LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
Information
- Symbol
- LFNG
- Type
- protein-coding
- Description
- LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
- Entrez Gene ID
- 3955
- Genome
- hg19
- Position
- chr7:2,559,408-2,568,063
- Genome
- hg38
- Position
- chr7:2,519,774-2,528,429
- MIM
- 602576 OMIM
- HGNC
- HGNC:6560 HGNC
- Ensembl
- ENSG00000106003 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 56 |
Likely benign | 0 | 224 |
Conflicting classifications of pathogenicity | 0 | 14 |
not provided | 2 | 0 |
Uncertain significance | 0 | 184 |
Ranking
ClinVar | |
---|---|
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0 |
![]() |
0 |
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58 |
![]() |
404 |
![]() |
10 |
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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Search word | : | |
Filtering | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | SCDO3 |
MIM | 602576 OMIM |
HGNC | HGNC:6560 HGNC |
Ensembl | ENSG00000106003 Ensembl |
AllianceGenome | HGNC:6560 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000359574.7 | hg38 | chr7 | 2,519,862 | 2,529,177 | 9,316 |
ENST00000402045.5 | hg38 | chr7 | 2,517,863 | 2,528,429 | 10,567 |
ENST00000402506.5 | hg38 | chr7 | 2,512,529 | 2,528,427 | 15,899 |
ENST00000338732.7 | hg38 | chr7 | 2,518,554 | 2,528,427 | 9,874 |
ENST00000222725.10 | hg38 | chr7 | 2,519,774 | 2,528,429 | 8,656 |
ENST00000402506.5 | hg19 | chr7 | 2,552,163 | 2,568,061 | 15,899 |
ENST00000402045.5 | hg19 | chr7 | 2,557,497 | 2,568,063 | 10,567 |
ENST00000338732.7 | hg19 | chr7 | 2,558,188 | 2,568,061 | 9,874 |
ENST00000222725.10 | hg19 | chr7 | 2,559,408 | 2,568,063 | 8,656 |
ENST00000359574.7 | hg19 | chr7 | 2,559,496 | 2,568,811 | 9,316 |
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