Details for: HARS2
Associated with
Other Information
Genular Protein ID: 3817950628
Symbol: SYHM_HUMAN
Name: Histidine--tRNA ligase, mitochondrial
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 7755634
Title: A novel gene oriented in a head-to-head configuration with the human histidyl-tRNA synthetase (HRS) gene encodes an mRNA that predicts a polypeptide homologous to HRS.
PubMed ID: 7755634
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15372022
Title: The DNA sequence and comparative analysis of human chromosome 5.
PubMed ID: 15372022
DOI: 10.1038/nature02919
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: 17081983
Title: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.
PubMed ID: 17081983
PubMed ID: 19608861
Title: Lysine acetylation targets protein complexes and co-regulates major cellular functions.
PubMed ID: 19608861
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 21406692
Title: System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation.
PubMed ID: 21406692
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 24275569
Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
PubMed ID: 24275569
PubMed ID: 25944712
Title: N-terminome analysis of the human mitochondrial proteome.
PubMed ID: 25944712
PubMed ID: 21464306
Title: Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.
PubMed ID: 21464306
PubMed ID: 31449985
Title: Novel HARS2 missense variants identified in individuals with sensorineural hearing impairment and Perrault syndrome.
PubMed ID: 31449985
Sequence Information:
- Length: 506
- Mass: 56888
- Checksum: E1CE879837AE26E7
- Sequence:
MPLLGLLPRR AWASLLSQLL RPPCASCTGA VRCQSQVAEA VLTSQLKAHQ EKPNFIIKTP KGTRDLSPQH MVVREKILDL VISCFKRHGA KGMDTPAFEL KETLTEKYGE DSGLMYDLKD QGGELLSLRY DLTVPFARYL AMNKVKKMKR YHVGKVWRRE SPTIVQGRYR EFCQCDFDIA GQFDPMIPDA ECLKIMCEIL SGLQLGDFLI KVNDRRIVDG MFAVCGVPES KFRAICSSID KLDKMAWKDV RHEMVVKKGL APEVADRIGD YVQCHGGVSL VEQMFQDPRL SQNKQALEGL GDLKLLFEYL TLFGIADKIS FDLSLARGLD YYTGVIYEAV LLQTPTQAGE EPLNVGSVAA GGRYDGLVGM FDPKGHKVPC VGLSIGVERI FYIVEQRMKT KGEKVRTTET QVFVATPQKN FLQERLKLIA ELWDSGIKAE MLYKNNPKLL TQLHYCESTG IPLVVIIGEQ ELKEGVIKIR SVASREEVAI KRENFVAEIQ KRLSES
Genular Protein ID: 2353386120
Symbol: B4DDN8_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 362
- Mass: 40449
- Checksum: 2644BD420F0E6500
- Sequence:
MVVREKILDL VISCFKRHGA RGMDTPAFEL KDFDIAGQFD PMIPDAECLK IMCEILSGLQ LGDFLIKVND RRIVDGMFAV CGVPESKFRA IGSSIDKLDK MAWKDVRHEM VVKKGLAPEV ADRIGDYVQC HGGVSLVEQM FQDPRLSQNK QALEGLGDLK LLFEYLTLFG IADKISFDLS LARGLDYYTG VIYEAVLLQT PTQAGEEPLN VGSVAAGGRY DGLVGMFDPK GHKVPCVGLS IGVERIFYIV EQRMKTKGEK VRTTETQVFV ATPQKNFLQE RLKLIAELWD SGIKAEMLYK NNPKLLTQLH YCESTGIPLV VIIGEQELKE GVIKIRSVAS REEVAIKREN FVAEIQKRLS ES
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.