IWS1 interacts with SUPT6H, CTD assembly factor 1
Information
- Symbol
- IWS1
- Type
- protein-coding
- Description
- interacts with SUPT6H, CTD assembly factor 1
- Entrez Gene ID
- 55677
- Genome
- hg19
- Position
- chr2:128,238,388-128,284,065
- Genome
- hg38
- Position
- chr2:127,480,812-127,526,489
- HGNC
- HGNC:25467 HGNC
- Ensembl
- ENSG00000163166 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 60 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
68 |
 |
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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| 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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000637187.2 | hg38 | chr2 | 127,480,810 | 127,526,510 | 45,701 |
| ENST00000295321.9 | hg38 | chr2 | 127,480,812 | 127,526,489 | 45,678 |
| ENST00000637187.2 | hg19 | chr2 | 128,238,386 | 128,284,086 | 45,701 |
| ENST00000295321.9 | hg19 | chr2 | 128,238,388 | 128,284,065 | 45,678 |
| Key | Value |
|---|---|
| strand | - |
| start | 128,238,382 |
| Gene Symbol | IWS1 |
| Entrez GeneId | 55,677 |
| Chr Band | 2q14.3 |
| end | 128,284,086 |
| chr | chr2 |
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