Genomic Map
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Target Gene Details
Entrez Gene ID: | 128866 |
Gene Name: | charged multivesicular body protein 4B |
Gene Aliases: |
C20orf178, CHMP4A, CTPP3, CTRCT31, SNF7, SNF7-2, Shax1, VPS32B, Vps32-2, dJ553F4.4 |
Location: |
Chr.20:33811304-33854367 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CHMP4B | NM_176812.4 | NP_789782.1 | ||
| AB100261.1 | BAC79375.1 | |||
| AY329085.1 | AAQ91194.1 | |||
| AY726594.1 | ||||
| BC033859.1 | AAH33859.1 | |||
| CT001913.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv585930 | Chr.20:33779897 - 33839036 on Build GRCh38 | Gain |
 CHMP4B
ZNF341-AS1
ZNF341
|
| nsv518926 | Chr.20:33741162 - 33902088 on Build GRCh38 | Gain |
CHMP4B
ZNF341-AS1
ZNF341
|
| nsv833961 | Chr.20:33605380 - 33836992 on Build GRCh38 | Loss |
CBFA2T2
C20orf144
CHMP4B
PXMP4
E2F1
ZNF341-AS1
ZNF341
ACTL10
NECAB3
|
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Additional Information:
For this assay, SNP(s) [rs112613324] 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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