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Category

30 results for T10B5.4

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T10B5.4

(Caenorhabditis elegans)

Gene

Name: N-acetyltransferase domain-containing protein

Synonyms: CELE_T10B5.4

Source: WB:WBGene00020390

Biotype: protein coding gene

Symbol: T10B5.4 (Cel)

Symbol: T10B5.4

Cross References: T10B5.4...WB:T10B5.4...T10B5.4

Allele/Variant (26)

AANATL7

(Drosophila melanogaster)

Gene

Name: Arylalkylamine N-acetyltransferase-like 7

Synonyms: CG13759, BcDNA:AT19803, DmAANATL7, Arylalkylamine N-Acetyltransferase-like 7, CT33239, EG:BACR25B3.5, Arylalkylamine N-Acetyltransferase Like 7

Source: FB:FBgn0040376

Biotype: protein coding gene

Strict Orthology Symbols: T10B5.4

Allele/Variant (87)

N-acetyltransferase activity

Gene Ontology

Source: GO:0008080

Synonyms: Not Available

Branch: molecular function

Genes: T10B5.4 (Cel)

Genes Annotated with this GO Term (405)

acyltransferase activity, transferring groups other than amino-acyl groups

Gene Ontology

Source: GO:0016747

Synonyms:

transferase activity, transferring acyl groups other than amino-acyl groups
transferase activity, transferring groups other than amino-acyl groups

Branch: molecular function

Genes: T10B5.4 (Cel)

Genes Annotated with this GO Term (1423)

(WBcel235)V:1870452C>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870452C>A

Genes: T10B5.4 (Cel), knl-3 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870452C>A

Gene Cross References: T10B5.4

(WBcel235)V:1870675C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870675C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: stop_gained, 3_prime_UTR_variant, synonymous_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870675C>T

Gene Cross References: T10B5.4

(WBcel235)V:1871305G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871305G>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871305G>A

Gene Cross References: T10B5.4

(WBcel235)V:1870547A>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870547A>T

Genes: T10B5.4 (Cel), knl-3 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870547A>T

Gene Cross References: T10B5.4

(WBcel235)V:1870655T>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870655T>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870655T>A

Gene Cross References: T10B5.4

(WBcel235)V:1871622C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871622C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871622C>T

Gene Cross References: T10B5.4

(WBcel235)V:1870871G>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870871G>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870871G>T

Gene Cross References: T10B5.4

(WBcel235)V:1871265G>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871265G>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871265G>T

Gene Cross References: T10B5.4

(WBcel235)V:1870778T>C

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870778T>C

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870778T>C

Gene Cross References: T10B5.4

(WBcel235)V:1871008C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871008C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: splice_region_variant, missense_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871008C>T

Gene Cross References: T10B5.4

(WBcel235)V:1871482C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871482C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871482C>T

Gene Cross References: T10B5.4

(WBcel235)V:1870460T>G

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870460T>G

Genes: T10B5.4 (Cel), knl-3 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870460T>G

Gene Cross References: T10B5.4

(WBcel235)V:1870994T>C

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870994T>C

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870994T>C

Gene Cross References: T10B5.4

(WBcel235)V:1870608C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870608C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870608C>T

Gene Cross References: T10B5.4

(WBcel235)V:1871130C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871130C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: splice_region_variant, synonymous_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871130C>T

Gene Cross References: T10B5.4

(WBcel235)V:1870857C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870857C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870857C>T

Gene Cross References: T10B5.4

(WBcel235)V:1871729T>C

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871729T>C

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 5_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871729T>C

Gene Cross References: T10B5.4

(WBcel235)V:1871687G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871687G>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871687G>A

Gene Cross References: T10B5.4

(WBcel235)V:1871799G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871799G>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 5_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871799G>A

Gene Cross References: T10B5.4

(WBcel235)V:1870905G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870905G>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870905G>A

Gene Cross References: T10B5.4

(WBcel235)V:1871127C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871127C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871127C>T

Gene Cross References: T10B5.4

(WBcel235)V:1870866G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870866G>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870866G>A

Gene Cross References: T10B5.4

(WBcel235)V:1871370G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871370G>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871370G>A

Gene Cross References: T10B5.4

(WBcel235)V:1870708C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870708C>T

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, start_lost, 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870708C>T

Gene Cross References: T10B5.4

(WBcel235)V:1870854G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1870854G>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1870854G>A

Gene Cross References: T10B5.4

(WBcel235)V:1871014T>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003283.11:g.1871014T>A

Genes: T10B5.4 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, splice_donor_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)V:1871014T>A

Gene Cross References: T10B5.4

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