The SMO gene homepage

General information
Gene symbol SMO
Gene name smoothened, frizzled family receptor
Chromosome 7
Chromosomal band q32.1
Imprinted Unknown
Genomic reference NG_023340.1
Transcript reference NM_005631.4
Exon/intron information NM_005631.4 exon/intron table
Associated with diseases BCC1, CRJS, PHLS
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 53
Unique public DNA variants reported 36
Individuals with public variants 282
Hidden variants 1
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 April 19, 2024
Version SMO:240419

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_005631.4.
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/SMO
HGNC 11119
Entrez Gene 6608
PubMed articles SMO
OMIM - Gene 601500
OMIM - Diseases BCC1 (carcinoma, basal cell, susceptibility to, type 1 (BCC-1))
CRJS (Curry-Jones syndrome, somatic mosaic (CRJS))
PHLS (Pallister-Hall-like syndrome)
HGMD SMO
GeneCards SMO
GeneTests SMO
Orphanet SMO


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019464 7 smoothened, frizzled family receptor NM_005631.4 NP_005622.1 53


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