XIST (X inactive specific transcript)

Gene
Gene miRNA Gene ontology Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7503
Gene name Gene Name - the full gene name approved by the HGNC.
X inactive specific transcript
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
XIST
Synonyms (NCBI Gene) Gene synonyms aliases
DXS1089, DXS399E, LINC00001, NCRNA00001, SXI1, swd66
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq13.2
Summary Summary of gene provided in NCBI Entrez Gene.
X inactivation is an early developmental process in mammalian females that transcriptionally silences one of the pair of X chromosomes, thus providing dosage equivalence between males and females. The process is regulated by several factors, including a r
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Gene ontology Other IDs Associated diseases
Show/Hide all(8)
miRTarBase ID miRNA Experiments Reference
MIRT003171 hsa-miR-210-3p immunoprecipitaion, Luciferase reporter assay, Microarray, qRT-PCR 19826008
MIRT003171 hsa-miR-210-3p immunoprecipitaion, Luciferase reporter assay, Microarray, qRT-PCR 19826008
MIRT731182 hsa-miR-152-3p qRT-PCR/Luciferase reporter assay, Western blot 25578780
MIRT731182 hsa-miR-152-3p qRT-PCR/Luciferase reporter assay, Western blot 25578780
MIRT734229 hsa-miR-106a-5p Flow cytometry, Luciferase reporter assay, qRT-PCR 33400246
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene miRNA Gene ontology Other IDs Associated diseases
Show/Hide all(2)
GO ID Ontology Definition Evidence Reference
GO:0009048 Process Dosage compensation by inactivation of X chromosome IEA
GO:0016458 Process Gene silencing IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Associated diseases
MIM HGNC e!Ensembl
314670 12810 ENSG00000229807
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene miRNA Gene ontology Other IDs Associated diseases
Show/Hide Causal Diseases (1)
Causal
Disease term Disease name dbSNP ID References
Skewed x inactivation X INACTIVATION, FAMILIAL SKEWED, 1 (disorder) rs773396320
Show/Hide Text Mining Associations (126)
Associations from Text Mining
Disease Name Relationship Type References
Abortion Spontaneous Associate 37914735
Acute Kidney Injury Associate 31914881
Adenocarcinoma of Lung Associate 28961027, 31419261, 33771173
Alzheimer Disease Associate 36928034
Antiphospholipid Syndrome Stimulate 37914735
Aortic Dissection Associate 26339353
Arthritis Rheumatoid Associate 34165008, 37814309
Asthma Associate 33998076
Astrocytoma Associate 32647207
Atherosclerosis Associate 31539155, 32345778