The NBAS gene homepage

General information
Gene symbol NBAS
Gene name neuroblastoma amplified sequence
Chromosome 2
Chromosomal band p24.3
Imprinted Unknown
Genomic reference NG_032964.1
Transcript reference NM_015909.3
Exon/intron information NM_015909.3 exon/intron table
Associated with diseases LFIT2, SOPH
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 274
Unique public DNA variants reported 189
Individuals with public variants 27
Hidden variants 8
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 February 26, 2024
Version NBAS:240226

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_015909.3.
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 https://www.LOVD.nl/NBAS
HGNC 15625
Entrez Gene 51594
PubMed articles NBAS
OMIM - Gene 608025
OMIM - Diseases LFIT2 (failure, liver, transient, infantile, type 2 (LFIT-2))
SOPH (stature, short, optic nerve atrophy, and pelger-huet anomaly (SOPH))
HGMD NBAS
GeneCards NBAS
GeneTests NBAS
Orphanet NBAS


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00014309 2 transcript variant 1 NM_015909.3 NP_056993.2 274


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