KRTAP10-7 keratin associated protein 10-7
Information
- Symbol
- KRTAP10-7
- Type
- protein-coding
- Description
- keratin associated protein 10-7
- Entrez Gene ID
- 386675
- Genome
- hg19
- Position
- chr21:46,020,497-46,022,091
- Genome
- hg38
- Position
- chr21:44,600,597-44,602,174
- HGNC
- HGNC:22970 HGNC
- Ensembl
- ENSG00000272804 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 1 |
Likely benign | 0 | 13 |
not provided | 1 | 0 |
Uncertain significance | 0 | 38 |
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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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
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 | |||||
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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 | |||
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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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | KAP10.7 |
SYNONYM | KAP18.7 |
SYNONYM | KRTAP18-7 |
HGNC | HGNC:22970 HGNC |
Ensembl | ENSG00000272804 Ensembl |
AllianceGenome | HGNC:22970 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000609664.2 | hg38 | chr21 | 44,600,597 | 44,602,174 | 1,578 |
ENST00000609664.2 | hg19 | chr21 | 46,020,497 | 46,022,091 | 1,595 |
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