17q12, explained for kidsdeletion syndrome · static snapshot
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Gene + body-part link Learning, talking and behaviour 19 supporting sources confidence 97% novelty 55%

The gene ACACA shows up in 13 stories together with learning, talking and behaviour

We read 13 stories that talk about both the gene ACACA and learning, talking and behaviour. That does not prove one causes the other, but they keep showing up together.

How this was derived

This is about what shows up together in the articles. It is not proof that one thing causes the other.

Generated 2026-11-13, last changed yesterday. Dedup key assoc:ACACA:neurodevelopment. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (4 quotes)

…ch suggested that some people may be sensitive to the dose changes in genes located in the chromosome 17q12 region. A variable phenotype of epilepsy, intellectual disability, and schizophrenia caused by a 12p13.33-p13.32 terminal microdeletion was identified in a Korean family. Among the six candidate genes in this region…
…number variation in bipolar disorder. Mol. Psychiatry. 2016;21:89-93. doi: 10.1038/mp.2014.174. 9. Mefford H.C., Batshaw M.L., Hoffman E.P. Genomics, Intellectual Disability, and Autism. N. Engl. J. Med. 2012;366:733-743. doi: 10.1056/NEJMra1114194. 10. Srivastava A.K., Schwartz C.E. Intellectual disability and autism spe…
…4 , 45 ]. Approximately 30-40% of individuals with DiGeorge syndrome meet diagnostic criteria for ASD [ 46 ]. FXS, the most common inherited cause of intellectual disability, is also strongly associated with ASD, with prevalence estimates indicating that around 50% of males and 16% of females with FXS receive an ASD diagn…
…velopmental and epileptic encephalopathies (DEEs, [MIM: 308350]), a severe group of epilepsies characterized by early-onset, intractable seizures and developmental delay. In contrast, genes discovered for the milder, more common forms of epilepsies - genetic generalized epilepsy (GGE [MIM: 600669]) and non-acquired fo…

Supporting documents (47)

StorySourcePublishedSeenRelevance
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 yesterday 1.00
Identification of novel driver risk genes in CNV loci associated wi... pmc 2024-01-01 yesterday 0.45
HNF1β, LHX1, and GGNBP2 deletion contributed to kidney and reproduc... pmc 2024-01-01 yesterday 1.00
Prenatal diagnosis of 17q12 copy number variants in fetuses via chr... pmc 2024-01-01 yesterday 1.00
HNF1B Transcription Factor: Key Regulator in Renal Physiology and P... pmc 2024-01-01 yesterday 1.00
A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deleti... pmc 2024-01-01 yesterday 1.00
Prenatal diagnosis of familial transmission of 17q12 microduplicati... pubmed 2016-12-01 yesterday 1.00
The individual and global impact of copy-number variants on complex... pubmed 2022-04-07 yesterday 1.00
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pubmed 2026-01-01 yesterday 1.00
Exome sequencing of 20,979 individuals with epilepsy reveals shared... pmc 2024-01-01 yesterday 1.00
In-Depth Phenotyping of PIGW -Related Disease and Its Role in 17q12... pmc 2024-01-01 yesterday 1.00
Delineation of the Genetic Architecture and Clinical Polymorphism o... pmc 2024-01-01 yesterday 1.00
Psychosis of Epilepsy: An Update on Clinical Classification and Mechanism pmc 2025-01-01 yesterday 1.00
Decreased T helper 1 cell function underlies recurrent sinopulmonar... pmc 2025-01-01 yesterday 1.00
Case-based learning: a case of maturity-onset diabetes of the young... pmc 2025-01-01 yesterday 1.00
Severe neonatal cholestasis in HNF1β deficiency: a case report and ... pmc 2025-01-01 yesterday 1.00
Autism Spectrum Disorder: Genetic Mechanisms and Inheritance Patterns pmc 2025-01-01 yesterday 1.00
ESC models of autism with copy-number variations reveal cell-type-s... pmc 2025-01-01 yesterday 1.00
Diabetes associated with HNF1B: beyond Occam’s razor—A case report pmc 2025-01-01 yesterday 1.00
Persistent Tic Disorders Are Associated With 17q12 Duplications pmc 2025-01-01 yesterday 1.00
Cognitive deterioration in patients undergoing hemodialysis: how va... pmc 2025-01-01 yesterday 1.00
A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-on... pmc 2025-01-01 yesterday 1.00
Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebell... pmc 2025-01-01 yesterday 1.00
Unexpected genomic architecture in a sporadic case of C1-INH Heredi... pmc 2025-01-01 yesterday 1.00
Assessing the clinical application value of SNP-array in fetal cent... pmc 2025-01-01 yesterday 1.00
Phenotypic differences and similarities of monozygotic twins with m... pubmed 2019-07-01 yesterday 1.00
Reversed cortico-medullary differentiation in kidneys on fetal magn... pmc 2025-01-01 yesterday 1.00
Comparing Copy Number Variations in a Danish Case Cohort of Individ... pubmed 2022-01-01 yesterday 1.00
HNF1B variant without hyperglycaemia as a cause of isolated profoun... pubmed 2023-02-09 yesterday 1.00
Fetal agenesis of corpus callosum: chromosomal copy number abnormal... pubmed 2024-07-30 yesterday 1.00
Prenatal Diagnosis of Malformations of Cortical Development: A Revi... pmc 2026-01-01 yesterday 1.00
Prenatally diagnosed 17q12 microdeletion syndrome with a novel asso... pubmed 2012-01-01 yesterday 1.00
Structural variations in evolutionary novel genomic regions: new in... pmc 2026-01-01 yesterday 1.00
17q12 deletion and duplication syndrome in Denmark-A clinical cohor... pubmed 2016-11-01 yesterday 1.00
The Importance of Molecular Testing in the Diagnosis of Genetic Syn... pmc 2026-01-01 yesterday 1.00
Epilepsy as a Component of the Dysmorphic–Neurodevelopmental Phenot... pmc 2026-01-01 yesterday 1.00
Prenatal Ultrasound–Detected Structural Anomalies Associated with A... pmc 2026-01-01 yesterday 1.00
Transient neonatal diabetes mellitus as an early diagnostic clue to... pmc 2026-01-01 yesterday 1.00
17q12 deletion syndrome presenting with chronic pancreatitis: a case report pmc 2026-01-01 yesterday 1.00
A familial case report of 17q12 recurrent deletion syndrome: clinic... pmc 2026-01-01 yesterday 1.00
The effect of human-specific genetic variants on neuronal spinogenesis pmc 2026-01-01 yesterday 1.00
Chromosomal Microarray Analysis in Critically Ill Neonates and Chil... pmc 2026-01-01 yesterday 1.00
Accurate diagnosis and heterogeneity analysis of a 17q12 deletion s... pubmed 2021-07-01 yesterday 1.00
[Clinical and genetic analysis of a fetus with 17q12 microdeletion ... pubmed 2023-06-10 yesterday 1.00
Prenatal diagnosis and perinatal findings of 17q12 microdeletion en... pubmed 2024-01-01 yesterday 1.00
Prenatal diagnosis, ultrasound findings, and pregnancy outcome of 1... pubmed 2024-12-01 yesterday 1.00
Case-based learning: a case of maturity-onset diabetes of the young... pubmed 2025-04-01 yesterday 1.00