Variant #0000046858 (NC_000022.10:g.36962409C>G, NM_006078.3:c.427G>C (CACNG2))
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.36962409C>G |
DNA change (hg38) |
g.36566362C>G |
Published as |
- |
ISCN |
- |
DB-ID |
CACNG2_000001 See all 2 reported entries |
Variant remarks |
expression cloning in HEK293 cells using coIP shows decreased stargazin binding to GluR1/R2 AMPAR subunits; decreased miniEPSC amplitude and frequency in transfected hippocampal neurons; reduced cell GluR1 surface expression in transfected hippocampal neurons and HEK293 cells |
Reference |
PubMed: Hamdan 2011 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2014-11-14 19:43:27 +01:00 (CET) |
Date last edited |
2020-07-17 12:29:06 +02:00 (CEST) |

Variant on transcripts
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