Version: 8.0.0
Date: Tue Jan 28 2025
554 results for fbxo43
Allele/Variant

Fbxo43tm1.1Kald

(Mus musculus)
Allele/Variant
Source: MGI:6201341
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Fbxo43 (Mmu)
Genes: Fbxo43 (Mmu)
Symbol: Fbxo43tm1.1Kald

Fbxo43tm1.2Kald

(Mus musculus)
Allele/Variant
Source: MGI:6201342
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Fbxo43 (Mmu)
Genes: Fbxo43 (Mmu)
Symbol: Fbxo43tm1.2Kald

Fbxo43em2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7299022
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Fbxo43 (Mmu)
Genes: Fbxo43 (Mmu)
Symbol: Fbxo43em2Gpt

Fbxo43em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7299021
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Fbxo43 (Mmu)
Genes: Fbxo43 (Mmu)
Symbol: Fbxo43em1Gpt

sa13745

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-12170
Genes: fbxo43 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: fbxo43 (Dre)

(GRCh38)8:100142126G>A

(Homo sapiens)
Allele/Variant
Source: rs754320394
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100142126G>A

(GRCh38)8:100134292G>A

(Homo sapiens)
Allele/Variant
Source: rs768989830
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100134292G>A

(GRCh38)8:100140700G>C

(Homo sapiens)
Allele/Variant
Source: rs199780921
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140700G>C

(GRCh38)8:100140884C>A

(Homo sapiens)
Allele/Variant
Source: rs954142586
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140884C>A

(GRCh38)8:100141572A>C

(Homo sapiens)
Allele/Variant
Source: rs373258172
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141572A>C

(GRCh38)8:100140700G>A

(Homo sapiens)
Allele/Variant
Source: rs199780921
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140700G>A

(GRCh38)8:100134364C>T

(Homo sapiens)
Allele/Variant
Source: rs373092371
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100134364C>T

(GRCh38)8:100141395C>T

(Homo sapiens)
Allele/Variant
Source: rs1171227939
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141395C>T

(GRCh38)8:100133950C>T

(Homo sapiens)
Allele/Variant
Source: rs370561864
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100133950C>T

(GRCh38)8:100137646A>T

(Homo sapiens)
Allele/Variant
Source: rs759048586
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100137646A>T

(GRCh38)8:100141337A>G

(Homo sapiens)
Allele/Variant
Source: rs376577612
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141337A>G

(GRCh38)8:100141707C>T

(Homo sapiens)
Allele/Variant
Source: rs748362105
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141707C>T

(GRCh38)8:100133938C>T

(Homo sapiens)
Allele/Variant
Source: rs954702094
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100133938C>T

(GRCh38)8:100140744T>C

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.100140744T>C
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140744T>C

(GRCh38)8:100140843C>T

(Homo sapiens)
Allele/Variant
Source: rs1215477131
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140843C>T

(GRCh38)8:100140915G>A

(Homo sapiens)
Allele/Variant
Source: rs373156415
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140915G>A

(GRCh38)8:100140986C>T

(Homo sapiens)
Allele/Variant
Source: rs748943275
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140986C>T

(GRCh38)8:100141205T>C

(Homo sapiens)
Allele/Variant
Source: rs530844525
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141205T>C

(GRCh38)8:100141209A>T

(Homo sapiens)
Allele/Variant
Source: rs373910464
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141209A>T

(GRCh38)8:100141548C>T

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.100141548C>T
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141548C>T

(GRCh38)8:100145110C>A

(Homo sapiens)
Allele/Variant
Source: rs1387007809
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100145110C>A

(GRCh38)8:100142062G>A

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.100142062G>A
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100142062G>A

(GRCh38)8:100141935G>A

(Homo sapiens)
Allele/Variant
Source: rs553559355
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141935G>A

(GRCh38)8:100141483A>C

(Homo sapiens)
Allele/Variant
Source: rs369057548
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141483A>C

(GRCh38)8:100141567C>A

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.100141567C>A
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141567C>A

(GRCh38)8:100141848C>T

(Homo sapiens)
Allele/Variant
Source: rs745750597
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141848C>T

(GRCh38)8:100141940T>C

(Homo sapiens)
Allele/Variant
Source: rs1421611544
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141940T>C

(GRCh38)8:100140685G>C

(Homo sapiens)
Allele/Variant
Source: rs201016433
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140685G>C

(GRCh38)8:100133821C>T

(Homo sapiens)
Allele/Variant
Source: rs202056051
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100133821C>T

(GRCh38)8:100140761A>G

(Homo sapiens)
Allele/Variant
Source: rs267601676
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140761A>G

(GRCh38)8:100140976C>G

(Homo sapiens)
Allele/Variant
Source: rs1223084666
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100140976C>G

(GRCh38)8:100141102C>T

(Homo sapiens)
Allele/Variant
Source: rs371117490
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141102C>T

(GRCh38)8:100141949G>A

(Homo sapiens)
Allele/Variant
Source: rs201306425
Genes: FBXO43 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:100141949G>A

(mRatBN7.2)7:67335519T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321148057
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67335519T>C

(mRatBN7.2)7:67335650C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321130532
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67335650C>T

(mRatBN7.2)7:67336074T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321148124
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67336074T>G

(mRatBN7.2)7:67342202A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321115625
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67342202A>C

(mRatBN7.2)7:67334543T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321152848
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67334543T>G

(mRatBN7.2)7:67336402T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.67336402T>A
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67336402T>A

(mRatBN7.2)7:67337679T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.67337679T>C
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67337679T>C

(mRatBN7.2)7:67340187G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321148063
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67340187G>A

(mRatBN7.2)7:67340356T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321044364
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67340356T>C

(mRatBN7.2)7:67333740G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321053951
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67333740G>C

(mRatBN7.2)7:67336404T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.67336404T>A
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67336404T>A

(mRatBN7.2)7:67335990G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321148286
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67335990G>A