The TRPM7 gene homepage

General information
Gene symbol TRPM7
Gene name transient receptor potential cation channel, subfamily M, member 7
Chromosome 15
Chromosomal band q21
Imprinted Unknown
Genomic reference NG_021363.1
Transcript reference NM_017672.4
Exon/intron information NM_017672.4 exon/intron table
Associated with diseases sclerosis, lateral, amyotrophic/Parkinsonism/dementia complex 1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 7
Unique public DNA variants reported 7
Individuals with public variants 3
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated April 05, 2022
Version TRPM7:220405

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_017672.4.
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
HGNC 17994
Entrez Gene 54822
PubMed articles TRPM7
OMIM - Gene 605692
OMIM - Diseases sclerosis, lateral, amyotrophic/Parkinsonism/dementia complex 1
GeneCards TRPM7
GeneTests TRPM7
Orphanet TRPM7

Active transcripts




NCBI ID     

NCBI Protein ID     

00021912 15 transient receptor potential cation channel, subfamily M, member 7 NM_017672.4 NP_060142.3 7

Copyright & disclaimer
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