CIMIP2B ciliary microtubule inner protein 2B
Information
- Symbol
- CIMIP2B
- Type
- protein-coding
- Description
- ciliary microtubule inner protein 2B
- Entrez Gene ID
- 730112
- Genome
- hg19
- Position
- chr9:35,561,828-35,563,875
- Genome
- hg38
- Position
- chr9:35,561,831-35,563,878
- HGNC
- HGNC:34242 HGNC
- Ensembl
- ENSG00000215187 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 50 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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54 |
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2 |
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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| 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 | FAM166B |
| HGNC | HGNC:34242 HGNC |
| Ensembl | ENSG00000215187 Ensembl |
| AllianceGenome | HGNC:34242 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000447837.1 | hg38 | chr9 | 35,561,949 | 35,563,899 | 1,951 |
| ENST00000399742.7 | hg38 | chr9 | 35,561,831 | 35,563,878 | 2,048 |
| ENST00000492890.5 | hg38 | chr9 | 35,561,831 | 35,563,874 | 2,044 |
| ENST00000492890.5 | hg19 | chr9 | 35,561,828 | 35,563,871 | 2,044 |
| ENST00000399742.7 | hg19 | chr9 | 35,561,828 | 35,563,875 | 2,048 |
| ENST00000447837.1 | hg19 | chr9 | 35,561,946 | 35,563,896 | 1,951 |
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