88 results for Y116A8C.3

Y116A8C.3

(Caenorhabditis elegans)
Gene
Name: DUF19 domain-containing protein
Synonyms: CELE_Y116A8C.3
Source: WB:WBGene00013784
Biotype: protein coding gene
Symbol: Y116A8C.3 (Cel)
Symbol: Y116A8C.3
Cross References: WB:Y116A8C.3...Y116A8C.3...Y116A8C.3

Y116A8C.30

(Caenorhabditis elegans)
Gene
Name: NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12
Synonyms: CELE_Y116A8C.30
Source: WB:WBGene00013807
Biotype: protein coding gene
Symbol: Y116A8C.30 (Cel)
Symbol: Y116A8C.30

Y116A8C.33

(Caenorhabditis elegans)
Gene
Name: Domain of unknown function WSN domain-containing protein
Synonyms: CELE_Y116A8C.33
Source: WB:WBGene00013809
Biotype: protein coding gene
Symbol: Y116A8C.33 (Cel)
Symbol: Y116A8C.33

Y116A8C.38

(Caenorhabditis elegans)
Gene
Name: Tyrosine-protein kinase
Synonyms: CELE_Y116A8C.38
Source: WB:WBGene00013811
Biotype: protein coding gene
Symbol: Y116A8C.38 (Cel)
Symbol: Y116A8C.38

Y116A8C.37

(Caenorhabditis elegans)
Gene
Name: Tyrosine-protein phosphatase domain-containing protein
Synonyms: CELE_Y116A8C.37
Source: WB:WBGene00013810
Biotype: protein coding gene
Symbol: Y116A8C.37 (Cel)
Symbol: Y116A8C.37

NDUFAF2

(Homo sapiens)
Gene
Name: NADH:ubiquinone oxidoreductase complex assembly factor 2
Synonyms: NADH dehydrogenase 1 alpha subcomplex assembly factor 2, Myc-induced mitochondrial protein, MC1DN10, mimitin, FLJ22398, B17.2L, NDUFA12-like protein, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 2, NADH dehydrogenase (ubiquinone) complex I, assembly factor 2, NDUFA12L, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2, mimitin, mitochondrial, MMTN, B17.2-like
Source: HGNC:28086
Biotype: protein coding gene
Strict Orthology Symbols: Y116A8C.30

CG43346

(Drosophila melanogaster)
Gene
Name: Not Available
Synonyms: CG9243
Source: FB:FBgn0263051
Biotype: protein coding gene
Strict Orthology Symbols: Y116A8C.30

Ndufaf2

(Rattus norvegicus)
Gene
Name: NADH:ubiquinone oxidoreductase complex assembly factor 2
Synonyms: NADH dehydrogenase (ubiquinone) complex I, assembly factor 2, LOC361894, Ndufa12-like, RGD1560158, hypothetical LOC361894, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2, mimitin, mitochondrial, Ndufa12l, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 2
Source: RGD:1560158
Biotype: protein coding gene
Strict Orthology Symbols: Y116A8C.30

Ndufaf2

(Mus musculus)
Gene
Name: NADH:ubiquinone oxidoreductase complex assembly factor 2
Synonyms: expressed sequence C86051, mimitin, Ndufa12-like, RGD1560158, C86051, RIKEN cDNA 1810058I14 gene, 1810058I14Rik, Ndufa12l
Source: MGI:1922847
Biotype: protein coding gene
Strict Orthology Symbols: Y116A8C.30

Source: DOID:0112075
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF2 gene on chromosome 5q12.1.
Genes: Y116A8C.30 (Cel)

ndufaf2

(Xenopus tropicalis)
Gene
Name: NADH:ubiquinone oxidoreductase complex assembly factor 2
Synonyms: ndufaf2, NADH:ubiquinone oxidoreductase complex assembly factor 2
Source: Xenbase:XB-GENE-6031729
Biotype: gene
Strict Orthology Symbols: Y116A8C.30

Source: GO:0032981
Synonyms:
  • mitochondrial NADH dehydrogenase complex (ubiquinone) assembly
  • mitochondrial complex I assembly
Branch: biological process
Genes: Y116A8C.30 (Cel)

Source: GO:0004715
Synonyms:
  • ATP:protein-L-tyrosine O-phosphotransferase (non-specific) activity
  • ATP:protein-tyrosine O-phosphotransferase activity
Branch: molecular function
Genes: Y116A8C.38 (Cel)

Source: GO:0004725
Synonyms:
  • PPT-phosphatase activity
  • PTP-phosphatase activity
Branch: molecular function
Genes: Y116A8C.37 (Cel)

Source: GO:0006470
Synonyms:
  • protein amino acid dephosphorylation
Branch: biological process
Genes: Y116A8C.37 (Cel)

Source: GO:0004713
Synonyms:
  • protein-tyrosine kinase activity
Branch: molecular function
Genes: Y116A8C.38 (Cel)

Gene Ontology
Source: GO:0016310
Synonyms: Not Available
Branch: biological process
Genes: Y116A8C.38 (Cel)

Source: GO:0004672
Synonyms:
  • protamine kinase activity
Branch: molecular function
Genes: Y116A8C.38 (Cel)

Source: GO:0006468
Synonyms:
  • protein amino acid phosphorylation
Branch: biological process
Genes: Y116A8C.38 (Cel)

(WBcel235)IV:16917027A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917027A>G
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917027A>G
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917112A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917112A>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917112A>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917133C>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917133C>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917133C>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916338T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916338T>C
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916338T>C
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916349A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916349A>C
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916349A>C
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916988T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916988T>C
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916988T>C
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916146G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916146G>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916146G>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916180T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916180T>C
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916180T>C
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917169C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917169C>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917169C>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917517T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917517T>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917517T>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916438C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916438C>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916438C>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916559C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916559C>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916559C>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916612C>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916612C>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916612C>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916991C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916991C>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916991C>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917267G>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917267G>C
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917267G>C
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917319A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917319A>G
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917319A>G
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917366G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917366G>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917366G>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917541C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917541C>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917541C>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916501G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916501G>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916501G>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916581T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916581T>C
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916581T>C
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916560C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916560C>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916560C>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917307G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917307G>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917307G>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916158T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916158T>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916158T>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917369G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917369G>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917369G>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917151A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917151A>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917151A>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917400C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917400C>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917400C>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16917490C>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16917490C>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16917490C>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916202G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916202G>A
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916202G>A
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916300C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916300C>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916300C>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916513A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916513A>T
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916513A>T
Gene Cross References: Y116A8C.3

(WBcel235)IV:16916459T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.16916459T>C
Genes: Y116A8C.3 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:16916459T>C
Gene Cross References: Y116A8C.3