MGAT4D MGAT4 family member D
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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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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 | GnT1IP |
MIM | 610310 OMIM |
HGNC | HGNC:43619 HGNC |
Ensembl | ENSG00000205301 Ensembl |
AllianceGenome | HGNC:43619 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000515354.5 | hg38 | chr4 | 140,442,262 | 140,498,353 | 56,092 |
ENST00000503109.6 | hg38 | chr4 | 140,449,956 | 140,498,222 | 48,267 |
ENST00000511113.6 | hg38 | chr4 | 140,442,262 | 140,498,293 | 56,032 |
ENST00000511113.6 | hg19 | chr4 | 141,363,416 | 141,419,447 | 56,032 |
ENST00000515354.5 | hg19 | chr4 | 141,363,416 | 141,419,507 | 56,092 |
ENST00000503109.6 | hg19 | chr4 | 141,371,110 | 141,419,376 | 48,267 |
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