C4A

1HZF, 4FXG, 4FXK, 4XAM

C4A
C4A
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauC4A, C4, C4A2, C4A3, C4A4, C4A6, C4AD, C4S, CO4, CPAMD2, RG, complement component 4A (Rodgers blood group), complement C4A (Rodgers blood group)
Dynodwyr allanolOMIM: 120810 HomoloGene: 36030 GeneCards: C4A
Patrwm RNA pattern


Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001252204
NM_007293

n/a

RefSeq (protein)

NP_001239133
NP_009224

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 C4A yw C4A a elwir hefyd yn Complement C4A (Rodgers blood group) (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 6, band 6p21.33.[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 C4A.

  • C4
  • RG
  • C4S
  • CO4
  • C4A2
  • C4A3
  • C4A4
  • C4A6
  • C4AD
  • CPAMD2

Llyfryddiaeth

  • "Complement factor C4 activation in patients with hereditary angioedema. ". Clin Biochem. 2017. PMID 28412283.
  • "Re-evaluation of low-resolution crystal structures via interactive molecular-dynamics flexible fitting (iMDFF): a case study in complement C4. ". Acta Crystallogr D Struct Biol. 2016. PMID 27599733.
  • "Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD). ". J Neuroinflammation. 2016. PMID 27090374.
  • "Effect of major histocompatibility complex haplotype matching by C4 and MICA genotyping on acute graft versus host disease in unrelated hematopoietic stem cell transplantation. ". Hum Immunol. 2016. PMID 26602146.
  • "Genome-Wide Copy Number Variation Scan Identifies Complement Component C4 as Novel Susceptibility Gene for Crohn's Disease.". Inflamm Bowel Dis. 2016. PMID 26595553.

Cyfeiriadau

  1. "Human PubMed Reference:".
  2. C4A - Cronfa NCBI

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