MARCHF2 membrane associated ring-CH-type finger 2
Information
- Symbol
- MARCHF2
- Type
- protein-coding
- Description
- membrane associated ring-CH-type finger 2
- Entrez Gene ID
- 51257
- Genome
- hg19
- Position
- chr19:8,483,289-8,503,901
- Genome
- hg38
- Position
- chr19:8,418,405-8,439,017
- MIM
- 613332 OMIM
- HGNC
- HGNC:28038 HGNC
- Ensembl
- ENSG00000099785 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 40 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
44 |
 |
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
| 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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| 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 | HSPC240 |
| SYNONYM | MARCH-II |
| SYNONYM | MARCH2 |
| SYNONYM | RNF172 |
| MIM | 613332 OMIM |
| HGNC | HGNC:28038 HGNC |
| Ensembl | ENSG00000099785 Ensembl |
| AllianceGenome | HGNC:28038 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000601283.5 | hg38 | chr19 | 8,413,305 | 8,438,731 | 25,427 |
| ENST00000215555.7 | hg38 | chr19 | 8,413,305 | 8,439,017 | 25,713 |
| ENST00000381035.8 | hg38 | chr19 | 8,413,270 | 8,439,004 | 25,735 |
| ENST00000602117.1 | hg38 | chr19 | 8,418,405 | 8,439,017 | 20,613 |
| ENST00000381035.8 | hg19 | chr19 | 8,478,154 | 8,503,888 | 25,735 |
| ENST00000601283.5 | hg19 | chr19 | 8,478,189 | 8,503,615 | 25,427 |
| ENST00000215555.7 | hg19 | chr19 | 8,478,189 | 8,503,901 | 25,713 |
| ENST00000602117.1 | hg19 | chr19 | 8,483,289 | 8,503,901 | 20,613 |
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