FECH

4MK4, 1HRK, 2HRC, 2HRE, 2PNJ, 2PO5, 2PO7, 2QD1, 2QD2, 2QD3, 2QD4, 2QD5, 3AQI, 3HCN, 3HCO, 3HCP, 3HCR, 3W1W, 4F4D, 4KLA, 4KLC, 4KLR, 4KMM

FECH
FECH
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauFECH, EPP, FCE, ferrochelatase, EPP1
Dynodwyr allanolOMIM: 612386 HomoloGene: 113 GeneCards: FECH
EC number4.98.1.1
Patrwm RNA pattern


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

NM_000140
NM_001012515
NM_001371094
NM_001371095
NM_001374778

n/a

RefSeq (protein)

NP_000131
NP_001012533
NP_001358023
NP_001358024
NP_001361707

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 FECH yw FECH a elwir hefyd yn Ferrochelatase, mitochondrial a Ferrochelatase (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 18, band 18q21.31.[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 FECH.

  • EPP
  • FCE

Llyfryddiaeth

  • "Human Ferrochelatase: Insights for the Mechanism of Ferrous Iron Approaching Protoporphyrin IX by QM/MM and QTCP Free Energy Studies. ". J Chem Inf Model. 2016. PMID 27801584.
  • "A Novel Mutation in the FECH Gene in a Czech Family with Erythropoietic Protoporphyria and a Population Study of IVS3-48C Variant Contributing to the Disease. ". Folia Biol (Praha). 2015. PMID 26789144.
  • "Incomplete erythropoietic protoporphyria caused by a splice site modulator homozygous IVS3-48C polymorphism in the ferrochelatase gene. ". Br J Dermatol. 2016. PMID 26280465.
  • "Antisense oligonucleotide-based therapy in human erythropoietic protoporphyria. ". Am J Hum Genet. 2014. PMID 24680888.
  • "New mutation identified in two sisters with adult-onset erythropoietic protoporphyria.". Clin Exp Dermatol. 2013. PMID 23600449.

Cyfeiriadau

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

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