MORF4L2 mortality factor 4 like 2
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 6 | 0 |
| Uncertain significance | 0 | 10 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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10 |
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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
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | MORFL2 |
| SYNONYM | MRGX |
| MIM | 300409 OMIM |
| HGNC | HGNC:16849 HGNC |
| Ensembl | ENSG00000123562 Ensembl |
| AllianceGenome | HGNC:16849 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000441076.7 | hg38 | chrX | 103,675,498 | 103,686,699 | 11,202 |
| ENST00000433176.6 | hg38 | chrX | 103,675,500 | 103,688,158 | 12,659 |
| ENST00000360458.5 | hg38 | chrX | 103,675,496 | 103,688,064 | 12,569 |
| ENST00000451301.5 | hg38 | chrX | 103,675,500 | 103,686,818 | 11,319 |
| ENST00000360458.5 | hg19 | chrX | 102,930,424 | 102,942,992 | 12,569 |
| ENST00000441076.7 | hg19 | chrX | 102,930,426 | 102,941,627 | 11,202 |
| ENST00000451301.5 | hg19 | chrX | 102,930,428 | 102,941,746 | 11,319 |
| ENST00000433176.6 | hg19 | chrX | 102,930,428 | 102,943,086 | 12,659 |
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