Phospho-AP-1 (T231) Polyclonal Antibody, 50ul Pipette Filler Diseases associated with RGAG1 include

Diseases associated with RGAG1 include non-syndromic x-linked intellectual disability

and it is located in a cluster with three other family members on chromosome 7

and is considered to be a strong candidate gene for learning defects associated with Down syndrome

with 1 or more amino acids following the C-terminal glycine-glycine residues of the mature UBL protein

and ionic requirements

Phospho-AP-1 (T231) Polyclonal Antibody, 50ul Pipette Filler Diseases associated with RGAG1 includeJUN is the putative transforming gene of avian sarcoma virus 17. It encodes a protein which is highly similar to the viral protein, and which interacts directly with specific target DNA sequences to regulate gene expression. This gene is intronless and is mapped to 1p32 p31, a chromosomal region involved in both translocations and deletions in human malignancies.