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Proteins/UNIPROT:Q9Y6X0

SETBP1

Protein·UNIPROT:Q9Y6X0

Open in the graph

Curated compounds routed: 0

What the reference databases state

Inferred

Inferred — not reported by a source. Evidence key

GenCC submitters' classifications

3 rows

complex neurodevelopmental disorder has a germline basis in SETBP1DiseaseGenCC HGNC:15573|MONDO:0100038Inferred only
intellectual disability, autosomal dominant 29 has a germline basis in SETBP1DiseaseGenCC HGNC:15573|MONDO:0014482Inferred only
Schinzel-Giedion syndrome has a germline basis in SETBP1DiseaseGenCC HGNC:15573|MONDO:0010010Inferred only

Statements

5 statements

5 statements · 3 reference databases · Subject: SETBP1 · Sources: gene ontology, Hetionet, WikiPathways

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APP interacts with SETBP1ProteinHetionet hetionet:interacts:26040-351Inferred only
SET interacts with SETBP1ProteinHetionet hetionet:interacts:26040-6418Inferred only
SETBP1 participates in Histone modificationsPathwayWikiPathways WP2369Inferred only
SETBP1 regulates regulation of DNA-templated transcriptionBiological processgene ontology Q9Y6X0|GO:0006355Inferred only
LRSAM1 decreases the expression of SETBP1ProteinHetionet hetionet:regulates:90678-26040Inferred only

Other names

3 names

Resolves to: SETBP1

Also called: KIAA0437SEBSET-binding protein

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