Predicted to enable K63-linked polyubiquitin modification-dependent protein binding activity. Predicted to be involved in DNA repair. Predicted to act upstream of or within DNA damage response. Part of ATR-ATRIP complex. Is expressed in several structures, including alimentary system; brain; cardiovascular system; eye; and genitourinary system. Used to study Seckel syndrome. Orthologous to human ATRIP (ATR interacting protein); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; bisphenol A; triptonide.
Type:
protein-coding
Previously known as:
ATM and Rad3 related interacting protein; ATR-interacting protein; Atrip
[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in increased expression of ATRIP mRNA
[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in increased expression of ATRIP mRNA
[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in increased expression of ATRIP mRNA
[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in increased expression of ATRIP mRNA