Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79899
Gene name Gene Name - the full gene name approved by the HGNC.
Proline rich 5 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PRR5L
Synonyms (NCBI Gene) Gene synonyms aliases
PROTOR2
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p13-p12
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029915 hsa-miR-26b-5p Microarray 19088304
MIRT497095 hsa-miR-3125 PAR-CLIP 22291592
MIRT497094 hsa-miR-3916 PAR-CLIP 22291592
MIRT497093 hsa-miR-6859-5p PAR-CLIP 22291592
MIRT497092 hsa-miR-27b-5p PAR-CLIP 22291592
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001933 Process Negative regulation of protein phosphorylation IMP 22609986
GO:0005515 Function Protein binding IPI 21964062, 32296183
GO:0009968 Process Negative regulation of signal transduction IEA
GO:0010762 Process Regulation of fibroblast migration IEA
GO:0010762 Process Regulation of fibroblast migration IMP 22609986
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611728 25878 ENSG00000135362
Protein
UniProt ID Q6MZQ0
Protein name Proline-rich protein 5-like (Protein observed with Rictor-2) (Protor-2)
Protein function Associates with the mTORC2 complex that regulates cellular processes including survival and organization of the cytoskeleton (PubMed:17461779). Regulates the activity of the mTORC2 complex in a substrate-specific manner preventing for instance t
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08539 HbrB 47 152 HbrB-like Domain
Sequence
MTRGFAPILPVEFHKMGSFRRPRPRFMSSPVLSDLPRFQAARQALQLSSSSAWNSVQTAV
INVFKGGGLQSNELYALNENIRRLLKSELGSFITDYFQNQLLAKGLFFVEEKIKLCEGEN
RIEVLAEVWDHFFTETLPTLQAIFYPVQGQEL
TIRQISLLGFRDLVLLKVKLGDLLLLAQ
SKLPSSIVQMLLILQSVHEPTGPSESYLQLEELVKQVVSPFLGISGDRSFSGPTYTLARR
HSRVRPKVTVLNYASPITAVSRPLNEMVLTPLTEQEGEAYLEKCGSVRRHTVANAHSDIQ
LLAMATMMHSGLGEEASSENKCLLLPPSFPPPHRQCSSEPNITDNPDGLEEGARGSQEGS
ELNCASLS
Sequence length 368
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  mTOR signaling pathway  
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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
Asthma Asthma, Asthma (childhood onset) N/A N/A GWAS
Crohn Disease Crohn's disease N/A N/A GWAS
Dermatitis Atopic dermatitis N/A N/A GWAS
Eczema Eczema N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Juvenile Associate 25540605
Breast Neoplasms Stimulate 27314662
Breast Neoplasms Associate 27314662
Dermatitis Atopic Associate 33901562
Drug Hypersensitivity Associate 29679657