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MIRAGE
Transcription elongation factor, mitochondrial
Summary
- UniProt ID
- Q96QE5
- Gene Symbol
-
- C17orf42
- TEFM
- Gene ID
- 79736
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Disease variant
- Mitochondrion nucleoid
- Primary mitochondrial disease
- Reference proteome
- Transcription regulation
- Transit peptide
- Gene Ontology (GO)
| GO Term |
|---|
| mitochondrial nucleoid |
| ribonucleoprotein complex |
| mitochondrion |
| mitochondrial matrix |
| GO Term |
|---|
| oxidative phosphorylation |
| mitochondrial transcription |
| transcription elongation by mitochondrial RNA polymerase |
| GO Term |
|---|
| DNA polymerase processivity factor activity |
| RNA binding |
Sequence
MSGSVLFTAGERWRCFLTPSRSSLYWALHNFCCRKKSTTPKKITPNVTFCDENAKEPENALDKLFSSEQQASILHVLNTASTKELEAFRLLRGRRSINIVEHRENFGPFQNLESLMNVPLFKYKSTVQVCNSILCPKTGREKRKSPENRFLRKLLKPDIERERLKAVNSIISIVFGTRRIAWAHLDRKLTVLDWQQSDRWSLMRGIYSSSVYLEEISSIISKMPKADFYVLEKTGLSIQNSSLFPILLHFHIMEAMLYALLNKTFAQDGQHQVLSMNRNAVGKHFELMIGDSRTSGKELVKQFLFDSILKADPRVFFPSDKIVHYRQMFLSTELQRVEELYDSLLQAIAFYELAVFDSQP
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 125 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060286 | combined oxidative phosphorylation deficiency |
