======= WDR60 =======
== Gene Information ==
* **Official Symbol**: WDR60
* **Official Name**: WD repeat domain 60
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=55112|55112]]
* **UniProt**: [[https://www.uniprot.org/uniprot/Q8WVS4|Q8WVS4]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=WDR60&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20WDR60|Open PubMed]]
* **OMIM**: N/A
== Function Summary ==
* **Entrez Summary**: 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) and may facilitate the 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. The encoded protein contains four WD repeats and may play a role in the formation of cilia. Mutations in this gene have been associated with short-rib polydactyly and Jeune syndromes. [provided by RefSeq, Mar 2014].
* **UniProt Summary**: May play a role in ciliogenesis. {ECO:0000269|PubMed:23910462}.
No Pfam Domain information is available for this gene.
|interphase microtubule organizing center|
|dynein heavy chain binding|
|cytoplasmic dynein complex|
|pericentriolar material|
|dynein light chain binding|
|ATP-dependent microtubule motor activity, plus-end-directed|
|ciliary base|
|intraciliary transport involved in cilium assembly|
|ciliary tip|
|intraciliary transport|
|protein transport along microtubule|
|microtubule-based protein transport|
|embryonic skeletal system morphogenesis|
|spindle pole|
|embryonic skeletal system development|
|transport along microtubule|
|cytoskeleton-dependent intracellular transport|
|microtubule-based transport|
|cilium|
|skeletal system morphogenesis|
|protein-containing complex localization|
|microtubule-based movement|
|embryonic organ morphogenesis|
|cilium assembly|
|cilium organization|
|embryonic organ development|
|plasma membrane bounded cell projection assembly|
|cell projection assembly|
|centrosome|
|skeletal system development|
|embryonic morphogenesis|
|chordate embryonic development|
|embryo development ending in birth or egg hatching|
|microtubule-based process|
|organelle assembly|
|animal organ morphogenesis|
|embryo development|
|intracellular protein transport|
|plasma membrane bounded cell projection organization|
|cell projection organization|
|protein transport|
|intracellular transport|
|peptide transport|
|movement of cell or subcellular component|
|amide transport|
|cellular protein localization|
|cellular macromolecule localization|
|extracellular space|
|establishment of protein localization|
|establishment of localization in cell|
|nitrogen compound transport|
\\
=== CRISPR Data ===
^Screen^Score^
|[[:results:exp123|GSK-LSD1 10μM R03 exp123]]|-2.24|
|[[:results:exp476|Dihydrosphingosine 8μM R08 exp476]]|1.72|
|[[:results:exp37|Wortmannin 0.5μM R00 exp37]]|1.75|
No correlation found to any other genes in chemogenomics.
Global Fraction of Cell Lines Where Essential: 0/739
^Tissue^Fraction Of Cell Lines Where Essential^
|1290807.0|0/1|
|909776.0|0/1|
|bile duct|0/28|
|blood|0/28|
|bone|0/26|
|breast|0/33|
|central nervous system|0/56|
|cervix|0/4|
|colorectal|0/17|
|esophagus|0/13|
|fibroblast|0/1|
|gastric|0/16|
|kidney|0/21|
|liver|0/20|
|lung|0/75|
|lymphocyte|0/16|
|ovary|0/26|
|pancreas|0/24|
|peripheral nervous system|0/16|
|plasma cell|0/15|
|prostate|0/1|
|skin|0/24|
|soft tissue|0/9|
|thyroid|0/2|
|upper aerodigestive|0/22|
|urinary tract|0/29|
|uterus|0/5|
== Essentiality in NALM6 ==
* **Essentiality Rank**: 4863
* **Expression level (log2 read counts)**: 4.89
{{:chemogenomics:nalm6 dist.png?nolink |}}