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Protein-coding gene in the species Homo sapiens

PARD6A

PARD6A
All data from the card 18
Aliases
PARD6A, PAR-6A, PAR6, PAR6C, PAR6alpha, TAX40, TIP-40, par-6 family cell polarity regulator alpha
External IDs
OMIM: 607484; MGI: 1927223; GeneCards: PARD6A
PDB
Ortholog search: PDBe RCSB
Chr.
Chromosome 16 (human)
Band
16q22.1
End
67,662,774 bp
Chr.
Chromosome 8 (mouse)
Band
8|8 D3
End
106,430,128 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
50855
Ensembl
ENSG00000102981
UniProt
Q9NPB6
RefSeq (mRNA)
NM_001037281NM_016948
RefSeq (protein)
NP_001032358NP_058644
Location (UCSC)
Chr 16: 67.66 – 67.66 Mb

Partitioning defective 6 homolog alpha is a protein that in humans is encoded by the PARD6A gene.

Function

This gene is a member of the PAR6 family and encodes a protein with a PSD95/Discs-large/ZO1 (PDZ) domain and a semi-Cdc42/Rac interactive binding (CRIB) domain. This cell membrane protein is involved in asymmetrical cell division and cell polarization processes as a member of a multi-protein complex. The protein also has a role in the epithelial-to-mesenchymal transition (EMT) that characterizes the invasive phenotype associated with metastatic carcinomas. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

A recent study shows that Par6 associates with PKC-ι but not with PKC-zeta in melanoma. Oncogenic PKC-iota can promote melanoma cell invasion by up-regulating PKC-ι/Par6 pathway during EMT. PKC-ι inhibition or knockdown resulted an increase E-cadherin and RhoA levels while decreasing total Vimentin, phophorylated Vimentin (S39) and Par6 in metastatic melanoma cells. These results suggested that PKC-ι is involved in signaling pathways which upregulate EMT in melanoma.

Interactions

PARD6A has been shown to interact with:

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Text from Wikipedia, CC BY-SA 4.0 · Source article