45 results for C03C10.2

C03C10.2

(Caenorhabditis elegans)
Gene
Name: Putative casein kinase I C03C10.2
Synonyms: CELE_C03C10.2
Source: WB:WBGene00007269
Biotype: protein coding gene
Symbol: C03C10.2 (Cel)
Symbol: C03C10.2
Cross References: C03C10.2...WB:C03C10.2...C03C10.2

Source: GO:0044024
Synonyms:
  • histone kinase activity (H2A-S1 specific)
  • histone serine kinase activity (H2A-S1 specific)
Branch: molecular function
Genes: C03C10.2 (Cel)

Source: GO:0106310
Synonyms:
  • protein-serine kinase activity
Branch: molecular function
Genes: C03C10.2 (Cel)

Gene Ontology
Source: GO:0016310
Synonyms: Not Available
Branch: biological process
Genes: C03C10.2 (Cel)

Source: GO:0004672
Synonyms:
  • protamine kinase activity
Branch: molecular function
Genes: C03C10.2 (Cel)

Source: GO:0006468
Synonyms:
  • protein amino acid phosphorylation
Branch: biological process
Genes: C03C10.2 (Cel)

Source: GO:0004674
Synonyms:
  • protein serine kinase activity
  • protein serine-threonine kinase activity
Branch: molecular function
Genes: C03C10.2 (Cel)

(WBcel235)III:4091186T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091186T>G
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091186T>G
Gene Cross References: C03C10.2

(WBcel235)III:4091411G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091411G>A
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091411G>A
Gene Cross References: C03C10.2

(WBcel235)III:4091338C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091338C>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091338C>T
Gene Cross References: C03C10.2

(WBcel235)III:4092884T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092884T>C
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092884T>C
Gene Cross References: C03C10.2

(WBcel235)III:4091661G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091661G>A
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091661G>A
Gene Cross References: C03C10.2

(WBcel235)III:4093090A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4093090A>G
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4093090A>G
Gene Cross References: C03C10.2

(WBcel235)III:4091760C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091760C>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091760C>T
Gene Cross References: C03C10.2

(WBcel235)III:4091633G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091633G>A
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091633G>A
Gene Cross References: C03C10.2

(WBcel235)III:4091864G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091864G>A
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091864G>A
Gene Cross References: C03C10.2

(WBcel235)III:4092186C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092186C>T
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092186C>T
Gene Cross References: C03C10.2

(WBcel235)III:4091909A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091909A>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091909A>T
Gene Cross References: C03C10.2

(WBcel235)III:4091660G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091660G>A
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091660G>A
Gene Cross References: C03C10.2

(WBcel235)III:4092525T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092525T>G
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092525T>G
Gene Cross References: C03C10.2

(WBcel235)III:4092576A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092576A>C
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092576A>C
Gene Cross References: C03C10.2

(WBcel235)III:4092757G>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092757G>C
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092757G>C
Gene Cross References: C03C10.2

(WBcel235)III:4092888C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092888C>T
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092888C>T
Gene Cross References: C03C10.2

(WBcel235)III:4091431G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091431G>A
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091431G>A
Gene Cross References: C03C10.2

(WBcel235)III:4092680A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092680A>C
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092680A>C
Gene Cross References: C03C10.2

(WBcel235)III:4091521G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091521G>A
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091521G>A
Gene Cross References: C03C10.2

(WBcel235)III:4091654C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091654C>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091654C>T
Gene Cross References: C03C10.2

(WBcel235)III:4091903C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091903C>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091903C>T
Gene Cross References: C03C10.2

(WBcel235)III:4092365C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092365C>T
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092365C>T
Gene Cross References: C03C10.2

Source: GO:0006338
Synonyms:
  • ATP-dependent chromatin remodeling
  • ATP-dependent chromatin remodelling
Branch: biological process
Genes: C03C10.2 (Cel)

(WBcel235)III:4092005T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092005T>G
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092005T>G
Gene Cross References: C03C10.2

(WBcel235)III:4091081C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091081C>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091081C>T
Gene Cross References: C03C10.2

(WBcel235)III:4091089C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091089C>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091089C>T
Gene Cross References: C03C10.2

(WBcel235)III:4091217G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091217G>A
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091217G>A
Gene Cross References: C03C10.2

(WBcel235)III:4091248C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091248C>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091248C>T
Gene Cross References: C03C10.2

(WBcel235)III:4091446A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091446A>C
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091446A>C
Gene Cross References: C03C10.2

(WBcel235)III:4093120G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4093120G>A
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4093120G>A
Gene Cross References: C03C10.2

(WBcel235)III:4091591C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091591C>T
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091591C>T
Gene Cross References: C03C10.2

(WBcel235)III:4092154A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092154A>G
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092154A>G
Gene Cross References: C03C10.2

(WBcel235)III:4091436T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4091436T>G
Genes: C03C10.5 (Cel), C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4091436T>G
Gene Cross References: C03C10.2

(WBcel235)III:4092663G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003281.10:g.4092663G>A
Genes: C03C10.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)III:4092663G>A
Gene Cross References: C03C10.2

Gene Ontology
Source: GO:0007165
Synonyms:
  • signaling cascade
  • signaling pathway
Branch: biological process
Genes: C03C10.2 (Cel)

Gene Ontology
Source: GO:0005524
Synonyms:
  • Mg-ATP binding
  • MgATP binding
Branch: molecular function
Genes: C03C10.2 (Cel)

Gene Ontology
Source: GO:0005634
Synonyms:
  • cell nucleus
  • horsetail nucleus
Branch: cellular component
Genes: C03C10.2 (Cel)

Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: C03C10.2 (Cel)