9m46
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Crystal structure of IQSEC2 CC domain
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Structural highlights
DiseaseIQEC2_HUMAN Severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome;X-linked non-syndromic intellectual disability. The disease is caused by mutations affecting the gene represented in this entry. FunctionIQEC2_HUMAN Is a guanine nucleotide exchange factor for the ARF GTP-binding proteins.[1] References
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This page was last modified 09:18, 22 October 2025.