8,462 results for camk4
Source: GO:0006954
Synonyms:
  • inflammation
Branch: biological process
Genes: Camk4 (Mmu)...CAMK4 (Hsa)...Camk4 (Rno)

Gene Ontology
Source: GO:0098794
Synonyms: Not Available
Branch: cellular component
Genes: Camk4 (Mmu)...CAMK4 (Hsa)...Camk4 (Rno)

Source: GO:0106310
Synonyms:
  • protein-serine kinase activity
Branch: molecular function
Genes: Camk4 (Mmu)...CAMK4 (Hsa)...Camk4 (Rno)

Source: GO:0002250
Synonyms:
  • acquired immune response
  • immune memory response
Branch: biological process
Genes: Camk4 (Mmu)...CAMK4 (Hsa)...Camk4 (Rno)

Source: GO:0006468
Synonyms:
  • protein amino acid phosphorylation
Branch: biological process
Genes: Camk4 (Mmu)...CAMK4 (Hsa)...camk4 (Dre)...Camk4 (Rno)

Source: GO:0035556
Synonyms:
  • intracellular signal transduction pathway
  • intracellular signaling cascade
Branch: biological process
Genes: Camk4 (Mmu)...CAMK4 (Hsa)...camk4 (Dre)...Camk4 (Rno)

Source: GO:0098978
Synonyms: Not Available
Branch: cellular component
Genes: Camk4 (Mmu)...CAMK4 (Hsa)...Camk4 (Rno)

Source: GO:0045893
Synonyms:
  • activation of gene-specific transcription
  • activation of transcription, DNA-dependent
Branch: biological process
Genes: Camk4 (Mmu)...CAMK4 (Hsa)...Camk4 (Rno)

Gene Ontology
Source: GO:0016310
Synonyms: Not Available
Branch: biological process
Genes: camk4 (Dre)

Source: GO:0004672
Synonyms:
  • protamine kinase activity
Branch: molecular function
Genes: CAMK4 (Hsa)...camk4 (Dre)

Source: GO:0004674
Synonyms:
  • protein serine kinase activity
  • protein serine-threonine kinase activity
Branch: molecular function
Genes: CAMK4 (Hsa)...camk4 (Dre)

Allele/Variant
Source: rs753581560
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111224521C>G

Allele/Variant
Source: NC_000005.10:g.111482929A>G
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111482929A>G

Allele/Variant
Source: rs767800747
Genes: CAMK4 (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)5:111376875A>G

Allele/Variant
Source: rs6886469
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484418T>G

Allele/Variant
Source: rs207466323
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111371525G>T

Allele/Variant
Source: rs988750749
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111473377C>G

Allele/Variant
Source: rs991922432
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111224604G>T

Allele/Variant
Source: rs1748087413
Genes: CAMK4 (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)5:111224643C>T

Allele/Variant
Source: rs207466325
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111448189G>T

Allele/Variant
Source: rs754120828
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484210G>T

Allele/Variant
Source: rs35548075
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111446758G>A

Allele/Variant
Source: rs1755482400
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111482896C>T

Allele/Variant
Source: NC_000005.10:g.111484113C>G
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484113C>G

Allele/Variant
Source: rs143979132
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484371A>G

Allele/Variant
Source: rs760133605
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111478500A>G

Allele/Variant
Source: NC_000005.10:g.111482885T>C
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111482885T>C

Allele/Variant
Source: rs207466324
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111398307C>A

Allele/Variant
Source: rs564406339
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484269A>G

Allele/Variant
Source: NC_000005.10:g.111374914T>C
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111374914T>C

Allele/Variant
Source: rs778752233
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111473355A>G

Allele/Variant
Source: rs143584280
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111482806G>A

Allele/Variant
Source: rs1561515242
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111482938G>A

Allele/Variant
Source: NC_000005.10:g.111484280G>C
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484280G>C

Allele/Variant
Source: rs376502428
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484146G>A

Allele/Variant
Source: rs370357101
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111224545C>T

Allele/Variant
Source: rs140425791
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111478483A>T

Allele/Variant
Source: rs1406556113
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111224572C>G

Allele/Variant
Source: rs267600313
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111446775C>T

Allele/Variant
Source: rs377764169
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111449207T>G

Allele/Variant
Source: rs56360861
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484438A>G

Allele/Variant
Source: rs1440926092
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111484158A>G

Allele/Variant
Source: rs371085970
Genes: CAMK4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:111394739G>A

Gene Ontology
Source: GO:0016301
Synonyms:
  • phosphokinase activity
Branch: molecular function
Genes: camk4 (Dre)

Gene Ontology
Source: GO:0007165
Synonyms:
  • signaling cascade
  • signaling pathway
Branch: biological process
Genes: Camk4 (Rno)...Camk4 (Mmu)...CAMK4 (Hsa)

Gene Ontology
Source: GO:0000166
Synonyms: Not Available
Branch: molecular function
Genes: camk4 (Dre)

Source: GO:0070062
Synonyms:
  • exosome
  • extracellular vesicular exosome
Branch: cellular component
Genes: CAMK4 (Hsa)

Gene Ontology
Source: GO:0005524
Synonyms:
  • Mg-ATP binding
  • MgATP binding
Branch: molecular function
Genes: camk4 (Dre)...Camk4 (Mmu)...Camk4 (Rno)...CAMK4 (Hsa)

(mRatBN7.2)18:24771952T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323076740
Genes: Camk4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:24771952T>A

(mRatBN7.2)18:24773888C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323148847
Genes: Camk4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:24773888C>A