Gene

wdr19

ID
ZDB-GENE-090313-277
Name
WD repeat domain 19
Symbol
wdr19 Nomenclature History
Previous Names
  • si:dkey-251e24.6
Type
protein_coding_gene
Location
Chr: 1 Mapping Details/Browsers
Description
Involved in cilium assembly. Predicted to localize to cilium and intraciliary transport particle A. Human ortholog(s) of this gene implicated in several diseases, including Caroli disease; Senior-Loken syndrome; Sensenbrenner syndrome; asphyxiating thoracic dystrophy 5; and nephronophthisis 13. Orthologous to human WDR19 (WD repeat domain 19).
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
1 Figure from Ryan et al., 2017
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With wdr19 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
asphyxiating thoracic dystrophy 5 Alliance Short-rib thoracic dysplasia 5 with or without polydactyly 614376
cranioectodermal dysplasia 4 Alliance Cranioectodermal dysplasia 4 614378
nephronophthisis 13 Alliance Nephronophthisis 13 614377
Senior-Loken syndrome 8 616307
?Spermatogenic failure 72 619867
Associated With wdr19 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
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