The ATP6V1A gene homepage

General information
Gene symbol ATP6V1A
Gene name ATPase, H+ transporting, lysosomal 70kDa, V1 subunit A
Chromosome 3
Chromosomal band q13.31
Imprinted Unknown
Genomic reference NG_047012.1
Transcript reference NM_001690.3
Exon/intron information NM_001690.3 exon/intron table
Associated with diseases ARCL2D, EICEE3
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 15
Unique public DNA variants reported 14
Individuals with public variants 7
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated April 19, 2024
Version ATP6V1A:240419

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001690.3.
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
Homepage URL https://www.LOVD.nl/ATP6V1A
HGNC 851
Entrez Gene 523
PubMed articles ATP6V1A
OMIM - Gene 607027
OMIM - Diseases ARCL2D (cutis laxa, autosomal recessive, type IID (ARCL2D))
EICEE3 (encephalopathy, epileptic, infantile or early childhood, type 42 (EICEE3))
HGMD ATP6V1A
GeneCards ATP6V1A
GeneTests ATP6V1A
Orphanet ATP6V1A


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00003100 3 ATPase, H+ transporting, lysosomal 70kDa, V1 subunit A NM_001690.3 NP_001681.2 15


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