MARS
gjen i llojit Homo sapiens
nënklasë e
gjen kodues i proteinave[6]
found in taxon
genetic association
Charcot-Marie-Tooth disease axonal type 2U[9]
severe early-onset pulmonary alveolar proteinosis due to MARS deficiency[10]
kromozom
strand orientation
genomic start
genomic end
cytogenetic location
12q13.3[2]
HomoloGene ID
90878[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 ensembl Release 106, ENSG00000166986
- ^ a b c d e f NCBI Gene, 15 maj 2022, 4141
- ^ UMLS 2023, 15 qershor 2023, inferred by common HGNC mappings on source and on Wikidata
- ^ Online Mendelian Inheritance in Man, 19 gusht 2019
- ^ a b NCBI Gene, 10 prill 2022, 4141
- ^ Ensembl Release 87, ENSG00000166986
- ^ UniProt, 6 korrik 2017, P56192
- ^ H0YI94, 20 mars 2016, UniProt, anglisht
- ^ P56192, 13 gusht 2019, UniProt
- ^ Open Targets Platform, 24 gusht 2023, https://platform.opentargets.org/evidence/ENSG00000166986/MONDO_0014206, inferred from an Open Targets association score over 0.7
- ^ a b c d e HomoloGene build68, 90878
- ^ a b c d e f g h i j Bgee, 20 prill 2022, https://bgee.org/bgee15_0/gene/ENSG00000166986
- ^ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069