Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
56288
Gene name Gene Name - the full gene name approved by the HGNC.
Par-3 family cell polarity regulator
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PARD3
Synonyms (NCBI Gene) Gene synonyms aliases
ASIP, Baz, PAR3, PAR3alpha, PARD-3, PARD3A, PPP1R118, SE2-5L16, SE2-5LT1, SE2-5T2
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10p11.22-p11.21
Summary Summary of gene provided in NCBI Entrez Gene.
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 varia
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs199923448 C>A,T Risk-factor, uncertain-significance Coding sequence variant, missense variant
rs557643577 A>G Risk-factor Intron variant
rs757259023 C>T Risk-factor Coding sequence variant, genic downstream transcript variant, missense variant
rs762921297 T>A Risk-factor Coding sequence variant, intron variant, missense variant
rs781461462 G>A,C,T Pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT006686 hsa-miR-483-3p qRT-PCR, Western blot 22101077
MIRT039030 hsa-miR-766-3p CLASH 23622248
MIRT038900 hsa-miR-93-3p CLASH 23622248
MIRT692565 hsa-miR-106a-5p HITS-CLIP 23313552
MIRT692564 hsa-miR-106b-5p HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000226 Process Microtubule cytoskeleton organization IBA 21873635
GO:0005515 Function Protein binding IPI 10934474, 11257119, 14676191, 15161933, 15254234, 17057644, 17979178, 18838552, 19893486, 22579248, 22653443, 25241761, 26496610, 26766442, 28514442, 31980649
GO:0005546 Function Phosphatidylinositol-4,5-bisphosphate binding ISS
GO:0005547 Function Phosphatidylinositol-3,4,5-trisphosphate binding ISS
GO:0005829 Component Cytosol TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606745 16051 ENSG00000148498
Protein
UniProt ID Q8TEW0
Protein name Partitioning defective 3 homolog (PAR-3) (PARD-3) (Atypical PKC isotype-specific-interacting protein) (ASIP) (CTCL tumor antigen se2-5) (PAR3-alpha)
Protein function Adapter protein involved in asymmetrical cell division and cell polarization processes (PubMed:10954424, PubMed:27925688). Seems to play a central role in the formation of epithelial tight junctions (PubMed:27925688). Targets the phosphatase PTE
PDB 2KOM
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12053 Par3_HAL_N_term 1 83 N-terminal of Par3 and HAL proteins Family
PF00595 PDZ 461 545 PDZ domain Domain
PF00595 PDZ 590 680 PDZ domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed. {ECO:0000269|PubMed:12234671}.
Sequence
MKVTVCFGRTRVVVPCGDGHMKVFSLIQQAVTRYRKAIAKDPNYWIQVHRLEHGDGGILD
LDDILCDVADDKDRLVAVFDEQD
PHHGGDGTSASSTGTQSPEIFGSELGTNNVSAFQPYQ
ATSEIEVTPSVLRANMPLHVRRSSDPALIGLSTSVSDSNFSSEEPSRKNPTRWSTTAGFL
KQNTAGSPKTCDRKKDENYRSLPRDTSNWSNQFQRDNARSSLSASHPMVGKWLEKQEQDE
DGTEEDNSRVEPVGHADTGLEHIPNFSLDDMVKLVEVPNDGGPLGIHVVPFSARGGRTLG
LLVKRLEKGGKAEHENLFRENDCIVRINDGDLRNRRFEQAQHMFRQAMRTPIIWFHVVPA
ANKEQYEQLSQSEKNNYYSSRFSPDSQYIDNRSVNSAGLHTVQRAPRLNHPPEQIDSHSR
LPHSAHPSGKPPSAPASAPQNVFSTTVSSGYNTKKIGKRLNIQLKKGTEGLGFSITSRDV
TIGGSAPIYVKNILPRGAAIQDGRLKAGDRLIEVNGVDLVGKSQEEVVSLLRSTKMEGTV
SLLVF
RQEDAFHPRELNAEPSQMQIPKETKAEDEDIVLTPDGTREFLTFEVPLNDSGSAG
LGVSVKGNRSKENHADLGIFVKSIINGGAASKDGRLRVNDQLIAVNGESLLGKTNQDAME
TLRRSMSTEGNKRGMIQLIV
ARRISKCNELKSPGSPPGPELPIETALDDRERRISHSLYS
GIEGLDESPSRNAALSRIMGESGKYQLSPTVNMPQDDTVIIEDDRLPVLPPHLSDQSSSS
SHDDVGFVTADAGTWAKAAISDSADCSLSPDVDPVLAFQREGFGRQSMSEKRTKQFSDAS
QLDFVKTRKSKSMDLGIADETKLNTVDDQKAGSPSRDVGPSLGLKKSSSLESLQTAVAEV
TLNGDIPFHRPRPRIIRGRGCNESFRAAIDKSYDKPAVDDDDEGMETLEEDTEESSRSGR
ESVSTASDQPSHSLERQMNGNQEKGDKTDRKKDKTGKEKKKDRDKEKDKMKAKKGMLKGL
GDMFRFGKHRKDDKIEKTGKIKIQESFTSEEERIRMKQEQERIQAKTREFRERQARERDY
AEIQDFHRTFGCDDELMYGGVSSYEGSMALNARPQSPREGHMMDALYAQVKKPRNSKPSP
VDSNRSTPSNHDRIQRLRQEFQQAKQDEDVEDRRRTYSFEQPWPNARPATQSGRHSVSVE
VQMQRQRQEERESSQQAQRQYSSLPRQSRKNASSVSQDSWEQNYSPGEGFQSAKENPRYS
SYQGSRNGYLGGHGFNARVMLETQELLRQEQRRKEQQMKKQPPSEGPSNYDSYKKVQDPS
YAPPKGPFRQDVPPSPSQVARLNRLQTPEKGRPFYS
Sequence length 1356
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Rap1 signaling pathway
Chemokine signaling pathway
Endocytosis
Axon guidance
Hippo signaling pathway
Adherens junction
Tight junction
Human papillomavirus infection
  TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition)
Tight junction interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Prostate cancer Malignant neoplasm of prostate rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 28319090
Unknown
Disease term Disease name Evidence References Source
Mental Depression Mental Depression GWAS
Oligodendroglioma Oligodendroglioma GWAS
Restless Legs Syndrome Restless Legs Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Inhibit 27072891
Anencephaly Associate 28623428
Anodontia Associate 28844109
Atherosclerosis Associate 19592499
Breast Neoplasms Associate 34023783
Carcinogenesis Associate 24856572, 28844109, 33172988, 34023783
Carcinoma Hepatocellular Associate 23322019, 34040099, 36105681
Carcinoma Renal Cell Associate 24856572
Carcinoma Squamous Cell Associate 20215515, 25303977, 33172988, 34216486
Celiac Disease Associate 24386489