LRFN3 leucine rich repeat and fibronectin type III domain containing 3
Information
- Symbol
- LRFN3
- Type
- protein-coding
- Description
- leucine rich repeat and fibronectin type III domain containing 3
- Entrez Gene ID
- 79414
- Genome
- hg19
- Position
- chr19:36,427,276-36,437,526
- Genome
- hg38
- Position
- chr19:35,936,374-35,946,624
- MIM
- 612809 OMIM
- HGNC
- HGNC:28370 HGNC
- Ensembl
- ENSG00000126243 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 98 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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102 |
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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
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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 |
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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 |
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Target data | : |
MGeND data only
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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 |
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SYNONYM | FIGLER1 |
SYNONYM | SALM4 |
MIM | 612809 OMIM |
HGNC | HGNC:28370 HGNC |
Ensembl | ENSG00000126243 Ensembl |
AllianceGenome | HGNC:28370 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000588831.5 | hg38 | chr19 | 35,935,550 | 35,945,767 | 10,218 |
ENST00000246529.4 | hg38 | chr19 | 35,936,374 | 35,946,624 | 10,251 |
ENST00000588831.5 | hg19 | chr19 | 36,426,452 | 36,436,669 | 10,218 |
ENST00000246529.4 | hg19 | chr19 | 36,427,276 | 36,437,526 | 10,251 |
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