Assay Details
Target Gene Details
Entrez Gene ID: | 4099 |
Gene Name: | myelin associated glycoprotein |
Gene Aliases: |
GMA, S-MAG, SIGLEC-4A, SIGLEC4A, SPG75 |
Location: |
Chr.19:35292086-35313807 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MAG | NM_001199216.1 | NP_001186145.1 | ||
NM_002361.3 | NP_002352.1 | |||
NM_080600.2 | NP_542167.1 | |||
AK094545.1 | ||||
AK222649.1 | BAD96369.1 | |||
AK222680.1 | BAD96400.1 | |||
AK223562.1 | BAD97282.1 | |||
AK294644.1 | ||||
AK308976.1 | ||||
BC053347.1 | AAH53347.1 | |||
BC093045.1 | AAH93045.1 | |||
M29273.1 | AAA59545.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833810 | Chr.19:35291685 - 35481057 on Build GRCh38 | Gain | MIR5196 FFAR2 CD22 FFAR3 FFAR1 MAG LINC01531 |
esv2758758 | Chr.19:35220175 - 35396211 on Build GRCh38 | Loss | USF2 MIR5196 HAMP CD22 FFAR3 FAM187B FFAR1 MAG LSR |
nsv953283 | Chr.19:35247998 - 35314097 on Build GRCh38 | Deletion | USF2 HAMP MAG LSR |
nsv510765 | Chr.19:35217323 - 35399766 on Build GRCh38 | Deletion | USF2 MIR5196 HAMP CD22 FFAR3 FAM187B FFAR1 MAG LSR |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |