Genomic Map
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Target Gene Details
Entrez Gene ID: | 4155 |
Gene Name: | myelin basic protein |
Gene Aliases: |
- |
Location: |
Chr.18:76978833-77133708 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MBP | NM_001025081.1 | NP_001020252.1 | ||
| NM_001025090.1 | NP_001020261.1 | |||
| NM_001025092.1 | NP_001020263.1 | |||
| NM_001025101.1 | NP_001020272.1 | |||
| NM_002385.2 | NP_002376.1 | |||
| XM_011526009.2 | XP_011524311.1 | |||
| AK098402.1 | ||||
| AK128770.1 | ||||
| AK128788.1 | ||||
| AK289893.1 | ||||
| AK293922.1 | ||||
| AK296492.1 | ||||
| AK314553.1 | ||||
| BC008749.2 | ||||
| BC080654.1 | AAH80654.1 | |||
| BC101771.1 | ||||
| BC101773.1 | ||||
| BC143348.1 | ||||
| BC143350.1 | ||||
| BG766942.1 | ||||
| CB153535.1 | ||||
| CB156561.1 | ||||
| CR536534.1 | CAG38771.1 | |||
| CR541919.1 | CAG46717.1 | |||
| CR627018.1 | CAH10359.1 | |||
| M13577.1 | AAA59562.1 | |||
| M30047.1 | AAA59559.1 | |||
| M30515.1 | AAA59564.1 | |||
| M30516.1 | AAA59563.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2717388 | Chr.18:76288671 - 78160297 on Build GRCh38 | Deletion |
 LINC00908
LOC400661
GALR1
LOC101927651
ZNF516
LOC100131655
MBP
LOC101927989
LINC00683
C18orf65
LOC107987260
LINC01029
ZNF236
|
| nsv526525 | Chr.18:76992319 - 76993271 on Build GRCh38 | Loss |
MBP
|
| esv3643197 | Chr.18:76911767 - 77002929 on Build GRCh38 | Loss |
MBP
ZNF236
|
| nsv1063632 | Chr.18:76317786 - 77170410 on Build GRCh38 | Gain |
LINC00908
ZNF516
LOC100131655
LOC400661
MBP
LOC101927989
LINC00683
LOC101927651
C18orf65
LOC107987260
ZNF236
|
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Additional Information:
For this assay, SNP(s) [rs80192240] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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