CLEC4G C-type lectin domain family 4 member G
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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16 |
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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
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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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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 | DTTR431 |
SYNONYM | LP2698 |
SYNONYM | LSECtin |
SYNONYM | UNQ431 |
MIM | 616256 OMIM |
HGNC | HGNC:24591 HGNC |
Ensembl | ENSG00000182566 Ensembl |
AllianceGenome | HGNC:24591 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000678118.1 | hg38 | chr19 | 7,728,958 | 7,732,171 | 3,214 |
ENST00000676742.1 | hg38 | chr19 | 7,728,958 | 7,732,170 | 3,213 |
ENST00000328853.11 | hg38 | chr19 | 7,728,957 | 7,732,110 | 3,154 |
ENST00000328853.11 | hg19 | chr19 | 7,793,843 | 7,796,996 | 3,154 |
ENST00000676742.1 | hg19 | chr19 | 7,793,844 | 7,797,056 | 3,213 |
ENST00000678118.1 | hg19 | chr19 | 7,793,844 | 7,797,057 | 3,214 |
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