Gene

rlbp1.L

Species
Xenopus laevis
Symbol
rlbp1.L
Name
retinaldehyde binding protein 1
Synonyms
  • CRALBP
  • retinaldehyde binding protein 1
Biotype
gene
Automated Description
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).
XBXL Description
Phosphatidylinositol transfer protein SEC14 and related proteins
https://www.xenbase.org/gene/showgene.do?method=display&geneId=976302
Cross References
Additional Information
Literature

Orthology

Gene tree
Not Available
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
None
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
XL9.2
Viewer Help
100.124M100.126M100.128M100.130M100.132M100.134M100.136M100.138M100.140M

Sequence Details

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Expression

Primary Sources
Other Sources
None
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions