ವಿಕಿಪೀಡಿಯ

ASXL3

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protein-coding gene in the species Homo sapiens

External resources

RefSeq RNA ID
NM_030632[೧]
XM_005258356[೧]
XM_011526205[೧]
XM_011526206[೧]
XM_011526209[೧]
XM_011526212[೧]
XM_017026012[೧]
XM_024451269[೧]
Ensembl transcript ID
ENST00000593235[೨]
ENST00000269197[೨]
ENST00000585426[೨]
ENST00000586327[೨]
ENST00000586948[೨]
ENST00000588038[೨]
ENST00000590189[೨]
ENST00000590225[೨]
ENST00000590973[೨]
ENST00000592288[೨]
ENST00000592349[೨]
ENST00000592541[೨]
ENST00000593195[೨]
ENST00000647014[೨]
ENST00000642541[೨]
ENST00000681521[೨]
Entrez Gene ID
80816[೧]
UMLS CUI
C2239906[೩]
OMIM ID
615115[೪]
Ensembl gene ID
ENSG00000141431[೨]
HGNC ID
29357[೧]
HGNC gene symbol
ASXL3[೧]
Freebase ಐಡಿ
/m/0zrs7qc

ಉದಾಹರಣೆಗೆ

ವಂಶವಾಹಿ[೨]

ಉಪವರ್ಗ

protein-coding gene[೫]

found in taxon

Homo sapiens[೨]

encodes

ASXL transcriptional regulator 3[೬]

genetic association

Bainbridge Ropers Syndrome[೭][೮]

chromosome

human chromosome 18[೨]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

strand orientation

forward strand[೨]

genomic assembly: genome assembly GRCh38, Genome assembly GRCh37

genomic start

31158579[೨]

genomic assembly: Genome assembly GRCh37

chromosome: human chromosome 18

33578219[೨]

genomic assembly: genome assembly GRCh38

chromosome: human chromosome 18

genomic end

31331156[೨]

genomic assembly: Genome assembly GRCh37

chromosome: human chromosome 18

33751195[೨]

genomic assembly: genome assembly GRCh38

chromosome: human chromosome 18

cytogenetic location

18q12.1[೧]

HomoloGene ID

19371[೧]

ortholog

Asxl3[೯][೧೦]

found in taxon: house mouse

expressed in

buccal mucosa cell[೧೧]

series ordinal: 1

secondary oocyte[೧೧]

series ordinal: 2

ವೀರ್ಯ[೧೧]

series ordinal: 3

ವೃಷಣ[೧೧]

series ordinal: 4

ganglionic eminence[೧೧]

series ordinal: 5

Brodmann area 23[೧೧]

series ordinal: 6

middle temporal gyrus[೧೧]

series ordinal: 7

sural nerve[೧೧]

series ordinal: 8

endothelial cell[೧೧]

series ordinal: 9

ventricular zone[೧೧]

series ordinal: 10

exact match

http://identifiers.org/ncbigene/80816[೧೨]

Reference

  1. ↑ ೧.೦೦ ೧.೦೧ ೧.೦೨ ೧.೦೩ ೧.೦೪ ೧.೦೫ ೧.೦೬ ೧.೦೭ ೧.೦೮ ೧.೦೯ ೧.೧೦ ೧.೧೧ ೧.೧೨ NCBI Gene, ೧೫ ಮೇ 2022, 80816
  2. ↑ ೨.೦೦ ೨.೦೧ ೨.೦೨ ೨.೦೩ ೨.೦೪ ೨.೦೫ ೨.೦೬ ೨.೦೭ ೨.೦೮ ೨.೦೯ ೨.೧೦ ೨.೧೧ ೨.೧೨ ೨.೧೩ ೨.೧೪ ೨.೧೫ ೨.೧೬ ೨.೧೭ ೨.೧೮ ೨.೧೯ ೨.೨೦ ೨.೨೧ ೨.೨೨ ೨.೨೩ ೨.೨೪ ensembl Release 106, ENSG00000141431
  3. ↑ UMLS 2023, ೧೫ ಜೂನ್ 2023, inferred by common HGNC mappings on source and on Wikidata
  4. ↑ Online Mendelian Inheritance in Man, ೧೯ ಆಗಸ್ಟ್ 2019
  5. ↑ Ensembl Release 87, ENSG00000141431
  6. ↑ UniProt, ೬ ಜುಲೈ 2017, Q9C0F0
  7. ↑ Q9C0F0, ೧೩ ಆಗಸ್ಟ್ 2019, UniProt
  8. ↑ Open Targets Platform, ೨೪ ಆಗಸ್ಟ್ 2023, inferred from an Open Targets association score over 0.7, https://platform.opentargets.org/evidence/ENSG00000141431/Orphanet_352577
  9. ↑ HomoloGene build68, ೨೮ ನವೆಂಬರ್ 2015
  10. ↑ Orthologous MAtrix, https://omabrowser.org/oma/vps/Q9C0F0/
  11. ↑ ೧೧.೦೦ ೧೧.೦೧ ೧೧.೦೨ ೧೧.೦೩ ೧೧.೦೪ ೧೧.೦೫ ೧೧.೦೬ ೧೧.೦೭ ೧೧.೦೮ ೧೧.೦೯ Bgee, ೭ ಜೂನ್ 2024, https://www.bgee.org/gene/ENSG00000141431
  12. ↑ Identifiers.org, http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069
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