CLEC4C C-type lectin domain family 4 member C
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 24 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
30 |
 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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 | BDCA-2 |
| SYNONYM | BDCA2 |
| SYNONYM | CD303 |
| SYNONYM | CLECSF11 |
| SYNONYM | CLECSF7 |
| SYNONYM | DLEC |
| SYNONYM | HECL |
| SYNONYM | PRO34150 |
| MIM | 606677 OMIM |
| HGNC | HGNC:13258 HGNC |
| Ensembl | ENSG00000198178 Ensembl |
| AllianceGenome | HGNC:13258 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000360345.8 | hg38 | chr12 | 7,729,383 | 7,747,375 | 17,993 |
| ENST00000542353.5 | hg38 | chr12 | 7,729,415 | 7,749,473 | 20,059 |
| ENST00000540085.5 | hg38 | chr12 | 7,729,442 | 7,747,505 | 18,064 |
| ENST00000354629.9 | hg38 | chr12 | 7,729,415 | 7,751,605 | 22,191 |
| ENST00000360345.8 | hg19 | chr12 | 7,881,979 | 7,899,971 | 17,993 |
| ENST00000542353.5 | hg19 | chr12 | 7,882,011 | 7,902,069 | 20,059 |
| ENST00000354629.9 | hg19 | chr12 | 7,882,011 | 7,904,201 | 22,191 |
| ENST00000540085.5 | hg19 | chr12 | 7,882,038 | 7,900,101 | 18,064 |
Genome browser