Genomic Map
Back To TopAssay 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 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MAG | NM_001199216.1 | 5 | 685 | NP_001186145.1 |
| NM_002361.3 | 5 | 698 | NP_002352.1 | |
| NM_080600.2 | 5 | 698 | NP_542167.1 | |
| AK094545.1 | 6 | 544 | ||
| AK222649.1 | 5 | 623 | BAD96369.1 | |
| AK222680.1 | 5 | 601 | BAD96400.1 | |
| AK223562.1 | 5 | 659 | BAD97282.1 | |
| AK294644.1 | 5 | 592 | ||
| AK308976.1 | 5 | 610 | ||
| BC053347.1 | 5 | 590 | AAH53347.1 | |
| BC093045.1 | 5 | 650 | AAH93045.1 | |
| BI755065.1 | 5 | 648 | ||
| M29273.1 | 5 | 620 | 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 |
 CD22
MIR5196
FFAR1
LINC01531
FFAR2
MAG
FFAR3
|
| esv2758758 | Chr.19:35220175 - 35396211 on Build GRCh38 | Loss |
USF2
CD22
MIR5196
FFAR1
LSR
HAMP
FAM187B
MAG
FFAR3
|
| nsv953283 | Chr.19:35247998 - 35314097 on Build GRCh38 | Deletion |
USF2
LSR
HAMP
MAG
|
| nsv510765 | Chr.19:35217323 - 35399766 on Build GRCh38 | Deletion |
USF2
CD22
MIR5196
FFAR1
LSR
HAMP
FAM187B
MAG
FFAR3
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top