SAMM50

Protein-coding gene in the species Homo sapiens
SAMM50
Identifiers
AliasesSAMM50, OMP85, SAM50, TOB55, TRG-3, YNL026W, CGI-51, SAMM50 sorting and assembly machinery component
External IDsOMIM: 612058; MGI: 1915903; HomoloGene: 41034; GeneCards: SAMM50; OMA:SAMM50 - orthologs
Gene location (Human)
Chromosome 22 (human)
Chr.Chromosome 22 (human)[1]
Chromosome 22 (human)
Genomic location for SAMM50
Genomic location for SAMM50
Band22q13.31Start43,955,442 bp[1]
End44,010,531 bp[1]
Gene location (Mouse)
Chromosome 15 (mouse)
Chr.Chromosome 15 (mouse)[2]
Chromosome 15 (mouse)
Genomic location for SAMM50
Genomic location for SAMM50
Band15|15 E2Start84,076,442 bp[2]
End84,101,468 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • endothelial cell

  • vastus lateralis muscle

  • gastrocnemius muscle

  • thoracic diaphragm

  • triceps brachii muscle

  • body of tongue

  • deltoid muscle

  • left ventricle

  • left adrenal gland

  • right uterine tube
Top expressed in
  • Paneth cell

  • otic placode

  • saccule

  • medullary collecting duct

  • fossa

  • condyle

  • motor neuron

  • renal corpuscle

  • endocardial cushion

  • substantia nigra
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
  • protein binding
Cellular component
  • cytoplasm
  • integral component of membrane
  • mitochondrial inner membrane
  • outer membrane
  • mitochondrial outer membrane
  • extracellular exosome
  • membrane
  • mitochondrion
  • SAM complex
Biological process
  • cristae formation
  • protein insertion into mitochondrial outer membrane
  • mitochondrial respiratory chain complex assembly
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

25813

68653

Ensembl

ENSG00000100347

ENSMUSG00000022437

UniProt

Q9Y512

Q8BGH2

RefSeq (mRNA)

NM_015380

NM_178614

RefSeq (protein)

NP_056195

NP_848729

Location (UCSC)Chr 22: 43.96 – 44.01 MbChr 15: 84.08 – 84.1 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Sorting and assembly machinery component 50 homolog is a protein that in humans is encoded by the SAMM50 gene.[5][6]

Clinical significance

By means of exome sequencing, two variants - P377A and V231I on the SAMM50 gene were determined to have a potential relationship to the disease phenotype of Ezra, 9 year old male with Epilepsy, ESES, Hemiplegic Migraine, Exocrine Pancreatic Insuffiency, CSID, Global Apraxia, developmental regressions. History of torticollis, psychomotor regression, colitis as well as Carnitine Deficiency.

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000100347 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022437 – 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. ^ Humphries AD, Streimann IC, Stojanovski D, Johnston AJ, Yano M, Hoogenraad NJ, Ryan MT (Mar 2005). "Dissection of the mitochondrial import and assembly pathway for human Tom40". The Journal of Biological Chemistry. 280 (12): 11535–43. doi:10.1074/jbc.M413816200. PMID 15644312.
  6. ^ "Entrez Gene: SAMM50 sorting and assembly machinery component 50 homolog (S. cerevisiae)".

Further reading

  • Maruyama K, Sugano S (Jan 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (Oct 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
  • Lai CH, Chou CY, Ch'ang LY, Liu CS, Lin W (May 2000). "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics". Genome Research. 10 (5): 703–13. doi:10.1101/gr.10.5.703. PMC 310876. PMID 10810093.
  • Collins JE, Wright CL, Edwards CA, Davis MP, Grinham JA, Cole CG, Goward ME, Aguado B, Mallya M, Mokrab Y, Huckle EJ, Beare DM, Dunham I (2005). "A genome annotation-driven approach to cloning the human ORFeome". Genome Biology. 5 (10): R84. doi:10.1186/gb-2004-5-10-r84. PMC 545604. PMID 15461802.
  • Kozjak-Pavlovic V, Ross K, Benlasfer N, Kimmig S, Karlas A, Rudel T (Jun 2007). "Conserved roles of Sam50 and metaxins in VDAC biogenesis". EMBO Reports. 8 (6): 576–82. doi:10.1038/sj.embor.7400982. PMC 2002532. PMID 17510655.
  • Xie J, Marusich MF, Souda P, Whitelegge J, Capaldi RA (Jul 2007). "The mitochondrial inner membrane protein mitofilin exists as a complex with SAM50, metaxins 1 and 2, coiled-coil-helix coiled-coil-helix domain-containing protein 3 and 6 and DnaJC11". FEBS Letters. 581 (18): 3545–9. doi:10.1016/j.febslet.2007.06.052. PMID 17624330.
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