Version: 7.5.0
Date: Fri Dec 13 2024
All
All
Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Home
Data and Tools
Downloads
API
AllianceMine
JBrowse 2
Submit Data
Textpresso
Tools and Prototypes
COVID-19 Information
Members
FlyBase
Mouse Genome Database
Rat Genome Database
Saccharomyces Genome Database
WormBase
Xenbase
Zebrafish Information Network
Gene Ontology Consortium
News
News and Events
Release Notes
Event Calendar
About
About Us
Funding
Publications
Organization and Governance
Privacy, Warranty, Licensing, and Data Preservation Commitment
Working Groups
Help
FAQ / Known Issues
Glossary
Tutorials
User Documentation
Community
Alliance User Community
Mastodon
Bluesky
Contact Us
Cite Us
sa43578
ZFIN:ZDB-ALT-160601-9104
Allele of
ccng2
Danio rerio
Summary
Transgenic Constructs
Genomic Variant Information
Variant Molecular Consequences
Phenotypes
Disease Associations
Allele/Variant
sa43578
Species
Danio rerio
Symbol
sa43578
Category
allele
Allele of gene
ccng2
Transgenic Constructs
None
Synonyms
None
Description
Not Available
Additional Information
Literature
Transgenic Constructs
No data available
Genomic Variant Information
NC_007132.7:g.5802833G>A
Symbol
NC_007132.7:g.5802833G>A
Category
Variant
Variant type
point mutation
Overlaps
ccng2
Location
21:5802833
Nucleotide Change
G>A
Most Severe Consequence
splice donor variant
See all consequences
HGVS.g name
NC_007132.7:g.5802833G>A
(GRCz11)21:5802833G>A
Show All 3
HGVS.c name
ENSEMBL:ENSDART00000020603.1:c.573+1G>A
ENSEMBL:ENSDART00000151225.1:c.573+1G>A
Show All 5
HGVS.p name
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
ZFIN:ZDB-PUB-130425-4
All alleles with this variant
Download Variants Data
Genome location
Chr21:5800306...5807559
(7.25 kb)
Assembly version
GRCz11
Viewer Help
5.801M
5.802M
5.803M
5.804M
5.805M
5.806M
5.807M
Variant Types and Consequences
Only variants associated to alleles are shown in the graphics above. See all variants in
JBrowse
.
Variant Molecular Consequences
Predicted effect of NC_007132.7:g.5802833G>A
Variant
NC_007132.7:g.5802833G>A
Variant type:
point_mutation
Show all details
Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
No records match query. Try removing filters.
Showing 0 - 0 of 0 rows
10
10
25
100
per page
Phenotypes
No data available
Disease Associations
No data available
You need to enable JavaScript to run this app.