Details for: THG1L

Gene ID: 54974

Symbol: THG1L

Ensembl ID: ENSG00000113272

Description: tRNA-histidine guanylyltransferase 1 like

Associated with

Other Information

Genular Protein ID: 3861813934

Symbol: THG1_HUMAN

Name: Probable tRNA(His) guanylyltransferase

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 15459185

Title: Identification and characterization of a novel cytoplasm protein ICF45 that is involved in cell cycle regulation.

PubMed ID: 15459185

DOI: 10.1074/jbc.m406737200

PubMed ID: 11230166

Title: Towards a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.

PubMed ID: 11230166

DOI: 10.1101/gr.gr1547r

PubMed ID: 14702039

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

PubMed ID: 14702039

DOI: 10.1038/ng1285

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: 25008184

Title: IHG-1 increases mitochondrial fusion and bioenergetic function.

PubMed ID: 25008184

DOI: 10.2337/db13-1256

PubMed ID: 21059936

Title: tRNA(His) guanylyltransferase (THG1), a unique 3'-5' nucleotidyl transferase, shares unexpected structural homology with canonical 5'-3' DNA polymerases.

PubMed ID: 21059936

DOI: 10.1073/pnas.1010436107

PubMed ID: 27307223

Title: A mutation in the THG1L gene in a family with cerebellar ataxia and developmental delay.

PubMed ID: 27307223

DOI: 10.1007/s10048-016-0487-z

PubMed ID: 31168944

Title: Refining the phenotype of the THG1L (p.Val55Ala mutation)-related mitochondrial autosomal recessive congenital cerebellar ataxia.

PubMed ID: 31168944

DOI: 10.1002/ajmg.a.61196

PubMed ID: 30214071

Title: Genomic and phenotypic delineation of congenital microcephaly.

PubMed ID: 30214071

DOI: 10.1038/s41436-018-0140-3

Sequence Information:

  • Length: 298
  • Mass: 34831
  • Checksum: A6C941B75611C448
  • Sequence:
  • MWGACKVKVH DSLATISITL RRYLRLGATM AKSKFEYVRD FEADDTCLAH CWVVVRLDGR 
    NFHRFAEKHN FAKPNDSRAL QLMTKCAQTV MEELEDIVIA YGQSDEYSFV FKRKTNWFKR 
    RASKFMTHVA SQFASSYVFY WRDYFEDQPL LYPPGFDGRV VVYPSNQTLK DYLSWRQADC 
    HINNLYNTVF WALIQQSGLT PVQAQGRLQG TLAADKNEIL FSEFNINYNN ELPMYRKGTV 
    LIWQKVDEVM TKEIKLPTEM EGKKMAVTRT RTKPVPLHCD IIGDAFWKEH PEILDEDS

Genular Protein ID: 2404251855

Symbol: B4E366_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 166
  • Mass: 18948
  • Checksum: 6CE96057A098FCA6
  • Sequence:
  • MDRVMSTALC SSGKPIGLKE EPGFDGRVVV YPSNQTLKDY LSWRQADCHI NNLYNTVFWA 
    LIQQSGLTPV QAQGRLQGTL AADKNEILFS EFNINYNNEL PMYRKGTVLI WQKVDEVMTK 
    EIKLPTEMEG KKMAVTRTRT KPVPLHCDII GDAFWKEHPE ILDEDS

Genular Protein ID: 1683350846

Symbol: Q9H8R6_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 14702039

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

PubMed ID: 14702039

DOI: 10.1038/ng1285

Sequence Information:

  • Length: 173
  • Mass: 20157
  • Checksum: 70C1D8FFC116B416
  • Sequence:
  • MTHVASQFAS SYVFYWRDYF EDQPLLYPPG FDGRVVVYPS NQTLKDYLSW RQADCHINNL 
    YNTVFWALIQ QSGLTPVQAQ GRLQGTLAAD KNEILFSEFN INYNNELPMY RKGTVLIWQK 
    VDEVMTKEIK LPTEMEGKKM AVTRTRTKPV PLHCDIIGDA FWKEHPEILD EDS

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.