SEM1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SEM1 wild-type allele is located in the vicinity of 7q21.3 and is approximately 228 kb in length. This allele, which encodes 26 proteasome complex subunit SEM1 protein, is involved in the mediation of protein degradation. The gene may play a role in split hand/split foot malformation.

**Synonyms:** - C7orf76 - Chromosome 7 Open Reading Frame 76 Gene - DSS1 - Deleted In Split-Hand/Split-Foot 1 Gene - Deleted In Split-Hand/Split-Foot 1 Region - Deleted in Split-Hand/Foot 1 Gene - Deleted in Split-Hand/Split-Foot 1 Region Gene - ECD - FLJ42280 - SEM1 26S Proteasome Complex Subunit wt Allele - SEM1, 26S Proteasome Complex Subunit Gene - SHFD1 - SHFDG1 - SHFM1 - SHSF1 - Shfdg1 - Split Hand/Foot Malformation (Ectrodactyly) Type 1 Gene