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 Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MAG | NM_001199216.1 | 6 | 960 | NP_001186145.1 |
NM_002361.3 | 6 | 973 | NP_002352.1 | |
NM_080600.2 | 6 | 973 | NP_542167.1 | |
AK094545.1 | 7 | 819 | ||
AK222649.1 | 6 | 898 | BAD96369.1 | |
AK222680.1 | 6 | 876 | BAD96400.1 | |
AK223562.1 | 6 | 934 | BAD97282.1 | |
AK294644.1 | 6 | 867 | ||
AK308976.1 | 6 | 885 | ||
BC053347.1 | 6 | 865 | AAH53347.1 | |
BC093045.1 | 6 | 925 | AAH93045.1 | |
M29273.1 | 6 | 895 | 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 | LINC01531 FFAR1 CD22 FFAR2 MIR5196 MAG FFAR3 |
esv2758758 | Chr.19:35220175 - 35396211 on Build GRCh38 | Loss | FAM187B HAMP FFAR1 USF2 CD22 LSR MIR5196 MAG FFAR3 |
nsv953283 | Chr.19:35247998 - 35314097 on Build GRCh38 | Deletion | HAMP USF2 LSR MAG |
nsv510765 | Chr.19:35217323 - 35399766 on Build GRCh38 | Deletion | FAM187B HAMP FFAR1 USF2 CD22 LSR MIR5196 MAG FFAR3 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |