PTPN11
From Wikipedia, the free encyclopedia
| protein tyrosine phosphatase, non-receptor type 11
| |
| Identifiers | |
| Symbol(s) | PTPN11 NS1 |
| Entrez | 5781 |
| OMIM | 176876 |
| RefSeq | NM_002834 |
| UniProt | Q06124 |
| Other data | |
| Locus | Chr. 12 q24.1 |
PTPN11 is a gene for protein tyrosine phosphatase.
Defects are associated with both Noonan syndrome and Leopard syndrome
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