19694
240370099240372032240370556240370556Frame_Shift_DelC-p.S815fs
LIHCTCGA-G3-A3CJ-01exon_skip_19694
240370099240372032240370660240370660Frame_Shift_DelA-p.K850fs
COADTCGA-AD-6889-01exon_skip_19694
240370099240372032240370840240370840Frame_Shift_DelC-p.P909fs
COADTCGA-G4-6628-01exon_skip_19694
240370099240372032240370840240370840Frame_Shift_DelC-p.P909fs
STADTCGA-BR-8372-01exon_skip_19694
240370099240372032240370840240370840Frame_Shift_DelC-p.P909fs
STADTCGA-BR-8372-01exon_skip_19694
240370099240372032240370840240370840Frame_Shift_DelC-p.P913fs
UCECTCGA-B5-A0JR-01exon_skip_19694
240370099240372032240370840240370840Frame_Shift_DelC-p.P914fs
STADTCGA-BR-8590-01exon_skip_19694
240370099240372032240370873240370873Frame_Shift_DelC-p.I920fs
STADTCGA-BR-8590-01exon_skip_19694
240370099240372032240370873240370873Frame_Shift_DelC-p.I924fs
LIHCTCGA-DD-A39Y-01exon_skip_19694
240370099240372032240371005240371005Frame_Shift_DelC-p.P965fs
UCECTCGA-B5-A0K9-01exon_skip_19694
240370099240372032240371071240371071Frame_Shift_DelC-p.P991fs
LIHCTCGA-DD-A39Y-01exon_skip_19694
240370099240372032240371203240371203Frame_Shift_DelC-p.P1035fs
LIHCTCGA-DD-A3A0-01exon_skip_19694
240370099240372032240371203240371203Frame_Shift_DelC-p.P1035fs
LUADTCGA-44-4112-01exon_skip_19694
240370099240372032240371236240371236Frame_Shift_DelC-p.P1042fs
LUADTCGA-44-4112-01exon_skip_19694
240370099240372032240371236240371236Frame_Shift_DelC-p.P1046fs
COADTCGA-G4-6586-01exon_skip_19694
240370099240372032240371278240371278Frame_Shift_DelC-p.P1055fs
LIHCTCGA-BC-A3KG-01exon_skip_19694
240370099240372032240371335240371335Frame_Shift_DelC-p.P1079fs
LIHCTCGA-DD-A39Y-01exon_skip_19694
240370099240372032240371335240371335Frame_Shift_DelC-p.P1079fs
STADTCGA-HU-A4G9-01exon_skip_19694
240370099240372032240371335240371335Frame_Shift_DelC-p.P1075fs
LIHCTCGA-DD-A39Y-01exon_skip_19694
240370099240372032240371368240371368Frame_Shift_DelC-p.P1090fs
COADTCGA-CM-4746-01exon_skip_19694
240370099240372032240371401240371401Frame_Shift_DelC-p.I1096fs
LIHCTCGA-G3-A3CJ-01exon_skip_19694
240370099240372032240371467240371467Frame_Shift_DelC-p.P1123fs
LIHCTCGA-DD-A39Y-01exon_skip_19694
240370099240372032240371521240371521Frame_Shift_DelG-p.G1137fs
HNSCTCGA-F7-A624-01exon_skip_19694
240370099240372032240371608240371608Frame_Shift_DelC-p.P1167fs
LIHCTCGA-DD-A1EG-01exon_skip_19694
240370099240372032240371731240371731Frame_Shift_DelC-p.P1211fs
LUADTCGA-50-5066-02exon_skip_19694
240370099240372032240371883240371883Frame_Shift_DelA-p.P1257fs
LUADTCGA-55-8085-01exon_skip_19694
240370099240372032240370489240370489Nonsense_MutationCTp.R793*
BLCATCGA-4Z-AA7Q-01exon_skip_19694
240370099240372032240370516240370516Nonsense_MutationCTp.Q802*
LIHCTCGA-BD-A3EP-01exon_skip_19694
240370099240372032240370636240370636Nonsense_MutationGTp.E842X
THYMTCGA-X7-A8M3-01exon_skip_19694
240370099240372032240370636240370636Nonsense_MutationGTp.E842X
LUADTCGA-MP-A4TF-01exon_skip_19694
240370099240372032240371125240371125Nonsense_MutationGTp.G1005*
BLCATCGA-R3-A69X-01exon_skip_19706
240458122240458183240458166240458166Nonsense_MutationCTp.Q1400*
LIHCTCGA-DD-AADP-01exon_skip_19694
240370099240372032240370098240370098Splice_SiteGA.
ESCATCGA-2H-A9GJ-01exon_skip_19711
240519116240519208240519210240519210Splice_SiteTC.
ESCATCGA-2H-A9GJ-01exon_skip_19711
240519116240519208240519210240519210Splice_SiteTCe14+2

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
HEC59_ENDOMETRIUM240370099240372032240370419240370419Frame_Shift_DelC-p.C769fs
NCIH441_LUNG240370099240372032240370441240370441Frame_Shift_DelC-p.P777fs
RERFLCAD2_LUNG240370099240372032240370837240370837Frame_Shift_DelC-p.P914fs
HEC151_ENDOMETRIUM240370099240372032240370840240370840Frame_Shift_DelC-p.P914fs
HEC6_ENDOMETRIUM240370099240372032240371236240371236Frame_Shift_DelC-p.P1046fs
TGBC11TKB_STOMACH240370099240372032240371376240371377Frame_Shift_Ins-Cp.P1089fs
JHH7_LIVER240370099240372032240370858240370890In_Frame_DelCCCGGAGCGGGCATACCTCCTCCGCCGCCTCTA-p.PGAGIPPPPPL916del
NCIH460_LUNG240370099240372032240370169240370169Missense_MutationTAp.L686Q
HT115_LARGE_INTESTINE240370099240372032240370178240370178Missense_MutationACp.K689T
MM370_SKIN240370099240372032240370204240370204Missense_MutationCTp.P698S
NCIH720_LUNG240370099240372032240370285240370285Missense_MutationGAp.A725T
MCC26_SKIN240370099240372032240370300240370300Missense_MutationGAp.E730K
P31FUJ_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240370322240370322Missense_MutationGAp.R737K
HCC2998_LARGE_INTESTINE240370099240372032240370340240370340Missense_MutationCTp.S743L
NCIH1836_LUNG240370099240372032240370390240370390Missense_MutationGTp.V760L
EOL1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240370409240370409Missense_MutationGAp.R766H
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240370414240370414Missense_MutationCTp.P768S
COLO684_ENDOMETRIUM240370099240372032240370424240370424Missense_MutationCAp.P771H
COLO704_OVARY240370099240372032240370424240370424Missense_MutationCAp.P771H
KYSE450_OESOPHAGUS240370099240372032240370455240370455Missense_MutationCAp.F781L
SNU503_LARGE_INTESTINE240370099240372032240370477240370477Missense_MutationGAp.V789M
NCIH2110_LUNG240370099240372032240370481240370481Missense_MutationCAp.S790Y
UMUC3_URINARY_TRACT240370099240372032240370556240370556Missense_MutationCAp.S815Y
NCIH2135_LUNG240370099240372032240370589240370589Missense_MutationGTp.G826V
HEC108_ENDOMETRIUM240370099240372032240370605240370605Missense_MutationTAp.H831Q
SKMEL30_SKIN240370099240372032240370636240370636Missense_MutationGAp.E842K
EW11_BONE240370099240372032240370645240370645Missense_MutationGCp.V845L
CAL78_BONE240370099240372032240370660240370660Missense_MutationAGp.K850E
NCIH1563_LUNG240370099240372032240370705240370705Missense_MutationGCp.E865Q
NCIH2342_LUNG240370099240372032240370722240370722Missense_MutationGTp.M870I
SNU407_LARGE_INTESTINE240370099240372032240370732240370732Missense_MutationGTp.G874C
VMRCLCD_LUNG240370099240372032240370747240370747Missense_MutationCAp.P879T
M980513_SKIN240370099240372032240370747240370747Missense_MutationCTp.P879S
DMS273_LUNG240370099240372032240370778240370778Missense_MutationCAp.P889H
KMS26_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240370796240370796Missense_MutationCGp.A895G
HCC56_LARGE_INTESTINE240370099240372032240370841240370841Missense_MutationCAp.P910H
2313287_STOMACH240370099240372032240370859240370859Missense_MutationCTp.P916L
DMS454_LUNG240370099240372032240370862240370862Missense_MutationGCp.G917A
COLO792_SKIN240370099240372032240370876240370876Missense_MutationCTp.P922S
KASUMI2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240370883240370883Missense_MutationCTp.P924L
SCC4_UPPER_AERODIGESTIVE_TRACT240370099240372032240370979240370979Missense_MutationCTp.P956L
HCC202_BREAST240370099240372032240371012240371012Missense_MutationCAp.P967H
WIL2NS_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371014240371014Missense_MutationCAp.P968T
OUMS27_BONE240370099240372032240371018240371018Missense_MutationCTp.P969L
HEC1A_ENDOMETRIUM240370099240372032240371020240371020Missense_MutationCAp.L970I
HEC1_ENDOMETRIUM240370099240372032240371020240371020Missense_MutationCAp.L970I
HEC1B_ENDOMETRIUM240370099240372032240371020240371020Missense_MutationCAp.L970I
A101D_SKIN240370099240372032240371023240371023Missense_MutationCTp.P971S
HS294T_SKIN240370099240372032240371023240371023Missense_MutationCTp.P971S
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371045240371045Missense_MutationCAp.P978Q
KYSE510_OESOPHAGUS240370099240372032240371060240371060Missense_MutationGAp.G983E
RL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371080240371080Missense_MutationCTp.P990S
MEWO_SKIN240370099240372032240371083240371083Missense_MutationCTp.P991S
NCIH446_LUNG240370099240372032240371084240371084Missense_MutationCAp.P991Q
KASUMI1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371116240371116Missense_MutationCAp.P1002T
SW684_SOFT_TISSUE240370099240372032240371122240371122Missense_MutationCTp.P1004S
NCIH727_LUNG240370099240372032240371134240371134Missense_MutationAGp.I1008V
NB13_AUTONOMIC_GANGLIA240370099240372032240371150240371150Missense_MutationCGp.P1013R
HOP62_LUNG240370099240372032240371158240371158Missense_MutationGAp.G1016R
M980513_SKIN240370099240372032240371158240371158Missense_MutationGAp.G1016R
LS411N_LARGE_INTESTINE240370099240372032240371194240371194Missense_MutationGTp.A1028S
VAL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371210240371210Missense_MutationCTp.P1033L
NCIH446_LUNG240370099240372032240371216240371216Missense_MutationCAp.P1035Q
5637_URINARY_TRACT240370099240372032240371218240371218Missense_MutationCTp.L1036F
MEWO_SKIN240370099240372032240371221240371221Missense_MutationCTp.P1037S
KCL22_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371224240371224Missense_MutationGAp.G1038R
NCIH2135_LUNG240370099240372032240371240240371240Missense_MutationCAp.P1043H
JHUEM7_ENDOMETRIUM240370099240372032240371243240371243Missense_MutationCTp.P1044L
DOK_UPPER_AERODIGESTIVE_TRACT240370099240372032240371243240371243Missense_MutationCGp.P1044R
MDAMB231_BREAST240370099240372032240371243240371243Missense_MutationCTp.P1044L
RF48_STOMACH240370099240372032240371243240371243Missense_MutationCTp.P1044L
KYSE410_OESOPHAGUS240370099240372032240371257240371257Missense_MutationGAp.G1049R
HCC2157_BREAST240370099240372032240371261240371261Missense_MutationCTp.A1050V
KON_UPPER_AERODIGESTIVE_TRACT240370099240372032240371278240371279Missense_MutationCCTTp.P1056F
MM127_SKIN240370099240372032240371353240371353Missense_MutationCTp.P1081S
COLO679_SKIN240370099240372032240371353240371353Missense_MutationCTp.P1081S
MEWO_SKIN240370099240372032240371353240371353Missense_MutationCTp.P1081S
GRST_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371356240371356Missense_MutationGAp.G1082R
HKA1_SKIN240370099240372032240371369240371369Missense_MutationCTp.P1086L
SW962_VULVA240370099240372032240371371240371371Missense_MutationCAp.P1087T
HKA1_SKIN240370099240372032240371377240371378Missense_MutationCCTTp.P1089F
KARPAS45_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371398240371398Missense_MutationAGp.I1096V
COLO792_SKIN240370099240372032240371404240371404Missense_MutationCTp.P1098S
MM386_SKIN240370099240372032240371407240371407Missense_MutationCTp.P1099S
CHAGOK1_LUNG240370099240372032240371408240371408Missense_MutationCAp.P1099Q
NCIH810_LUNG240370099240372032240371410240371410Missense_MutationCAp.P1100T
NALM6_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371422240371422Missense_MutationGAp.G1104R
PATU8902_PANCREAS240370099240372032240371437240371437Missense_MutationCGp.P1109A
WM278_SKIN240370099240372032240371455240371455Missense_MutationGAp.G1115R
MELHO_SKIN240370099240372032240371468240371468Missense_MutationCTp.P1119L
AML193_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371488240371488Missense_MutationGAp.G1126R
CI1_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371488240371488Missense_MutationGAp.G1126R
ISTSL2_LUNG240370099240372032240371488240371488Missense_MutationGAp.G1126R
MEWO_SKIN240370099240372032240371489240371489Missense_MutationGAp.G1126E
NCIH2073_LUNG240370099240372032240371492240371492Missense_MutationCAp.A1127E
NCIH1993_LUNG240370099240372032240371492240371492Missense_MutationCAp.A1127E
NCIH1693_LUNG240370099240372032240371494240371494Missense_MutationGAp.G1128S
JHH2_LIVER240370099240372032240371495240371495Missense_MutationGTp.G1128V
SNU407_LARGE_INTESTINE240370099240372032240371512240371512Missense_MutationCAp.P1134T
RL_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371521240371521Missense_MutationGAp.G1137R
SNUC5_LARGE_INTESTINE240370099240372032240371524240371524Missense_MutationGAp.A1138T
UMUC14_URINARY_TRACT240370099240372032240371564240371564Missense_MutationTCp.I1151T
NCIH647_LUNG240370099240372032240371569240371569Missense_MutationCAp.P1153T
IGR1_SKIN240370099240372032240371584240371584Missense_MutationCTp.P1158S
SKMM2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371588240371588Missense_MutationGCp.G1159A
KMRC1_KIDNEY240370099240372032240371600240371600Missense_MutationCTp.P1163L
SH10TC_STOMACH240370099240372032240371617240371617Missense_MutationCTp.P1169S
K2_SKIN240370099240372032240371634240371635Missense_MutationCCTTp.P1175S
HKA1_SKIN240370099240372032240371635240371635Missense_MutationCTp.P1175S
CHL1_SKIN240370099240372032240371635240371635Missense_MutationCTp.P1175S
KMOE2_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371669240371669Missense_MutationCTp.P1186L
SW684_SOFT_TISSUE240370099240372032240371702240371702Missense_MutationCTp.P1197L
JURKAT_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371711240371711Missense_MutationCGp.P1200R
EW8_BONE240370099240372032240371788240371788Missense_MutationCAp.P1226T
MCC142_SKIN240370099240372032240371788240371788Missense_MutationCTp.P1226S
KU1919_URINARY_TRACT240370099240372032240371793240371794Missense_MutationACGAp.P1228T
KU1919_URINARY_TRACT240370099240372032240371794240371794Missense_MutationCAp.P1228T
NCIH1975_LUNG240370099240372032240371815240371815Missense_MutationCTp.P1235S
BFTC905_URINARY_TRACT240370099240372032240371818240371818Missense_MutationCAp.P1236T
IPC298_SKIN240370099240372032240371878240371878Missense_MutationAGp.T1256A
HMC18_BREAST240370099240372032240371945240371945Missense_MutationACp.Q1278P
CAL78_BONE240370099240372032240371946240371946Missense_MutationGCp.Q1278H
SISO_CERVIX240370099240372032240371960240371960Missense_MutationGAp.R1283K
GRST_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371960240371960Missense_MutationGAp.R1283K
CP66MEL_SKIN240370099240372032240371972240371972Missense_MutationTAp.I1287K
DL40_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240370099240372032240371986240371986Missense_MutationCAp.P1292T
IPC298_SKIN240370099240372032240371991240371991Missense_MutationGAp.M1293I
CL34_LARGE_INTESTINE240370099240372032240371998240371998Missense_MutationCGp.L1296V
SNU81_LARGE_INTESTINE240497187240497246240497194240497194Missense_MutationGTp.S1531I
SW1783_CENTRAL_NERVOUS_SYSTEM240497187240497246240497233240497233Missense_MutationGAp.R1544Q
NCIH2081_LUNG240519116240519208240519201240519201Missense_MutationTGp.I1617M
MOLP8_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240555811240555862240555814240555814Missense_MutationACp.K1621T
JHUEM7_ENDOMETRIUM240555811240555862240555840240555840Missense_MutationTCp.S1630P
HCC95_LUNG240555811240555862240555851240555851Missense_MutationGTp.E1633D
CAL148_BREAST240370099240372032240370141240370141Nonsense_MutationCTp.Q677*
HTCC3_THYROID240370099240372032240370150240370150Nonsense_MutationGTp.E680*
BHY_UPPER_AERODIGESTIVE_TRACT240370099240372032240370419240370419Nonsense_MutationCAp.C769*
NCIH1734_LUNG240370099240372032240370894240370894Nonsense_MutationGTp.G928*
HCT15_LARGE_INTESTINE240370099240372032240371974240371974Nonsense_MutationGTp.E1288*
HRT18_LARGE_INTESTINE240370099240372032240371974240371974Nonsense_MutationGTp.E1288*
RCHACV_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE240497187240497246240497232240497232Nonsense_MutationCTp.R1544*
CHAGOK1_LUNG240519116240519208240519155240519155Nonsense_MutationCGp.S1602*

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for FMN2

check button sQTL information located at the skipped exons.
Exon skip IDChromosomeThree exonsSkippped exonENSTCancer typeSNP idLocationDNA change (ref/var)P-value

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for FMN2


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for FMN2


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RelatedDrugs for FMN2

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
GeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for FMN2

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
FMN2C0007134Renal Cell Carcinoma1CTD_human