The RAI2 gene homepage

General information
Gene symbol RAI2
Gene name retinoic acid induced 2
Chromosome X
Chromosomal band p22
Imprinted Unknown
Genomic reference NG_016739.1
Transcript reference NM_021785.4
Associated with diseases -
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 14
Unique public DNA variants reported 13
Individuals with public variants 10
Hidden variants 1
Notes This gene sequence variant database has 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 RAI2:210917

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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
HGNC 9835
Entrez Gene 10742
PubMed articles RAI2
OMIM - Gene 300217
HGMD RAI2
GeneCards RAI2
GeneTests RAI2
Orphanet RAI2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001435 X transcript variant 2 NM_021785.4 NP_068557.3 14


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