KRTAP10-2 keratin associated protein 10-2
Information
- Symbol
- KRTAP10-2
- Type
- protein-coding
- Description
- keratin associated protein 10-2
- Entrez Gene ID
- 386679
- Genome
- hg19
- Position
- chr21:45,970,240-45,971,388
- Genome
- hg38
- Position
- chr21:44,550,357-44,551,505
- HGNC
- HGNC:22967 HGNC
- Ensembl
- ENSG00000205445 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
40 |
 |
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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| 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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| 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
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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 | KAP10.2 |
| SYNONYM | KAP18-2 |
| SYNONYM | KAP18.2 |
| SYNONYM | KRTAP10.2 |
| SYNONYM | KRTAP18-2 |
| SYNONYM | KRTAP18.2 |
| HGNC | HGNC:22967 HGNC |
| Ensembl | ENSG00000205445 Ensembl |
| AllianceGenome | HGNC:22967 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000391621.1 | hg38 | chr21 | 44,550,357 | 44,551,505 | 1,149 |
| ENST00000391621.1 | hg19 | chr21 | 45,970,240 | 45,971,388 | 1,149 |
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