NCR1 natural cytotoxicity triggering receptor 1
Information
- Symbol
- NCR1
- Type
- protein-coding
- Description
- natural cytotoxicity triggering receptor 1
- Entrez Gene ID
- 9437
- Genome
- hg19
- Position
- chr19:55,417,506-55,424,441
- Genome
- hg38
- Position
- chr19:54,906,148-54,913,073
- MIM
- 604530 OMIM
- HGNC
- HGNC:6731 HGNC
- Ensembl
- ENSG00000189430 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
34 |
![]() |
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 | CD335 |
SYNONYM | LY94 |
SYNONYM | NK-p46 |
SYNONYM | NKP46 |
MIM | 604530 OMIM |
HGNC | HGNC:6731 HGNC |
Ensembl | ENSG00000189430 Ensembl |
AllianceGenome | HGNC:6731 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000291890.9 | hg38 | chr19 | 54,906,148 | 54,913,073 | 6,926 |
ENST00000350790.9 | hg38 | chr19 | 54,906,181 | 54,912,973 | 6,793 |
ENST00000598576.5 | hg38 | chr19 | 54,906,156 | 54,912,959 | 6,804 |
ENST00000357397.5 | hg38 | chr19 | 54,906,188 | 54,912,871 | 6,684 |
ENST00000594765.5 | hg38 | chr19 | 54,906,163 | 54,916,140 | 9,978 |
ENST00000338835.9 | hg38 | chr19 | 54,906,181 | 54,912,973 | 6,793 |
ENST00000291890.9 | hg19 | chr19 | 55,417,506 | 55,424,441 | 6,936 |
ENST00000598576.5 | hg19 | chr19 | 55,417,514 | 55,424,327 | 6,814 |
ENST00000594765.5 | hg19 | chr19 | 55,417,521 | 55,427,508 | 9,988 |
ENST00000338835.9 | hg19 | chr19 | 55,417,539 | 55,424,341 | 6,803 |
ENST00000350790.9 | hg19 | chr19 | 55,417,539 | 55,424,341 | 6,803 |
ENST00000357397.5 | hg19 | chr19 | 55,417,546 | 55,424,239 | 6,694 |
Genome browser