About: PTPN11 wt Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • PTPN11 wt Allele
equivalentClass
OMIM_Number
  • 176876
GenBank_Accession_Number
  • NM_002834
Semantic_Type
  • Gene or Genome
Preferred_Name
  • PTPN11 wt Allele
UMLS_CUI
  • C1706044
GO_Annotation
  • non-membrane spanning protein tyrosine phosphatase activityGO:0004726TAS29-SEP-2003CGAP
  • protein tyrosine phosphatase activityGO:0004725TAS29-SEP-2003CGAP
  • signal transductionGO:0007165TAS29-SEP-2003CGAP
EntrezGene_ID
  • 5781
Legacy_Concept_Name
  • PTPN11_wt_Allele
HGNC_ID
  • HGNC:9644
FULL_SYN
  • SHP-2SYNCI
  • PTP-1DSYNCI
  • SH-PTP2SYNCI
  • SH-PTP3SYNCI
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11 (Noonan Syndrome 1) wt AlleleSYNCI
  • CFCSYNCI
  • NS1SYNCI
  • SHP2SYNCI
  • PTPN11 wt AllelePTNCI
  • BPTP3SYNCI
  • PTP2CSYNCI
Gene_Encodes_Product
  • Protein Tyrosine Phosphatase, Non-Receptor Type 11
DEFINITION
  • Human PTPN11 wild-type allele is located within 12q24 and is approximately 91 kb in length. This allele, which encodes tyrosine-protein phosphatase non-receptor type 11 protein, is involved in the dephosphorylation of protein-tyrosine phosphates. The PTPN11 gene is associated with severe congenital neutropenia as well as several forms of leukemia.NCI
DesignNote
  • Gene_Has_Function: Cell Morphogenesis
code
  • C49518
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