======= 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 |}}