Assay Details
Target Gene Details
| Entrez Gene ID: | 113655 | 
| Gene Name: | major facilitator superfamily domain containing 3 | 
| Gene Aliases: | - | 
| Location: | Chr.8:144508081-144511228 on Build GRCh38 | 
| Assay Gene Location: | Overlaps Intron 3 - Exon 4 | 
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID | 
|---|---|---|---|---|
| MFSD3 | NM_138431.2 | NP_612440.1 | ||
| NR_130120.1 | ||||
| XM_011516806.2 | XP_011515108.1 | |||
| XM_017013005.1 | XP_016868494.1 | |||
| BC011982.1 | AAH11982.1 | |||
| BF688676.1 | ||||
| DB520468.1 | 
Target Copy Number Variation Details
| DGV Version: | Release date: 2016-05-15, GRCh GRCh38 | 
| Target Variation | Location | CNV Subtype | Genes | 
|---|---|---|---|
| nsv470249 | Chr.8:143889098 - 144519234 on Build GRCh38 | Loss |  BOP1  ADCK5  LOC101928953  MFSD3  HSF1  HGH1  RECQL4  MIR6848  MIR939  MIR6846  MIR6847  OPLAH  SPATC1  SMPD5  FBXL6  MROH1  SCRT1  PPP1R16A  TMEM249  LRRC14  DGAT1  MIR661  EXOSC4  MIR1234  MIR6893  WDR97  CPSF1  LOC101928902  PARP10  FOXH1  PLEC  GRINA  MAF1  TONSL  MIR6849  CYHR1  TONSL-AS1  SLC39A4  CYC1  SCX  MIR7112  VPS28  GPT  KIFC2  SLC52A2  SHARPIN  GPAA1 | 
| nsv612951 | Chr.8:144479830 - 144677692 on Build GRCh38 | Loss |  LOC101928953  MFSD3  RECQL4  LRRC24  PPP1R16A  LRRC14  GPT  ARHGAP39  C8orf82 | 
| nsv831489 | Chr.8:144342140 - 144544026 on Build GRCh38 | Loss |  ADCK5  LOC101928953  MFSD3  RECQL4  MIR939  LRRC24  C8orf82  FBXL6  PPP1R16A  TMEM249  LRRC14  ARHGAP39  MIR1234  MIR6893  CPSF1  LOC101928902  FOXH1  TONSL  MIR6849  CYHR1  TONSL-AS1  SLC39A4  VPS28  GPT  KIFC2  SLC52A2 | 
| dgv1207n67 | Chr.8:144498396 - 144532417 on Build GRCh38 | Gain |  LOC101928953  MFSD3  RECQL4  LRRC24  PPP1R16A  LRRC14  GPT  ARHGAP39  C8orf82 | 
| dgv12439n54 | Chr.8:144438306 - 144525122 on Build GRCh38 | Loss |  FOXH1  LOC101928953  MFSD3  RECQL4  LRRC24  PPP1R16A  LRRC14  GPT  KIFC2  TONSL  CYHR1  TONSL-AS1 | 
| nsv612962 | Chr.8:144504742 - 144511458 on Build GRCh38 | Loss |  LOC101928953  MFSD3  RECQL4  GPT | 
| dgv907n27 | Chr.8:144416180 - 144525122 on Build GRCh38 | Loss |  FOXH1  LOC101928953  MFSD3  RECQL4  LRRC24  TONSL  CYHR1  TONSL-AS1  SLC39A4  VPS28  PPP1R16A  LRRC14  GPT  KIFC2  MIR6893 | 
| dgv12442n54 | Chr.8:144492696 - 144516381 on Build GRCh38 | Loss |  LOC101928953  MFSD3  RECQL4  PPP1R16A  GPT | 
| dgv12434n54 | Chr.8:144270080 - 144516801 on Build GRCh38 | Loss |  BOP1  ADCK5  LOC101928953  MFSD3  HSF1  RECQL4  MIR6848  MIR939  FBXL6  SCRT1  PPP1R16A  TMEM249  DGAT1  MIR1234  MIR6893  CPSF1  LOC101928902  FOXH1  TONSL  MIR6849  CYHR1  TONSL-AS1  SLC39A4  VPS28  GPT  KIFC2  SLC52A2 | 
| dgv12443n54 | Chr.8:144502322 - 144518490 on Build GRCh38 | Loss |  LOC101928953  MFSD3  RECQL4  LRRC14  GPT | 
| nsv515809 | Chr.8:143904439 - 144519234 on Build GRCh38 | Gain+Loss |  BOP1  ADCK5  LOC101928953  MFSD3  HSF1  HGH1  RECQL4  MIR6848  MIR939  MIR6846  MIR6847  OPLAH  SPATC1  SMPD5  FBXL6  MROH1  SCRT1  PPP1R16A  TMEM249  LRRC14  DGAT1  MIR661  EXOSC4  MIR1234  MIR6893  WDR97  CPSF1  LOC101928902  PARP10  FOXH1  PLEC  GRINA  MAF1  TONSL  MIR6849  CYHR1  TONSL-AS1  SLC39A4  CYC1  SCX  MIR7112  VPS28  GPT  KIFC2  SLC52A2  SHARPIN  GPAA1 | 
| nsv612940 | Chr.8:144436292 - 144613673 on Build GRCh38 | Loss |  FOXH1  LOC101928953  MFSD3  RECQL4  LRRC24  TONSL  C8orf82  CYHR1  TONSL-AS1  PPP1R16A  LRRC14  GPT  KIFC2  ARHGAP39 | 
| nsv428208 | Chr.8:144041826 - 144722291 on Build GRCh38 | Gain |  BOP1  ADCK5  LOC101928953  MFSD3  HSF1  HGH1  RECQL4  MIR6848  MIR939  MIR6846  LRRC24  MIR6847  ZNF251  C8orf82  OPLAH  SPATC1  SMPD5  FBXL6  MROH1  SCRT1  PPP1R16A  TMEM249  LRRC14  DGAT1  ARHGAP39  EXOSC4  MIR1234  MIR6893  WDR97  CPSF1  LOC101928902  FOXH1  MAF1  TONSL  MIR6849  CYHR1  TONSL-AS1  SLC39A4  CYC1  SCX  MIR7112  VPS28  GPT  KIFC2  SLC52A2  SHARPIN  GPAA1 | 
| esv29999 | Chr.8:144456732 - 144525122 on Build GRCh38 | Loss |  FOXH1  LOC101928953  MFSD3  RECQL4  LRRC24  PPP1R16A  LRRC14  GPT  KIFC2  CYHR1 | 
| nsv612965 | Chr.8:144508945 - 144516381 on Build GRCh38 | Loss |  MFSD3  RECQL4 | 
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| Set Membership: |  Intragenic  Non-exonic  DGV Variation | 
Panther Classification:
Gene Ontology Categories:
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