Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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8495 |
Gene nameGene Name - the full gene name approved by the HGNC.
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PPFIB scaffold protein 2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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PPFIBP2 |
SynonymsGene synonyms aliases
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Cclp1 |
ChromosomeChromosome number
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11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11p15.4 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the LAR protein-tyrosine phosphatase-interacting protein (liprin) family. The encoded protein is a beta liprin and plays a role in axon guidance and neuronal synapse development by recruiting LAR protein-tyrosine phosphatases |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q8ND30 |
Protein name |
Liprin-beta-2 (Protein tyrosine phosphatase receptor type f polypeptide-interacting protein-binding protein 2) (PTPRF-interacting protein-binding protein 2) |
Protein function |
May regulate the disassembly of focal adhesions. Did not bind receptor-like tyrosine phosphatases type 2A. |
PDB |
3QH9
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00536 |
SAM_1 |
556 → 620 |
SAM domain (Sterile alpha motif) |
Domain |
PF00536 |
SAM_1 |
631 → 691 |
SAM domain (Sterile alpha motif) |
Domain |
PF07647 |
SAM_2 |
715 → 785 |
SAM domain (Sterile alpha motif) |
Domain |
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Sequence |
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Sequence length |
876 |
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.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Prostate cancer |
Malignant neoplasm of prostate, Prostate carcinoma, Prostate cancer, familial |
rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 |
26443449, 29892016, 26443449, 29892016 |
Prostate cancer, hereditary |
PROSTATE CANCER, HEREDITARY, 1 |
rs387906327, rs193929331, rs74315365, rs10993994, rs397516896, rs794729219, rs121913349, rs587782641, rs1114167673, rs1597371666, rs2073394466 |
29892016 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Prostatic neoplasms |
Prostatic Neoplasms |
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26443449 |
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