LINGO4 leucine rich repeat and Ig domain containing 4
Information
- Symbol
- LINGO4
- Type
- protein-coding
- Description
- leucine rich repeat and Ig domain containing 4
- Entrez Gene ID
- 339398
- Genome
- hg19
- Position
- chr1:151,772,740-151,777,895
- Genome
- hg38
- Position
- chr1:151,800,264-151,805,419
- MIM
- 609794 OMIM
- HGNC
- HGNC:31814 HGNC
- Ensembl
- ENSG00000213171 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 86 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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88 |
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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 | DAAT9248 |
SYNONYM | LRRN6D |
SYNONYM | PRO34002 |
MIM | 609794 OMIM |
HGNC | HGNC:31814 HGNC |
Ensembl | ENSG00000213171 Ensembl |
AllianceGenome | HGNC:31814 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000368820.4 | hg38 | chr1 | 151,800,264 | 151,805,419 | 5,156 |
ENST00000368820.4 | hg19 | chr1 | 151,772,740 | 151,777,895 | 5,156 |
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