MARCHF10 membrane associated ring-CH-type finger 10
Information
- Symbol
- MARCHF10
- Type
- protein-coding
- Description
- membrane associated ring-CH-type finger 10
- Entrez Gene ID
- 162333
- Genome
- hg19
- Position
- chr17:60,778,676-60,885,705
- Genome
- hg38
- Position
- chr17:62,701,315-62,808,344
- MIM
- 613337 OMIM
- HGNC
- HGNC:26655 HGNC
- Ensembl
- ENSG00000173838 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 34 |
| Likely benign | 0 | 28 |
| Uncertain significance | 0 | 80 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
142 |
 |
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 | MARCH-X |
| SYNONYM | MARCH10 |
| SYNONYM | RNF190 |
| MIM | 613337 OMIM |
| HGNC | HGNC:26655 HGNC |
| Ensembl | ENSG00000173838 Ensembl |
| AllianceGenome | HGNC:26655 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000544856.6 | hg38 | chr17 | 62,704,948 | 62,808,290 | 103,343 |
| ENST00000456609.6 | hg38 | chr17 | 62,701,314 | 62,806,653 | 105,340 |
| ENST00000311269.10 | hg38 | chr17 | 62,701,314 | 62,808,314 | 107,001 |
| ENST00000583600.5 | hg38 | chr17 | 62,701,315 | 62,808,344 | 107,030 |
| ENST00000456609.6 | hg19 | chr17 | 60,778,675 | 60,884,014 | 105,340 |
| ENST00000311269.10 | hg19 | chr17 | 60,778,675 | 60,885,675 | 107,001 |
| ENST00000583600.5 | hg19 | chr17 | 60,778,676 | 60,885,705 | 107,030 |
| ENST00000544856.6 | hg19 | chr17 | 60,782,309 | 60,885,651 | 103,343 |
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