SLX4 SLX4 structure-specific endonuclease subunit
Information
- Symbol
- SLX4
- Type
- protein-coding
- Description
- SLX4 structure-specific endonuclease subunit
- Entrez Gene ID
- 84464
- Genome
- hg19
- Position
- chr16:3,631,182-3,661,607
- Genome
- hg38
- Position
- chr16:3,581,181-3,611,606
- MIM
- 613278 OMIM
- HGNC
- HGNC:23845 HGNC
- Ensembl
- ENSG00000188827 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 4 | 178 |
Likely pathogenic | 2 | 68 |
Benign | 14 | 216 |
Likely benign | 4 | 1,346 |
Conflicting classifications of pathogenicity | 0 | 172 |
not provided | 422 | 0 |
Uncertain significance | 26 | 2,394 |
Ranking
ClinVar | |
---|---|
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0 |
![]() |
0 |
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1,090 |
![]() |
2,932 |
![]() |
80 |
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 | BTBD12 |
SYNONYM | FANCP |
SYNONYM | MUS312 |
MIM | 613278 OMIM |
HGNC | HGNC:23845 HGNC |
Ensembl | ENSG00000188827 Ensembl |
AllianceGenome | HGNC:23845 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000294008.4 | hg38 | chr16 | 3,581,181 | 3,611,606 | 30,426 |
ENST00000294008.4 | hg19 | chr16 | 3,631,182 | 3,661,607 | 30,426 |
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