Selected-GenAtlas references SOURCE GeneCards NCBI Gene Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol TENT5A contributors: mct - updated : 18-11-2019
HGNC name terminal nucleotidyltransferase 5A
HGNC id 18345
Corresponding disease
OIXVIII osteogenesis imperfecta, type XVIII
Location 6q14      Physical location : -
Synonym name
  • retinal expressed gene C6orf37
  • chromosome 6 open reading frame 37
  • HBV X-transactivated gene 11 protein
  • family with sequence similarity 46, member A
  • Synonym symbol(s) FLJ20037, C6orf37, XTP11, FLJ31495, FAM46A
    DNA
    TYPE functioning gene
    STRUCTURE 3.00 kb     3 Exon(s)
    MAPPING cloned Y linked N status provisional
    RNA
    TRANSCRIPTS type messenger
    EXPRESSION
    Type widely
    constitutive of
       expressed in (based on citations)
    organ(s)
    SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
    Endocrineadrenal gland    
     neuroendocrinepituitary   
    Reproductivefemale systemuteruscervix  
    Respiratoryrespiratory tractlarynx   
    Visualeyeretina   
    tissue
    SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
    Blood / hematopoieticbone marrow   
    cell lineage
    cell lines
    fluid/secretion
    at STAGE
    physiological period pregnancy
    Text placenta
    PROTEIN
    PHYSICAL PROPERTIES globular
    STRUCTURE
    motifs/domains several conserved phosphorylation sites
    conjugated PhosphoP
    HOMOLOGY
    interspecies homolog to dog LOC481896
    ortholog to murine BC023892
    Homologene
    FAMILY FAM46 family
    CATEGORY unknown/unspecified
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm
    basic FUNCTION unknown
    CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
    cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) OIXVIII
    Susceptibility
    Variant & Polymorphism
    Candidate gene chromosome 6q-associated inherited retina disease
    Marker
    Therapy target
    ANIMAL & CELL MODELS