The GCM2 gene homepage

General information
Gene symbol GCM2
Gene name glial cells missing homolog 2 (Drosophila)
Chromosome 6
Chromosomal band p24.2
Imprinted Unknown
Genomic reference NG_008970.1
Transcript reference NM_004752.3
Exon/intron information NM_004752.3 exon/intron table
Associated with diseases FIH1, FIH2, HRPT4
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 1
Hidden variants 0
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 November 01, 2022
Version GCM2:221101

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_004752.3.
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 http://www.LOVD.nl/GCM2
HGNC 4198
Entrez Gene 9247
PubMed articles GCM2
OMIM - Gene 603716
OMIM - Diseases FIH1 (hypoparathyroidism, familial isolated, type 1 (FIH))
FIH2 (Hypoparathyroidism, familial isolated 2)
HRPT4 (Hyperparathyroidism 4)
HGMD GCM2
GeneCards GCM2
GeneTests GCM2
Orphanet GCM2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00008414 6 glial cells missing homolog 2 (Drosophila) NM_004752.3 NP_004743.1 7


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