======= XK =======
== Gene Information ==
* **Official Symbol**: XK
* **Official Name**: X-linked Kx blood group
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=7504|7504]]
* **UniProt**: [[https://www.uniprot.org/uniprot/P51811|P51811]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=XK&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20XK|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/314850|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008].
* **UniProt Summary**: May be involved in sodium-dependent transport of neutral amino acids or oligopeptides.
|XK-related|
|regulation of axon diameter|
|cellular magnesium ion homeostasis|
|magnesium ion homeostasis|
|regulation of cell projection size|
|skeletal muscle fiber development|
|myotube cell development|
|transporter activity|
|myotube differentiation|
|muscle fiber development|
|myelination|
|axon ensheathment|
|ensheathment of neurons|
|amino acid transport|
|skeletal muscle tissue development|
|skeletal muscle organ development|
|striated muscle cell development|
|muscle cell development|
|regulation of cell size|
|regulation of axonogenesis|
|striated muscle cell differentiation|
|muscle cell differentiation|
|striated muscle tissue development|
|organic acid transport|
|carboxylic acid transport|
|muscle organ development|
|muscle tissue development|
|regulation of cell morphogenesis involved in differentiation|
|regulation of cellular component size|
|cellular calcium ion homeostasis|
|calcium ion homeostasis|
|organic anion transport|
|cellular divalent inorganic cation homeostasis|
|muscle structure development|
|regulation of cell morphogenesis|
|divalent inorganic cation homeostasis|
|regulation of neuron projection development|
|regulation of anatomical structure size|
|cellular metal ion homeostasis|
|anion transport|
|metal ion homeostasis|
|cellular cation homeostasis|
|cellular ion homeostasis|
|regulation of neuron differentiation|
|regulation of plasma membrane bounded cell projection organization|
|cation homeostasis|
|regulation of cell projection organization|
|inorganic ion homeostasis|
|cellular chemical homeostasis|
|ion homeostasis|
|regulation of neurogenesis|
|cellular homeostasis|
|regulation of nervous system development|
|regulation of cell development|
|regulation of anatomical structure morphogenesis|
|chemical homeostasis|
|ion transport|
|generation of neurons|
|neurogenesis|
|homeostatic process|
|cell development|
|tissue development|
|regulation of cell differentiation|
|nitrogen compound transport|
\\
=== CRISPR Data ===
^Screen^Score^
|[[:results:exp362|GSK-J4 1μM R07 exp362]]|-1.74|
No correlation found to any other genes in chemogenomics.
Global Fraction of Cell Lines Where Essential: 0/694
^Tissue^Fraction Of Cell Lines Where Essential^
|1290807.0|0/1|
|909776.0|0/1|
|bile duct|0/28|
|blood|0/26|
|bone|0/26|
|breast|0/30|
|central nervous system|0/49|
|cervix|0/4|
|colorectal|0/17|
|esophagus|0/11|
|fibroblast|0/1|
|gastric|0/14|
|kidney|0/18|
|liver|0/19|
|lung|0/72|
|lymphocyte|0/16|
|ovary|0/25|
|pancreas|0/22|
|peripheral nervous system|0/15|
|plasma cell|0/12|
|prostate|0/1|
|skin|0/20|
|soft tissue|0/9|
|thyroid|0/2|
|upper aerodigestive|0/22|
|urinary tract|0/28|
|uterus|0/5|
== Essentiality in NALM6 ==
* **Essentiality Rank**: 16772
* **Expression level (log2 read counts)**: -2.64
{{:chemogenomics:nalm6 dist.png?nolink |}}