DNAJB6
protein-coding gene in the species Homo sapiens
mille alamklass
protein-coding gene[6]
found in taxon
Homo sapiens[3]
genetic association
autosomal dominant limb-girdle muscular dystrophy type 1E[9]
chromosome
strand orientation
genomic start
genomic end
cytogenetic location
7q36.3[1]
HomoloGene ID
38058[1]
ortholog
expressed in
täpne vaste
Viited
- ↑ 1,00 1,01 1,02 1,03 1,04 1,05 1,06 1,07 1,08 1,09 1,10 1,11 NCBI Gene, 15. mai 2022, 10049
- ↑ 2,0 2,1 2,2 2,3 NCBI Gene, 10. aprill 2022, 10049
- ↑ 3,00 3,01 3,02 3,03 3,04 3,05 3,06 3,07 3,08 3,09 3,10 3,11 3,12 3,13 3,14 3,15 3,16 3,17 3,18 3,19 3,20 3,21 3,22 3,23 3,24 3,25 3,26 ensembl Release 106, ENSG00000105993
- ↑ UMLS 2023, 15. juuni 2023, inferred by common HGNC mappings on source and on Wikidata
- ↑ Online Mendelian Inheritance in Man, 19. august 2019
- ↑ Ensembl Release 87, ENSG00000105993
- ↑ UniProt, 6. juuli 2017, O75190
- ↑ C9JB42, 21. märts 2016, UniProt, inglise keel
- ↑ Open Targets Platform, 24. august 2023, https://platform.opentargets.org/evidence/ENSG00000105993/Orphanet_34516, inferred from an Open Targets association score over 0.7
- ↑ 10,0 10,1 10,2 10,3 10,4 HomoloGene build68, 38058
- ↑ 11,0 11,1 11,2 Orthologous MAtrix, https://omabrowser.org/oma/vps/O75190/
- ↑ 12,00 12,01 12,02 12,03 12,04 12,05 12,06 12,07 12,08 12,09 Bgee, 7. juuni 2024, https://www.bgee.org/gene/ENSG00000105993
- ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069