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- Gene Symbol
- VAV2
- Assay Reference Genome
Location
Chr.9:133799380 on build GRCh38- Cytoband
- 9q34.2
Genomic Map
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Target Gene Details
Entrez Gene ID: | 7410 |
Gene Name: | vav guanine nucleotide exchange factor 2 |
Gene Aliases: |
VAV-2 |
Location: |
Chr.9:133761894-133992374 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| VAV2 | NM_001134398.1 | NP_001127870.1 | ||
| NM_003371.3 | NP_003362.2 | |||
| XM_005272213.1 | XP_005272270.1 | |||
| XM_017015108.1 | XP_016870597.1 | |||
| XM_017015109.1 | XP_016870598.1 | |||
| XM_017015110.1 | XP_016870599.1 | |||
| XM_017015111.1 | XP_016870600.1 | |||
| XM_017015112.1 | XP_016870601.1 | |||
| XM_017015113.1 | XP_016870602.1 | |||
| BC132965.1 | ||||
| BC132967.1 | ||||
| BQ050947.1 | ||||
| BX640754.1 | CAE45861.1 | |||
| S76992.1 | AAB34377.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2739138 | Chr.9:132727483 - 135521553 on Build GRCh38 | Deletion |
 FAM163B
MIR3689F
MRPS2
GBGT1
MIR6877
SURF1
MIR3689E
COL5A1-AS1
SNORD141A
AK8
ADAMTS13
SNORD36C
ABO
SURF4
LINC00094
MED22
RPL7A
C9orf116
LOC105376306
SNORD36A
LOC100996574
SLC2A6
COL5A1
LOC401557
LOC101928193
STKLD1
GTF3C5
FCN2
GFI1B
PPP1R26-AS1
MIR3689D1
MIR3689D2
OBP2B
SURF6
SNORD36B
SARDH
LOC101448202
DBH
TSC1
MIR3689A
ADAMTSL2
RALGDS
CELP
MIR4669
C9orf62
VAV2
CACFD1
LCN1
RNU6ATAC
MIR3689C
SNORD24
TMEM8C
DBH-AS1
MIR3689B
SURF2
WDR5
BRD3
REXO4
MIR548AW
RXRA
CEL
LOC100130548
LOC101928525
SPACA9
FCN1
PPP1R26
OLFM1
|
| nsv951802 | Chr.9:133753679 - 133815978 on Build GRCh38 | Deletion |
VAV2
|
| dgv95n68 | Chr.9:133728580 - 133915151 on Build GRCh38 | Loss |
VAV2
SARDH
|
| nsv482984 | Chr.9:133676624 - 133855751 on Build GRCh38 | Gain |
VAV2
SARDH
|
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Additional Information:
For this assay, SNP(s) [rs73663840] 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
|
Gene Ontology Categories:
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