PXK (PX domain containing serine/threonine kinase like)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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54899 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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PX domain containing serine/threonine kinase like |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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PXK |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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MONAKA, SLOB |
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Chromosome
Chromosome number
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3 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3p14.3 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a phox (PX) domain-containing protein which may be involved in synaptic transmission and the ligand-induced internalization and degradation of epidermal growth factors. Variations in this gene may be associated with susceptibility to sys |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | ||||||||||||||||
| UniProt ID | Q7Z7A4 | |||||||||||||||
| Protein name | PX domain-containing protein kinase-like protein (Modulator of Na,K-ATPase) (MONaKA) | |||||||||||||||
| Protein function | Binds to and modulates brain Na,K-ATPase subunits ATP1B1 and ATP1B3 and may thereby participate in the regulation of electrical excitability and synaptic transmission. May not display kinase activity. {ECO:0000250|UniProtKB:Q8BX57, ECO:0000303|P | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed in all tissues examined except in heart. Isoform 1 is expressed in high levels in the brain, skeletal muscle, spleen and testis. Isoform 7 expression has yet to be demonstrated. {ECO:0000269|PubMed:16142408}. | |||||||||||||||
| Sequence |
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| Sequence length | 578 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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