Hydin Gene Summary [Mouse]

Acts upstream of or within several processes, including cytoskeleton organization; trachea development; and ventricular system development. Located in axonemal central pair projection. Is expressed in choroid invagination; diencephalon roof plate; medulla oblongata part of 4th ventricle choroid plexus; and metencephalon part of 4th ventricle choroid plexus. Used to study hydrocephalus. Human ortholog(s) of this gene implicated in primary ciliary dyskinesia 5. Orthologous to human HYDIN (HYDIN axonemal central pair apparatus protein). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Hydin
Official Name
HYDIN, axonemal central pair apparatus protein [Source:MGI Symbol;Acc:MGI:2389007]
Ensembl ID
ENSMUSG00000059854
Bio databases IDs NCBI: 244653 Ensembl: ENSMUSG00000059854
Aliases HYDIN, axonemal central pair apparatus protein
Synonyms 1700034M11RIK, 4930545D19RIK, 4932703P14, A830061H17, AC069308.21gm4, CILD5, DKFZP434L0850, FLJ14665, Gm9558, hy-3, HYDIN1, HYDIN2, HYDIN axonemal central pair apparatus protein, HYDIN, axonemal central pair apparatus protein, hyrh, KIAA1864, PPP1R31
Species
Mouse, Mus musculus
OrthologiesHumanRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in mouse Hydin often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Arginine and glutamate-rich 1
  • Cgr1 family
  • Hydin Adenylate kinase-like domain
  • Ezrin/radixin/moesin, alpha-helical domain
  • UDM1_RNF168_RNF169-like
  • protein binding
  • PLC-beta C terminal
  • Troponin
  • MAP7 (E-MAP-115) family
  • Chromatin assembly factor 1 complex p150 subunit, N-terminal
  • Abnormal spindle-like microcephaly-assoc'd, ASPM-SPD-2-Hydin
  • ALMS motif
  • Domain of unknown function (DUF4200)

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • schizophrenia
  • hypertension
  • primary ciliary dyskinesia type 5
  • celiac disease
  • paroxysmal supraventricular tachycardia
  • primary ciliary dyskinesia
  • Alzheimer disease
  • chronic obstructive pulmonary disease
  • head and neck cancer
  • myopia
regulated by
regulates
role in cell
  • development
  • movement
  • beat
  • stalling

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • cilia
  • Mitochondria
  • sperm tail

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Hydin gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • ventricular system development
  • trachea development
  • epithelial cell development
  • cilium movement

Cellular Component

Where in the cell the gene product is active
  • axoneme

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.