Fanconi anemia, complementation group M
mammalian protein found in Mus musculus
Press Enter · cited answer in seconds
0 sources
Fanconi anemia, complementation group M
Summary
Fanconi anemia, complementation group M is a protein[1].
Key Facts
- Fanconi anemia, complementation group M's instance of is recorded as protein[2].
- Fanconi anemia, complementation group M's subclass of is recorded as protein[3].
- Fanconi anemia, complementation group M's UniProt protein ID is recorded as Q8BGE5[4].
- Fanconi anemia, complementation group M's RefSeq protein ID is recorded as NP_849243[5].
- Fanconi anemia, complementation group M's RefSeq protein ID is recorded as XP_006515403[6].
- Fanconi anemia, complementation group M's RefSeq protein ID is recorded as XP_006515404[7].
- Fanconi anemia, complementation group M's RefSeq protein ID is recorded as NP_001351376[8].
- Fanconi anemia, complementation group M's molecular function is recorded as nucleotide binding[9].
- Fanconi anemia, complementation group M's molecular function is recorded as nuclease activity[10].
- Fanconi anemia, complementation group M's molecular function is recorded as DNA binding[11].
- Fanconi anemia, complementation group M's molecular function is recorded as chromatin binding[12].
- Fanconi anemia, complementation group M's molecular function is recorded as hydrolase activity[13].
- Fanconi anemia, complementation group M's molecular function is recorded as ATP binding[14].
- Fanconi anemia, complementation group M's molecular function is recorded as helicase activity[15].
- Fanconi anemia, complementation group M's molecular function is recorded as 3'-5' DNA helicase activity[16].
- Fanconi anemia, complementation group M's cell component is recorded as FANCM-MHF complex[17].
- Fanconi anemia, complementation group M's cell component is recorded as Fanconi anaemia nuclear complex[18].
- Fanconi anemia, complementation group M's cell component is recorded as nucleus[19].
- Fanconi anemia, complementation group M's cell component is recorded as nucleoplasm[20].
- Fanconi anemia, complementation group M's biological process is recorded as resolution of meiotic recombination intermediates[21].
- Fanconi anemia, complementation group M's biological process is recorded as DNA repair[22].
- Fanconi anemia, complementation group M's biological process is recorded as replication fork processing[23].
- Fanconi anemia, complementation group M's biological process is recorded as cellular response to DNA damage stimulus[24].
- Fanconi anemia, complementation group M's biological process is recorded as nucleic acid phosphodiester bond hydrolysis[25].
- Fanconi anemia, complementation group M's biological process is recorded as DNA duplex unwinding[26].