RTN4RL2 reticulon 4 receptor like 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | NGRH1 |
SYNONYM | NgR2 |
MIM | 610462 OMIM |
HGNC | HGNC:23053 HGNC |
Ensembl | ENSG00000186907 Ensembl |
AllianceGenome | HGNC:23053 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000335099.8 | hg38 | chr11 | 57,460,528 | 57,477,534 | 17,007 |
ENST00000533205.5 | hg38 | chr11 | 57,460,857 | 57,468,884 | 8,028 |
ENST00000395120.2 | hg38 | chr11 | 57,460,866 | 57,468,630 | 7,765 |
ENST00000335099.8 | hg19 | chr11 | 57,228,001 | 57,245,007 | 17,007 |
ENST00000533205.5 | hg19 | chr11 | 57,228,330 | 57,236,357 | 8,028 |
ENST00000395120.2 | hg19 | chr11 | 57,228,339 | 57,236,103 | 7,765 |
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