NXT2 nuclear transport factor 2 like export factor 2

Information
Symbol
NXT2
Type
protein-coding
Description
nuclear transport factor 2 like export factor 2
Entrez Gene ID
55916
Genome
hg19
Position
chrX:108,779,010-108,787,913
Genome
hg38
Position
chrX:109,535,781-109,544,684
MIM
300320 OMIM
HGNC
HGNC:18151 HGNC
Ensembl
ENSG00000101888 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 6 0
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
6
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
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 P15-2
MIM 300320 OMIM
HGNC HGNC:18151 HGNC
Ensembl ENSG00000101888 Ensembl
AllianceGenome HGNC:18151
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000218004.5 hg38 chrX 109,535,781 109,544,684 8,904
ENST00000372103.1 hg38 chrX 109,537,118 109,543,206 6,089
ENST00000372107.5 hg38 chrX 109,536,664 109,542,974 6,311
ENST00000372106.6 hg38 chrX 109,536,844 109,544,698 7,855
ENST00000218004.5 hg19 chrX 108,779,010 108,787,913 8,904
ENST00000372107.5 hg19 chrX 108,779,893 108,786,203 6,311
ENST00000372106.6 hg19 chrX 108,780,073 108,787,927 7,855
ENST00000372103.1 hg19 chrX 108,780,347 108,786,435 6,089
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