Version: 8.0.0
Date: Tue Jan 28 2025
514 results for fbxo43
Allele/Variant Molecular Consequence: missense 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)8:100134292G>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)8:100140700G>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)8:100142062G>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)8:100141102C>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

(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

(mRatBN7.2)7:67345449G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321116424
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67345449G>A

(GRCm39)15:36152642C>T

(Mus musculus)
Allele/Variant
Source: rs257849157
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36152642C>T

(GRCm39)15:36153043T>G

(Mus musculus)
Allele/Variant
Source: rs32527458
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36153043T>G

(GRCm39)15:36157171G>A

(Mus musculus)
Allele/Variant
Source: rs243536649
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36157171G>A

(GRCm39)15:36160258A>G

(Mus musculus)
Allele/Variant
Source: rs219141298
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36160258A>G

(GRCm39)15:36159965A>G

(Mus musculus)
Allele/Variant
Source: rs32507277
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36159965A>G

(GRCm39)15:36166419A>C

(Mus musculus)
Allele/Variant
Source: rs223244847
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36166419A>C

(GRCm39)15:36166619C>T

(Mus musculus)
Allele/Variant
Source: rs263564276
Genes: Fbxo43 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:36166619C>T

(mRatBN7.2)7:67334037T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321115662
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67334037T>G

(mRatBN7.2)7:67334962T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321152870
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67334962T>A

(mRatBN7.2)7:67334181G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321115775
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67334181G>A

(mRatBN7.2)7:67334362G>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.67334362G>C
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67334362G>C

(mRatBN7.2)7:67335072T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321054073
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67335072T>C

(mRatBN7.2)7:67337716C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321152866
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67337716C>T

(mRatBN7.2)7:67341350C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320910723
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67341350C>T

(mRatBN7.2)7:67338440A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321011706
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67338440A>T

(mRatBN7.2)7:67340961G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321150603
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67340961G>A

(mRatBN7.2)7:67343128T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321044284
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67343128T>G

(mRatBN7.2)7:67341066A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.67341066A>G
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67341066A>G

(mRatBN7.2)7:67334527G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321148233
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67334527G>A

(mRatBN7.2)7:67341181A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.67341181A>G
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67341181A>G

(mRatBN7.2)7:67336406T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.67336406T>A
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67336406T>A

(mRatBN7.2)7:67336575A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321044421
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67336575A>G

(mRatBN7.2)7:67338185T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321153013
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67338185T>C

(mRatBN7.2)7:67339266A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321150598
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67339266A>G

(mRatBN7.2)7:67334101A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321115647
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67334101A>T

(mRatBN7.2)7:67335229C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321011828
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67335229C>G

(mRatBN7.2)7:67338685T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321054006
Genes: Fbxo43 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:67338685T>C