ANKAR ankyrin and armadillo repeat containing
Information
- Symbol
- ANKAR
- Type
- protein-coding
- Description
- ankyrin and armadillo repeat containing
- Entrez Gene ID
- 150709
- Genome
- hg19
- Position
- chr2:190,539,396-190,611,373
- Genome
- hg38
- Position
- chr2:189,674,670-189,746,647
- MIM
- 609803 OMIM
- HGNC
- HGNC:26350 HGNC
- Ensembl
- ENSG00000151687 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 22 |
Likely benign | 0 | 18 |
Uncertain significance | 0 | 124 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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164 |
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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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
MIM | 609803 OMIM |
HGNC | HGNC:26350 HGNC |
Ensembl | ENSG00000151687 Ensembl |
AllianceGenome | HGNC:26350 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000520309.5 | hg38 | chr2 | 189,675,985 | 189,746,644 | 70,660 |
ENST00000684021.1 | hg38 | chr2 | 189,674,670 | 189,746,647 | 71,978 |
ENST00000313581.4 | hg38 | chr2 | 189,676,427 | 189,746,649 | 70,223 |
ENST00000684021.1 | hg19 | chr2 | 190,539,396 | 190,611,373 | 71,978 |
ENST00000520309.5 | hg19 | chr2 | 190,540,711 | 190,611,370 | 70,660 |
ENST00000313581.4 | hg19 | chr2 | 190,541,153 | 190,611,375 | 70,223 |
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