About: PTPN12 wt Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • PTPN12 wt Allele
equivalentClass
OMIM_Number
  • 600079
GenBank_Accession_Number
  • NM_002835
Semantic_Type
  • Gene or Genome
Preferred_Name
  • PTPN12 wt Allele
UMLS_CUI
  • C1705342
GO_Annotation
  • soluble fractionGO:0005625TAS29-SEP-2003CGAP
  • protein amino acid dephosphorylationGO:0006470TAS29-SEP-2003CGAP
  • non-membrane spanning protein tyrosine phosphatase activityGO:0004726TAS29-SEP-2003CGAP
  • cytoplasmGO:0005737TAS29-SEP-2003CGAP
EntrezGene_ID
  • 5782
Legacy_Concept_Name
  • PTPN12_wt_Allele
HGNC_ID
  • HGNC:9645
FULL_SYN
  • PTPG1SYNCI
  • PTP-PESTSYNCI
  • PTPN12 wt AllelePTNCI
  • Protein Tyrosine Phosphatase, Non-Receptor Type 12 wt AlleleSYNCI
Gene_Encodes_Product
  • Protein Tyrosine Phosphatase, Non-Receptor Type 12
DEFINITION
  • Human PTPN12 wild-type allele is located in the vicinity of 7q11.23 and is approximately 103 kb in length. This allele, which encodes tyrosine-protein phosphatase non-receptor type 12 protein, plays a role in the dephosphorylation of protein-tyrosine phosphates. Defects in the PTPN12 gene are associated with colon cancer.NCI
code
  • C49520
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