MLF2 myeloid leukemia factor 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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
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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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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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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 | NTN4 |
MIM | 601401 OMIM |
HGNC | HGNC:7126 HGNC |
Ensembl | ENSG00000089693 Ensembl |
AllianceGenome | HGNC:7126 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000203630.10 | hg38 | chr12 | 6,747,996 | 6,753,141 | 5,146 |
ENST00000435120.5 | hg38 | chr12 | 6,748,004 | 6,752,916 | 4,913 |
ENST00000539187.5 | hg38 | chr12 | 6,748,795 | 6,767,475 | 18,681 |
ENST00000203630.10 | hg19 | chr12 | 6,857,162 | 6,862,307 | 5,146 |
ENST00000435120.5 | hg19 | chr12 | 6,857,170 | 6,862,082 | 4,913 |
ENST00000539187.5 | hg19 | chr12 | 6,857,961 | 6,876,641 | 18,681 |
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