Gene Gene information from NCBI Gene database.
Entrez ID 84552
Gene name Par-6 family cell polarity regulator gamma
Gene symbol PARD6G
Synonyms (NCBI Gene)
PAR-6GPAR6gamma
Chromosome 18
Chromosome location 18q23
miRNA miRNA information provided by mirtarbase database.
331
miRTarBase ID miRNA Experiments Reference
MIRT710384 hsa-miR-4740-3p HITS-CLIP 19536157
MIRT710383 hsa-miR-4524a-3p HITS-CLIP 19536157
MIRT710382 hsa-miR-223-5p HITS-CLIP 19536157
MIRT710381 hsa-miR-4446-5p HITS-CLIP 19536157
MIRT678449 hsa-miR-6814-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 11260256, 14676191, 17057644, 25852190, 28514442, 31980649, 32707033, 33961781
GO:0005634 Component Nucleus IBA
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol TAS
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608976 16076 ENSG00000178184
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BYG4
Protein name Partitioning defective 6 homolog gamma (PAR-6 gamma) (PAR6D)
Protein function Adapter protein involved in asymmetrical cell division and cell polarization processes. May play a role in the formation of epithelial tight junctions. The PARD6-PARD3 complex links GTP-bound Rho small GTPases to atypical protein kinase C protei
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00564 PB1 18 98 PB1 domain Domain
PF00595 PDZ 158 248 PDZ domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed, with a higher expression in fetal and adult kidney.
Sequence
MNRSFHKSQTLRFYDCSAVEVKSKFGAEFRRFSLDRHKPGKFEDFYKLVVHTHHISNSDV
TIGYADVHGDLLPINNDDNFCKAVSSANPLLRVFIQKR
EEAERGSLGAGSLCRRRRALGA
LRDEGPRRRAHLDIGLPRDFRPVSSIIDVDLVPETHRRVRLHRHGCEKPLGFYIRDGASV
RVTPHGLEKVPGIFISRMVPGGLAESTGLLAVNDEVLEVNGIEVAGKTLDQVTDMMIANS
HNLIVTVK
PANQRNNVVRGGRALGSSGPPSDGTAGFVGPPAPRVLQNFHPDEAESDEDND
VVIEGTLEPARPPQTPGAPAGSLSRVNGAGLAQRLQRDLALDGGLQRLLSSLRADPRHSL
ALPPGGVEEHGPAVTL
Sequence length 376
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Rap1 signaling pathway
Endocytosis
Axon guidance
Hippo signaling pathway
Tight junction
Human papillomavirus infection
  Tight junction interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OSTEOARTHRITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Muscular Dystrophy Duchenne Duchenne muscular dystrophy Pubtator 36935420 Associate
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 22989571
★☆☆☆☆
Found in Text Mining only