MARCHF7 membrane associated ring-CH-type finger 7
Information
- Symbol
- MARCHF7
- Type
- protein-coding
- Description
- membrane associated ring-CH-type finger 7
- Entrez Gene ID
- 64844
- Genome
- hg19
- Position
- chr2:160,569,017-160,627,538
- Genome
- hg38
- Position
- chr2:159,712,506-159,771,027
- MIM
- 613334 OMIM
- HGNC
- HGNC:17393 HGNC
- Ensembl
- ENSG00000136536 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 84 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
84 |
 |
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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| 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 | AXO |
| SYNONYM | AXOT |
| SYNONYM | MARCH-VII |
| SYNONYM | MARCH7 |
| SYNONYM | RNF177 |
| MIM | 613334 OMIM |
| HGNC | HGNC:17393 HGNC |
| Ensembl | ENSG00000136536 Ensembl |
| AllianceGenome | HGNC:17393 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000409175.6 | hg38 | chr2 | 159,712,506 | 159,771,027 | 58,522 |
| ENST00000259050.8 | hg38 | chr2 | 159,712,499 | 159,771,027 | 58,529 |
| ENST00000409591.5 | hg38 | chr2 | 159,733,965 | 159,767,409 | 33,445 |
| ENST00000539065.5 | hg38 | chr2 | 159,712,457 | 159,768,583 | 56,127 |
| ENST00000539065.5 | hg19 | chr2 | 160,568,968 | 160,625,094 | 56,127 |
| ENST00000259050.8 | hg19 | chr2 | 160,569,010 | 160,627,538 | 58,529 |
| ENST00000409175.6 | hg19 | chr2 | 160,569,017 | 160,627,538 | 58,522 |
| ENST00000409591.5 | hg19 | chr2 | 160,590,476 | 160,623,920 | 33,445 |
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