Split-Hand/Foot Malformation

A rare genetic disorder often inherited in an autosomal manner characterized by limb malformations including syndactyly, median clefts of the hands and/or feet, and partial or complete absence of fingers or toes. It may be associated with other skeletal and extraskeletal abnormalities. (NCI Thesaurus)

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Split

To separate or divide into distinct parts or portions.

Splicing Regulation Pathway

While transcriptional regulation is often viewed as the most prevalent way extracellular signals act to regulate gene expression, post-transcriptional regulation of splicing,…

Splicing Factor U2AF 35 kDa Subunit

Splicing factor U2AF 35 kDa subunit (240 aa, ~28 kDa) is encoded by the human U2AF1 gene. This protein is involved in…

Splicing Factor Proline-and Glutamine-Rich

Splicing factor, proline- and glutamine-rich protein (707 aa, ~76 kDa) is encoded by the human SFPQ gene. This protein may be involved…

Splicing Factor 3B Subunit 1

Splicing factor 3B subunit 1 (1304 aa, ~146 kDa) is encoded by the human SF3B1 gene. This protein is involved in the…

Splicer Device Component

A device designed to join pieces of a material into a continuous length.