Entity Details
| Primary name |
METTL5 |
| Entity type |
gene |
| Source |
Source Link |
Details
| PrimaryID | 29081 |
| RefseqGene | |
| Symbol | METTL5 |
| Name | methyltransferase 5, N6-adenosine |
| Chromosome | 2 |
| Location | 2q31.1 |
| TaxID | 9606 |
| Status | live |
| SourceGenome | genomic |
| SourceOrigin | natural |
| CreationDate | 2000-02-08 |
| ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 618665 | OMIM | Intellectual developmental disorder, autosomal recessive 72 (MRT72) | A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations. MRT72 patients manifest moderate to severe intellectual disability, microcephaly, and dysmorphic facial features. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions