MCPH1 Products

Description

MCPH-1 was identified in a screen for negative regulators of hTERT (human telomerase) expression. It has been implicated in chromosome condensation and DNA damage induced cellular responses. It may play a role in neurogenesis and regulation of the size of the cerebral cortex. Defects in MCPH1 are the cause of primary microcephaly 1.

Bioinformatics

Entrez	79648 Human
Uniprot	AAH30702.2 Human NM_024596 Human NP_078872 Human Q8NEM0 Human
Product By Gene ID	79648
Alternate Names	BRCT-repeat inhibitor of TERT expression 1 BRIT1 FLJ12847 MCT microcephalin 1 microcephalin microcephaly, primary autosomal recessive 1

Research Areas for MCPH1

Find related products by research area and learn more about each of the different research areas below.

DNA Repair