Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5063
Gene name Gene Name - the full gene name approved by the HGNC.
P21 (RAC1) activated kinase 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PAK3
Synonyms (NCBI Gene) Gene synonyms aliases
ARA, MRX30, MRX47, OPHN3, PAK-3, PAK3beta, XLID30, bPAK, beta-PAK
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq23
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a serine-threonine kinase and forms an activated complex with GTP-bound RAS-like (P21), CDC2 and RAC1. This protein may be necessary for dendritic development and for the rapid cytoskeletal reorganization in dendritic s
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs121434611 C>T Pathogenic Coding sequence variant, non coding transcript variant, stop gained, genic downstream transcript variant
rs121434612 C>T Pathogenic Coding sequence variant, non coding transcript variant, missense variant, genic downstream transcript variant
rs121434613 C>A Pathogenic Coding sequence variant, non coding transcript variant, missense variant, genic downstream transcript variant
rs121434614 G>C Pathogenic Coding sequence variant, non coding transcript variant, missense variant, genic downstream transcript variant
rs200474454 A>G Conflicting-interpretations-of-pathogenicity, uncertain-significance Non coding transcript variant, coding sequence variant, missense variant, genic downstream transcript variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018369 hsa-miR-335-5p Microarray 18185580
MIRT662985 hsa-miR-7109-3p HITS-CLIP 23824327
MIRT662984 hsa-miR-6819-3p HITS-CLIP 23824327
MIRT662983 hsa-miR-6877-3p HITS-CLIP 23824327
MIRT662982 hsa-miR-150-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000165 Process MAPK cascade IEA
GO:0000166 Function Nucleotide binding IEA
GO:0002223 Process Stimulatory C-type lectin receptor signaling pathway IEA
GO:0002223 Process Stimulatory C-type lectin receptor signaling pathway TAS
GO:0003824 Function Catalytic activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300142 8592 ENSG00000077264
Protein
UniProt ID O75914
Protein name Serine/threonine-protein kinase PAK 3 (EC 2.7.11.1) (Beta-PAK) (Oligophrenin-3) (p21-activated kinase 3) (PAK-3)
Protein function Serine/threonine protein kinase that plays a role in a variety of different signaling pathways including cytoskeleton regulation, cell migration, or cell cycle regulation. Plays a role in dendrite spine morphogenesis as well as synapse formation
PDB 6FD3
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00786 PBD 69 142 P21-Rho-binding domain Domain
PF00069 Pkinase 283 534 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Restricted to the nervous system. Highly expressed in postmitotic neurons of the developing and postnatal cerebral cortex and hippocampus. {ECO:0000269|PubMed:12890786}.
Sequence
MSDGLDNEEKPPAPPLRMNSNNRDSSALNHSSKPLPMAPEEKNKKARLRSIFPGGGDKTN
KKKEKERPEISLPSDFEHTIHVGFDAVTGEFTPDLYGSQMCPGKLPEGIPEQWARLLQTS
NITKLEQKKNPQAVLDVLKFYD
SKETVNNQKYMSFTSGDKSAHGYIAAHPSSTKTASEPP
LAPPVSEEEDEEEEEEEDENEPPPVIAPRPEHTKSIYTRSVVESIASPAVPNKEVTPPSA
ENANSSTLYRNTDRQRKKSKMTDEEILEKLRSIVSVGDPKKKYTRFEKIGQGASGTVYTA
LDIATGQEVAIKQMNLQQQPKKELIINEILVMRENKNPNIVNYLDSYLVGDELWVVMEYL
AGGSLTDVVTETCMDEGQIAAVCRECLQALDFLHSNQVIHRDIKSDNILLGMDGSVKLTD
FGFCAQITPEQSKRSTMVGTPYWMAPEVVTRKAYGPKVDIWSLGIMAIEMVEGEPPYLNE
NPLRALYLIATNGTPELQNPERLSAVFRDFLNRCLEMDVDRRGSAKELLQHPFL
KLAKPL
SSLTPLIIAAKEAIKNSSR
Sequence length 559
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  ErbB signaling pathway
Ras signaling pathway
Axon guidance
Focal adhesion
T cell receptor signaling pathway
Regulation of actin cytoskeleton
Pathogenic Escherichia coli infection
Salmonella infection
Human immunodeficiency virus 1 infection
Renal cell carcinoma
  Generation of second messenger molecules
CD28 dependent Vav1 pathway
Ephrin signaling
Sema3A PAK dependent Axon repulsion
VEGFR2 mediated vascular permeability
CD209 (DC-SIGN) signaling
RHO GTPases activate PAKs
MAPK6/MAPK4 signaling
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Mental retardation intellectual disability rs1569459580 N/A
Mental Retardation, X-Linked Intellectual disability, X-linked 30 rs121434611, rs121434612, rs121434613, rs121434614, rs780775497, rs1603378331, rs1603377813 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Agenesis Of Corpus Callosum corpus callosum, agenesis of N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Anxiety Associate 17853471
Attention Deficit Disorder with Hyperactivity Associate 17853471
Breast Neoplasms Associate 31987914
Carcinogenesis Associate 40028213
Cognition Disorders Associate 17853471, 18805672, 34014906
Developmental Disabilities Associate 32050918
Hydrocephalus Associate 17853471
Immune System Diseases Associate 34014906
Immunologic Deficiency Syndromes Associate 34014906
Infections Inhibit 16352537