Genomic Map
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Target Gene Details
Entrez Gene ID: | 682 |
Gene Name: | basigin (Ok blood group) |
Gene Aliases: |
5F7, CD147, EMMPRIN, OK, TCSF |
Location: |
Chr.19:571277-583493 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BSG | NM_001322243.1 | NP_001309172.1 | ||
| NM_001728.3 | NP_001719.2 | |||
| NM_198589.2 | NP_940991.1 | |||
| NM_198590.2 | NP_940992.1 | |||
| NM_198591.2 | NP_940993.1 | |||
| XM_017027173.1 | XP_016882662.1 | |||
| AB072923.1 | BAB88938.1 | |||
| AB085790.1 | BAC76828.1 | |||
| AB091680.1 | BAC67168.1 | |||
| AF548371.1 | AAN40694.1 | |||
| AK296858.1 | ||||
| AK297880.1 | ||||
| AK302231.1 | ||||
| AY358113.1 | AAQ88480.1 | |||
| BC009040.2 | AAH09040.1 | |||
| BG480530.1 | ||||
| BI464857.1 | ||||
| CB153773.1 | ||||
| D45131.1 | BAA08109.1 | |||
| DA007913.1 | ||||
| GU557064.1 | ||||
| GU557065.1 | ||||
| L10240.1 | AAA68936.1 | |||
| L20471.1 | AAB41120.1 | |||
| M87879.1 | AAA91084.1 | |||
| X64364.1 | CAA45716.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv428360 | Chr.19:232069 - 702131 on Build GRCh38 | Gain |
 TPGS1
C2CD4C
HCN2
ODF3L2
MIER2
CDC34
MADCAM1
PLPP2
SHC2
THEG
PRSS57
FSTL3
POLRMT
FGF22
BSG
RNF126
LOC101929060
GZMM
|
| esv3643355 | Chr.19:572192 - 582084 on Build GRCh38 | Gain |
BSG
|
| nsv577978 | Chr.19:294526 - 782854 on Build GRCh38 | Gain |
TPGS1
C2CD4C
PALM
HCN2
ODF3L2
LOC101928450
MIER2
CDC34
MADCAM1
MISP
SHC2
THEG
PRSS57
FSTL3
POLRMT
FGF22
BSG
RNF126
LOC101929060
GZMM
|
| nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
TPGS1
C2CD4C
ODF3L2
RNU6-9
THEG
R3HDM4
KISS1R
GPX4
LOC105372235
ARHGAP45
FGF22
PLPPR3
GZMM
TMEM259
MED16
PALM
HCN2
WDR18
POLR2E
AZU1
LOC101928450
GRIN3B
CDC34
MADCAM1
MIR3187
MISP
SHC2
PRTN3
CFD
ELANE
ARID3A
PRSS57
FSTL3
POLRMT
CNN2
BSG
RNF126
RNU6-2
PTBP1
ABCA7
MIR4745
|
| nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss |
TPGS1
C2CD4C
ODF3L2
RNU6-9
R3HDM4
KISS1R
LOC105372235
FGF22
PLPPR3
GZMM
MED16
PALM
HCN2
WDR18
AZU1
LOC101928450
GRIN3B
CDC34
MADCAM1
MIR3187
MISP
SHC2
PRTN3
CFD
ELANE
ARID3A
PRSS57
FSTL3
POLRMT
BSG
RNF126
PTBP1
MIR4745
|
| nsv578152 | Chr.19:572860 - 583812 on Build GRCh38 | Gain |
BSG
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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