RPA32 Polyclonal Antibody, 50ul Serum & Sample Tubes This gene resides in the

This gene resides in the same region of chromosome 3 as members of the transferrin superfamily

MMP12 may play a role in aneurysm formation and mutations in this gene are associated with lung function and chronic obstructive pulmonary disease (COPD)

Ectonucleotide pyrophosphatase/phosphodiesterase family member 3 encoded by ENPP3 belongs to a series of ectoenzymes that are involved in hydrolysis of extracellular nucleotides

and studies in rat suggest that alternative use of the two translation initiation sites results in N-terminally distinct protein isoforms with different subcellular localization

Very high expression levels of KSR1 inhibit MAPK signaling

RPA32 Polyclonal Antibody, 50ul Serum & Sample Tubes This gene resides in theRPA2 (Replication Protein A2) is a Protein Coding gene. Diseases associated with RPA2 include xeroderma pigmentosum, group a and ataxia telangiectasia. Among its related pathways are DNA strand elongation andFanconi anemia pathway. GO annotations related to this gene include nucleic acid binding and ubiquitin protein ligase binding. An important paralog of this gene is RPA4.