Aliases for NAP1L1 Gene
External Ids for NAP1L1 Gene
Previous GeneCards Identifiers for NAP1L1 Gene
This gene encodes a member of the nucleosome assembly protein (NAP) family. This protein participates in DNA replication and may play a role in modulating chromatin formation and contribute to the regulation of cell proliferation. Alternative splicing results in multiple transcript variants encoding different isoforms; however, not all have been fully described. [provided by RefSeq, Apr 2015]
GeneCards Summary for NAP1L1 Gene
NAP1L1 (Nucleosome Assembly Protein 1 Like 1) is a Protein Coding gene. Diseases associated with NAP1L1 include Transient Antenatal Bartter Syndrome and Antenatal Bartter Syndrome. An important paralog of this gene is NAP1L4.
UniProtKB/Swiss-Prot Summary for NAP1L1 Gene
Plays a key role in the regulation of embryonic neurogenesis (By similarity). Promotes the proliferation of neural progenitors and inhibits neuronal differentiation during cortical development (By similarity). Regulates neurogenesis via the modulation of RASSF10; regulates RASSF10 expression by promoting SETD1A-mediated H3K4 methylation at the RASSF10 promoter (By similarity).