Gene

rlbp1b

Species
Danio rerio
Symbol
rlbp1b
Name
retinaldehyde binding protein 1b
Synonyms
  • cralbpa
  • rlbp1
Biotype
protein coding gene
Automated Description
Predicted to enable phosphatidylinositol bisphosphate binding activity. Acts upstream of or within optokinetic behavior. Is expressed in optic vesicle; otic vesicle; pericardial region; pronephric duct; and sensory system. Human ortholog(s) of this gene implicated in Bothnia retinal dystrophy; Newfoundland cone-rod dystrophy; fundus albipunctatus; night blindness; and retinitis pigmentosa. Orthologous to human RLBP1 (retinaldehyde binding protein 1).
ZFIN Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR10174
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
None

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

Genome location
Assembly version
GRCz11
Viewer Help
19.106M19.108M19.110M19.112M19.114M19.116M19.118M

Sequence Details

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Expression

Primary Sources
Other Sources
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions