CLEC12A C-type lectin domain family 12 member A
Information
- Symbol
- CLEC12A
- Type
- protein-coding
- Description
- C-type lectin domain family 12 member A
- Entrez Gene ID
- 160364
- Genome
- hg19
- Position
- chr12:10,103,915-10,138,194
- Genome
- hg38
- Position
- chr12:9,951,316-9,985,595
- MIM
- 612088 OMIM
- HGNC
- HGNC:31713 HGNC
- Ensembl
- ENSG00000172322 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 30 |
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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| 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
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| Category | : |
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| 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 | CD371 |
| SYNONYM | CLL-1 |
| SYNONYM | CLL1 |
| SYNONYM | DCAL-2 |
| SYNONYM | MICL |
| MIM | 612088 OMIM |
| HGNC | HGNC:31713 HGNC |
| Ensembl | ENSG00000172322 Ensembl |
| AllianceGenome | HGNC:31713 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000304361.9 | hg38 | chr12 | 9,971,409 | 9,985,595 | 14,187 |
| ENST00000434319.6 | hg38 | chr12 | 9,971,435 | 9,984,241 | 12,807 |
| ENST00000350667.4 | hg38 | chr12 | 9,971,597 | 9,985,026 | 13,430 |
| ENST00000355690.8 | hg38 | chr12 | 9,951,316 | 9,985,595 | 34,280 |
| ENST00000355690.8 | hg19 | chr12 | 10,103,915 | 10,138,194 | 34,280 |
| ENST00000304361.9 | hg19 | chr12 | 10,124,008 | 10,138,194 | 14,187 |
| ENST00000434319.6 | hg19 | chr12 | 10,124,034 | 10,136,840 | 12,807 |
| ENST00000350667.4 | hg19 | chr12 | 10,124,196 | 10,137,625 | 13,430 |
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