Fancm - FA complementation group M Gene

Rattus norvegicus

Also known as RGD1307897

Gene ID: 314172 | Gene type: protein coding

About Fancm

Summary

Predicted to enable chromatin binding activity. Predicted to be involved in positive regulation of protein monoubiquitination; replication fork processing; and resolution of meiotic recombination intermediates. Predicted to be located in nucleoplasm. Predicted to be part of FANCM-MHF complex and Fanconi anaemia nuclear complex. Human ortholog(s) of this gene implicated in primary ovarian insufficiency 15 and spermatogenic failure 28. Orthologous to human FANCM (FA complementation group M). [provided by Alliance of Genome Resources, Apr 2022]

Protein Preferred Names

Protein Names

FA complementation group M

Fanconi anemia, complementation group M

Related Agents

Pre-clinical Phase

Bioactive Molecules (5)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-124325	PIP-199		≥98.0%	Unkown
HY-163573	FANCM-BTR PPI-IN-1		98.61%	Unkown
HY-RS04741	FANCM Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown
HY-RS18278	Fancm Mouse Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown
HY-RS24756	Fancm Rat Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Fancm	NCBI	NCBI:57697

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