Gene

mettl23

ID
ZDB-GENE-030131-10056
Name
methyltransferase 23, arginine
Symbol
mettl23 Nomenclature History
Previous Names
  • ik:tdsubc_1b12 (1)
  • si:ch73-366l1.2
  • xx:tdsubc_1b12
Type
protein_coding_gene
Location
Chr: 3 Mapping Details/Browsers
Description
Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human METTL23 (methyltransferase like 23).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With mettl23 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive intellectual developmental disorder 44 Alliance Intellectual developmental disorder, autosomal recessive 44 615942
Associated With mettl23 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR019410 Lysine methyltransferase
Homologous_superfamily IPR029063 S-adenosyl-L-methionine-dependent methyltransferase superfamily
Domain Details Per Protein
Protein Length Lysine methyltransferase S-adenosyl-L-methionine-dependent methyltransferase superfamily
UniProtKB:A0A0R4IMW2 225
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA mettl23-201 (1) Havana 1521 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations