Version: 8.1.0
Date: Fri Apr 18 2025
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Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Category
Allele/Variant
33
Gene Ontology
11
Gene
1
Filter
45
results
for
C03C10.2
Page 1 of 1
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
Allele/Variant (33)
histone H2AS1 kinase activity
Gene Ontology
Source:
GO:0044024
Synonyms:
histone kinase activity (H2A-S1 specific)
histone serine kinase activity (H2A-S1 specific)
Show All 3
Branch:
molecular function
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (841)
protein serine kinase activity
Gene Ontology
Source:
GO:0106310
Synonyms:
protein-serine kinase activity
Branch:
molecular function
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (1228)
phosphorylation
Gene Ontology
Source:
GO:0016310
Synonyms:
Not Available
Branch:
biological process
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (3408)
protein kinase activity
Gene Ontology
Source:
GO:0004672
Synonyms:
protamine kinase activity
Branch:
molecular function
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (3340)
protein phosphorylation
Gene Ontology
Source:
GO:0006468
Synonyms:
protein amino acid phosphorylation
Branch:
biological process
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (2710)
protein serine/threonine kinase activity
Gene Ontology
Source:
GO:0004674
Synonyms:
protein serine kinase activity
protein serine-threonine kinase activity
Show All 10
Branch:
molecular function
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (2523)
(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
chromatin remodeling
Gene Ontology
Source:
GO:0006338
Synonyms:
ATP-dependent chromatin remodeling
ATP-dependent chromatin remodelling
Show All 5
Branch:
biological process
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (4464)
(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
signal transduction
Gene Ontology
Source:
GO:0007165
Synonyms:
signaling cascade
signaling pathway
Show All 4
Branch:
biological process
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (10000)
ATP binding
Gene Ontology
Source:
GO:0005524
Synonyms:
Mg-ATP binding
MgATP binding
Branch:
molecular function
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (8374)
nucleus
Gene Ontology
Source:
GO:0005634
Synonyms:
cell nucleus
horsetail nucleus
Branch:
cellular component
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (10000)
cytoplasm
Gene Ontology
Source:
GO:0005737
Synonyms:
Not Available
Branch:
cellular component
Genes:
C03C10.2
(Cel)
Genes Annotated with this GO Term (10000)
Page 1 of 1
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