NCR3 natural cytotoxicity triggering receptor 3
Information
- Symbol
- NCR3
- Type
- protein-coding
- Description
- natural cytotoxicity triggering receptor 3
- Entrez Gene ID
- 259197
- Genome
- hg19
- Position
- chr6:31,556,672-31,560,783
- Genome
- hg38
- Position
- chr6:31,588,895-31,593,006
- MIM
- 611550 OMIM
- HGNC
- HGNC:19077 HGNC
- Ensembl
- ENSG00000204475 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Likely benign | 0 | 26 |
| not provided | 5 | 0 |
| Uncertain significance | 0 | 16 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
![]() |
4 |
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38 |
![]() |
2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 | 1C7 |
| SYNONYM | CD337 |
| SYNONYM | LY117 |
| SYNONYM | MALS |
| SYNONYM | NKp30 |
| MIM | 611550 OMIM |
| HGNC | HGNC:19077 HGNC |
| Ensembl | ENSG00000204475 Ensembl |
| AllianceGenome | HGNC:19077 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000340027.10 | hg38 | chr6 | 31,588,895 | 31,593,006 | 4,112 |
| ENST00000376071.4 | hg38 | chr6 | 31,589,297 | 31,592,749 | 3,453 |
| ENST00000376072.7 | hg38 | chr6 | 31,589,274 | 31,592,985 | 3,712 |
| ENST00000376073.8 | hg38 | chr6 | 31,588,895 | 31,592,985 | 4,091 |
| ENST00000376073.8 | hg19 | chr6 | 31,556,672 | 31,560,762 | 4,091 |
| ENST00000340027.10 | hg19 | chr6 | 31,556,672 | 31,560,783 | 4,112 |
| ENST00000376072.7 | hg19 | chr6 | 31,557,051 | 31,560,762 | 3,712 |
| ENST00000376071.4 | hg19 | chr6 | 31,557,074 | 31,560,526 | 3,453 |
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