CFLAR CASP8 and FADD like apoptosis regulator
Information
- Symbol
- CFLAR
- Type
- protein-coding
- Description
- CASP8 and FADD like apoptosis regulator
- Entrez Gene ID
- 8837
- Genome
- hg19
- Position
- chr2:201,980,887-202,041,410
- Genome
- hg38
- Position
- chr2:201,116,164-201,176,687
- MIM
- 603599 OMIM
- HGNC
- HGNC:1876 HGNC
- Ensembl
- ENSG00000003402 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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28 |
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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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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 | CASH |
SYNONYM | CASP8AP1 |
SYNONYM | CLARP |
SYNONYM | Casper |
SYNONYM | FLAME |
SYNONYM | FLAME-1 |
SYNONYM | FLAME1 |
SYNONYM | FLIP |
SYNONYM | I-FLICE |
SYNONYM | MRIT |
SYNONYM | c-FLIP |
SYNONYM | c-FLIPL |
SYNONYM | c-FLIPR |
SYNONYM | c-FLIPS |
SYNONYM | cFLIP |
MIM | 603599 OMIM |
HGNC | HGNC:1876 HGNC |
Ensembl | ENSG00000003402 Ensembl |
AllianceGenome | HGNC:1876 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000309955.8 | hg38 | chr2 | 201,116,164 | 201,176,687 | 60,524 |
ENST00000395148.6 | hg38 | chr2 | 201,116,407 | 201,139,877 | 23,471 |
ENST00000423241.6 | hg38 | chr2 | 201,118,491 | 201,164,110 | 45,620 |
ENST00000341582.10 | hg38 | chr2 | 201,116,207 | 201,164,279 | 48,073 |
ENST00000479953.6 | hg38 | chr2 | 201,132,984 | 201,163,157 | 30,174 |
ENST00000342795.9 | hg38 | chr2 | 201,116,239 | 201,154,576 | 38,338 |
ENST00000443227.5 | hg38 | chr2 | 201,116,154 | 201,164,162 | 48,009 |
ENST00000457277.5 | hg38 | chr2 | 201,129,866 | 201,163,559 | 33,694 |
ENST00000494258.5 | hg38 | chr2 | 201,132,779 | 201,140,735 | 7,957 |
ENST00000341222.10 | hg38 | chr2 | 201,116,167 | 201,141,598 | 25,432 |
ENST00000440180.5 | hg38 | chr2 | 201,129,503 | 201,141,602 | 12,100 |
ENST00000309955.8 | hg19 | chr2 | 201,980,887 | 202,041,410 | 60,524 |
ENST00000341222.10 | hg19 | chr2 | 201,980,890 | 202,006,321 | 25,432 |
ENST00000341582.10 | hg19 | chr2 | 201,980,930 | 202,029,002 | 48,073 |
ENST00000342795.9 | hg19 | chr2 | 201,980,962 | 202,019,299 | 38,338 |
ENST00000395148.6 | hg19 | chr2 | 201,981,130 | 202,004,600 | 23,471 |
ENST00000443227.5 | hg19 | chr2 | 201,980,877 | 202,028,885 | 48,009 |
ENST00000423241.6 | hg19 | chr2 | 201,983,214 | 202,028,833 | 45,620 |
ENST00000440180.5 | hg19 | chr2 | 201,994,226 | 202,006,325 | 12,100 |
ENST00000457277.5 | hg19 | chr2 | 201,994,589 | 202,028,282 | 33,694 |
ENST00000494258.5 | hg19 | chr2 | 201,997,502 | 202,005,458 | 7,957 |
ENST00000479953.6 | hg19 | chr2 | 201,997,707 | 202,027,880 | 30,174 |
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