Genomic Map
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Target Gene Details
Entrez Gene ID: | 64750 |
Gene Name: | SMAD specific E3 ubiquitin protein ligase 2 |
Gene Aliases: |
- |
Location: |
Chr.17:64542282-64662268 on Build GRCh38 |
Assay Gene Location: | Within Intron 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SMURF2 | NM_022739.3 | NP_073576.1 | ||
| XM_005257585.3 | XP_005257642.1 | |||
| XM_011525128.1 | XP_011523430.1 | |||
| AF301463.1 | AAG25641.1 | |||
| AF310676.1 | AAG45422.1 | |||
| AY014180.1 | AAG50421.1 | |||
| BC093876.1 | AAH93876.1 | |||
| BC111945.1 | AAI11946.1 | |||
| CR936721.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1066765 | Chr.17:64520760 - 65128185 on Build GRCh38 | Gain |
 MIR4315-2
LOC146880
PLEKHM1P1
AMZ2P1
GNA13
MIR6080
LOC100507002
CEP95
SMURF2
LRRC37A3
|
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Additional Information:
For this assay, SNP(s) [rs77357262] 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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