Version: 8.0.0
Date: Tue Jan 28 2025
2,734 results for pxk

pxk

(Danio rerio)
Gene
Name: PX domain containing serine/threonine kinase
Synonyms: si:dkeyp-87e7.1, sb:eu550
Source: ZFIN:ZDB-GENE-050208-393
Biotype: protein coding gene
Symbol: pxk (Dre)
Symbol: pxk
Automated Gene Synopsis: Orthologous to human PXK (PX domain containing serine/threonine kinase like).
Strict Orthology Symbols: pxk

Pxk

(Mus musculus)
Gene
Name: PX domain containing serine/threonine kinase
Synonyms: DNA segment, Chr 14, ERATO Doi 813, expressed, D14Ertd813e, MONaKA, C230080L11Rik, RIKEN cDNA C230080L11 gene
Source: MGI:1289230
Biotype: protein coding gene
Symbol: Pxk (Mmu)
Symbol: Pxk
Automated Gene Synopsis: Orthologous to human PXK (PX domain containing serine/threonine kinase like).
Strict Orthology Symbols: pxk
Alleles: Pxk (Mmu)

PXK

(Homo sapiens)
Gene
Name: PX domain containing serine/threonine kinase like
Synonyms: PX ser/thr kinase v2, modulator of Na,K-ATPase long form, PX serine/threonine kinase, PX domain-containing protein kinase-like protein, MONaKA, FLJ20335, SLOB
Source: HGNC:23326
Biotype: protein coding gene
Symbol: PXK (Hsa)
Symbol: PXK
Strict Orthology Symbols: pxk

Pxk

(Rattus norvegicus)
Gene
Name: PX domain containing serine/threonine kinase like
Synonyms: PX domain containing serine/threonine kinase, PX serine/threonine kinase, PX domain-containing protein kinase-like protein, MONaKA, modulator of Na,K-ATPase, MGC114238
Source: RGD:727819
Biotype: protein coding gene
Symbol: Pxk (Rno)
Symbol: Pxk
Gene Synopsis: Orthologous to human PXK (PX domain containing serine/threonine kinase like); INTERACTS WITH 17alpha-ethynylestradiol
Automated Gene Synopsis: Orthologous to human PXK (PX domain containing serine/threonine kinase like).
Strict Orthology Symbols: pxk

pxk

(Xenopus tropicalis)
Gene
Name: PX domain containing serine/threonine kinase
Synonyms: pxk, PX domain containing serine/threonine kinase
Source: Xenbase:XB-GENE-952529
Biotype: gene
Symbol: pxk
Symbol: pxk (Xtr)
Automated Gene Synopsis: Orthologous to human PXK (PX domain containing serine/threonine kinase like).
Synonyms: pxk...pxk...pxk
Strict Orthology Symbols: pxk

pxk.S

(Xenopus laevis)
Gene
Name: PX domain containing serine/threonine kinase
Synonyms: PX domain containing serine/threonine kinase, pxk.S
Source: Xenbase:XB-GENE-952532
Biotype: gene
Symbol: pxk.S (Xla)
Automated Gene Synopsis: Orthologous to human PXK (PX domain containing serine/threonine kinase like).
Strict Orthology Symbols: pxk
Symbol: pxk.S

Pxkem1(IMPC)Tcp

(Mus musculus)
Allele/Variant
Source: MGI:6385270
Genes: Pxk (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Pxk (Mmu)
Genes: Pxk (Mmu)
Symbol: Pxkem1(IMPC)Tcp

Pxkem1(IMPC)Tcp/Pxkem1(IMPC)Tcp [background:] C57BL/6N-Pxkem1(IMPC)Tcp/Tcp

(Mus musculus)
Model
Id: MGI:6696874
Synonyms: Not Available
Symbol: Pxk/Pxk [background:] C57BL/6N-Pxk/Tcp (Mmu)
Genes: Pxk (Mmu)
Alleles: Pxk (Mmu)
Name: Pxk/Pxk [background:] C57BL/6N-Pxk/Tcp

CG8726

(Drosophila melanogaster)
Gene
Name: Not Available
Synonyms: Not Available
Source: FB:FBgn0033244
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human PXK (PX domain containing serine/threonine kinase like).
Strict Orthology Symbols: pxk

polycythemia due to hypoxia

Disease
Source: DOID:2835
Definition: Not Available
Genes: PXK (Hsa)...Pxk (Rno)...Pxk (Mmu)...pxk (Dre)...pxk (Xtr)

negative regulation of monoatomic ion transport

Gene Ontology
Source: GO:0043271
Synonyms:
  • down regulation of ion transport
  • down-regulation of ion transport
Branch: biological process
Genes: PXK (Hsa)...Pxk (Rno)...Pxk (Mmu)

negative regulation of ATP-dependent activity

Gene Ontology
Source: GO:0032780
Synonyms:
  • down regulation of ATPase activity
  • down-regulation of ATPase activity
Branch: biological process
Genes: Pxk (Mmu)...Pxk (Rno)...PXK (Hsa)

modulation of chemical synaptic transmission

Gene Ontology
Source: GO:0050804
Synonyms:
  • modulation of synaptic transmission
  • regulation of chemical synaptic transmission
Branch: biological process
Genes: PXK (Hsa)...Pxk (Mmu)...pxk (Dre)...Pxk (Rno)

phosphatidylinositol binding

Gene Ontology
Source: GO:0035091
Synonyms:
  • phosphoinositide binding
Branch: molecular function
Genes: PXK (Hsa)...Pxk (Mmu)...pxk (Dre)...Pxk (Rno)

centriolar satellite

Gene Ontology
Source: GO:0034451
Synonyms: Not Available
Branch: cellular component
Genes: PXK (Hsa)...Pxk (Mmu)...Pxk (Rno)

actin binding

Gene Ontology
Source: GO:0003779
Synonyms:
  • membrane associated actin binding
Branch: molecular function
Genes: Pxk (Rno)...Pxk (Mmu)...pxk (Dre)...PXK (Hsa)

inflammatory response

Gene Ontology
Source: GO:0006954
Synonyms:
  • inflammation
Branch: biological process
Genes: Pxk (Mmu)...Pxk (Rno)...PXK (Hsa)

protein kinase activity

Gene Ontology
Source: GO:0004672
Synonyms:
  • protamine kinase activity
Branch: molecular function
Genes: Pxk (Rno)...Pxk (Mmu)...pxk (Dre)...PXK (Hsa)

protein-containing complex

Gene Ontology
Source: GO:0032991
Synonyms:
  • macromolecular complex
  • macromolecule complex
Branch: cellular component
Genes: Pxk (Rno)...Pxk (Mmu)...PXK (Hsa)

kinase activity

Gene Ontology
Source: GO:0016301
Synonyms:
  • phosphokinase activity
Branch: molecular function
Genes: pxk (Dre)...PXK (Hsa)

phosphorylation

Gene Ontology
Source: GO:0016310
Synonyms: Not Available
Branch: biological process
Genes: pxk (Dre)

protein phosphorylation

Gene Ontology
Source: GO:0006468
Synonyms:
  • protein amino acid phosphorylation
Branch: biological process
Genes: pxk (Dre)...PXK (Hsa)

nucleotide binding

Gene Ontology
Source: GO:0000166
Synonyms: Not Available
Branch: molecular function
Genes: PXK (Hsa)

ATP binding

Gene Ontology
Source: GO:0005524
Synonyms:
  • Mg-ATP binding
  • MgATP binding
Branch: molecular function
Genes: pxk (Dre)...PXK (Hsa)...Pxk (Rno)...Pxk (Mmu)

sa32380

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-1643
Genes: pxk (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: pxk (Dre)

sa16786

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-12963
Genes: pxk (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: pxk (Dre)

transferase activity

Gene Ontology
Source: GO:0016740
Synonyms: Not Available
Branch: molecular function
Genes: pxk (Dre)

cytosol

Gene Ontology
Source: GO:0005829
Synonyms: Not Available
Branch: cellular component
Genes: Pxk (Mmu)...PXK (Hsa)...Pxk (Rno)

plasma membrane

Gene Ontology
Source: GO:0005886
Synonyms:
  • bacterial inner membrane
  • cell membrane
Branch: cellular component
Genes: Pxk (Mmu)...pxk (Dre)...PXK (Hsa)...Pxk (Rno)

cytoplasm

Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: pxk (Dre)...PXK (Hsa)...Pxk (Rno)...Pxk (Mmu)

nucleus

Gene Ontology
Source: GO:0005634
Synonyms:
  • cell nucleus
  • horsetail nucleus
Branch: cellular component
Genes: PXK (Hsa)...Pxk (Rno)...Pxk (Mmu)

(GRCh38)3:58397638C>T

(Homo sapiens)
Allele/Variant
Source: rs377744341
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58397638C>T

(GRCh38)3:58409545G>A

(Homo sapiens)
Allele/Variant
Source: rs140556006
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58409545G>A

(GRCh38)3:58410115A>T

(Homo sapiens)
Allele/Variant
Source: rs140203295
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58410115A>T

(GRCh38)3:58390585T>A

(Homo sapiens)
Allele/Variant
Source: rs1363158507
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58390585T>A

(GRCh38)3:58424908G>C

(Homo sapiens)
Allele/Variant
Source: rs376301093
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58424908G>C

(GRCh38)3:58399371A>G

(Homo sapiens)
Allele/Variant
Source: rs143160176
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58399371A>G

(GRCh38)3:58412901C>G

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.58412901C>G
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58412901C>G

(GRCh38)3:58397708C>T

(Homo sapiens)
Allele/Variant
Source: rs201628646
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58397708C>T

(GRCh38)3:58397720T>C

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.58397720T>C
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58397720T>C

(GRCh38)3:58403905T>G

(Homo sapiens)
Allele/Variant
Source: rs781470461
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58403905T>G

(GRCh38)3:58424866G>A

(Homo sapiens)
Allele/Variant
Source: rs138144401
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58424866G>A

(GRCh38)3:58391835G>A

(Homo sapiens)
Allele/Variant
Source: rs56401437
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58391835G>A

(GRCh38)3:58424782C>G

(Homo sapiens)
Allele/Variant
Source: rs755110801
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58424782C>G

(GRCh38)3:58424821C>A

(Homo sapiens)
Allele/Variant
Source: rs2062602283
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58424821C>A

(GRCh38)3:58424842C>T

(Homo sapiens)
Allele/Variant
Source: rs773826594
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58424842C>T

(GRCh38)3:58390582A>G

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.58390582A>G
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58390582A>G

(GRCh38)3:58390623C>T

(Homo sapiens)
Allele/Variant
Source: rs745755795
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58390623C>T

(GRCh38)3:58382619A>T

(Homo sapiens)
Allele/Variant
Source: rs770219681
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58382619A>T

(GRCh38)3:58382520G>A

(Homo sapiens)
Allele/Variant
Source: rs375318244
Genes: PXK (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:58382520G>A