LOC108348031 (-)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 108348031 |
| Gene name | - |
| Gene symbol | LOC108348031 |
| Synonyms (NCBI Gene) |
-
|
| Chromosome | 19 |
| Chromosome location | 19p13.3 |
| Summary | This genomic element is located in an intron of the GNG7 (G protein subunit gamma 7) gene. It was defined as a tissue-specific transcribed enhancer based on the co-occurrence of H3K4me1, H3K27ac and DNase hypersensitive epigenetic marks with the presence |
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Related Genes
Genes most often co-reported with LOC108348031 across shared curated disease and pathway associations.
0
|
|
|
Diseases Linked via Similar Genes
Diseases curated for genes most similar to LOC108348031 (see Related Genes above), that are NOT already directly curated for LOC108348031 itself -- a lead worth checking, not a confirmed association.
0
|
|