NAV3 neuron navigator 3

Information
Symbol
NAV3
Type
protein-coding
Description
neuron navigator 3
Entrez Gene ID
89795
Genome
hg19
Position
chr12:78,224,674-78,606,790
Genome
hg38
Position
chr12:77,830,894-78,213,010
MIM
611629 OMIM
HGNC
HGNC:15998 HGNC
Ensembl
ENSG00000067798 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 18
Likely benign 0 10
Uncertain significance 0 204
Ranking
ClinVar
0
0
0
232
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM POMFIL1
SYNONYM STEERIN3
SYNONYM unc53H3
MIM 611629 OMIM
HGNC HGNC:15998 HGNC
Ensembl ENSG00000067798 Ensembl
AllianceGenome HGNC:15998
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000397909.7 hg38 chr12 77,830,894 78,213,010 382,117
ENST00000644176.1 hg38 chr12 78,036,257 78,211,465 175,209
ENST00000536525.6 hg38 chr12 77,831,289 78,210,638 379,350
ENST00000397909.7 hg19 chr12 78,224,674 78,606,790 382,117
ENST00000536525.6 hg19 chr12 78,225,069 78,604,418 379,350
ENST00000644176.1 hg19 chr12 78,430,037 78,605,245 175,209
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