UniProt | Protein Name |
---|---|
P55265 |
|
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 | ||
double-stranded RNA binding | ||
double-stranded RNA adenosine deaminase activity | ||
double-stranded RNA adenosine deaminase activity |
Gene Ontology |
---|
adenosine deaminase activity |
double-stranded RNA binding |
tRNA-specific adenosine deaminase activity |
InterPro |
---|
Adenosine deaminase/editase |
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:225154 |
|
ORPHA:41 |
|
ORPHA:51 |
|
OMIM:615010 |
|
OMIM:127400 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
103 | Xenbase:XB-GENE-854473 | ||
56417 | Xenbase:XB-GENE-854473 | MOUSE38974 | |
58119 | DANRE10647 | ||
81635 | RATNO23342 | ||
457349 | PANTR22416 | ||
505134 | BOVIN25836 | ||
718759 | MACMU23499 | ||
100020840 | MONDO11851 | ||
100056984 | HORSE34484 | ||
100220215 | TAEGU14296 |
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 7, 2025