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Neidio i'r cynnwys
Wicipedia
Chwilio

MSH2

Oddi ar Wicipedia
MSH2
Strwythurau
PDBHuman UniProt search:PDBeRCSB
Rhestr o ddynodwyr PDB

2O8B,2O8C,2O8D,2O8E,2O8F,3THW,3THX,3THY,3THZ

Dynodwyr
CyfenwauMSH2, mutS homolog 2, COCA1, FCC1, HNPCC, HNPCC1, LCFS2, hMMRCS2, MSH-2
Dynodwyr allanolOMIM:609309HomoloGene:210GeneCards:MSH2
PatrwmRNA pattern
Rhagor o gyfeiriadau
Ontoleg y genyn
Gweithrediad moleciwlaiddDNA binding
nucleotide binding
protein homodimerization activity
mismatched DNA binding
dinucleotide insertion or deletion binding
ADP binding
centromeric DNA binding
oxidized purine DNA binding
single-stranded DNA binding
damaged DNA binding
ATPase activity
protein C-terminus binding
GO:0001948, GO:0016582 protein binding
single thymine insertion binding
four-way junction DNA binding
MutLalpha complex binding
enzyme binding
double-stranded DNA binding
dinucleotide repeat insertion binding
ATP binding
protein kinase binding
magnesium ion binding
single guanine insertion binding
guanine/thymine mispair binding
Y-form DNA binding
heteroduplex DNA loop binding
double-strand/single-strand DNA junction binding
ATP-dependent activity, acting on DNA
chromatin binding
Cydrannau o'r gellMutSbeta complex
bilen
MutSalpha complex
nucleoplasm
mismatch repair complex
cnewyllyn cell
Cromosom
Prosesau biolegolGO:1904089 negative regulation of neuron apoptotic process
germ cell development
male gonad development
postreplication repair
determination of adult lifespan
in utero embryonic development
cellular response to DNA damage stimulus
oxidative phosphorylation
maintenance of DNA repeat elements
positive regulation of helicase activity
somatic recombination of immunoglobulin gene segments
intrinsic apoptotic signaling pathway in response to DNA damage
negative regulation of DNA recombination
somatic recombination of immunoglobulin genes involved in immune response
DNA mismatch repair
B cell differentiation
B cell mediated immunity
GO:0100026 DNA repair
positive regulation of isotype switching to IgA isotypes
positive regulation of isotype switching to IgG isotypes
double-strand break repair
meiotic gene conversion
response to X-ray
response to UV-B
somatic hypermutation of immunoglobulin genes
mitotic intra-S DNA damage checkpoint signaling
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator
negative regulation of reciprocal meiotic recombination
isotype switching
protein localization to chromatin
DNA recombination
Sources:Amigo /QuickGO
Orthologau
SpeciesBod dynolLlygoden
Entrez

4436

n/a

Ensembl

ENSG00000095002

n/a

UniProt

P43246

n/a

RefSeq (mRNA)

NM_000251
NM_001258281

n/a

RefSeq (protein)

NP_000242
NP_001245210

n/a

Lleoliad (UCSC)n/an/a
PubMed search[1]n/a
Wicidata
Gweld/Golygu Bod dynol

Protein sy'n cael ei godio yn ycorff dynol gan y genynMSH2 ywMSH2 a elwir hefyd ynMutS homolog 2 (Saesneg). Segment oDNA yw'rgenyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom dynol 2, band 2p21-p16.3.[2]

Cyfystyron

[golygu |golygu cod]

Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn MSH2.

  • FCC1
  • COCA1
  • HNPCC
  • LCFS2
  • HNPCC1

Llyfryddiaeth

[golygu |golygu cod]
  • "Predicting the impact of Lynch syndrome-causing missense mutations from structural calculations.". PLoS Genet. 2017. PMID 28422960.
  • "Overexpression of MutSα Complex Proteins Predicts Poor Prognosis in Oral Squamous Cell Carcinoma.". Medicine (Baltimore). 2016. PMID 27258499.
  • "Causes of Cancer Death Among First-Degree Relatives in Japanese Families with Lynch Syndrome.". Anticancer Res. 2016. PMID 27069191.
  • "Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.". Proc Natl Acad Sci U S A. 2016. PMID 26951660.
  • "A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.". Carcinogenesis. 2016. PMID 26498247.

Cyfeiriadau

[golygu |golygu cod]
  1. "Human PubMed Reference:".
  2. MSH2 - Cronfa NCBI
Wedi dod o "https://cy.wikipedia.org/w/index.php?title=MSH2&oldid=4493976"
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