View RAI1 gene homepage

General information
Gene symbol RAI1
Gene name retinoic acid induced 1
Chromosome 17
Chromosomal band p11.2
Imprinted Unknown
Genomic reference NG_007101.2
Transcript reference NM_030665.3
Exon/intron information NM_030665.3
Associated with diseases ID, SMS
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 15
Unique public DNA variants reported 13
Individuals with public variants 15
Hidden variants 0
Notes Establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created May 01, 2012
Date last updated October 24, 2015
Version RAI1:151024

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
Homepage URL
HGNC 9834
Entrez Gene 10743
PubMed articles RAI1
OMIM - Gene 607642
OMIM - Diseases SMS (Smith-Magenis syndrome (SMS))
GeneCards RAI1
GeneTests RAI1

Active transcripts




NCBI ID     

NCBI Protein ID     

00000081 17 retinoic acid induced 1 NM_030665.3 NP_109590.3 15

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