FYN FYN proto-oncogene, Src family tyrosine kinase
Information
- Symbol
- FYN
- Type
- protein-coding
- Description
- FYN proto-oncogene, Src family tyrosine kinase
- Entrez Gene ID
- 2534
- Genome
- hg19
- Position
- chr6:111,981,535-112,194,655
- Genome
- hg38
- Position
- chr6:111,660,332-111,873,452
- MIM
- 137025 OMIM
- HGNC
- HGNC:4037 HGNC
- Ensembl
- ENSG00000010810 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 12 |
| Likely benign | 0 | 2 |
| not provided | 9 | 12 |
| Uncertain significance | 0 | 24 |
Ranking
| ClinVar | |
|---|---|
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0 |
![]() |
0 |
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2 |
![]() |
36 |
![]() |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| 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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| 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
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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 | SLK |
| SYNONYM | SYN |
| SYNONYM | p59-FYN |
| MIM | 137025 OMIM |
| HGNC | HGNC:4037 HGNC |
| Ensembl | ENSG00000010810 Ensembl |
| AllianceGenome | HGNC:4037 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000368682.8 | hg38 | chr6 | 111,660,332 | 111,873,452 | 213,121 |
| ENST00000354650.7 | hg38 | chr6 | 111,660,332 | 111,873,452 | 213,121 |
| ENST00000229471.8 | hg38 | chr6 | 111,661,282 | 111,759,131 | 97,850 |
| ENST00000368667.6 | hg38 | chr6 | 111,661,282 | 111,793,886 | 132,605 |
| ENST00000368678.8 | hg38 | chr6 | 111,661,286 | 111,873,430 | 212,145 |
| ENST00000368682.8 | hg19 | chr6 | 111,981,535 | 112,194,655 | 213,121 |
| ENST00000229471.8 | hg19 | chr6 | 111,982,485 | 112,080,334 | 97,850 |
| ENST00000354650.7 | hg19 | chr6 | 111,981,535 | 112,194,655 | 213,121 |
| ENST00000368667.6 | hg19 | chr6 | 111,982,485 | 112,115,089 | 132,605 |
| ENST00000368678.8 | hg19 | chr6 | 111,982,489 | 112,194,633 | 212,145 |
| Key | Value |
|---|---|
| strand | - |
| UniProt | OG |
| start | 111,981,534 |
| Gene Symbol | FYN |
| Entrez GeneId | 2,534 |
| Chr Band | 6q21 |
| end | 112,194,654 |
| chr | chr6 |
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