NXT1 nuclear transport factor 2 like export factor 1
Information
- Symbol
- NXT1
- Type
- protein-coding
- Description
- nuclear transport factor 2 like export factor 1
- Entrez Gene ID
- 29107
- Genome
- hg19
- Position
- chr20:23,331,428-23,335,408
- Genome
- hg38
- Position
- chr20:23,350,791-23,354,771
- MIM
- 605811 OMIM
- HGNC
- HGNC:15913 HGNC
- Ensembl
- ENSG00000132661 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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12 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | MTR2 |
SYNONYM | P15 |
MIM | 605811 OMIM |
HGNC | HGNC:15913 HGNC |
Ensembl | ENSG00000132661 Ensembl |
AllianceGenome | HGNC:15913 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000254998.3 | hg38 | chr20 | 23,350,791 | 23,354,771 | 3,981 |
ENST00000254998.3 | hg19 | chr20 | 23,331,428 | 23,335,408 | 3,981 |
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