| Health / Medical Topics |
SIX1 wt Allele
Human SIX1 wild-type allele is located in the vicinity of 14q23.1 and is approximately 3 kb in length. This allele, which encodes homeobox protein SIX1, may play a role in skeletal muscle development. Mutation of the gene is associated with both autosomal dominant deafness type 23 and branchiootic syndrome type 3. (NCI Thesaurus)
YOU MAY ALSO LIKE
This gene may be involved in limb development.
Six-twelve leukemia (5362 bp) is encoded by the human STL gene. This non-coding RNA may play a role in B-cell acute lymphoblastic…
Six times per year.
Six times per week.
Six times per month.
Six times per day.
