INSC INSC spindle orientation adaptor protein
Information
- Symbol
- INSC
- Type
- protein-coding
- Description
- INSC spindle orientation adaptor protein
- Entrez Gene ID
- 387755
- Genome
- hg19
- Position
- chr11:15,133,970-15,268,754
- Genome
- hg38
- Position
- chr11:15,112,424-15,247,208
- MIM
- 610668 OMIM
- HGNC
- HGNC:33116 HGNC
- Ensembl
- ENSG00000188487 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 88 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
96 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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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| 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 | 610668 OMIM |
| HGNC | HGNC:33116 HGNC |
| Ensembl | ENSG00000188487 Ensembl |
| AllianceGenome | HGNC:33116 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000424273.5 | hg38 | chr11 | 15,149,102 | 15,247,206 | 98,105 |
| ENST00000530161.5 | hg38 | chr11 | 15,149,108 | 15,246,076 | 96,969 |
| ENST00000528567.5 | hg38 | chr11 | 15,149,102 | 15,246,526 | 97,425 |
| ENST00000379556.8 | hg38 | chr11 | 15,114,923 | 15,247,208 | 132,286 |
| ENST00000379554.7 | hg38 | chr11 | 15,112,424 | 15,247,208 | 134,785 |
| ENST00000525218.1 | hg38 | chr11 | 15,149,108 | 15,246,076 | 96,969 |
| ENST00000379554.7 | hg19 | chr11 | 15,133,970 | 15,268,754 | 134,785 |
| ENST00000379556.8 | hg19 | chr11 | 15,136,469 | 15,268,754 | 132,286 |
| ENST00000528567.5 | hg19 | chr11 | 15,170,648 | 15,268,072 | 97,425 |
| ENST00000424273.5 | hg19 | chr11 | 15,170,648 | 15,268,752 | 98,105 |
| ENST00000530161.5 | hg19 | chr11 | 15,170,654 | 15,267,622 | 96,969 |
| ENST00000525218.1 | hg19 | chr11 | 15,170,654 | 15,267,622 | 96,969 |
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