ASB11 ankyrin repeat and SOCS box containing 11
Information
- Symbol
- ASB11
- Type
- protein-coding
- Description
- ankyrin repeat and SOCS box containing 11
- Entrez Gene ID
- 140456
- Genome
- hg19
- Position
- chrX:15,299,819-15,333,762
- Genome
- hg38
- Position
- chrX:15,281,697-15,315,640
- MIM
- 300626 OMIM
- HGNC
- HGNC:17186 HGNC
- Ensembl
- ENSG00000165192 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 8 |
| not provided | 7 | 0 |
| Uncertain significance | 0 | 42 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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52 |
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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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| Category | : |
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| 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
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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 | : |
|
| 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 |
|---|---|
| MIM | 300626 OMIM |
| HGNC | HGNC:17186 HGNC |
| Ensembl | ENSG00000165192 Ensembl |
| AllianceGenome | HGNC:17186 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000480796.6 | hg38 | chrX | 15,281,697 | 15,315,640 | 33,944 |
| ENST00000380470.7 | hg38 | chrX | 15,281,697 | 15,315,624 | 33,928 |
| ENST00000344384.8 | hg38 | chrX | 15,282,319 | 15,314,559 | 32,241 |
| ENST00000380470.7 | hg19 | chrX | 15,299,819 | 15,333,746 | 33,928 |
| ENST00000480796.6 | hg19 | chrX | 15,299,819 | 15,333,762 | 33,944 |
| ENST00000344384.8 | hg19 | chrX | 15,300,441 | 15,332,681 | 32,241 |
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