SMCR7L

Mitochondrial dynamic protein MID51 (MID51) also known as mitochondrial elongation factor 1 (MIEF1) or Smith-Magenis syndrome chromosome region candidate gene 7 protein-like (SMCR7L) is a protein that in humans is encoded by the SMCR7L gene.[5][6][7]

MIEF1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMIEF1, HSU79252, MID51, SMCR7L, dJ1104E15.3, mitochondrial elongation factor 1, AltMIEF1-MP
External IDsOMIM: 615497 MGI: 2146020 HomoloGene: 10374 GeneCards: MIEF1
Gene location (Human)
Chr.Chromosome 22 (human)[1]
Band22q13.1Start39,499,432 bp[1]
End39,518,132 bp[1]
RNA expression pattern




More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

54471

239555

Ensembl

ENSG00000100335

ENSMUSG00000022412

UniProt

L0R8F8

Q8BGV8

RefSeq (mRNA)

NM_001304564
NM_013298
NM_019008

NM_178719
NM_001357659
NM_001357660

RefSeq (protein)

NP_001291493
NP_061881

NP_848834
NP_001344588
NP_001344589

Location (UCSC)Chr 22: 39.5 – 39.52 MbChr 15: 80.23 – 80.25 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

The SMCR7L gene codes for a protein that has been called MiD51/MIEF1 and shown to regulate mitochondrial fission by interacting with the proteins Drp1 and FIS1.[8]

References

  1. GRCh38: Ensembl release 89: ENSG00000100335 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000022412 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Wiemann S; Weil B; Wellenreuther R; Gassenhuber J; Glassl S; Ansorge W; Bocher M; Blocker H; Bauersachs S; Blum H; Lauber J; Dusterhoft A; Beyer A; Kohrer K; Strack N; Mewes HW; Ottenwalder B; Obermaier B; Tampe J; Heubner D; Wambutt R; Korn B; Klein M; Poustka A (Mar 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072. PMID 11230166.
  6. Andersson B; Wentland MA; Ricafrente JY; Liu W; Gibbs RA (Jun 1996). "A "double adaptor" method for improved shotgun library construction". Anal Biochem. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474.
  7. "Entrez Gene: SMCR7L Smith-Magenis syndrome chromosome region, candidate 7-like".
  8. Dikov, D.; Reichert, A. S. (2011). "How to split up: Lessons from mitochondria". The EMBO Journal. 30 (14): 2751–2753. doi:10.1038/emboj.2011.219. PMC 3160261. PMID 21772324.

Further reading


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