Version: 8.0.0
Date: Tue Jan 28 2025
1,409 results for aifm1
Allele/Variant

Aifm1tm1.2Geno

(Mus musculus)
Allele/Variant
Source: MGI:6728504
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Aifm1 (Mmu)
Genes: Aifm1 (Mmu)
Symbol: Aifm1tm1.2Geno

Aifm1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7376192
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Aifm1 (Mmu)
Genes: Aifm1 (Mmu)
Symbol: Aifm1em1Gpt

Aifm1tm2Pngr

(Mus musculus)
Allele/Variant
Source: MGI:3686777
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Aifm1 (Mmu)
Genes: Aifm1 (Mmu)
Symbol: Aifm1tm2Pngr

Aifm1em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7626368
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Aifm1 (Mmu)
Genes: Aifm1 (Mmu)
Symbol: Aifm1em1Smoc

Aifm1tm2.1Pngr

(Mus musculus)
Allele/Variant
Source: MGI:3851178
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Aifm1 (Mmu)
Genes: Aifm1 (Mmu)
Symbol: Aifm1tm2.1Pngr

Aifm1Hq

(Mus musculus)
Allele/Variant
Source: MGI:1861097
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: mitochondrial complex I deficiency
Variant Name: Not Available
Symbol: Aifm1 (Mmu)
Genes: Aifm1 (Mmu)
Symbol: Aifm1Hq

Aifm1tm1.1Geno

(Mus musculus)
Allele/Variant
Source: MGI:6728503
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Aifm1 (Mmu)
Genes: Aifm1 (Mmu)
Symbol: Aifm1tm1.1Geno

Aifm1em1Kazk

(Mus musculus)
Allele/Variant
Source: MGI:7716593
Genes: Aifm1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Aifm1 (Mmu)
Genes: Aifm1 (Mmu)
Symbol: Aifm1em1Kazk

Gt(ROSA)26Sortm8(Aifm1)Jhai

(Mus musculus)
Allele/Variant
Source: MGI:5470252
Genes: Gt(ROSA)26Sor (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Gt(ROSA)26SorAifm1)Jhai>
Construct Expressed Component: Aifm1 (Mmu)

Gt(ROSA)26Sortm9(Aifm1*)Jhai

(Mus musculus)
Allele/Variant
Source: MGI:5470253
Genes: Gt(ROSA)26Sor (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Gt(ROSA)26SorAifm1*)Jhai>
Construct Expressed Component: Aifm1 (Mmu)

sa40408

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-6628
Genes: aifm1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: aifm1 (Dre)

sa33579

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-2488
Genes: aifm1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: aifm1 (Dre)

sa1710

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-10273
Genes: aifm1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: aifm1 (Dre)

(mRatBN7.2)X:127686317G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323565468
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127686317G>A

(mRatBN7.2)X:127653398T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051356.1:g.127653398T>C
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127653398T>C

(mRatBN7.2)X:127678468A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323720118
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127678468A>G

(mRatBN7.2)X:127670259T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323750549
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127670259T>C

(mRatBN7.2)X:127688552A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323689235
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127688552A>G

(mRatBN7.2)X:127665967C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051356.1:g.127665967C>T
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127665967C>T

(mRatBN7.2)X:127663671A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051356.1:g.127663671A>G
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127663671A>G

(mRatBN7.2)X:127664251C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323692801
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127664251C>T

(mRatBN7.2)X:127677204G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323726979
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127677204G>T

(mRatBN7.2)X:127680280T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323270494
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127680280T>C

(mRatBN7.2)X:127657073G>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051356.1:g.127657073G>T
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127657073G>T

(mRatBN7.2)X:127665956T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051356.1:g.127665956T>C
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127665956T>C

(mRatBN7.2)X:127656092G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051356.1:g.127656092G>A
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127656092G>A

(mRatBN7.2)X:127672077A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323565471
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127672077A>G

(mRatBN7.2)X:127673440G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323692932
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127673440G>A

(mRatBN7.2)X:127683782G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323741930
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127683782G>T

(mRatBN7.2)X:127665022G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051356.1:g.127665022G>A
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127665022G>A

(mRatBN7.2)X:127670149T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323720133
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127670149T>C

(mRatBN7.2)X:127674468G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323621067
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127674468G>A

(mRatBN7.2)X:127654622A>C

(Rattus norvegicus)
Allele/Variant
Source: rs8171724
Genes: Aifm1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:127654622A>C

(GRCh38)X:130133383C>T

(Homo sapiens)
Allele/Variant
Source: NC_000023.11:g.130133383C>T
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, splice_donor_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133383C>T

(GRCh38)X:130136652G>A

(Homo sapiens)
Allele/Variant
Source: rs2030352383
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136652G>A

(GRCh38)X:130136687C>T

(Homo sapiens)
Allele/Variant
Source: rs1057521792
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136687C>T

(GRCh38)X:130129579A>T

(Homo sapiens)
Allele/Variant
Source: rs863223899
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130129579A>T

(GRCh38)X:130145463C>T

(Homo sapiens)
Allele/Variant
Source: rs748492632
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130145463C>T

(GRCh38)X:130136638C>T

(Homo sapiens)
Allele/Variant
Source: NC_000023.11:g.130136638C>T
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130136638C>T

(GRCh38)X:130129508G>A

(Homo sapiens)
Allele/Variant
Source: rs1057515766
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130129508G>A

(GRCh38)X:130147231A>C

(Homo sapiens)
Allele/Variant
Source: rs139842860
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130147231A>C

(GRCh38)X:130147479A>G

(Homo sapiens)
Allele/Variant
Source: rs368859964
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130147479A>G

(GRCh38)X:130149545A>G

(Homo sapiens)
Allele/Variant
Source: rs1139851
Genes: RAB33A (Hsa), AIFM1 (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)X:130149545A>G

(GRCh38)X:130130000G>A

(Homo sapiens)
Allele/Variant
Source: rs1455517770
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130000G>A

(GRCh38)X:130130045G>A

(Homo sapiens)
Allele/Variant
Source: NC_000023.11:g.130130045G>A
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130045G>A

(GRCh38)X:130133352G>C

(Homo sapiens)
Allele/Variant
Source: NC_000023.11:g.130133352G>C
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133352G>C

(GRCh38)X:130130138T>C

(Homo sapiens)
Allele/Variant
Source: rs2030004639
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130130138T>C

(GRCh38)X:130133412C>T

(Homo sapiens)
Allele/Variant
Source: rs1424829478
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133412C>T

(GRCh38)X:130133164G>A

(Homo sapiens)
Allele/Variant
Source: rs145415514
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133164G>A

(GRCh38)X:130133297G>C

(Homo sapiens)
Allele/Variant
Source: rs2030179917
Genes: RAB33A (Hsa), AIFM1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:130133297G>C