Variant #0000164567 (NC_000007.13:g.144098161del, NM_001080413.3:c.822del (NOBOX))
Chromosome |
7 |
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.144098161del |
DNA change (hg38) |
g.144401068del |
Published as |
- |
ISCN |
- |
DB-ID |
NOBOX_000001 See all 2 reported entries |
Variant remarks |
cDNA expression cloning in 293FT cells showed normal protein expression (truncated), reduced (0.2) GDF9 promoter activation and reduced gene expression activation of CPSF4L, MYOT, RFPL4A, UNC13C, GDF9, NLRP14 and RSPO2 |
Reference |
PubMed: Li 2017 |
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 |
2017-03-24 15:25:24 +01:00 (CET) |
Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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