FREM2 gene homepage

General information
Gene symbol FREM2
Gene name FRAS1 related extracellular matrix protein 2
Chromosome 13
Chromosomal band q13.3
Imprinted Unknown
Genomic reference NG_008125.2
Transcript reference NM_207361.4
Exon/intron information NM_207361.4 exon/intron table
Associated with diseases Fraser, ID
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 145
Unique public DNA variants reported 138
Individuals with public variants 3
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 August 28, 2017
Version FREM2:170828

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_207361.4.
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 https://www.LOVD.nl/FREM2
HGNC 25396
Entrez Gene 341640
PubMed articles FREM2
OMIM - Gene 608945
OMIM - Diseases Fraser (Fraser syndrome)
HGMD FREM2
GeneCards FREM2
GeneTests FREM2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00008132 13 FRAS1 related extracellular matrix protein 2 NM_207361.4 NP_997244.3 145


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