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Paper Details

Evolutionary Landscape of <i>SOX</i> Genes to Inform Genotype-to-Phenotype Relationships.
Genes (Basel)
2
2023
1890 open-reading frame, A379V, C, COSMIC human variants, Campomelic Dysplasia, E137K, Genes, HMG, HMG box, HMG-box, High Mobility Group, K88R, R104G, R159G, SOX, SOX proteins, SOX transcription factor family, SOX14, SOX15, SOX15 R104G, SOX18, SOX2 HMG-box-flanking region, SOX7, SOX8, SOX8 R159G, SOX9 dimerization region, SOXF, amino acid, amino acids, cardiovascular complications, gene family, human, intellectual disability, musculature abnormality, ortholog, rs143587868, rs199932938, rs201931544, seizures
Author NameAffiliation
Timothy J TricheCenter for Epigenetics, Van Andel Research Institute
Timothy J TricheCenter for Epigenetics, Van Andel Research Institute
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink