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PRR5L (proline rich 5 like)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79899
Gene nameGene Name - the full gene name approved by the HGNC.
Proline rich 5 like
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
PRR5L
SynonymsGene synonyms aliases
PROTOR2
ChromosomeChromosome number
11
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11p13-p12
miRNAmiRNA 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:0001934 Process Positive regulation of protein phosphorylation IEA
GO:0005515 Function Protein binding IPI 21964062, 32296183
GO:0009968 Process Negative regulation of signal transduction IEA
GO:0010762 Process Regulation of fibroblast migration IMP 22609986
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
  mTOR signaling pathway  
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Arthritis Systemic onset juvenile chronic arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 23603761
Asthma Asthma, Childhood asthma rs324981, rs121912630, rs150116809, rs4950928, rs708494, rs1581842283 30929738, 31619474, 30929738
Dermatitis Dermatitis, Atopic rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 26482879
Rheumatoid arthritis Rheumatoid Arthritis, Systemic Juvenile rs3766379, rs3792876, rs2071592, rs3087456, rs587776843, rs1566328963, rs2240340, rs1557787212 23603761
Unknown
Disease name Disease term dbSNP ID References
Achoo syndrome Autosomal dominant compelling helio ophthalmic outburst syndrome 27182965
Eczema Eczema 30595370
Oligoarticular arthritis Oligoarticular Juvenile Idiopathic Arthritis 23603761
Pauciarticular chronic arthritis Juvenile pauciarticular chronic arthritis 23603761

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