Health / Medical Topics |
RUNX2 wt Allele
Human RUNX2 wild-type allele is located in the vicinity of 6p21 and is approximately 223 kb in length. This allele, which encodes runt-related transcription factor 2 protein, is involved in osteoblastic differentiation, skeletal morphogenesis and hematopoietic stem cell differentiation. Mutation of the gene is associated with cleidocranial dysplasia. (NCI Thesaurus)
YOU MAY ALSO LIKE
This gene plays a role in both transcription and cell differentiation.
Human RUNX1T1 wild-type allele is located in the vicinity of 8q22 and is approximately 136 kb in length. This allele, which encodes…
This gene plays a role in transcriptional regulation and hematopoiesis.
A fusion protein encoded by the RUNX1/ZNF687 fusion gene. This protein is comprised of part of the N-terminal runt domain of the…
A fusion gene that results from a chromosomal translocation t(1;21)(q21;q22) which fuses the first 3 exons of the RUNX1 gene to exon…
A fusion protein encoded by the RUNX1/ZFPM2 fusion gene. This protein is comprised of the N-terminal runt domain of the runt-related transcription…