Details for: TENT5A

Gene ID: 55603

Symbol: TENT5A

Ensembl ID: ENSG00000112773

Description: terminal nucleotidyltransferase 5A

Associated with

Other Information

Genular Protein ID: 2966469567

Symbol: TET5A_HUMAN

Name: N/A

UniProtKB Accession Codes:

Q96IP4 A8K7U4 Q5TF86 Q8NFZ9 Q9BW32 Q9NXV5

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 BRENDA 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 1 CTD 1 ChEBI 4 ChiTaRS 1 DMDM 1 DNASU 1 DisGeNET 1 EC 1 EMBL 9 EPD 1 Ensembl 2 ExpressionAtlas 1 GO 8 GeneCards 1 GeneTree 1 GeneWiki 1 Genevisible 1 GenomeRNAi 1 HGNC 2 HOGENOM 1 HPA 1 InParanoid 1 IntAct 1 InterPro 1 KEGG 1 MANE-Select 1 MIM 3 MalaCards 1 MassIVE 1 MaxQB 1 NCBI Taxonomy 1 OpenTargets 1 Orphanet 1 OrthoDB 1 PANTHER 2 PDB 3 PDBsum 2 PIR 1 PRO 1 PathwayCommons 1 PaxDb 1 PeptideAtlas 1 Pfam 1 PharmGKB 1 Pharos 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 2 Pumba 1 RNAct 1 RefSeq 1 Rhea 4 SMART 1 SMR 1 STRING 1 SignaLink 1 TreeFam 1 UCSC 1 UniProtKB 1 VEuPathDB 1 eggNOG 1 iPTMnet 1 jPOST 1 neXtProt 1

Citations:

PubMed ID: 12054608

Title: Identification and characterization of C6orf37, a novel candidate human retinal disease gene on chromosome 6q14.

PubMed ID: 12054608

DOI: 10.1016/s0006-291x(02)00228-0

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: 33882302

Title: Cytoplasmic polyadenylation by TENT5A is required for proper bone formation.

PubMed ID: 33882302

DOI: 10.1016/j.celrep.2021.109015

PubMed ID: 29358272

Title: FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta.

PubMed ID: 29358272

DOI: 10.1136/jmedgenet-2017-104999

PubMed ID: 16545789

Title: Identification of a novel VNTR polymorphism in C6orf37 and its association with colorectal cancer risk in Chinese population.

PubMed ID: 16545789

DOI: 10.1016/j.cca.2005.12.043

Sequence Information:

  • Length: 442
  • Mass: 49666
  • Checksum: C72092C590C1E369
  • Sequence:
    • MAEGEGYFAM SEDELACSPY IPLGGDFGGG DFGGGDFGGG DFGGGGSFGG HCLDYCESPT 
AHCNVLNWEQ VQRLDGILSE TIPIHGRGNF PTLELQPSLI VKVVRRRLAE KRIGVRDVRL 
NGSAASHVLH QDSGLGYKDL DLIFCADLRG EGEFQTVKDV VLDCLLDFLP EGVNKEKITP 
LTLKEAYVQK MVKVCNDSDR WSLISLSNNS GKNVELKFVD SLRRQFEFSV DSFQIKLDSL 
LLFYECSENP MTETFHPTII GESVYGDFQE AFDHLCNKII ATRNPEEIRG GGLLKYCNLL 
VRGFRPASDE IKTLQRYMCS RFFIDFSDIG EQQRKLESYL QNHFVGLEDR KYEYLMTLHG 
VVNESTVCLM GHERRQTLNL ITMLAIRVLA DQNVIPNVAN VTCYYQPAPY VADANFSNYY 
IAQVQPVFTC QQQTYSTWLP CN

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.