The ITGA7 gene homepage

This database is one of the gene variant databases from the Leiden Muscular Dystrophy pages
General information
Gene symbol ITGA7
Gene name integrin, alpha 7
Chromosome 12
Chromosomal band q13
Imprinted Unknown
Genomic reference NG_012343.1
Transcript reference NM_002206.2
Exon/intron information NM_002206.2 exon/intron table
Associated with diseases dystrophy, muscular, congenital, due to integrin alpha-7 deficiency
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (2) Global Variome, with Curator vacancy and Johan den Dunnen
Total number of public variants reported 99
Unique public DNA variants reported 80
Individuals with public variants 146
Hidden variants 17
Download all this gene's data Download all data
Notes This database is one of the gene variant databases from the:
Date created March 01, 2010
Date last updated November 01, 2021
Version ITGA7:211101

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_002206.2.
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/ITGA7
HGNC 6143
Entrez Gene 3679
PubMed articles ITGA7
OMIM - Gene 600536
OMIM - Diseases dystrophy, muscular, congenital, due to integrin alpha-7 deficiency
HGMD ITGA7
GeneCards ITGA7
GeneTests ITGA7
Orphanet ITGA7


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00010188 12 transcript variant 2 NM_002206.2 NP_002197.2 99


Copyright & disclaimer
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