PTPRM (protein tyrosine phosphatase receptor type M)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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5797 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Protein tyrosine phosphatase receptor type M |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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PTPRM |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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PTPRL1, R-PTP-MU, RPTPM, RPTPU, hR-PTPu |
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Chromosome
Chromosome number
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18 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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18p11.23 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic tran |
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miRNA
miRNA 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 IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||||||||||||||||||||||
| UniProt ID | P28827 | ||||||||||||||||||||||||||||||||||||||||
| Protein name | Receptor-type tyrosine-protein phosphatase mu (Protein-tyrosine phosphatase mu) (R-PTP-mu) (EC 3.1.3.48) | ||||||||||||||||||||||||||||||||||||||||
| Protein function | Receptor protein-tyrosine phosphatase that mediates homotypic cell-cell interactions and plays a role in adipogenic differentiation via modulation of p120 catenin/CTNND1 phosphorylation (PubMed:10753936, PubMed:17761881). Promotes CTNND1 dephosp | ||||||||||||||||||||||||||||||||||||||||
| PDB | 1RPM , 2C9A , 2V5Y , 8A16 , 8A17 | ||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence | |||||||||||||||||||||||||||||||||||||||||
| Sequence length | 1452 | ||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||||||||||||||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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