FLT3LG fms related receptor tyrosine kinase 3 ligand
Information
- Symbol
- FLT3LG
- Type
- protein-coding
- Description
- fms related receptor tyrosine kinase 3 ligand
- Entrez Gene ID
- 2323
- Genome
- hg19
- Position
- chr19:49,977,818-49,989,488
- Genome
- hg38
- Position
- chr19:49,474,561-49,486,231
- MIM
- 600007 OMIM
- HGNC
- HGNC:3766 HGNC
- Ensembl
- ENSG00000090554 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
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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24 |
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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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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 | FL |
SYNONYM | FLG3L |
SYNONYM | FLT3L |
MIM | 600007 OMIM |
HGNC | HGNC:3766 HGNC |
Ensembl | ENSG00000090554 Ensembl |
AllianceGenome | HGNC:3766 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000597551.6 | hg38 | chr19 | 49,474,215 | 49,486,231 | 12,017 |
ENST00000600429.5 | hg38 | chr19 | 49,474,252 | 49,486,151 | 11,900 |
ENST00000594009.5 | hg38 | chr19 | 49,474,561 | 49,486,231 | 11,671 |
ENST00000595510.1 | hg38 | chr19 | 49,474,602 | 49,482,391 | 7,790 |
ENST00000596435.5 | hg38 | chr19 | 49,474,228 | 49,486,231 | 12,004 |
ENST00000204637.6 | hg38 | chr19 | 49,474,236 | 49,486,231 | 11,996 |
ENST00000597551.6 | hg19 | chr19 | 49,977,472 | 49,989,488 | 12,017 |
ENST00000596435.5 | hg19 | chr19 | 49,977,485 | 49,989,488 | 12,004 |
ENST00000204637.6 | hg19 | chr19 | 49,977,493 | 49,989,488 | 11,996 |
ENST00000600429.5 | hg19 | chr19 | 49,977,509 | 49,989,408 | 11,900 |
ENST00000594009.5 | hg19 | chr19 | 49,977,818 | 49,989,488 | 11,671 |
ENST00000595510.1 | hg19 | chr19 | 49,977,859 | 49,985,648 | 7,790 |
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