View STIL gene homepage

General information
Gene symbol STIL
Gene name SCL/TAL1 interrupting locus
Chromosome 1
Chromosomal band p32
Imprinted Unknown
Genomic reference NG_012126.1
Transcript reference NM_001048166.1
Exon/intron information NM_001048166.1
Associated with diseases ID, MCPH-7
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 2
Unique public DNA variants reported 2
Individuals with public variants 2
Hidden variants 0
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 November 28, 2016
Version STIL:161128

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 http://www.LOVD.nl/STIL
HGNC 10879
Entrez Gene 6491
PubMed articles STIL
OMIM - Gene 181590
OMIM - Diseases MCPH-7 (microcephaly, type 7, autosomal recessive (MCPH-7))
HGMD STIL
GeneCards STIL
GeneTests STIL


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024204 1 transcript variant 1 NM_001048166.1 NP_001041631.1 2


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