AFG3L2 gene homepage

General information
Gene symbol AFG3L2
Gene name AFG3 like matrix AAA peptidase subunit 2
Chromosome 18
Chromosomal band p11.21
Imprinted Unknown
Genomic reference NC_000018.9
Transcript reference NM_006796.2
Associated with diseases OPA, SCA
Citation reference(s) -
Curators (1) XY Liu
Total number of public variants reported 4
Unique public DNA variants reported 4
Individuals with public variants 4
Hidden variants 0
Date created June 13, 2017
Date last updated June 23, 2017
Version AFG3L2:170623

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 315
Entrez Gene 10939
PubMed articles AFG3L2
OMIM - Gene 604581
OMIM - Diseases OPA (Optic Atrophy)
SCA (Spinocerebellar Degenerations)
HGMD AFG3L2
GeneCards AFG3L2
GeneTests AFG3L2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000267 18 AFG3-like AAA ATPase 2 NM_006796.2 NP_006787.2 4


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