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See other MFSD7 CNV Assays ›
Gene Symbol
MFSD7
Assay Reference Genome
Location

Chr.4:684532 on build GRCh38
Cytoband
4p16.3
Assay ID Hs02135983_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 84179

Gene Name:

 major facilitator superfamily domain containing 7

Gene Aliases:

 LP2561

Location:

 Chr.4:676205-689468 on Build GRCh38

Assay Gene Location:

 Within Exon 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
MFSD7 NM_001294341.1 6 1108 NP_001281270.1
NM_001294342.1 4 751 NP_001281271.1
NM_032219.3 6 1105 NP_115595.2
XM_005272297.1 4 841 XP_005272354.1
XM_005272299.4 6 1135 XP_005272356.1
XM_006713918.1 6 762 XP_006713981.1
XM_006713919.1 4 844 XP_006713982.1
XM_011513568.1 6 1912 XP_011511870.1
XM_011513571.1 7 932 XP_011511873.1
XM_011513572.1 4 928 XP_011511874.1
XM_011513573.2 6 1135 XP_011511875.1
XM_011513574.1 5 901 XP_011511876.1
XM_011513575.2 5 1680 XP_011511877.1
XM_017008700.1 XP_016864189.1
AK025922.1 4 583 BAB15283.1
AK292010.1 6 1003
AY203936.1 2 454 AAP34459.1
AY358401.1 6 810 AAQ88767.1
BC030246.1 6 848 AAH30246.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv593206 Chr.4:632173 - 741362 on Build GRCh38 Loss MFSD7 MYL5 LOC101928521 PDE6B PCGF3 ATP5I
esv2759217 Chr.4:609419 - 937566 on Build GRCh38 Loss MFSD7 MYL5 CPLX1 LOC101928521 PDE6B PCGF3 LOC100129917 GAK LOC107986211 TMEM175 ATP5I
nsv822425 Chr.4:546316 - 1420011 on Build GRCh38 Loss CPLX1 PDE6B PCGF3 LOC100130872 MFSD7 CRIPAK LOC101928521 MAEA RNF212 NKX1-1 CTBP1-AS LOC107986211 ATP5I SPON2 CTBP1 CTBP1-AS2 MYL5 FGFRL1 UVSSA LOC100129917 GAK TMEM175 DGKQ TMED11P LOC105374344 LOC101928548 SLC26A1 IDUA
nsv829834 Chr.4:671688 - 781736 on Build GRCh38 Loss MFSD7 MYL5 PCGF3 LOC100129917 LOC107986211 ATP5I
nsv950325 Chr.4:620112 - 796912 on Build GRCh38 Deletion MFSD7 MYL5 CPLX1 LOC101928521 PDE6B PCGF3 LOC100129917 LOC107986211 ATP5I
nsv593208 Chr.4:674211 - 688444 on Build GRCh38 Loss MFSD7 MYL5 ATP5I
nsv508986 Chr.4:527899 - 756994 on Build GRCh38 Insertion MFSD7 MYL5 LOC101928521 PDE6B PCGF3 LOC107986211 ATP5I PIGG
nsv10413 Chr.4:673415 - 690512 on Build GRCh38 Gain MFSD7 MYL5 ATP5I

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More Information


Set Membership:

 Intragenic Exonic DGV Variation

Panther Classification:

Molecular Function -

secondary carrier transporter

Gene Ontology Categories:

Function(s)


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