KRTAP9-9 keratin associated protein 9-9
Information
- Symbol
- KRTAP9-9
- Type
- protein-coding
- Description
- keratin associated protein 9-9
- Entrez Gene ID
- 81870
- Genome
- hg19
- Position
- chr17:39,411,636-39,412,616
- Genome
- hg38
- Position
- chr17:41,255,384-41,256,364
- HGNC
- HGNC:16773 HGNC
- Ensembl
- ENSG00000198083 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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30 |
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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 |
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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 |
---|---|
SYNONYM | KAP9.5 |
SYNONYM | KAP9.9 |
SYNONYM | KRTAP9-5 |
SYNONYM | KRTAP9.9 |
HGNC | HGNC:16773 HGNC |
Ensembl | ENSG00000198083 Ensembl |
AllianceGenome | HGNC:16773 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000394008.1 | hg38 | chr17 | 41,255,384 | 41,256,364 | 981 |
ENST00000394008.1 | hg19 | chr17 | 39,411,636 | 39,412,616 | 981 |
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