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3 Possible Causes for Mutation in the NR2F2 Gene

  • Multiple Types of Congenital Heart Defects 4

    Safely perform and accurately interpret pediatric imaging studies with this concise, highly illustrated resource! Written by Lane F. Donnelly, MD, Fundamentals of Pediatric Imaging, 2nd Edition, covers the essential concepts residents and practitioners need to know, laying a solid foundation for understanding the[…][books.google.com]

  • Optic Atrophy-Intellectual Disability Syndrome

    Syndromes Bosch-Boonstra-Schaaf optic atrophy syndrome Genetic Category Rare Single Gene Mutation, Syndromic Associated Disorders EPS, ID, ASD, ADHD, DD/NDD Relevance to[gene.sfari.org] Autism Reports / Total Reports 5 / 11 Rare Variants / Common Variants 34 / 0 Aliases NR2F1, BBOAS, BBSOAS, COUP-TFI, EAR-3, EAR3, ERBAL3, NR2F2, SVP44, TCFCOUP1, TFCOUP1 Associated[gene.sfari.org]

  • Situs Inversus

    CHTD4 ( OMIM ) is caused by mutation in the NR2F2 gene ( OMIM ) on chromosome 15q26. CHTD5 ( OMIM ) is caused by mutation in the GATA5 gene ( OMIM ) on chromosome 20q13.[mendelian.co] CHTD2 ( OMIM ) is caused by mutation in the TAB2 gene ( OMIM ) on chromosome 6q25.[mendelian.co]

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