adenosine deaminase RNA specific
| UniProt | Protein Name |
|---|---|
| P55265 |
|
| A0AAQ5BGH8 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| osteoblast differentiation |
|
|
| hematopoietic progenitor cell differentiation |
|
|
| somatic diversification of immune receptors via somatic mutation |
|
|
| adenosine to inosine editing |
|
|
| adenosine to inosine editing |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| DNA binding |
|
|
| RNA binding |
|
|
| RNA binding |
|
|
| double-stranded RNA binding |
|
|
| double-stranded RNA adenosine deaminase activity |
|
| Gene Ontology |
|---|
| adenosine deaminase activity |
| adenosine to inosine editing |
| double-stranded RNA binding |
| tRNA-specific adenosine deaminase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050629 | Aicardi-Goutieres syndrome | |
| DOID:0060257 | dyschromatosis symmetrica hereditaria | |
| DOID:11166 | Human papillomavirus infectious disease | |
| DOID:5082 | liver cirrhosis |
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000054 | Micropenis |
| HP:0000252 | Microcephaly |
| HP:0000369 | Low-set ears |
| HP:0000444 | Convex nasal ridge |
| HP:0000496 | Abnormality of eye movement |
| HP:0000501 | Glaucoma |
| HP:0000508 | Ptosis |
| HP:0000625 | Eyelid coloboma |
| Disease ID | Disease Name |
|---|---|
| ORPHA:41 |
|
| ORPHA:51 |
|
| OMIM:127400 |
|
| ORPHA:225154 |
|
| OMIM:615010 |
|
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