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SUMF1 and autism spectrum disorder are reported together in 2 articles.
Gene
SUMF1
- HGNC
- HGNC:20376
3articles
3mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Autism spectrum disorder
- HPO
- HP:0000729
881articles
881mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
2 records shown · first 60Boolean Modeling of Biological Network Applied to Protein-Protein Interaction Network of Autism Patients.
PMID 39194544 | PMCID PMC11352122 | DOI 10.3390/biology13080606 · Biology · 2024 · 8 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | SUMF1 | “The aim is to examine how patients' genetic variations in INTS6L, USP9X, RSK4, FGF5, FLNA, SUMF1, and IDS affect mTOR and Wnt cell signaling convergence.” | 0.98 | hgnc_dict_v1 |
| phenotype | autism spectrum disorder | “Boolean Modeling of Biological Network Applied to Protein-Protein Interaction Network of Autism Patients.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | INTS6L | “The aim is to examine how patients' genetic variations in INTS6L, USP9X, RSK4, FGF5, FLNA, SUMF1, and IDS affect mTOR and Wnt cell signaling convergence.” | 0.98 | hgnc_dict_v1 |
| gene | USP9X | “The aim is to examine how patients' genetic variations in INTS6L, USP9X, RSK4, FGF5, FLNA, SUMF1, and IDS affect mTOR and Wnt cell signaling convergence.” | 0.98 | hgnc_dict_v1 |
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.
PMID 28720891 | PMCID PMC5515956 | DOI 10.1038/s41598-017-06033-1 · Scientific reports · 2017 · 15 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | SUMF1 | “Examples include SUMF1, KDM5B and MXRA5 (Known-ASD genes), PRODH2 and KCTD21 (implicated in schizophrenia), as well as USP9X and SMS (implicated in intellectual disability).” | 0.98 | hgnc_dict_v1 |
| phenotype | autism spectrum disorder | “Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | GLT8D1 | “Our pipeline uncovered variants in 15 ASD-candidate genes, including 5 (GLT8D1, HTATSF1, OR6C65, ITIH6 and DDX26B) that have not been reported in any human condition.” | 0.98 | hgnc_dict_v1 |
| gene | HTATSF1 | “Our pipeline uncovered variants in 15 ASD-candidate genes, including 5 (GLT8D1, HTATSF1, OR6C65, ITIH6 and DDX26B) that have not been reported in any human condition.” | 0.98 | hgnc_dict_v1 |