DDX20 gene
E1555615
UNEXPLORED
The DDX20 gene encodes a DEAD-box RNA helicase involved in RNA processing and the assembly and function of small nuclear ribonucleoprotein (snRNP) complexes.
All labels observed (1)
| Label | Occurrences |
|---|---|
| DDX20 gene canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T22796874 — resolving that mention is where its identity was fixed. The disambiguator weighed these candidate entities and picked the highlighted one (or “None”, minting a new entity). This is how homonymy is resolved: the same surface form can point to different entities.
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: DDX20 gene Context triple: [Gemin3, encodedBy, DDX20 gene]
-
A.
TAF15 gene
The TAF15 gene encodes a multifunctional RNA-binding protein involved in transcription regulation and RNA processing, and is implicated in certain cancers through gene fusions.
-
B.
HTT gene
The HTT gene encodes the huntingtin protein, and mutations in this gene—particularly CAG trinucleotide repeat expansions—cause Huntington's disease, a progressive neurodegenerative disorder.
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C.
SMN2
SMN2 is a human gene that produces a backup form of survival motor neuron protein and is a key therapeutic target in spinal muscular atrophy.
-
D.
GRIN2A
GRIN2A is a gene that encodes the GluN2A subunit of NMDA-type glutamate receptors, which are critical for synaptic plasticity, learning, and memory in the brain.
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E.
5q13 (SMN1)
5q13 (SMN1) is a gene located on chromosome 5 whose proper function is critical for motor neuron survival and whose mutations are the primary cause of spinal muscular atrophy.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: DDX20 gene Target entity description: The DDX20 gene encodes a DEAD-box RNA helicase involved in RNA processing and the assembly and function of small nuclear ribonucleoprotein (snRNP) complexes.
-
A.
TAF15 gene
The TAF15 gene encodes a multifunctional RNA-binding protein involved in transcription regulation and RNA processing, and is implicated in certain cancers through gene fusions.
-
B.
HTT gene
The HTT gene encodes the huntingtin protein, and mutations in this gene—particularly CAG trinucleotide repeat expansions—cause Huntington's disease, a progressive neurodegenerative disorder.
-
C.
SMN2
SMN2 is a human gene that produces a backup form of survival motor neuron protein and is a key therapeutic target in spinal muscular atrophy.
-
D.
GRIN2A
GRIN2A is a gene that encodes the GluN2A subunit of NMDA-type glutamate receptors, which are critical for synaptic plasticity, learning, and memory in the brain.
-
E.
5q13 (SMN1)
5q13 (SMN1) is a gene located on chromosome 5 whose proper function is critical for motor neuron survival and whose mutations are the primary cause of spinal muscular atrophy.
- F. None of above. chosen
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.