The NOBOX gene homepage

General information
Gene symbol NOBOX
Gene name NOBOX oogenesis homeobox
Chromosome 7
Chromosomal band q35
Imprinted Unknown
Genomic reference NG_028979.1
Transcript reference NM_001080413.3
Exon/intron information NM_001080413.3 exon/intron table
Associated with diseases POF, POF5
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 15
Unique public DNA variants reported 14
Individuals with public variants 11
Hidden variants 0
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 May 09, 2022
Version NOBOX:220509

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_001080413.3.
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
HGNC 22448
Entrez Gene 135935
PubMed articles NOBOX
OMIM - Gene 610934
OMIM - Diseases POF5 (ovarian failure, premature, type 5 (POF5))
GeneCards NOBOX
GeneTests NOBOX
Orphanet NOBOX

Active transcripts




NCBI ID     

NCBI Protein ID     

00014662 7 NOBOX oogenesis homeobox NM_001080413.3 NP_001073882.3 15

Copyright & disclaimer
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