The SH3GL1 gene homepage

General information
Gene symbol SH3GL1
Gene name SH3-domain GRB2-like 1
Chromosome 19
Chromosomal band p13.3
Imprinted Unknown
Genomic reference NG_028084.1
Transcript reference NM_003025.3
Exon/intron information NM_003025.3 exon/intron table
Associated with diseases AML
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 2
Unique public DNA variants reported 2
Individuals with public variants 1
Hidden variants -
Download all this gene's data Download all data
Notes This database was established with financial support of the Leiden University Medical Center (LUMC).
Date created May 03, 2013
Date last updated July 15, 2020
Version SH3GL1:200715

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_003025.3.
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/SH3GL1
HGNC 10830
Entrez Gene 6455
PubMed articles SH3GL1
OMIM - Gene 601768
OMIM - Diseases AML (leukemia, myeloid, acute (AML))
HGMD SH3GL1
GeneCards SH3GL1
GeneTests SH3GL1
Orphanet SH3GL1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00018846 19 transcript variant 1 NM_003025.3 NP_003016.1 2


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