AP4M1 involved in several pathways and played different roles in them. We selected most pathways AP4M1 participated on our site, such as Lysosome, which may be useful for your reference. Also, other proteins which involved in the same pathway with AP4M1 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name |
Pathway Related Protein |
| Lysosome |
ARSB; CD68; TCEAL4; AP3M1; CTSJ; ATP6V0A1B; CTPS1B; AP1S3; MANBA; AP1G2 |
AP4M1 has several biochemical functions, for example, protein binding, transporter activity. Some of the functions are cooperated with other proteins, some of the functions could acted by AP4M1 itself. We selected most functions AP4M1 had, and list some proteins which have the same functions with AP4M1. You can find most of the proteins on our site.
| Function |
Related Protein |
| protein binding |
RIC8; CTNNBIP1; RAB7L1; AP1G1; CDX1; CCP110; DPH1; BSG; DPP3; CCL18 |
| transporter activity |
ASNA1; ABCC6; AQP8B; FABP4; SLC17A9; CDH17; ABCA9; MIPA; AP3S1; HIAT1 |
AP4M1 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with AP4M1 here. Most of them are supplied by our site. Hope this information will be useful for your research of AP4M1.
USP47; tax; ZBTB22; CHTF8; DDX52; b4dnw0_human; SF3B2; H3F3B; CBX4; LCMT2; RALA; IMPDH2; HMGA1; CDK11B; AKT2; GALNT2; NPAT
Abdollahpour, H; Alawi, M; et al. An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS 23:256-259(2015).
Jameel, M; Klar, J; et al. A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency. BMC MEDICAL GENETICS 15:-(2014).
