ASB9 ankyrin repeat and SOCS box containing 9
Information
- Symbol
- ASB9
- Type
- protein-coding
- Description
- ankyrin repeat and SOCS box containing 9
- Entrez Gene ID
- 140462
- Genome
- hg19
- Position
- chrX:15,262,109-15,288,205
- Genome
- hg38
- Position
- chrX:15,243,987-15,270,083
- MIM
- 300890 OMIM
- HGNC
- HGNC:17184 HGNC
- Ensembl
- ENSG00000102048 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 7 | 0 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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20 |
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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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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
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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 | 300890 OMIM |
HGNC | HGNC:17184 HGNC |
Ensembl | ENSG00000102048 Ensembl |
AllianceGenome | HGNC:17184 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000380485.7 | hg38 | chrX | 15,243,987 | 15,270,061 | 26,075 |
ENST00000380488.9 | hg38 | chrX | 15,243,987 | 15,270,083 | 26,097 |
ENST00000380483.7 | hg38 | chrX | 15,243,987 | 15,270,051 | 26,065 |
ENST00000546332.1 | hg38 | chrX | 15,243,989 | 15,270,467 | 26,479 |
ENST00000380483.7 | hg19 | chrX | 15,262,109 | 15,288,173 | 26,065 |
ENST00000380485.7 | hg19 | chrX | 15,262,109 | 15,288,183 | 26,075 |
ENST00000380488.9 | hg19 | chrX | 15,262,109 | 15,288,205 | 26,097 |
ENST00000546332.1 | hg19 | chrX | 15,262,111 | 15,288,589 | 26,479 |
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