hydin

ID

ZDB-GENE-050419-219

Name

HYDIN axonemal central pair apparatus protein

Symbol

hydin Nomenclature History

Previous Names

si:ch211-245p7.3
si:ch73-22b10.1
si:ch73-22b10.2

Type

protein_coding_gene

Location

Chr: 18 Mapping Details/Browsers

Genome Assembly

GRCz12tu

Annotation Status

Current

Description

Predicted to be involved in axonemal central apparatus assembly and cilium movement. Predicted to be located in cytoplasm. Predicted to be active in axoneme. Human ortholog(s) of this gene implicated in primary ciliary dyskinesia 5. Orthologous to human HYDIN (HYDIN axonemal central pair apparatus protein).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

No data available

Cross-Species Comparison

High Throughput Data

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Daniocell

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 hydin Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
primary ciliary dyskinesia 5	Alliance	Ciliary dyskinesia, primary, 5	608647

Associated With hydin Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Domain	IPR033768	Hydin adenylate kinase-like domain
Domain	IPR053879	HYDIN/VesB/CFA65-like, Ig-like domain
Family	IPR033305	Hydrocephalus-inducing-like
Homologous_superfamily	IPR013783	Immunoglobulin-like fold
Homologous_superfamily	IPR027417	P-loop containing nucleoside triphosphate hydrolase