dynamin 1 like
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial fission |
|
|
| mitochondrial fission |
|
|
| mitochondrial fission |
|
|
| mitochondrial fission |
|
|
| calcium ion transport |
|
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytoplasm |
|
|
| cytoplasm |
|
|
| cytoplasm |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| GTPase activity |
|
|
| GTPase activity |
|
|
| GTPase activity |
|
|
| GTPase activity |
|
|
| GTPase activator activity |
|
| Gene Ontology |
|---|
| GTP binding |
| microtubule binding |
| nucleotide binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070347 | encephalopathy due to defective mitochondrial and peroxisomal fission 1 | |
| DOID:0111438 | optic atrophy 5 |
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000135 | Hypogonadism |
| HP:0000252 | Microcephaly |
| HP:0000307 | Pointed chin |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000486 | Strabismus |
| HP:0000490 | Deeply set eye |
| HP:0000505 | Visual impairment |
| HP:0000508 | Ptosis |
| Disease ID | Disease Name |
|---|---|
| OMIM:610708 |
|
| OMIM:614388 |
|
| ORPHA:330050 |
|
| ORPHA:98673 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: April 6, 2026