CLEC4A C-type lectin domain family 4 member A
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 26 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
32 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CD367 |
| SYNONYM | CLECSF6 |
| SYNONYM | DCIR |
| SYNONYM | DDB27 |
| SYNONYM | HDCGC13P |
| SYNONYM | LLIR |
| SYNONYM | hDCIR |
| MIM | 605306 OMIM |
| HGNC | HGNC:13257 HGNC |
| Ensembl | ENSG00000111729 Ensembl |
| AllianceGenome | HGNC:13257 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000229332.12 | hg38 | chr12 | 8,123,617 | 8,138,607 | 14,991 |
| ENST00000352620.9 | hg38 | chr12 | 8,123,879 | 8,138,287 | 14,409 |
| ENST00000345999.9 | hg38 | chr12 | 8,123,853 | 8,138,604 | 14,752 |
| ENST00000360500.5 | hg38 | chr12 | 8,123,879 | 8,138,287 | 14,409 |
| ENST00000229332.12 | hg19 | chr12 | 8,276,213 | 8,291,203 | 14,991 |
| ENST00000345999.9 | hg19 | chr12 | 8,276,449 | 8,291,200 | 14,752 |
| ENST00000352620.9 | hg19 | chr12 | 8,276,475 | 8,290,883 | 14,409 |
| ENST00000360500.5 | hg19 | chr12 | 8,276,475 | 8,290,883 | 14,409 |
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