Gene data
NPAS3- Name
- neuronal PAS domain protein 3
- Type
- protein-coding
- Position
- 32,934,396–33,820,863 (+)
- Aliases
- MOP6, PASD6, bHLHe12
- Ensembl
- ENSG00000151322
- RefSeq RNA
- NM_001164749.2, NM_001165893.2, NM_001394988.1, NM_001394989.1, NM_022123.3
- RefSeq protein
- NP_001158221.1, NP_001159365.1, NP_001381917.1, NP_001381918.1, NP_071406.1
This gene encodes a member of the basic helix-loop-helix and PAS domain-containing family of transcription factors. The encoded protein is localized to the nucleus and may regulate genes involved in neurogenesis. Chromosomal abnormalities that affect the coding potential of this gene are associated with schizophrenia and cognitive disability. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009].
Gene Ontology
Biological process
Molecular function
Cellular component
via MyGene.info
Gene · Ensembl
neuronal PAS domain protein 3
- Symbol
- NPAS3
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 14:32,934,396-33,820,863
- Strand
- Forward (+)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 9 more facts
- HomoloGene ID
- 8461
- exact match
- identifiers.org/ncbigene/64067
- genetic association
- schizophrenia
- found in taxon
- Homo sapiens
- genomic end
- 33820863
- genomic start
- 32934396
- chromosome
- human chromosome 14
- cytogenetic location
- 14q13.1
- expressed in
- entorhinal cortex
via Wikidata · CC0