DCAF12L1 DDB1 and CUL4 associated factor 12 like 1
Information
- Symbol
- DCAF12L1
- Type
- protein-coding
- Description
- DDB1 and CUL4 associated factor 12 like 1
- Entrez Gene ID
- 139170
- Genome
- hg19
- Position
- chrX:125,683,366-125,686,797
- Genome
- hg38
- Position
- chrX:126,549,383-126,552,814
- HGNC
- HGNC:29395 HGNC
- Ensembl
- ENSG00000198889 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 6 |
Likely benign | 0 | 8 |
not provided | 6 | 0 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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32 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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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Category | : |
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Search word | : | |
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
|
Category | : |
|
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 | KIAA1892L |
SYNONYM | WDR40B |
HGNC | HGNC:29395 HGNC |
Ensembl | ENSG00000198889 Ensembl |
AllianceGenome | HGNC:29395 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000371126.3 | hg38 | chrX | 126,549,383 | 126,552,814 | 3,432 |
ENST00000371126.3 | hg19 | chrX | 125,683,366 | 125,686,797 | 3,432 |
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