Gene

rp1l1b

ID
ZDB-GENE-091204-67
Name
rp1 like 1b
Symbol
rp1l1b Nomenclature History
Previous Names
  • si:dkey-33i22.3
Type
protein_coding_gene
Location
Chr: 20 Mapping Details/Browsers
Description
Predicted to be involved in axoneme assembly; photoreceptor cell development; and retina development in camera-type eye. Predicted to localize to axoneme. Human ortholog(s) of this gene implicated in occult macular dystrophy and retinitis pigmentosa. Orthologous to human RP1L1 (RP1 like 1).
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 rp1l1b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
occult macular dystrophy Alliance Occult macular dystrophy 613587
retinitis pigmentosa 88 Alliance Retinitis pigmentosa 88 618826
Associated With rp1l1b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR003533 Doublecortin domain
Homologous_superfamily IPR036572 Doublecortin domain superfamily
Domain Details Per Protein
Protein Length Doublecortin domain Doublecortin domain superfamily
UniProtKB:A0A8M9PT86 3898
UniProtKB:E7F542 3919
UniProtKB:A0A8M9PPV2 3864
Transcripts
Genome Browsers
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