XB-FEAT-6036017: Difference between revisions
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=nlgn4x= | =nlgn4x= | ||
This is the community wiki page for the gene ''nlgn4x'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase | This is the community wiki page for the gene ''nlgn4x'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
05.08.2018 | |||
Human name has changed for Entrez Gene: 57502. From neuroligin 4, X-linked to neuroligin 4 X-linked. | |||
=summary from NCBI= | |||
This gene encodes a member of the type-B carboxylesterase/lipase protein family. The encoded protein belongs to a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. The encoded protein interacts with discs large homolog 4 (DLG4). Mutations in this gene have been associated with autism and Asperger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] | |||
Latest revision as of 08:39, 8 May 2018
nlgn4x
This is the community wiki page for the gene nlgn4x please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
05.08.2018 Human name has changed for Entrez Gene: 57502. From neuroligin 4, X-linked to neuroligin 4 X-linked.
summary from NCBI
This gene encodes a member of the type-B carboxylesterase/lipase protein family. The encoded protein belongs to a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. The encoded protein interacts with discs large homolog 4 (DLG4). Mutations in this gene have been associated with autism and Asperger syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]