Details for: FARS2

Gene ID: 10667

Symbol: FARS2

Ensembl ID: ENSG00000145982

Description: phenylalanyl-tRNA synthetase 2, mitochondrial

Associated with

Other Information

Genular Protein ID: 3616789888

Symbol: SYFM_HUMAN

Name: Phenylalanine--tRNA ligase, mitochondrial

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 10329163

Title: Expression and characterization of a human mitochondrial phenylalanyl-tRNA synthetase.

PubMed ID: 10329163

DOI: 10.1006/jmbi.1999.2708

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 14574404

Title: The DNA sequence and analysis of human chromosome 6.

PubMed ID: 14574404

DOI: 10.1038/nature02055

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 19608861

Title: Lysine acetylation targets protein complexes and co-regulates major cellular functions.

PubMed ID: 19608861

DOI: 10.1126/science.1175371

PubMed ID: 25944712

Title: N-terminome analysis of the human mitochondrial proteome.

PubMed ID: 25944712

DOI: 10.1002/pmic.201400617

PubMed ID: 18611382

Title: The tRNA-induced conformational activation of human mitochondrial phenylalanyl-tRNA synthetase.

PubMed ID: 18611382

DOI: 10.1016/j.str.2008.03.020

PubMed ID: 19549855

Title: Eukaryotic cytosolic and mitochondrial phenylalanyl-tRNA synthetases catalyze the charging of tRNA with the meta-tyrosine.

PubMed ID: 19549855

DOI: 10.1073/pnas.0905212106

PubMed ID: 22833457

Title: Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy.

PubMed ID: 22833457

DOI: 10.1093/hmg/dds294

PubMed ID: 22499341

Title: Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes.

PubMed ID: 22499341

DOI: 10.1136/jmedgenet-2012-100836

PubMed ID: 26553276

Title: A newly identified missense mutation in FARS2 causes autosomal-recessive spastic paraplegia.

PubMed ID: 26553276

DOI: 10.1002/humu.22930

Sequence Information:

  • Length: 451
  • Mass: 52357
  • Checksum: 1E5CC647A4A7193B
  • Sequence:
  • MVGSALRRGA HAYVYLVSKA SHISRGHQHQ AWGSRPPAAE CATQRAPGSV VELLGKSYPQ 
    DDHSNLTRKV LTRVGRNLHN QQHHPLWLIK ERVKEHFYKQ YVGRFGTPLF SVYDNLSPVV 
    TTWQNFDSLL IPADHPSRKK GDNYYLNRTH MLRAHTSAHQ WDLLHAGLDA FLVVGDVYRR 
    DQIDSQHYPI FHQLEAVRLF SKHELFAGIK DGESLQLFEQ SSRSAHKQET HTMEAVKLVE 
    FDLKQTLTRL MAHLFGDELE IRWVDCYFPF THPSFEMEIN FHGEWLEVLG CGVMEQQLVN 
    SAGAQDRIGW AFGLGLERLA MILYDIPDIR LFWCEDERFL KQFCVSNINQ KVKFQPLSKY 
    PAVINDISFW LPSENYAEND FYDLVRTIGG DLVEKVDLID KFVHPKTHKT SHCYRITYRH 
    MERTLSQREV RHIHQALQEA AVQLLGVEGR F

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.