Gene

rpgrip1l

ID
ZDB-GENE-081104-81
Name
RPGRIP1 like
Symbol
rpgrip1l Nomenclature History
Previous Names
  • si:ch1073-301i20.1 (1)
Type
protein_coding_gene
Location
Chr: 25 Mapping Details/Browsers
Description
Involved in embryonic pattern specification. Human ortholog(s) of this gene implicated in several diseases, including COACH syndrome; Joubert syndrome 7; Meckel syndrome 5; retinitis pigmentosa 3; and vascular dementia. Orthologous to human RPGRIP1L (RPGRIP1 like).
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
4 figures from 2 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With rpgrip1l Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Joubert syndrome 7 Alliance Joubert syndrome 7 611560
Meckel syndrome 5 Alliance Meckel syndrome 5 611561
?COACH syndrome 3 619113
Associated With rpgrip1l Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR000008 C2 domain
Domain IPR021656 RPGR-interacting protein 1, first C2 domain
Domain IPR041091 RPGRIP1, C-terminal
Family IPR031139 RPGRIP1 family
Homologous_superfamily IPR035892 C2 domain superfamily
Domain Details Per Protein
Protein Length C2 domain C2 domain superfamily RPGR-interacting protein 1, first C2 domain RPGRIP1, C-terminal RPGRIP1 family
UniProtKB:E7F4E7 1256
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