Gene

zgc:154077

ID
ZDB-GENE-061110-34
Name
zgc:154077
Symbol
zgc:154077 Nomenclature History
Previous Names
None
Type
protein_coding_gene
Location
Chr: 25 Mapping Details/Browsers
Description
Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human C12orf4 (chromosome 12 open reading frame 4).
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 zgc:154077 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive intellectual developmental disorder 66 Alliance Intellectual developmental disorder, autosomal recessive 66 618221
Associated With zgc:154077 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR019311 Protein of unknown function DUF2362
Domain Details Per Protein
Protein Length Protein of unknown function DUF2362
UniProtKB:A0JMN9 551
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA zgc:154077-201 (1) Havana 2541 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