CLEC18A C-type lectin domain family 18 member A
Information
- Symbol
- CLEC18A
- Type
- protein-coding
- Description
- C-type lectin domain family 18 member A
- Entrez Gene ID
- 348174
- Genome
- hg19
- Position
- chr16:69,984,810-69,997,889
- Genome
- hg38
- Position
- chr16:69,950,907-69,963,986
- MIM
- 616571 OMIM
- HGNC
- HGNC:30388 HGNC
- Ensembl
- ENSG00000157322 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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62 |
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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 |
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 | |||
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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 | MRCL |
SYNONYM | MRCL1 |
SYNONYM | MRLP2 |
MIM | 616571 OMIM |
HGNC | HGNC:30388 HGNC |
Ensembl | ENSG00000157322 Ensembl |
AllianceGenome | HGNC:30388 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000449317.6 | hg38 | chr16 | 69,951,233 | 69,963,984 | 12,752 |
ENST00000568461.5 | hg38 | chr16 | 69,950,986 | 69,963,986 | 13,001 |
ENST00000393701.6 | hg38 | chr16 | 69,950,907 | 69,963,986 | 13,080 |
ENST00000288040.11 | hg38 | chr16 | 69,951,334 | 69,963,986 | 12,653 |
ENST00000615430.4 | hg38 | chr16 | 69,950,705 | 69,964,347 | 13,643 |
ENST00000615430.4 | hg19 | chr16 | 69,984,608 | 69,998,250 | 13,643 |
ENST00000393701.6 | hg19 | chr16 | 69,984,810 | 69,997,889 | 13,080 |
ENST00000568461.5 | hg19 | chr16 | 69,984,889 | 69,997,889 | 13,001 |
ENST00000449317.6 | hg19 | chr16 | 69,985,136 | 69,997,887 | 12,752 |
ENST00000288040.11 | hg19 | chr16 | 69,985,237 | 69,997,889 | 12,653 |
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