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Category

8,485 results for acoxl

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ACOXL

(Homo sapiens)

Gene

Name: acyl-CoA oxidase like

Synonyms: FLJ11042, acyl-CoA oxidase-like protein, acyl-coenzyme A oxidase-like protein, ACOX4, acyl-CoA oxidase-like

Source: HGNC:25621

Biotype: protein coding gene

Symbol: ACOXL (Hsa)

Symbol: ACOXL

Strict Orthology Symbols: acoxl

Allele/Variant (41)

acoxl

(Danio rerio)

Gene

Name: acyl-CoA oxidase-like

Synonyms: si:ch211-205h19.1

Source: ZFIN:ZDB-GENE-081107-18

Biotype: protein coding gene

Symbol: acoxl (Dre)

Symbol: acoxl

Automated Gene Synopsis: Orthologous to human ACOXL (acyl-CoA oxidase like).

Strict Orthology Symbols: acoxl

Allele/Variant (2)

Acoxl

(Mus musculus)

Gene

Name: acyl-Coenzyme A oxidase-like

Synonyms: 1200014P05Rik, AV025673, expressed sequence AV025673, RIKEN cDNA 1200014P05 gene

Source: MGI:1921371

Biotype: protein coding gene

Symbol: Acoxl (Mmu)

Symbol: Acoxl

Automated Gene Synopsis: Orthologous to human ACOXL (acyl-CoA oxidase like).

Strict Orthology Symbols: acoxl

Alleles: Acoxl (Mmu)...Acoxl (Mmu)

Acoxl

(Rattus norvegicus)

Gene

Name: acyl-CoA oxidase-like

Synonyms: acyl-Coenzyme A oxidase-like, LOC296138

Source: RGD:1306814

Biotype: protein coding gene

Symbol: Acoxl (Rno)

Symbol: Acoxl

Gene Synopsis: Orthologous to human ACOXL (acyl-CoA oxidase like); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine;

Automated Gene Synopsis: Orthologous to human ACOXL (acyl-CoA oxidase like).

Strict Orthology Symbols: acoxl

Alleles: Acoxl (Rno)

acoxl

(Xenopus tropicalis)

Gene

Name: acyl-CoA oxidase like

Synonyms: acoxl, acyl-CoA oxidase like, LOC108716607

Source: Xenbase:XB-GENE-990149

Biotype: gene

Symbol: acoxl

Symbol: acoxl (Xtr)

Automated Gene Synopsis: Orthologous to human ACOXL (acyl-CoA oxidase like).

Synonyms: acoxl...acoxl...acoxl

Strict Orthology Symbols: acoxl

ACOXL-AS1

(Homo sapiens)

Gene

Name: ACOXL antisense RNA 1

Synonyms: LOC400997, uncharacterized LOC400997

Source: HGNC:41112

Biotype: ncRNA gene

Symbol: ACOXL-AS1 (Hsa)

Symbol: ACOXL-AS1

Acoxl^em1(IMPC)Mbp

(Mus musculus)

Allele/Variant

Source: MGI:6140125

Genes: Acoxl (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Acoxl (Mmu)

Genes: Acoxl (Mmu)

Symbol: Acoxl^em1(IMPC)Mbp

Acoxl^{Tn(sb-T2/Bart3)2.342Mcwi}

(Rattus norvegicus)

Allele/Variant

Source: RGD:2314337

Genes: Acoxl (Rno)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Acoxl (Rno)

Genes: Acoxl (Rno)

Symbol: Acoxl^{Tn(sb-T2/Bart3)2.342Mcwi}

Acoxl^em9Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7309347

Genes: Acoxl (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Acoxl (Mmu)

Genes: Acoxl (Mmu)

Symbol: Acoxl^em9Gpt

Gene (1)

Acoxl^em1(IMPC)Mbp/Acoxl^em1(IMPC)Mbp [background:] C57BL/6NCrl-Acoxl^em1(IMPC)Mbp/Mmucd

(Mus musculus)

Model

Id: MGI:6461039

Synonyms: Not Available

Symbol: Acoxl/Acoxl [background:] C57BL/6NCrl-Acoxl/Mmucd (Mmu)

Genes: Acoxl (Mmu)

Alleles: Acoxl (Mmu)

Name: Acoxl/Acoxl [background:] C57BL/6NCrl-Acoxl/Mmucd

Gene (1)

POX1

(Saccharomyces cerevisiae)

Gene

Name: Not Available

Synonyms: FOX1, YGL205W

Source: SGD:S000003173

Biotype: protein coding gene

Strict Orthology Symbols: acoxl

acyl-CoA oxidase activity

Gene Ontology

Source: GO:0003997

Synonyms:

acyl coenzyme A oxidase activity
acyl-CoA:oxygen 2-oxidoreductase activity

Branch: molecular function

Genes: acoxl (Dre)...Acoxl (Rno)...ACOXL (Hsa)...Acoxl (Mmu)

Genes Annotated with this GO Term (39)

fatty acid beta-oxidation using acyl-CoA oxidase

Gene Ontology

Source: GO:0033540

Synonyms: Not Available

Branch: biological process

Genes: acoxl (Dre)...Acoxl (Rno)...ACOXL (Hsa)...Acoxl (Mmu)

Genes Annotated with this GO Term (46)

F344-Acoxl^{Tn(sb-T2/Bart3)2.342Mcwi}

(Rattus norvegicus)

Model

Id: RGD:2314340

Synonyms: F344-AcoxlTn(sb-T2/Bart3)2.342Mcwi

Genes: Acoxl (Rno)

Alleles: Acoxl (Rno)

Name: F344-<Acoxl

Gene (1)

fatty acid binding

Gene Ontology

Source: GO:0005504

Synonyms: Not Available

Branch: molecular function

Genes: acoxl (Dre)...Acoxl (Rno)...ACOXL (Hsa)...Acoxl (Mmu)

Genes Annotated with this GO Term (227)

oxidoreductase activity, acting on the CH-CH group of donors

Gene Ontology

Source: GO:0016627

Synonyms:

oxidoreductase activity, acting on the CH-CH group of donors, other acceptors

Branch: molecular function

Genes: acoxl (Dre)...ACOXL (Hsa)

Genes Annotated with this GO Term (355)

FAD binding

Gene Ontology

Source: GO:0071949

Synonyms:

oxidized flavin adenine dinucleotide binding
oxidized flavine-adenine dinucleotide binding

Branch: molecular function

Genes: ACOXL (Hsa)...Acoxl (Mmu)...acoxl (Dre)...Acoxl (Rno)

Genes Annotated with this GO Term (237)

fatty acid beta-oxidation

Gene Ontology

Source: GO:0006635

Synonyms: Not Available

Branch: biological process

Genes: ACOXL (Hsa)...Acoxl (Mmu)...acoxl (Dre)

Genes Annotated with this GO Term (302)

flavin adenine dinucleotide binding

Gene Ontology

Source: GO:0050660

Synonyms:

FAD or FADH2 binding
flavine-adenine dinucleotide binding

Branch: molecular function

Genes: ACOXL (Hsa)...Acoxl (Mmu)...acoxl (Dre)...Acoxl (Rno)

Genes Annotated with this GO Term (542)

peroxisome

Gene Ontology

Source: GO:0005777

Synonyms:

peroxisomal
peroxisome vesicle

Branch: cellular component

Genes: ACOXL (Hsa)...Acoxl (Mmu)...acoxl (Dre)...Acoxl (Rno)

Genes Annotated with this GO Term (889)

peroxisomal matrix

Gene Ontology

Source: GO:0005782

Synonyms:

peroxisomal lumen

Branch: cellular component

Genes: ACOXL (Hsa)

Genes Annotated with this GO Term (156)

fatty acid metabolic process

Gene Ontology

Source: GO:0006631

Synonyms:

fatty acid metabolism

Branch: biological process

Genes: ACOXL (Hsa)...acoxl (Dre)

Genes Annotated with this GO Term (1653)

oxidoreductase activity

Gene Ontology

Source: GO:0016491

Synonyms:

oxidoreductase activity, acting on other substrates
redox activity

Branch: molecular function

Genes: ACOXL (Hsa)...acoxl (Dre)

Genes Annotated with this GO Term (4673)

sa13812

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-131217-12230

Genes: acoxl (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: acoxl (Dre)

sa14022

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-131217-12424

Genes: acoxl (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_donor_variant

Diseases: Not Available

Variant Name: Not Available

Genes: acoxl (Dre)

molecular_function

Gene Ontology

Source: GO:0003674

Synonyms:

molecular function

Branch: molecular function

Genes: ACOXL (Hsa)

Genes Annotated with this GO Term (10000)

(GRCh38)2:110799020A>T

(Homo sapiens)

Allele/Variant

Source: rs933453806

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110799020A>T

(GRCh38)2:110841387C>G

(Homo sapiens)

Allele/Variant

Source: rs749321633

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110841387C>G

(GRCh38)2:110933623G>A

(Homo sapiens)

Allele/Variant

Source: rs1265915879

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110933623G>A

(GRCh38)2:110794154A>G

(Homo sapiens)

Allele/Variant

Source: rs201529913

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110794154A>G

(GRCh38)2:110798706A>T

(Homo sapiens)

Allele/Variant

Source: rs748517725

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110798706A>T

(GRCh38)2:110933631A>G

(Homo sapiens)

Allele/Variant

Source: rs367553833

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110933631A>G

(GRCh38)2:110805388C>T

(Homo sapiens)

Allele/Variant

Source: NC_000002.12:g.110805388C>T

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110805388C>T

(GRCh38)2:110908856C>T

(Homo sapiens)

Allele/Variant

Source: rs778800133

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110908856C>T

(GRCh38)2:110933494C>T

(Homo sapiens)

Allele/Variant

Source: NC_000002.12:g.110933494C>T

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110933494C>T

(GRCh38)2:110987117C>T

(Homo sapiens)

Allele/Variant

Source: rs561949547

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110987117C>T

(GRCh38)2:110784804A>G

(Homo sapiens)

Allele/Variant

Source: rs887505142

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110784804A>G

(GRCh38)2:110933634G>A

(Homo sapiens)

Allele/Variant

Source: rs2060560004

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110933634G>A

(GRCh38)2:110987148A>G

(Homo sapiens)

Allele/Variant

Source: rs2062969247

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110987148A>G

(GRCh38)2:110805324T>C

(Homo sapiens)

Allele/Variant

Source: rs145955915

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110805324T>C

(GRCh38)2:110784811T>A

(Homo sapiens)

Allele/Variant

Source: rs771820899

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110784811T>A

(GRCh38)2:110805366G>T

(Homo sapiens)

Allele/Variant

Source: rs527716900

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110805366G>T

(GRCh38)2:110987198G>A

(Homo sapiens)

Allele/Variant

Source: rs267598834

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, start_lost, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110987198G>A

(GRCh38)2:110794107C>A

(Homo sapiens)

Allele/Variant

Source: rs1684993535

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110794107C>A

(GRCh38)2:110799023G>A

(Homo sapiens)

Allele/Variant

Source: rs764902890

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110799023G>A

(GRCh38)2:110801675A>G

(Homo sapiens)

Allele/Variant

Source: rs1226948911

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110801675A>G

(GRCh38)2:110987118G>A

(Homo sapiens)

Allele/Variant

Source: rs763217979

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110987118G>A

(GRCh38)2:110768447C>T

(Homo sapiens)

Allele/Variant

Source: rs752696818

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110768447C>T

(GRCh38)2:110841385A>G

(Homo sapiens)

Allele/Variant

Source: rs777944015

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, stop_lost

Diseases: Not Available

Variant Name: (GRCh38)2:110841385A>G

(GRCh38)2:110798641C>T

(Homo sapiens)

Allele/Variant

Source: rs551873770

Genes: ACOXL (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)2:110798641C>T

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