CFB
gjen i llojit Homo Sapiens
nënklasë e
gjen kodues i proteinave[6]
found in taxon
encodes
Complement factor B[7]
genetic association
age related macular degeneration 14[9]
atypical hemolytic-uremic syndrome with b factor anomaly[10]
kromozom
strand orientation
genomic start
genomic end
cytogenetic location
6p21.33[2]
HomoloGene ID
1292[2]
Gene Atlas image
ortholog
expressed in
përputhje e saktë
Reference
- ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu ensembl Release 106, ENSG00000243649
- ^ a b c d e f NCBI Gene, 15 maj 2022, 629
- ^ UMLS 2023, 15 qershor 2023, inferred by common HGNC mappings on source and on Wikidata
- ^ OpenAlex, 26 janar 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ^ Online Mendelian Inheritance in Man, 19 gusht 2019
- ^ NCBI homo sapiens annotation release 107, 15 dhjetor 2016, 629
- ^ UniProt, 16 mars 2017, P00751
- ^ 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 maj 2020
- ^ P00751, 13 gusht 2019, UniProt
- ^ Open Targets Platform, 24 gusht 2023, https://platform.opentargets.org/evidence/ENSG00000243649/MONDO_0013042, inferred from an Open Targets association score over 0.7
- ^ a b c d e HomoloGene build68, 1292
- ^ Orthologous MAtrix, https://omabrowser.org/oma/vps/P00751/
- ^ a b c d e f g h i j Bgee, 28 prill 2022, https://bgee.org/bgee15_0/gene/ENSG00000243649
- ^ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069