NOD1 nucleotide binding oligomerization domain containing 1
Information
- Symbol
- NOD1
- Type
- protein-coding
- Description
- nucleotide binding oligomerization domain containing 1
- Entrez Gene ID
- 10392
- Genome
- hg19
- Position
- chr7:30,464,143-30,518,400
- Genome
- hg38
- Position
- chr7:30,424,527-30,478,784
- MIM
- 605980 OMIM
- HGNC
- HGNC:16390 HGNC
- Ensembl
- ENSG00000106100 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 12 |
| Likely benign | 0 | 24 |
| not provided | 0 | 50 |
| Uncertain significance | 0 | 102 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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138 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| 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 | CARD4 |
| SYNONYM | CLR7.1 |
| SYNONYM | NLRC1 |
| SYNONYM | hNod1 |
| MIM | 605980 OMIM |
| HGNC | HGNC:16390 HGNC |
| Ensembl | ENSG00000106100 Ensembl |
| AllianceGenome | HGNC:16390 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000222823.9 | hg38 | chr7 | 30,424,527 | 30,478,784 | 54,258 |
| ENST00000222823.9 | hg19 | chr7 | 30,464,143 | 30,518,400 | 54,258 |
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