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Fusion gene ID: 13379 |
FusionGeneSummary for FGF2_FREM3 |
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Fusion gene information | Fusion gene name: FGF2_FREM3 | Fusion gene ID: 13379 | Hgene | Tgene | Gene symbol | FGF2 | FREM3 | Gene ID | 2258 | 166752 |
Gene name | fibroblast growth factor 13 | FRAS1 related extracellular matrix 3 | |
Synonyms | FGF-13|FGF2|FHF-2|FHF2 | - | |
Cytomap | Xq26.3-q27.1 | 4q31.21 | |
Type of gene | protein-coding | protein-coding | |
Description | fibroblast growth factor 13fibroblast growth factor homologous factor 2 | FRAS1-related extracellular matrix protein 3 | |
Modification date | 20180519 | 20180329 | |
UniProtAcc | P09038 | P0C091 | |
Ensembl transtripts involved in fusion gene | ENST00000264498, ENST00000608478, | ENST00000329798, ENST00000508899, | |
Fusion gene scores | * DoF score | 1 X 1 X 1=1 | 1 X 1 X 1=1 |
# samples | 1 | 1 | |
** MAII score | log2(1/1*10)=3.32192809488736 | log2(1/1*10)=3.32192809488736 | |
Context | PubMed: FGF2 [Title/Abstract] AND FREM3 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | FGF2 | GO:0000165 | MAPK cascade | 12244047 |
![]() (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | LD | SARC | TCGA-DX-A1L1-01A | FGF2 | chr4 | 123748507 | + | FREM3 | chr4 | 144548913 | - |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
In-frame | ENST00000264498 | ENST00000329798 | FGF2 | chr4 | 123748507 | + | FREM3 | chr4 | 144548913 | - |
5CDS-intron | ENST00000264498 | ENST00000508899 | FGF2 | chr4 | 123748507 | + | FREM3 | chr4 | 144548913 | - |
In-frame | ENST00000608478 | ENST00000329798 | FGF2 | chr4 | 123748507 | + | FREM3 | chr4 | 144548913 | - |
5CDS-intron | ENST00000608478 | ENST00000508899 | FGF2 | chr4 | 123748507 | + | FREM3 | chr4 | 144548913 | - |
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FusionProtFeatures for FGF2_FREM3 |
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Hgene | Tgene |
FGF2 | FREM3 |
Extracellular matrix protein which may play a role incell adhesion. {ECO:0000250}. |
![]() * Minus value of BPloci means that the break pointn is located before the CDS. |
- In-frame and retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | FGF2 | chr4:123748507 | chr4:144548913 | ENST00000264498 | + | 1 | 3 | 179_181 | 192 | 289 | Motif | Cell attachment site%3B atypical |
Tgene | >FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 1764_1862 | 1758 | 2140 | Domain | Note=Calx-beta 1 |
Tgene | >FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 1875_1985 | 1758 | 2140 | Domain | Note=Calx-beta 2 |
Tgene | >FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 2000_2106 | 1758 | 2140 | Domain | Note=Calx-beta 3 |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | >FGF2 | chr4:123748507 | chr4:144548913 | ENST00000264498 | + | 1 | 3 | 221_223 | 192 | 289 | Motif | Cell attachment site%3B atypical |
Hgene | >FGF2 | chr4:123748507 | chr4:144548913 | ENST00000264498 | + | 1 | 3 | 261_277 | 192 | 289 | Region | Heparin-binding |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 1069_1171 | 1758 | 2140 | Repeat | CSPG 7 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 1192_1285 | 1758 | 2140 | Repeat | CSPG 8 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 1306_1404 | 1758 | 2140 | Repeat | CSPG 9 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 1425_1516 | 1758 | 2140 | Repeat | CSPG 10 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 1536_1625 | 1758 | 2140 | Repeat | CSPG 11 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 1659_1756 | 1758 | 2140 | Repeat | CSPG 12 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 306_409 | 1758 | 2140 | Repeat | CSPG 1 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 432_522 | 1758 | 2140 | Repeat | CSPG 2 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 543_677 | 1758 | 2140 | Repeat | CSPG 3 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 702_807 | 1758 | 2140 | Repeat | CSPG 4 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 828_920 | 1758 | 2140 | Repeat | CSPG 5 |
Tgene | FREM3 | chr4:123748507 | chr4:144548913 | ENST00000329798 | - | 1 | 8 | 948_1040 | 1758 | 2140 | Repeat | CSPG 6 |
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FusionGeneSequence for FGF2_FREM3 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_FGF2_ENST00000264498_chr4_123748507_+_FREM3_ENST00000329798_chr4_144548913_-_574aa LVGVGGGDVEDVTPRPGGCQISGRGARGCNGIPGAAAWEAALPRRRPRRHPSVNPRSRAAGSPRTRGRRTEERPSGSRLGDRGRGRALPG GRLGGRGRGRAPERVGGRGRGRGTAAPRAAPAARGSRPGPAGTMAAGSITTLPALPEDGGSGAFPPGHFKDPKRLYCKNGGFFLRIHPDG RVDGVREKSDPHRGNKLTNQPFHLNWAWICLEKEYYIVDEDSTFLEVTLTRRGYLGETSFISIGTKDETAKKDKDFKWKTNKQIQFNPGQ TTATWRVRIIPDNEYETSETFQIILSEPLMAVLEFPEMATVEIVDPGDESTVYIPEAEYKIEEDIGELLIPVRRSGDASQELIVICSTRQ GSATGTISSTVLFSDYISRPEDHTSILHFDKNETQKTCQVLIIDDSLYEEEESFSVSLRLPVGGQLGARFPTTKVTILADRYDEPVLHFG DAEYHVNESARYVEVCVWRRGTDLSQPSSIAVRSRKSEQESAEAGTDYVGISRNLDFAPGVRMQTFQVTILDDLGQPTLEGPEKFELLLQ >In-frame_FGF2_ENST00000608478_chr4_123748507_+_FREM3_ENST00000329798_chr4_144548913_-_441aa MAAGSITTLPALPEDGGSGAFPPGHFKDPKRLYCKNGGFFLRIHPDGRVDGVREKSDPHRGNKLTNQPFHLNWAWICLEKEYYIVDEDST FLEVTLTRRGYLGETSFISIGTKDETAKKDKDFKWKTNKQIQFNPGQTTATWRVRIIPDNEYETSETFQIILSEPLMAVLEFPEMATVEI VDPGDESTVYIPEAEYKIEEDIGELLIPVRRSGDASQELIVICSTRQGSATGTISSTVLFSDYISRPEDHTSILHFDKNETQKTCQVLII DDSLYEEEESFSVSLRLPVGGQLGARFPTTKVTILADRYDEPVLHFGDAEYHVNESARYVEVCVWRRGTDLSQPSSIAVRSRKSEQESAE |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_FGF2_ENST00000264498_chr4_123748507_+_FREM3_ENST00000329798_chr4_144548913_-_1722nt CTGGTGGGTGTGGGGGGTGGAGATGTAGAAGATGTGACGCCGCGGCCCGGCGGGTGCCAGATTAGCGGACGCGGTGCCCGCGGTTGCAAC GGGATCCCGGGCGCTGCAGCTTGGGAGGCGGCTCTCCCCAGGCGGCGTCCGCGGAGACACCCATCCGTGAACCCCAGGTCCCGGGCCGCC GGCTCGCCGCGCACCAGGGGCCGGCGGACAGAAGAGCGGCCGAGCGGCTCGAGGCTGGGGGACCGCGGGCGCGGCCGCGCGCTGCCGGGC GGGAGGCTGGGGGGCCGGGGCCGGGGCCGTGCCCCGGAGCGGGTCGGAGGCCGGGGCCGGGGCCGGGGGACGGCGGCTCCCCGCGCGGCT CCAGCGGCTCGGGGATCCCGGCCGGGCCCCGCAGGGACCATGGCAGCCGGGAGCATCACCACGCTGCCCGCCTTGCCCGAGGATGGCGGC AGCGGCGCCTTCCCGCCCGGCCACTTCAAGGACCCCAAGCGGCTGTACTGCAAAAACGGGGGCTTCTTCCTGCGCATCCACCCCGACGGC CGAGTTGACGGGGTCCGGGAGAAGAGCGACCCTCACAGAGGAAATAAACTAACAAATCAGCCTTTCCATCTAAACTGGGCTTGGATTTGT TTGGAGAAAGAGTACTACATTGTGGATGAAGATTCCACATTCTTAGAAGTGACCCTTACACGCAGAGGATACCTTGGAGAAACATCATTT ATCAGCATTGGTACCAAAGATGAAACTGCAAAAAAAGACAAAGATTTCAAATGGAAGACCAATAAACAGATCCAGTTCAATCCTGGACAG ACTACAGCCACATGGAGGGTGAGAATTATACCTGACAATGAATATGAGACTTCAGAGACCTTCCAGATCATTCTGTCTGAACCTCTCATG GCTGTACTGGAGTTTCCAGAAATGGCAACGGTTGAAATTGTAGACCCTGGAGATGAATCAACAGTTTATATTCCAGAGGCGGAATACAAA ATAGAAGAGGACATTGGGGAACTTTTGATTCCAGTAAGACGATCTGGAGATGCAAGCCAGGAACTAATCGTCATTTGCTCCACACGTCAA GGTTCTGCCACAGGCACGATTTCTTCCACAGTGTTATTCTCTGATTACATCTCACGTCCAGAAGACCACACCAGCATCCTCCACTTTGAC AAGAATGAGACACAGAAGACCTGCCAGGTCCTGATCATTGATGACTCCCTTTATGAAGAGGAGGAATCCTTCAGCGTTTCACTTAGGCTG CCAGTGGGAGGACAGCTGGGAGCCAGATTCCCCACCACTAAGGTGACTATTCTGGCTGATCGTTATGATGAACCTGTCCTGCACTTTGGG GATGCTGAATATCACGTCAATGAAAGTGCTCGCTACGTGGAGGTTTGTGTTTGGAGAAGAGGCACTGATCTTTCCCAACCATCATCCATC GCCGTGCGCTCCAGAAAGTCAGAGCAGGAGTCAGCAGAAGCTGGAACAGATTATGTTGGTATCAGCCGAAACCTGGACTTTGCTCCAGGC GTGCGCATGCAGACATTCCAAGTGACCATCCTTGATGACCTGGGACAGCCTACCTTGGAAGGCCCAGAGAAGTTTGAATTACTTCTTCAG ATGCCTATGGGTGCAGTGCTTGGAGAACCAAATAAAACTACCATTTTCATCGAGGACACCATCACGGACTGTAAGCAGAGTGCTTGTAGT >In-frame_FGF2_ENST00000608478_chr4_123748507_+_FREM3_ENST00000329798_chr4_144548913_-_1323nt ATGGCAGCCGGGAGCATCACCACGCTGCCCGCCTTGCCCGAGGATGGCGGCAGCGGCGCCTTCCCGCCCGGCCACTTCAAGGACCCCAAG CGGCTGTACTGCAAAAACGGGGGCTTCTTCCTGCGCATCCACCCCGACGGCCGAGTTGACGGGGTCCGGGAGAAGAGCGACCCTCACAGA GGAAATAAACTAACAAATCAGCCTTTCCATCTAAACTGGGCTTGGATTTGTTTGGAGAAAGAGTACTACATTGTGGATGAAGATTCCACA TTCTTAGAAGTGACCCTTACACGCAGAGGATACCTTGGAGAAACATCATTTATCAGCATTGGTACCAAAGATGAAACTGCAAAAAAAGAC AAAGATTTCAAATGGAAGACCAATAAACAGATCCAGTTCAATCCTGGACAGACTACAGCCACATGGAGGGTGAGAATTATACCTGACAAT GAATATGAGACTTCAGAGACCTTCCAGATCATTCTGTCTGAACCTCTCATGGCTGTACTGGAGTTTCCAGAAATGGCAACGGTTGAAATT GTAGACCCTGGAGATGAATCAACAGTTTATATTCCAGAGGCGGAATACAAAATAGAAGAGGACATTGGGGAACTTTTGATTCCAGTAAGA CGATCTGGAGATGCAAGCCAGGAACTAATCGTCATTTGCTCCACACGTCAAGGTTCTGCCACAGGCACGATTTCTTCCACAGTGTTATTC TCTGATTACATCTCACGTCCAGAAGACCACACCAGCATCCTCCACTTTGACAAGAATGAGACACAGAAGACCTGCCAGGTCCTGATCATT GATGACTCCCTTTATGAAGAGGAGGAATCCTTCAGCGTTTCACTTAGGCTGCCAGTGGGAGGACAGCTGGGAGCCAGATTCCCCACCACT AAGGTGACTATTCTGGCTGATCGTTATGATGAACCTGTCCTGCACTTTGGGGATGCTGAATATCACGTCAATGAAAGTGCTCGCTACGTG GAGGTTTGTGTTTGGAGAAGAGGCACTGATCTTTCCCAACCATCATCCATCGCCGTGCGCTCCAGAAAGTCAGAGCAGGAGTCAGCAGAA GCTGGAACAGATTATGTTGGTATCAGCCGAAACCTGGACTTTGCTCCAGGCGTGCGCATGCAGACATTCCAAGTGACCATCCTTGATGAC CTGGGACAGCCTACCTTGGAAGGCCCAGAGAAGTTTGAATTACTTCTTCAGATGCCTATGGGTGCAGTGCTTGGAGAACCAAATAAAACT |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_FGF2_ENST00000264498_chr4_123748507_+_FREM3_ENST00000329798_chr4_144548913_-_2099nt CGGCCCCAGAAAACCCGAGCGAGTAGGGGGCGGCGCGCAGGAGGGAGGAGAACTGGGGGCGCGGGAGGCTGGTGGGTGTGGGGGGTGGAG ATGTAGAAGATGTGACGCCGCGGCCCGGCGGGTGCCAGATTAGCGGACGCGGTGCCCGCGGTTGCAACGGGATCCCGGGCGCTGCAGCTT GGGAGGCGGCTCTCCCCAGGCGGCGTCCGCGGAGACACCCATCCGTGAACCCCAGGTCCCGGGCCGCCGGCTCGCCGCGCACCAGGGGCC GGCGGACAGAAGAGCGGCCGAGCGGCTCGAGGCTGGGGGACCGCGGGCGCGGCCGCGCGCTGCCGGGCGGGAGGCTGGGGGGCCGGGGCC GGGGCCGTGCCCCGGAGCGGGTCGGAGGCCGGGGCCGGGGCCGGGGGACGGCGGCTCCCCGCGCGGCTCCAGCGGCTCGGGGATCCCGGC CGGGCCCCGCAGGGACCATGGCAGCCGGGAGCATCACCACGCTGCCCGCCTTGCCCGAGGATGGCGGCAGCGGCGCCTTCCCGCCCGGCC ACTTCAAGGACCCCAAGCGGCTGTACTGCAAAAACGGGGGCTTCTTCCTGCGCATCCACCCCGACGGCCGAGTTGACGGGGTCCGGGAGA AGAGCGACCCTCACAGAGGAAATAAACTAACAAATCAGCCTTTCCATCTAAACTGGGCTTGGATTTGTTTGGAGAAAGAGTACTACATTG TGGATGAAGATTCCACATTCTTAGAAGTGACCCTTACACGCAGAGGATACCTTGGAGAAACATCATTTATCAGCATTGGTACCAAAGATG AAACTGCAAAAAAAGACAAAGATTTCAAATGGAAGACCAATAAACAGATCCAGTTCAATCCTGGACAGACTACAGCCACATGGAGGGTGA GAATTATACCTGACAATGAATATGAGACTTCAGAGACCTTCCAGATCATTCTGTCTGAACCTCTCATGGCTGTACTGGAGTTTCCAGAAA TGGCAACGGTTGAAATTGTAGACCCTGGAGATGAATCAACAGTTTATATTCCAGAGGCGGAATACAAAATAGAAGAGGACATTGGGGAAC TTTTGATTCCAGTAAGACGATCTGGAGATGCAAGCCAGGAACTAATCGTCATTTGCTCCACACGTCAAGGTTCTGCCACAGGCACGATTT CTTCCACAGTGTTATTCTCTGATTACATCTCACGTCCAGAAGACCACACCAGCATCCTCCACTTTGACAAGAATGAGACACAGAAGACCT GCCAGGTCCTGATCATTGATGACTCCCTTTATGAAGAGGAGGAATCCTTCAGCGTTTCACTTAGGCTGCCAGTGGGAGGACAGCTGGGAG CCAGATTCCCCACCACTAAGGTGACTATTCTGGCTGATCGTTATGATGAACCTGTCCTGCACTTTGGGGATGCTGAATATCACGTCAATG AAAGTGCTCGCTACGTGGAGGTTTGTGTTTGGAGAAGAGGCACTGATCTTTCCCAACCATCATCCATCGCCGTGCGCTCCAGAAAGTCAG AGCAGGAGTCAGCAGAAGCTGGAACAGATTATGTTGGTATCAGCCGAAACCTGGACTTTGCTCCAGGCGTGCGCATGCAGACATTCCAAG TGACCATCCTTGATGACCTGGGACAGCCTACCTTGGAAGGCCCAGAGAAGTTTGAATTACTTCTTCAGATGCCTATGGGTGCAGTGCTTG GAGAACCAAATAAAACTACCATTTTCATCGAGGACACCATCACGGACTGTAAGCAGAGTGCTTGTAGTTCCTTTGATTGAAAGACTTTAA GAGGGAAAAAAACAGCCAAGATATGTCTCCTAACAACAGAATGAAACTCTACTGTTTATAGATCTTAGCAATTCTGGGATATCAGTGATA TTGTACTGTCATTGGTGTTATATTCTGGTGATATGTGGAAATGTAATTTATATGACTGCATGGAGATAGAAATATATATACCTAGAAAAC ATTGAGCCCACAAATAATTAGACTGTGTTCATGTTCTTTTTCTATTTTGTTTTACTTTGTTTCTGAGGCAAGTAAGAAATCCACTGTGAT >In-frame_FGF2_ENST00000608478_chr4_123748507_+_FREM3_ENST00000329798_chr4_144548913_-_1976nt GCCAGATTAGCGGACGCGGTGCCCGCGGTTGCAACGGGATCCCGGGCGCTGCAGCTTGGGAGGCGGCTCTCCCCAGGCGGCGTCCGCGGA GACACCCATCCGTGAACCCCAGGTCCCGGGCCGCCGGCTCGCCGCGCACCAGGGGCCGGCGGACAGAAGAGCGGCCGAGCGGCTCGAGGC TGGGGGACCGCGGGCGCGGCCGCGCGCTGCCGGGCGGGAGGCTGGGGGGCCGGGGCCGGGGCCGTGCCCCGGAGCGGGTCGGAGGCCGGG GCCGGGGCCGGGGGACGGCGGCTCCCCGCGCGGCTCCAGCGGCTCGGGGATCCCGGCCGGGCCCCGCAGGGACCATGGCAGCCGGGAGCA TCACCACGCTGCCCGCCTTGCCCGAGGATGGCGGCAGCGGCGCCTTCCCGCCCGGCCACTTCAAGGACCCCAAGCGGCTGTACTGCAAAA ACGGGGGCTTCTTCCTGCGCATCCACCCCGACGGCCGAGTTGACGGGGTCCGGGAGAAGAGCGACCCTCACAGAGGAAATAAACTAACAA ATCAGCCTTTCCATCTAAACTGGGCTTGGATTTGTTTGGAGAAAGAGTACTACATTGTGGATGAAGATTCCACATTCTTAGAAGTGACCC TTACACGCAGAGGATACCTTGGAGAAACATCATTTATCAGCATTGGTACCAAAGATGAAACTGCAAAAAAAGACAAAGATTTCAAATGGA AGACCAATAAACAGATCCAGTTCAATCCTGGACAGACTACAGCCACATGGAGGGTGAGAATTATACCTGACAATGAATATGAGACTTCAG AGACCTTCCAGATCATTCTGTCTGAACCTCTCATGGCTGTACTGGAGTTTCCAGAAATGGCAACGGTTGAAATTGTAGACCCTGGAGATG AATCAACAGTTTATATTCCAGAGGCGGAATACAAAATAGAAGAGGACATTGGGGAACTTTTGATTCCAGTAAGACGATCTGGAGATGCAA GCCAGGAACTAATCGTCATTTGCTCCACACGTCAAGGTTCTGCCACAGGCACGATTTCTTCCACAGTGTTATTCTCTGATTACATCTCAC GTCCAGAAGACCACACCAGCATCCTCCACTTTGACAAGAATGAGACACAGAAGACCTGCCAGGTCCTGATCATTGATGACTCCCTTTATG AAGAGGAGGAATCCTTCAGCGTTTCACTTAGGCTGCCAGTGGGAGGACAGCTGGGAGCCAGATTCCCCACCACTAAGGTGACTATTCTGG CTGATCGTTATGATGAACCTGTCCTGCACTTTGGGGATGCTGAATATCACGTCAATGAAAGTGCTCGCTACGTGGAGGTTTGTGTTTGGA GAAGAGGCACTGATCTTTCCCAACCATCATCCATCGCCGTGCGCTCCAGAAAGTCAGAGCAGGAGTCAGCAGAAGCTGGAACAGATTATG TTGGTATCAGCCGAAACCTGGACTTTGCTCCAGGCGTGCGCATGCAGACATTCCAAGTGACCATCCTTGATGACCTGGGACAGCCTACCT TGGAAGGCCCAGAGAAGTTTGAATTACTTCTTCAGATGCCTATGGGTGCAGTGCTTGGAGAACCAAATAAAACTACCATTTTCATCGAGG ACACCATCACGGACTGTAAGCAGAGTGCTTGTAGTTCCTTTGATTGAAAGACTTTAAGAGGGAAAAAAACAGCCAAGATATGTCTCCTAA CAACAGAATGAAACTCTACTGTTTATAGATCTTAGCAATTCTGGGATATCAGTGATATTGTACTGTCATTGGTGTTATATTCTGGTGATA TGTGGAAATGTAATTTATATGACTGCATGGAGATAGAAATATATATACCTAGAAAACATTGAGCCCACAAATAATTAGACTGTGTTCATG |
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FusionGenePPI for FGF2_FREM3 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
FGF2 | SDC1, SDC2, SDC4, CSNK2A1, CSNK2A2, CSNK2B, GPC3, RPS19, VTN, FGFBP1, SDC3, FGFR1, GPC4, RPL6, THBS1, CRYAB, PRMT1, TUBG1, TMEFF1, IFI16, COMT, FGFR2, PRKACA, CD44, TES | FREM3 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for FGF2_FREM3 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | FGF2 | P09038 | DB00364 | Sucralfate | Fibroblast growth factor 2 | small molecule | approved |
Hgene | FGF2 | P09038 | DB00686 | Pentosan Polysulfate | Fibroblast growth factor 2 | small molecule | approved |
Hgene | FGF2 | P09038 | DB00877 | Sirolimus | Fibroblast growth factor 2 | small molecule | approved|investigational |
Hgene | FGF2 | P09038 | DB01109 | Heparin | Fibroblast growth factor 2 | small molecule | approved|investigational |
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RelatedDiseases for FGF2_FREM3 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | FGF2 | C0525045 | Mood Disorders | 3 | PSYGENET |
Hgene | FGF2 | C0151744 | Myocardial Ischemia | 2 | CTD_human |
Hgene | FGF2 | C0008924 | Cleft Lip | 1 | CTD_human |
Hgene | FGF2 | C0008925 | Cleft Palate | 1 | CTD_human |
Hgene | FGF2 | C0011581 | Depressive disorder | 1 | CTD_human |
Hgene | FGF2 | C0014549 | Tonic-Clonic Epilepsy | 1 | CTD_human |
Hgene | FGF2 | C0017638 | Glioma | 1 | CTD_human |
Hgene | FGF2 | C0017639 | Gliosis | 1 | CTD_human |
Hgene | FGF2 | C0018800 | Cardiomegaly | 1 | CTD_human |
Hgene | FGF2 | C0019284 | Diaphragmatic Hernia | 1 | CTD_human |
Hgene | FGF2 | C0021368 | Inflammation | 1 | CTD_human |
Hgene | FGF2 | C0022658 | Kidney Diseases | 1 | CTD_human |
Hgene | FGF2 | C0023890 | Liver Cirrhosis | 1 | CTD_human |
Hgene | FGF2 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Hgene | FGF2 | C0025500 | Mesothelioma | 1 | CTD_human |
Hgene | FGF2 | C0027726 | Nephrotic Syndrome | 1 | CTD_human |
Hgene | FGF2 | C0027746 | Nerve Degeneration | 1 | CTD_human |
Hgene | FGF2 | C0029172 | Oral Submucous Fibrosis | 1 | CTD_human |
Hgene | FGF2 | C0031030 | Periapical Periodontitis | 1 | CTD_human |
Hgene | FGF2 | C0033054 | Prenatal Exposure Delayed Effects | 1 | CTD_human |
Hgene | FGF2 | C0033578 | Prostatic Neoplasms | 1 | CTD_human |
Hgene | FGF2 | C0034069 | Pulmonary Fibrosis | 1 | CTD_human |
Hgene | FGF2 | C0035126 | Reperfusion Injury | 1 | CTD_human |
Hgene | FGF2 | C0036341 | Schizophrenia | 1 | PSYGENET |
Hgene | FGF2 | C0036572 | Seizures | 1 | CTD_human |
Hgene | FGF2 | C0040028 | Thrombocythemia, Essential | 1 | CTD_human |
Hgene | FGF2 | C0085109 | Corneal Neovascularization | 1 | CTD_human |
Hgene | FGF2 | C0085207 | Gestational Diabetes | 1 | CTD_human |
Hgene | FGF2 | C0236736 | Cocaine-Related Disorders | 1 | CTD_human |
Hgene | FGF2 | C0751955 | Brain Infarction | 1 | CTD_human |
Tgene | FREM3 | C1269683 | Major Depressive Disorder | 2 | CTD_human;PSYGENET |
Tgene | FREM3 | C0041696 | Unipolar Depression | 1 | PSYGENET |