The MCF2 gene homepage

General information
Gene symbol MCF2
Gene name MCF.2 cell line derived transforming sequence
Chromosome X
Chromosomal band q26.3-q27.1
Imprinted Not imprinted
Genomic reference NG_016439.1
Transcript reference NM_005369.4
Exon/intron information NM_005369.4 exon/intron table
Associated with diseases -
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 54
Unique public DNA variants reported 39
Individuals with public variants 127
Hidden variants 5
Download all this gene's data Download all data
Notes This gene sequence variant databasehas been initiated based on the data reported by Tarpey et al. (2009) A systematic, large-scale resequencing screen of the X-chromosome coding exons in mental retardation. Nat.Genet. 41: 535-543. Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created March 06, 2009
Date last updated September 17, 2021
Version MCF2:210917

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_005369.4.
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 http://www.LOVD.nl/MCF2
HGNC 6940
Entrez Gene 4168
PubMed articles MCF2
OMIM - Gene 311030
HGMD MCF2
GeneCards MCF2
GeneTests MCF2
Orphanet MCF2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000372 X transcript variant 2 NM_005369.4 NP_005360.3 54


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