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Neidio i'r cynnwys
Wicipedia
Chwilio

F10

Oddi ar Wicipedia
F10
Strwythurau
PDBHuman UniProt search:PDBeRCSB
Rhestr o ddynodwyr PDB

1C5M,1EZQ,1F0R,1F0S,1FAX,1FJS,1G2L,1G2M,1HCG,1IOE,1IQE,1IQF,1IQG,1IQH,1IQI,1IQJ,1IQK,1IQL,1IQM,1IQN,1KSN,1LPG,1LPK,1LPZ,1LQD,1MQ5,1MQ6,1NFU,1NFW,1NFX,1NFY,1P0S,1V3X,1WU1,1XKA,1XKB,1Z6E,2BMG,2BOH,2BOK,2BQ6,2BQ7,2BQW,2CJI,2D1J,2EI6,2EI7,2EI8,2FZZ,2G00,2GD4,2H9E,2J2U,2J34,2J38,2J4I,2J94,2J95,2JKH,2P16,2P3F,2P3T,2P3U,2P93,2P94,2P95,2PHB,2PR3,2Q1J,2RA0,2UWL,2UWO,2UWP,2VH0,2VH6,2VVC,2VVU,2VVV,2VWL,2VWM,2VWN,2VWO,2W26,2W3I,2W3K,2WYG,2WYJ,2XBV,2XBW,2XBX,2XBY,2XC0,2XC4,2XC5,2Y5F,2Y5G,2Y5H,2Y7X,2Y7Z,2Y80,2Y81,2Y82,3CEN,3CS7,3ENS,3FFG,3HPT,3IIT,3K9X,3KL6,3Q3K,3SW2,3TK5,3TK6,4A7I,3KQB,3KQC,3KQD,3KQE,3LIW,3M36,3M37,4BTI,4BTT,4BTU,4Y6D,4Y71,4Y76,4Y79,4Y7A,4Y7B,4ZHA,4ZH8,5K0H

Dynodwyr
CyfenwauF10, FX, FXA, coagulation factor X
Dynodwyr allanolOMIM:613872HomoloGene:30976GeneCards:F10
PatrwmRNA pattern
Rhagor o gyfeiriadau
Ontoleg y genyn
Gweithrediad moleciwlaiddcalcium ion binding
GO:0070122 peptidase activity
GO:0001948, GO:0016582 protein binding
serine-type peptidase activity
serine-type endopeptidase activity
phospholipid binding
hydrolase activity
Cydrannau o'r gellendoplasmic reticulum lumen
intrinsic component of external side of plasma membrane
Cellbilen
extracellular region
Golgi lumen
extracellular space
Prosesau biolegolhemostasis
positive regulation of protein kinase B signaling
positive regulation of cell migration
blood coagulation
proteolysis
endoplasmic reticulum to Golgi vesicle-mediated transport
blood coagulation, extrinsic pathway
Sources:Amigo /QuickGO
Orthologau
SpeciesBod dynolLlygoden
Entrez

2159

n/a

Ensembl

ENSG00000126218

n/a

UniProt

P00742

n/a

RefSeq (mRNA)

NM_000504
NM_001312674
NM_001312675

n/a

RefSeq (protein)

NP_000495
NP_001299603
NP_001299604

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 genynF10 ywF10 a elwir hefyd ynCoagulation factor X (Saesneg). Segment oDNA yw'rgenyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom dynol 13, band 13q34.[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 F10.

  • FX
  • FXA

Llyfryddiaeth

[golygu |golygu cod]
  • "Rendering factor Xa zymogen-like as a therapeutic strategy to treat bleeding.". Curr Opin Hematol. 2017. PMID 28692575.
  • "[Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree].". Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID 27264807.
  • "Novel Anthranilamide-Based FXa Inhibitors: Drug Design, Synthesis and Biological Evaluation.". Molecules. 2016. PMID 27089317.
  • "A family with factor X deficiency from Argentina: a compound heterozygosis because of the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys).". Blood Coagul Fibrinolysis. 2016. PMID 27031279.
  • "Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency.". Blood Coagul Fibrinolysis. 2016. PMID 26891460.

Cyfeiriadau

[golygu |golygu cod]
  1. "Human PubMed Reference:".
  2. F10 - Cronfa NCBI
Wedi dod o "https://cy.wikipedia.org/w/index.php?title=F10&oldid=4493543"
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