CD300LG CD300 molecule like family member g
Information
- Symbol
- CD300LG
- Type
- protein-coding
- Description
- CD300 molecule like family member g
- Entrez Gene ID
- 146894
- Genome
- hg19
- Position
- chr17:41,924,544-41,941,007
- Genome
- hg38
- Position
- chr17:43,847,176-43,863,639
- MIM
- 610520 OMIM
- HGNC
- HGNC:30455 HGNC
- Ensembl
- ENSG00000161649 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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64 |
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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 | CLM-9 |
SYNONYM | CLM9 |
SYNONYM | NEPMUCIN |
SYNONYM | TREM-4 |
SYNONYM | TREM4 |
MIM | 610520 OMIM |
HGNC | HGNC:30455 HGNC |
Ensembl | ENSG00000161649 Ensembl |
AllianceGenome | HGNC:30455 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000700726.1 | hg38 | chr17 | 43,847,176 | 43,863,623 | 16,448 |
ENST00000377203.8 | hg38 | chr17 | 43,847,148 | 43,857,997 | 10,850 |
ENST00000293396.12 | hg38 | chr17 | 43,847,156 | 43,857,760 | 10,605 |
ENST00000586233.5 | hg38 | chr17 | 43,847,156 | 43,858,040 | 10,885 |
ENST00000317310.5 | hg38 | chr17 | 43,847,176 | 43,863,639 | 16,464 |
ENST00000539718.5 | hg38 | chr17 | 43,847,148 | 43,858,234 | 11,087 |
ENST00000588884.1 | hg38 | chr17 | 43,847,153 | 43,849,909 | 2,757 |
ENST00000377203.8 | hg19 | chr17 | 41,924,516 | 41,935,365 | 10,850 |
ENST00000539718.5 | hg19 | chr17 | 41,924,516 | 41,935,602 | 11,087 |
ENST00000588884.1 | hg19 | chr17 | 41,924,521 | 41,927,277 | 2,757 |
ENST00000293396.12 | hg19 | chr17 | 41,924,524 | 41,935,128 | 10,605 |
ENST00000586233.5 | hg19 | chr17 | 41,924,524 | 41,935,408 | 10,885 |
ENST00000700726.1 | hg19 | chr17 | 41,924,544 | 41,940,991 | 16,448 |
ENST00000317310.5 | hg19 | chr17 | 41,924,544 | 41,941,007 | 16,464 |
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