MFF
Appearance
gjen i llojit Homo Sapiens
nënklasë e
gjen kodues i proteinave[6]
found in taxon
genetic association
leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome[9]
lethal encephalopathy due to mitochondrial and peroxisomal fission defect[10]
kromozom
strand orientation
genomic start
genomic end
cytogenetic location
2q36.3[1]
HomoloGene ID
137341[1]
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 NCBI Gene, 15 maj 2022, 56947
- ^ a b c d e f g NCBI Gene, 10 prill 2022, 56947
- ^ 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 ensembl Release 106, ENSG00000168958
- ^ UMLS 2023, 15 qershor 2023, inferred by common HGNC mappings on source and on Wikidata
- ^ Online Mendelian Inheritance in Man, 19 gusht 2019
- ^ Ensembl Release 87, ENSG00000168958
- ^ UniProt, 6 korrik 2017, Q9GZY8
- ^ C9JU19, 20 mars 2016, anglisht, UniProt
- ^ Q9GZY8, 13 gusht 2019, UniProt
- ^ Open Targets Platform, 24 gusht 2023, inferred from an Open Targets association score over 0.7, https://platform.opentargets.org/evidence/ENSG00000168958/Orphanet_330050
- ^ a b HomoloGene build68, 137341
- ^ a b Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9GZY8/
- ^ a b c d e f g h i j Bgee, 7 qershor 2024, https://www.bgee.org/gene/ENSG00000168958
- ^ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069