TIRAP TIR domain containing adaptor protein
Information
- Symbol
- TIRAP
- Type
- protein-coding
- Description
- TIR domain containing adaptor protein
- Entrez Gene ID
- 114609
- Genome
- hg19
- Position
- chr11:126,153,005-126,163,139
- Genome
- hg38
- Position
- chr11:126,283,110-126,293,244
- MIM
- 606252 OMIM
- HGNC
- HGNC:17192 HGNC
- Ensembl
- ENSG00000150455 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 20 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 16 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
4 |
 |
38 |
 |
4 |
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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| Category | : |
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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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| Category | : |
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| 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 | : |
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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 | BACTS1 |
| SYNONYM | Mal |
| SYNONYM | MyD88-2 |
| SYNONYM | wyatt |
| MIM | 606252 OMIM |
| HGNC | HGNC:17192 HGNC |
| Ensembl | ENSG00000150455 Ensembl |
| AllianceGenome | HGNC:17192 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000700489.1 | hg38 | chr11 | 126,283,001 | 126,296,129 | 13,129 |
| ENST00000700488.1 | hg38 | chr11 | 126,282,497 | 126,296,129 | 13,633 |
| ENST00000700490.1 | hg38 | chr11 | 126,283,046 | 126,296,158 | 13,113 |
| ENST00000700495.1 | hg38 | chr11 | 126,290,471 | 126,296,158 | 5,688 |
| ENST00000700492.1 | hg38 | chr11 | 126,283,131 | 126,293,234 | 10,104 |
| ENST00000700491.1 | hg38 | chr11 | 126,283,094 | 126,293,117 | 10,024 |
| ENST00000392680.6 | hg38 | chr11 | 126,283,118 | 126,294,684 | 11,567 |
| ENST00000392679.6 | hg38 | chr11 | 126,283,093 | 126,294,933 | 11,841 |
| ENST00000392678.7 | hg38 | chr11 | 126,283,110 | 126,293,244 | 10,135 |
| ENST00000700488.1 | hg19 | chr11 | 126,152,392 | 126,166,024 | 13,633 |
| ENST00000700489.1 | hg19 | chr11 | 126,152,896 | 126,166,024 | 13,129 |
| ENST00000700490.1 | hg19 | chr11 | 126,152,941 | 126,166,053 | 13,113 |
| ENST00000392679.6 | hg19 | chr11 | 126,152,988 | 126,164,828 | 11,841 |
| ENST00000700491.1 | hg19 | chr11 | 126,152,989 | 126,163,012 | 10,024 |
| ENST00000392678.7 | hg19 | chr11 | 126,153,005 | 126,163,139 | 10,135 |
| ENST00000392680.6 | hg19 | chr11 | 126,153,013 | 126,164,579 | 11,567 |
| ENST00000700492.1 | hg19 | chr11 | 126,153,026 | 126,163,129 | 10,104 |
| ENST00000700495.1 | hg19 | chr11 | 126,160,366 | 126,166,053 | 5,688 |
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