WDR26

WDR26
Identifiers
Aliases	WDR26, CDW2, GID7, MIP2, WD repeat domain 26, SKDEAS
External IDs	OMIM: 617424; MGI: 1923825; HomoloGene: 11857; GeneCards: WDR26; OMA:WDR26 - orthologs
Gene location (Human)
Chr.	Chromosome 1 (human)
End	224,437,033 bp
Gene location (Mouse)
Chr.	Chromosome 1 (mouse)
End	181,039,566 bp
RNA expression pattern
	Top expressed in
	sperm; ; secondary oocyte; ; mucosa of pharynx; ; epithelium of colon; ; bone marrow cell; ; stromal cell of endometrium; ; trabecular bone; ; oral cavity; ; skin of thigh; ; amniotic fluid;
	Top expressed in
	aortic valve; ; ascending aorta; ; human fetus; ; Rostral migratory stream; ; blood; ; tibiofemoral joint; ; parotid gland; ; left lung lobe; ; skin of external ear; ; epithelium of lens;
	More reference expression data
	More reference expression data
Orthologs
	80232
	226757
	ENSG00000162923
	ENSMUSG00000038733
	Q9H7D7
	Q8C6G8
	NM_001115113; NM_025160; NM_001379403
	NM_145514
	NP_001108585; NP_079436; NP_001366332
NP_663489; NP_001390510; NP_001390511; NP_001390512; NP_001390513;
	NP_001390514; NP_001390515; NP_001390516; NP_001390517; NP_001390518
	Wikidata
View/Edit Human	View/Edit Mouse

WD repeat-containing protein 26 is a protein that in humans is encoded by the WDR26 gene.^[5]

Function

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation.^[5]

Clinical significance

Pathogenic variants of the gene cause Skraban–Deardorff syndrome.^[6]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000162923 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000038733 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
1 2 "Entrez Gene: WDR26 WD repeat domain 26".
↑ Gross A, Müller J, Chrustowicz J, Strasser A, Gottemukkala K, Sherpa D, et al. (2024-04-04). "Skraban–Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly". FEBS Letters. 598 (9). Cambridge, England: Federation of European Biochemical Societies: 978–994. doi:10.1002/1873-3468.14866. ISSN 1873-3468. PMC 7616460. PMID 38575527.

Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, et al. (Nov 2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. 127 (3): 635–648. doi:10.1016/j.cell.2006.09.026. PMID 17081983. S2CID 7827573.
Higa LA, Wu M, Ye T, Kobayashi R, Sun H, Zhang H (Nov 2006). "CUL4-DDB1 ubiquitin ligase interacts with multiple WD40-repeat proteins and regulates histone methylation". Nature Cell Biology. 8 (11): 1277–1283. doi:10.1038/ncb1490. PMID 17041588. S2CID 22180568.
Zhu Y, Wang Y, Xia C, Li D, Li Y, Zeng W, et al. (Oct 2004). "WDR26: a novel Gbeta-like protein, suppresses MAPK signaling pathway". Journal of Cellular Biochemistry. 93 (3): 579–587. doi:10.1002/jcb.20175. PMID 15378603. S2CID 86601953.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (Oct 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–156. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Maruyama K, Sugano S (Jan 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–174. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.

This article on a gene on human chromosome 1 is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000162923 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000038733 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] 1 2 "Entrez Gene: WDR26 WD repeat domain 26".

[Gross_2024-6] Gross A, Müller J, Chrustowicz J, Strasser A, Gottemukkala K, Sherpa D, et al. (2024-04-04). "Skraban–Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly". FEBS Letters. 598 (9). Cambridge, England: Federation of European Biochemical Societies: 978–994. doi:10.1002/1873-3468.14866. ISSN 1873-3468. PMC 7616460. PMID 38575527.

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WDR26

Function

Clinical significance

References

Further reading