Gene

prdm12a

ID
ZDB-GENE-080623-1
Name
PR domain containing 12a
Symbol
prdm12a Nomenclature History
Previous Names
  • prdm12
Type
protein_coding_gene
Location
Chr: 5 Mapping Details/Browsers
Description
Human ortholog(s) of this gene implicated in hereditary sensory and autonomic neuropathy type 8. Is expressed in hindbrain; peripheral olfactory organ; and tegmentum. Orthologous to human PRDM12 (PR/SET domain 12).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
2 figures from Sun et al., 2008
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 prdm12a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
hereditary sensory and autonomic neuropathy type 8 Alliance Neuropathy, hereditary sensory and autonomic, type VIII 616488
Associated With prdm12a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
No data available
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Citations