FCN2

2J0G, 2J0H, 2J0Y, 2J1G, 2J2P, 2J3F, 2J3G, 2J3O, 2J3U, 2J61, 4NYT, 4R9J, 4R9T

FCN2
FCN2
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauFCN2, EBP-37, FCNL, P35, ficolin-2, ficolin 2
Dynodwyr allanolOMIM: 601624 HomoloGene: 3031 GeneCards: FCN2
Patrwm RNA pattern
Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez

2220

n/a

Ensembl

n/a

n/a

UniProt

Q15485

n/a

RefSeq (mRNA)

NM_004108
NM_015837
NM_015838
NM_015839

n/a

RefSeq (protein)

NP_004099
NP_056652

n/a

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

Protein sy'n cael ei godio yn y corff dynol gan y genyn FCN2 yw FCN2 a elwir hefyd yn Ficolin 2 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom dynol 9, band 9q34.3.[2]

Cyfystyron

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 FCN2.

  • P35
  • FCNL
  • EBP-37
  • ficolin-2

Llyfryddiaeth

  • "The prevalence of the variants of the L-ficolin gene (FCN2) in the arctic populations of East Siberia. ". Immunogenetics. 2017. PMID 28391359.
  • "FCN2 c.772G>T polymorphism is associated with chronic adenoiditis and/or tonsillitis, but not -4 A>G and -602 G>A. ". Int J Pediatr Otorhinolaryngol. 2016. PMID 27368434.
  • "The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection. ". J Innate Immun. 2016. PMID 27355483.
  • "Ficolin Gene Polymorphisms in Systemic Lupus Erythematosus and Rheumatoid Arthritis. ". Ann Hum Genet. 2016. PMID 26464189.
  • "Association of the FCN2 Gene Single Nucleotide Polymorphisms with Susceptibility to Pulmonary Tuberculosis.". PLoS One. 2015. PMID 26379154.

Cyfeiriadau

  1. ↑ "Human PubMed Reference:".
  2. ↑ FCN2 - Cronfa NCBI

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