rs146237502

This variant is located in the NSMCE2 gene.

ClinVar annotation

Likely Benign☆☆☆
2 submitters

not provided; NSMCE2-related disorder

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About NSMCE2

This gene encodes a member of a family of E3 small ubiquitin-related modifier (SUMO) ligases that mediates the attachment of a SUMO protein to proteins involved in nuclear transport, transcription, chromosome segregation and DNA repair. The encoded protein is part of the structural maintenance of chromosomes (SMC) 5/6 complex which plays a key role genome maintenance, facilitating chromosome segregation and suppressing mitotic recombination. A knockout of the orthologous mouse gene is lethal prior to embryonic day 10.5. Naturally occurring mutations in this gene, that abolish the SUMO ligase activity, are associated with primordial dwarfism and extreme insulin resistance. [provided by RefSeq, Mar 2017]

View all NSMCE2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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