DRC12 dynein regulatory complex subunit 12 homolog
Information
- Symbol
- DRC12
- Type
- protein-coding
- Description
- dynein regulatory complex subunit 12 homolog
- Entrez Gene ID
- 283152
- Genome
- hg19
- Position
- chr11:119,060,965-119,067,479
- Genome
- hg38
- Position
- chr11:119,190,256-119,196,769
- HGNC
- HGNC:27446 HGNC
- Ensembl
- ENSG00000248712 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 20 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
22 |
 |
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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| 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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| 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 | CCDC153 |
| HGNC | HGNC:27446 HGNC |
| Ensembl | ENSG00000248712 Ensembl |
| AllianceGenome | HGNC:27446 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000503566.7 | hg38 | chr11 | 119,190,254 | 119,195,841 | 5,588 |
| ENST00000415318.2 | hg38 | chr11 | 119,190,256 | 119,196,769 | 6,514 |
| ENST00000503566.7 | hg19 | chr11 | 119,060,963 | 119,066,551 | 5,589 |
| ENST00000415318.2 | hg19 | chr11 | 119,060,965 | 119,067,479 | 6,515 |
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