CFB

Lehekülje sisu ei toetata teistes keeltes.

protein-coding gene in the species Homo sapiens

Välised allikad

Freebase
Microsoft Academic ID
Ensembl transcript ID
Entrez Gene ID
HGNC ID
UMLS CUI
HGNC gene symbol
OpenAlex ID
OMIM ID
Ensembl gene ID
RefSeq RNA ID

üksikjuht nähtusest

mille alamklass

protein-coding gene[6]

found in taxon

Homo sapiens[1]

encodes

Complement factor B[7]

genetic association

maakuli degeneratsioon[8]

määramismeetod: Ülegenoomne assotsiatsiooniuuring, TAS

age related macular degeneration 14[9]
atypical hemolytic-uremic syndrome with b factor anomaly[10]

chromosome

human chromosome 6[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

forward strand[1]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

31945650[1]

chromosome: human chromosome 6

genomic assembly: genome assembly GRCh38

31895475[1]

chromosome: human chromosome 6

genomic assembly: Genome assembly GRCh37

genomic end

31952084[1]

chromosome: human chromosome 6

genomic assembly: genome assembly GRCh38

31919861[1]

chromosome: human chromosome 6

genomic assembly: Genome assembly GRCh37

cytogenetic location

6p21.33[2]

HomoloGene ID

1292[2]

Gene Atlas image

ortholog

Cfb[11][12]

found in taxon: koduhiir

Cfb[11]

found in taxon: rändrott

bfb[11]

found in taxon: Danio rerio

cfb[11]

found in taxon: Danio rerio

cfbl[11]

found in taxon: Danio rerio

expressed in

right lobe of liver[13]

järjekorranumber: 1

Sapipõis[13]

järjekorranumber: 2

Ussripik[13]

järjekorranumber: 3

Kaksteistsõrmiksool[13]

järjekorranumber: 4

islet of Langerhans[13]

järjekorranumber: 5

gastric mucosa[13]

järjekorranumber: 6

right coronary artery[13]

järjekorranumber: 7

neerud[13]

järjekorranumber: 8

upper lobe of left lung[13]

järjekorranumber: 9

Ülenev aort[13]

järjekorranumber: 10

Viited

  1. 1,00 1,01 1,02 1,03 1,04 1,05 1,06 1,07 1,08 1,09 1,10 1,11 1,12 1,13 1,14 1,15 1,16 1,17 1,18 1,19 1,20 1,21 1,22 1,23 1,24 1,25 1,26 1,27 1,28 1,29 1,30 1,31 1,32 1,33 1,34 1,35 1,36 1,37 1,38 1,39 1,40 1,41 1,42 1,43 1,44 1,45 1,46 1,47 1,48 1,49 1,50 1,51 1,52 1,53 1,54 1,55 1,56 1,57 1,58 1,59 1,60 1,61 1,62 1,63 1,64 1,65 1,66 1,67 1,68 1,69 1,70 1,71 1,72 1,73 1,74 1,75 1,76 1,77 1,78 1,79 1,80 1,81 1,82 1,83 1,84 1,85 1,86 1,87 1,88 1,89 1,90 1,91 1,92 1,93 1,94 1,95 1,96 1,97 1,98 ensembl Release 106, ENSG00000243649
  2. 2,0 2,1 2,2 2,3 2,4 2,5 NCBI Gene, 15. mai 2022, 629
  3. UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
  4. OpenAlex, 26. jaanuar 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  5. Online Mendelian Inheritance in Man, 19. august 2019
  6. NCBI homo sapiens annotation release 107, 15. detsember 2016, 629
  7. UniProt, 16. märts 2017, P00751
  8. Phenocarta, Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10871&ncbiId=629, http://www.genome.gov/gwastudies/index.cfm?gene=CFB, 25. mai 2020
  9. P00751, 13. august 2019, UniProt
  10. Open Targets Platform, 24. august 2023, https://platform.opentargets.org/evidence/ENSG00000243649/MONDO_0013042, inferred from an Open Targets association score over 0.7
  11. 11,0 11,1 11,2 11,3 11,4 HomoloGene build68, 1292
  12. Orthologous MAtrix, https://omabrowser.org/oma/vps/P00751/
  13. 13,00 13,01 13,02 13,03 13,04 13,05 13,06 13,07 13,08 13,09 Bgee, 28. aprill 2022, https://bgee.org/bgee15_0/gene/ENSG00000243649
  14. Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069