Gene

prom1a

ID
ZDB-GENE-030131-1577
Name
prominin 1a
Symbol
prom1a Nomenclature History
Previous Names
  • prom1
  • proml1
  • fb75c01
  • wu:fb75c01
Type
protein_coding_gene
Location
Chr: 14 Mapping Details/Browsers
Description
Predicted to have cholesterol binding activity. Predicted to localize to several cellular components, including endoplasmic reticulum-Golgi intermediate compartment; microvillus; and prominosome. Human ortholog(s) of this gene implicated in cone-rod dystrophy 12 and retinitis pigmentosa 41. Is expressed in gill; muscle; nervous system; otic vesicle; and pleuroperitoneal region. Orthologous to human PROM1 (prominin 1).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
12 figures from 4 publications
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 prom1a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
cone-rod dystrophy 12 Alliance Cone-rod dystrophy 12 612657
retinitis pigmentosa 41 Alliance Retinitis pigmentosa 41 612095
Stargardt disease Alliance Stargardt disease 4 603786
Macular dystrophy, retinal, 2 608051
Associated With prom1a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR008795 Prominin
Domain Details Per Protein
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
Name Type Antigen Genes Isotype Host Organism Assay Source Citations
Ab1-prom1a polyclonal Rabbit
1
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations