MIMT1 (MER1 repeat containing imprinted transcript 1)

Gene
Gene Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100073347
Gene name Gene Name - the full gene name approved by the HGNC.
MER1 repeat containing imprinted transcript 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MIMT1
Synonyms (NCBI Gene) Gene synonyms aliases
LINC00067, MIM1, NCRNA00067
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.43
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Other IDs Associated diseases
MIM HGNC e!Ensembl
620407 33464 ENSG00000268654
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene Other IDs Associated diseases
Show/Hide Unknown Diseases (2)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Diabetes Triglyceride levels in non-type 2 diabetes N/A N/A GWAS
Show/Hide Text Mining Associations (4)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Colorectal Neoplasms Inhibit 36727289
Melanoma Associate 31432325
Melanoma Amelanotic Associate 31432325
Neoplasms Inhibit 36727289