FOXN3 (original) (raw)

From Wikipedia, the free encyclopedia

Protein-coding gene in the species Homo sapiens

FOXN3
Identifiers
Aliases FOXN3, C14orf116, CHES1, PRO1635, forkhead box N3
External IDs OMIM: 602628; MGI: 1918625; HomoloGene: 3809; GeneCards: FOXN3; OMA:FOXN3 - orthologs
Gene location (Human)Chromosome 14 (human)Chr.Chromosome 14 (human)[1]Chromosome 14 (human)Genomic location for FOXN3Genomic location for FOXN3Band14q31.3-q32.11Start89,124,871 bp[1]End89,619,149 bp[1]
Gene location (Mouse)Chromosome 12 (mouse)Chr.Chromosome 12 (mouse)[2]Chromosome 12 (mouse)Genomic location for FOXN3Genomic location for FOXN3Band12|12 EStart99,156,337 bp[2]End99,529,841 bp[2]
RNA expression patternBgeeHuman Mouse (ortholog)Top expressed inparaflocculus of cerebellumtendon of biceps brachiinipplesaphenous veinskin of hipskin of armmucosa of paranasal sinusskin of thighsynovial jointSkeletal muscle tissue of rectus abdominisTop expressed inzygotesecondary oocytehandascending aortasoleus muscleRostral migratory streamtibialis anterior musclefootgastrocnemius muscleaortic valveMore reference expression dataBioGPSMore reference expression data
Gene ontologyMolecular function DNA binding protein C-terminus binding protein binding DNA-binding transcription factor activity sequence-specific DNA binding DNA-binding transcription factor activity, RNA polymerase II-specific Cellular component nucleus Biological process cell cycle mitotic G2 DNA damage checkpoint signaling negative regulation of transcription, DNA-templated regulation of transcription, DNA-templated transcription, DNA-templated craniofacial suture morphogenesis cell differentiation positive regulation of transcription, DNA-templated regulation of transcription by RNA polymerase II Sources:Amigo / QuickGO
OrthologsSpeciesHuman MouseEntrez111271375EnsemblENSG00000053254ENSMUSG00000033713UniProtO00409Q499D0RefSeq (mRNA)NM_005197NM_001085471NM_183186RefSeq (protein)NP_001078940NP_005188NP_899009Location (UCSC)Chr 14: 89.12 – 89.62 MbChr 12: 99.16 – 99.53 MbPubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Forkhead box protein N3 is a protein that in humans is encoded by the FOXN3 gene.[5][6]

This gene is a member of the forkhead/winged helix transcription factor family. Checkpoints are eukaryotic DNA damage-inducible cell cycle arrests at G1 and G2. Checkpoint suppressor 1 suppresses multiple yeast checkpoint mutations including mec1, rad9, rad53 and dun1 by activating a MEC1-independent checkpoint pathway. Alternative splicing is observed at the locus, resulting in distinct isoforms.[6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000053254Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000033713Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Pati D, Keller C, Groudine M, Plon SE (Jun 1997). "Reconstitution of a MEC1-independent checkpoint in yeast by expression of a novel human fork head cDNA". Mol Cell Biol. 17 (6): 3037–46. doi:10.1128/MCB.17.6.3037. PMC 232156. PMID 9154802.
  6. ^ a b "Entrez Gene: CHES1 checkpoint suppressor 1".