Sequence Detail

ID/Version

Q80W93 Q8BRL9 Q8CDF4 Q3UQ06 Q68ED1 (UniProt | EBI)

Last sequence update: 2011-04-05
Last annotation update: 2024-01-24

Sequence description from provider

RecName: Full=Hydrocephalus-inducing protein;AltName: Full=Protein Hy-3;

Provider

SWISS-PROT

Sequence

Polypeptide 5154 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Hydin	HYDIN, axonemal central pair apparatus protein	15	97	3	11

Sequence references in MGI

J:83437 Davy BE, et al., Congenital hydrocephalus in hy3 mice is caused by a frameshift mutation in Hydin, a large novel gene. Hum Mol Genet. 2003 May 15;12(10):1163-70
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:135322 Lechtreck KF, et al., Mutations in Hydin impair ciliary motility in mice. J Cell Biol. 2008 Feb 11;180(3):633-43
J:277764 Zheng J, et al., Microtubule-bundling protein Spef1 enables mammalian ciliary central apparatus formation. J Mol Cell Biol. 2019 Jan 1;11(1):67-77
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89
J:303071 Miyata H, et al., Testis-enriched kinesin KIF9 is important for progressive motility in mouse spermatozoa. FASEB J. 2020 Apr;34(4):5389-5400