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- NCIT_C102800 IAO_0000115 "Human RELN wild-type allele is located in the vicinity of 7q22 and is approximately 518 kb in length. This allele, which encodes reelin protein, plays a role in extracellular matrix proteolysis, signal transduction and neuronal development. Mutation of the gene is associated with lissencephaly type 2." @default.
- NCIT_C102800 NCIT_NHC0 "C102800" @default.
- NCIT_C102800 NCIT_P100 "600514" @default.
- NCIT_C102800 NCIT_P102 "NM_005045" @default.
- NCIT_C102800 NCIT_P106 "Gene or Genome" @default.
- NCIT_C102800 NCIT_P108 "RELN wt Allele" @default.
- NCIT_C102800 NCIT_P207 "C3539667" @default.
- NCIT_C102800 NCIT_P321 "5649" @default.
- NCIT_C102800 NCIT_P98 "A polymorphic GGC triplet repeat located in the 5'-UTR region of the RELN gene, which numbers from 8 to 10 in the normal population, is increased in autistic patients to carry 4 to 23 additional repeats. (UniProt)" @default.
- NCIT_C102800 NCIT_P98 "Somatic mutation of the RELN gene may be associated with early T-cell precursor acute lymphoblastic leukemia. (Nature. 2012; 481:157-163.)" @default.
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- NCIT_C102800 hasExactSynonym "LIS2" @default.
- NCIT_C102800 hasExactSynonym "PRO1598" @default.
- NCIT_C102800 hasExactSynonym "RELN wt Allele" @default.
- NCIT_C102800 hasExactSynonym "RL" @default.
- NCIT_C102800 hasExactSynonym "Reelin wt Allele" @default.
- NCIT_C102800 type Class @default.
- NCIT_C102800 isDefinedBy ncit.owl @default.
- NCIT_C102800 label "RELN wt Allele" @default.
- NCIT_C102800 subClassOf NCIT_C102799 @default.
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- NCIT_C102800 subClassOf NCIT_C16612 @default.
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