MARCHF9 membrane associated ring-CH-type finger 9
Information
- Symbol
- MARCHF9
- Type
- protein-coding
- Description
- membrane associated ring-CH-type finger 9
- Entrez Gene ID
- 92979
- Genome
- hg19
- Position
- chr12:58,148,886-58,154,194
- Genome
- hg38
- Position
- chr12:57,755,103-57,760,411
- MIM
- 613336 OMIM
- HGNC
- HGNC:25139 HGNC
- Ensembl
- ENSG00000139266 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 48 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
48 |
 |
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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| 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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| 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-IX |
| SYNONYM | MARCH9 |
| SYNONYM | RNF179 |
| MIM | 613336 OMIM |
| HGNC | HGNC:25139 HGNC |
| Ensembl | ENSG00000139266 Ensembl |
| AllianceGenome | HGNC:25139 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000548358.1 | hg38 | chr12 | 57,757,487 | 57,759,416 | 1,930 |
| ENST00000266643.6 | hg38 | chr12 | 57,755,103 | 57,760,411 | 5,309 |
| ENST00000266643.6 | hg19 | chr12 | 58,148,886 | 58,154,194 | 5,309 |
| ENST00000548358.1 | hg19 | chr12 | 58,151,270 | 58,153,199 | 1,930 |
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