PARD3
Sign in to saveAlso known as ASIP, Baz, PAR3, PAR3alpha, PARD-3, PARD3A, PPP1R118, SE2-5L16
Partitioning defective 3 homolog is a protein that in humans is encoded by the PARD3 gene.
Gene data
PARD3- Name
- par-3 family cell polarity regulator
- Type
- protein-coding
- Position
- 34,109,560–34,815,419 (−)
- Aliases
- ASIP, Baz, PAR3, PAR3alpha, PARD-3, PARD3A, PPP1R118, SE2-5L16, SE2-5LT1, SE2-5T2
- Ensembl
- ENSG00000148498
- RefSeq RNA
- NM_001184785.2, NM_001184786.2, NM_001184787.2, NM_001184788.2, NM_001184789.2
- RefSeq protein
- NP_001171714.1, NP_001171715.1, NP_001171716.1, NP_001171717.1, NP_001171718.1
This gene encodes a member of the PARD protein family. PARD family members interact with other PARD family members and other proteins; they affect asymmetrical cell division and direct polarized cell growth. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
par-3 family cell polarity regulator
- Symbol
- PARD3
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 10:34,109,560-34,815,424
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Image
- Protein PARD3 PDB 2KOM.png
Show 5 more facts
- HomoloGene ID
- 10489
- exact match
- identifiers.org/ncbigene/56288
- genomic end
- 35104253
- genomic start
- 34398488
- cytogenetic location
- 10p11.22-p11.21
via Wikidata · CC0
~1 min read
Article
4 sectionsContents
- Function
- Interactions
- References
- Further reading
Partitioning defective 3 homolog is a protein that in humans is encoded by the PARD3 gene.
== Function ==