SETD4 SET domain containing 4
Information
- Symbol
- SETD4
- Type
- protein-coding
- Description
- SET domain containing 4
- Entrez Gene ID
- 54093
- Genome
- hg19
- Position
- chr21:37,406,839-37,432,559
- Genome
- hg38
- Position
- chr21:36,034,541-36,060,261
- HGNC
- HGNC:1258 HGNC
- Ensembl
- ENSG00000185917 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | C21orf18 |
SYNONYM | C21orf27 |
HGNC | HGNC:1258 HGNC |
Ensembl | ENSG00000185917 Ensembl |
AllianceGenome | HGNC:1258 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000399215.5 | hg38 | chr21 | 36,034,541 | 36,060,261 | 25,721 |
ENST00000399212.5 | hg38 | chr21 | 36,034,541 | 36,060,526 | 25,986 |
ENST00000332131.9 | hg38 | chr21 | 36,034,541 | 36,060,526 | 25,986 |
ENST00000399207.5 | hg38 | chr21 | 36,043,698 | 36,060,245 | 16,548 |
ENST00000399208.6 | hg38 | chr21 | 36,043,686 | 36,060,364 | 16,679 |
ENST00000399205.5 | hg38 | chr21 | 36,043,686 | 36,060,313 | 16,628 |
ENST00000399201.5 | hg38 | chr21 | 36,043,686 | 36,079,389 | 35,704 |
ENST00000399215.5 | hg19 | chr21 | 37,406,839 | 37,432,559 | 25,721 |
ENST00000399212.5 | hg19 | chr21 | 37,406,839 | 37,432,824 | 25,986 |
ENST00000332131.9 | hg19 | chr21 | 37,406,839 | 37,432,824 | 25,986 |
ENST00000399205.5 | hg19 | chr21 | 37,415,984 | 37,432,611 | 16,628 |
ENST00000399208.6 | hg19 | chr21 | 37,415,984 | 37,432,662 | 16,679 |
ENST00000399201.5 | hg19 | chr21 | 37,415,984 | 37,451,687 | 35,704 |
ENST00000399207.5 | hg19 | chr21 | 37,415,996 | 37,432,543 | 16,548 |
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