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- NCIT_C186685 IAO_0000115 "Human ELP1 wild-type allele is located in the vicinity of 9q31.3 and is approximately 67 kb in length. This allele, which encodes elongator complex protein 1, plays a role in the modification of tRNA. Mutation of the gene is associated with familial dysautonomia and predisposition for medulloblastoma." @default.
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- NCIT_C186685 NCIT_P106 "Gene or Genome" @default.
- NCIT_C186685 NCIT_P108 "ELP1 wt Allele" @default.
- NCIT_C186685 NCIT_P208 "CL1779156" @default.
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- NCIT_C186685 referenceCount "1" @default.
- NCIT_C186685 hasExactSynonym "DYS" @default.
- NCIT_C186685 hasExactSynonym "Dysautonomia (Riley-Day Syndrome, Hereditary Sensory Autonomic Neuropathy Type III) Gene" @default.
- NCIT_C186685 hasExactSynonym "ELP1 wt Allele" @default.
- NCIT_C186685 hasExactSynonym "ELP1, Yeast, Homolog of Gene" @default.
- NCIT_C186685 hasExactSynonym "Elongator Acetyltransferase Complex Subunit 1 wt Allele" @default.
- NCIT_C186685 hasExactSynonym "Elongator Acetyltransferase Complex, Subunit 1 Gene" @default.
- NCIT_C186685 hasExactSynonym "FD" @default.
- NCIT_C186685 hasExactSynonym "IKAP" @default.
- NCIT_C186685 hasExactSynonym "IKBKAP" @default.
- NCIT_C186685 hasExactSynonym "IKI3" @default.
- NCIT_C186685 hasExactSynonym "Inhibitor of Kappa Light Polypeptide Gene Enhancer In B-Cells, Kinase Complex-Associated Protein Gene" @default.
- NCIT_C186685 hasExactSynonym "TOT1" @default.
- NCIT_C186685 type Class @default.
- NCIT_C186685 isDefinedBy ncit.owl @default.
- NCIT_C186685 label "ELP1 wt Allele" @default.
- NCIT_C186685 subClassOf B8064d925ecfc589967a1b18121d5eaba @default.
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