NAV3 (Entrez ID: 89795)

Entrez Gene ID	89795
Official Gene Symbol	NAV3 (GeneCards)
Full name	neuron navigator 3
Location	12q21.2
Other ids	Vega : OTTHUMG00000170001 MIM : 611629 HGNC : HGNC:15998 Ensembl : ENSG00000067798
Other names	POMFIL1, nc53H3, STEERIN3
Summary	This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. Multiple alternatively spliced transcript variants for this gene have been described but only one has had its full-length nature determined. [provided by RefSeq, Jul 2008]

Variants

Found 15 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
16082	89795	NAV3	12	78793967	78793967	Asymptomatic	HiSeq X Ten
16108	89795	NAV3	12	78686956	78686956	Asymptomatic	HiSeq X Ten
16262	89795	NAV3	12	78895285	78895285	Asymptomatic	HiSeq X Ten
16293	89795	NAV3	12	78412099	78412099	Asymptomatic	HiSeq X Ten
16349	89795	NAV3	12	78397344	78397344	Asymptomatic	HiSeq X Ten
16488	89795	NAV3	12	78635039	78635039	Asymptomatic	HiSeq X Ten
16489	89795	NAV3	12	78660068	78660068	Asymptomatic	HiSeq X Ten
16573	89795	NAV3	12	78867752	78867752	Asymptomatic	HiSeq X Ten
16814	89795	NAV3	12	78768882	78768882	Asymptomatic	HiSeq X Ten
16895	89795	NAV3	12	78486076	78486076	Cockayne syndrome	HiSeq X Ten
23663	89795	NAV3	12	78897459	78897459	Asymptomatic	HiSeq X Ten Single cell Sequencing Cell cloning
23702	89795	NAV3	12	79174747	79174747	Asymptomatic	HiSeq X Ten Single cell Sequencing Cell cloning
27454	89795	NAV3	12	78664545	78664545	Asymptomatic	HiSeq X Ten Single cell Sequencing Cell cloning
29356	89795	NAV3	12	78511923	78511923	Autism Spectrum Disorders	HiSeq X Ten Single cell Sequencing Cell cloning MiSeq
34710	89795	NAV3	12	78571018	78571018	Asymptomatic	HiSeq X Ten Single cell Sequencing Cell cloning MiSeq Whole Exome Sequencing Target Amplicon Sequencing Pyrosequencing