FTCDNL1 formiminotransferase cyclodeaminase N-terminal like
Information
- Symbol
- FTCDNL1
- Type
- protein-coding
- Description
- formiminotransferase cyclodeaminase N-terminal like
- Entrez Gene ID
- 348751
- Genome
- hg19
- Position
- chr2:200,683,084-200,715,915
- Genome
- hg38
- Position
- chr2:199,818,361-199,851,192
- MIM
- 614308 OMIM
- HGNC
- HGNC:48661 HGNC
- Ensembl
- ENSG00000226124 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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2 |
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | FONG |
MIM | 614308 OMIM |
HGNC | HGNC:48661 HGNC |
Ensembl | ENSG00000226124 Ensembl |
AllianceGenome | HGNC:48661 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000420128.6 | hg38 | chr2 | 199,809,272 | 199,851,192 | 41,921 |
ENST00000703582.1 | hg38 | chr2 | 199,818,628 | 199,850,886 | 32,259 |
ENST00000420922.6 | hg38 | chr2 | 199,760,550 | 199,850,873 | 90,324 |
ENST00000416668.5 | hg38 | chr2 | 199,760,544 | 199,851,173 | 90,630 |
ENST00000622774.2 | hg38 | chr2 | 199,818,361 | 199,851,192 | 32,832 |
ENST00000416668.5 | hg19 | chr2 | 200,625,267 | 200,715,896 | 90,630 |
ENST00000420922.6 | hg19 | chr2 | 200,625,273 | 200,715,596 | 90,324 |
ENST00000420128.6 | hg19 | chr2 | 200,673,995 | 200,715,915 | 41,921 |
ENST00000622774.2 | hg19 | chr2 | 200,683,084 | 200,715,915 | 32,832 |
ENST00000703582.1 | hg19 | chr2 | 200,683,351 | 200,715,609 | 32,259 |
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