NMRK2 nicotinamide riboside kinase 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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 |
Prediction | |||||
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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 |
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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 | ITGB1BP3 |
SYNONYM | MIBP |
SYNONYM | NRK2 |
MIM | 608705 OMIM |
HGNC | HGNC:17871 HGNC |
Ensembl | ENSG00000077009 Ensembl |
AllianceGenome | HGNC:17871 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000593949.1 | hg38 | chr19 | 3,933,607 | 3,942,369 | 8,763 |
ENST00000168977.7 | hg38 | chr19 | 3,933,069 | 3,942,416 | 9,348 |
ENST00000599576.5 | hg38 | chr19 | 3,933,116 | 3,942,413 | 9,298 |
ENST00000616156.4 | hg38 | chr19 | 3,933,103 | 3,942,414 | 9,312 |
ENST00000168977.7 | hg19 | chr19 | 3,933,067 | 3,942,414 | 9,348 |
ENST00000616156.4 | hg19 | chr19 | 3,933,101 | 3,942,412 | 9,312 |
ENST00000599576.5 | hg19 | chr19 | 3,933,114 | 3,942,411 | 9,298 |
ENST00000593949.1 | hg19 | chr19 | 3,933,605 | 3,942,367 | 8,763 |
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