Version: 8.0.0
Date: Tue Jan 28 2025
133 results for btg1
Allele/Variant

Btg1em1(IMPC)Mbp

(Mus musculus)
Allele/Variant
Source: MGI:6148075
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btg1 (Mmu)
Genes: Btg1 (Mmu)
Symbol: Btg1em1(IMPC)Mbp

Btg1em4Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7296041
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btg1 (Mmu)
Genes: Btg1 (Mmu)
Symbol: Btg1em4Gpt

Btg1em1Flv

(Mus musculus)
Allele/Variant
Source: MGI:6404518
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btg1 (Mmu)
Genes: Btg1 (Mmu)
Symbol: Btg1em1Flv

Btg1tm1Ftir

(Mus musculus)
Allele/Variant
Source: MGI:5825483
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btg1 (Mmu)
Genes: Btg1 (Mmu)
Symbol: Btg1tm1Ftir

Btg1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7296040
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btg1 (Mmu)
Genes: Btg1 (Mmu)
Symbol: Btg1em1Gpt

Btg1bem5Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7296042
Genes: Btg1b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btg1b (Mmu)
Genes: Btg1b (Mmu)
Symbol: Btg1bem5Gpt

Tg(Btg1-EGFP)HW278Gsat

(Mus musculus)
Allele/Variant
Source: MGI:4846889
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tg(Btg1-EGFP)HW278Gsat

Gt(ROSA)26Sorem1(Btg1)Meln

(Mus musculus)
Allele/Variant
Source: MGI:7430731
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)26SorBtg1)Meln>

Gt(ROSA)26Sortm1(Btg1*)Meln

(Mus musculus)
Allele/Variant
Source: MGI:7430724
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)26SorBtg1*)Meln>

(GRCh38)8:17245134C>A

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.17245134C>A
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17245134C>A
Gene Synonyms: BTG1 binding factor 1

(GRCh38)8:17243133T>C

(Homo sapiens)
Allele/Variant
Source: rs1810418480
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17243133T>C
Gene Synonyms: BTG1 binding factor 1

(GRCh38)8:17234811G>A

(Homo sapiens)
Allele/Variant
Source: rs771925219
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17234811G>A
Gene Synonyms: BTG1 binding factor 1

(GRCh38)8:17230748T>C

(Homo sapiens)
Allele/Variant
Source: rs1808502366
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17230748T>C
Gene Synonyms: BTG1 binding factor 1

(GRCh38)8:17245139G>A

(Homo sapiens)
Allele/Variant
Source: rs766330962
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17245139G>A
Gene Synonyms: BTG1 binding factor 1

(GRCh38)8:17246679G>A

(Homo sapiens)
Allele/Variant
Source: rs117960717
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17246679G>A
Gene Synonyms: BTG1 binding factor 1

(GRCh38)8:17246633C>G

(Homo sapiens)
Allele/Variant
Source: rs113175413
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17246633C>G
Gene Synonyms: BTG1 binding factor 1

sa12374

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-2114
Genes: btg1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: btg1 (Dre)

(GRCh38)12:92145428C>T

(Homo sapiens)
Allele/Variant
Source: rs533912735
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92145428C>T

(GRCh38)12:92144118G>A

(Homo sapiens)
Allele/Variant
Source: rs1246644859
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92144118G>A

(GRCh38)12:92145484C>A

(Homo sapiens)
Allele/Variant
Source: rs1263908473
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92145484C>A

(GRCh38)12:92145520T>G

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.92145520T>G
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92145520T>G

(GRCh38)12:92144126C>T

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.92144126C>T
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92144126C>T

(GRCh38)12:92144199T>C

(Homo sapiens)
Allele/Variant
Source: rs375522490
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92144199T>C

(GRCh38)12:92145500T>C

(Homo sapiens)
Allele/Variant
Source: rs2136950034
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92145500T>C

(mRatBN7.2)7:31341738C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105552662
Genes: Btg1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:31341738C>T

(GRCm39)10:96453618C>G

(Mus musculus)
Allele/Variant
Source: rs230014368
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96453618C>G

(GRCm39)10:96456725T>C

(Mus musculus)
Allele/Variant
Source: rs234667175
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96456725T>C

(GRCm39)10:96457065A>T

(Mus musculus)
Allele/Variant
Source: rs221753393
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96457065A>T

(GRCm39)10:96457936G>A

(Mus musculus)
Allele/Variant
Source: rs246518792
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96457936G>A

(GRCm39)10:96453571T>G

(Mus musculus)
Allele/Variant
Source: rs245045563
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96453571T>G

(GRCm39)10:96453575C>T

(Mus musculus)
Allele/Variant
Source: rs216438113
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96453575C>T

(GRCm39)10:96458483G>A

(Mus musculus)
Allele/Variant
Source: rs247650763
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96458483G>A

(GRCm39)10:96456388C>T

(Mus musculus)
Allele/Variant
Source: rs265644514
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96456388C>T

(GRCm39)10:96452905C>T

(Mus musculus)
Allele/Variant
Source: rs244483011
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96452905C>T

(mRatBN7.2)7:31342499C>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.31342499C>G
Genes: Btg1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:31342499C>G

(mRatBN7.2)7:31342157C>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.31342157C>G
Genes: Btg1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:31342157C>G

(GRCm39)10:96455758C>G

(Mus musculus)
Allele/Variant
Source: rs253741213
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96455758C>G

(GRCm39)10:96457998G>A

(Mus musculus)
Allele/Variant
Source: rs586716815
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96457998G>A

(GRCm39)10:96456062T>C

(Mus musculus)
Allele/Variant
Source: rs247140722
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96456062T>C

(GRCm39)10:96458448G>A

(Mus musculus)
Allele/Variant
Source: rs213019275
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96458448G>A

(GRCm39)10:96457449A>C

(Mus musculus)
Allele/Variant
Source: rs261215583
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96457449A>C

(GRCm39)10:96457917C>T

(Mus musculus)
Allele/Variant
Source: rs222243437
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96457917C>T

(GRCm39)10:96453724A>G

(Mus musculus)
Allele/Variant
Source: rs251400389
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96453724A>G

(GRCm39)10:96456832T>C

(Mus musculus)
Allele/Variant
Source: rs46644661
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96456832T>C

(mRatBN7.2)7:31343632T>G

(Rattus norvegicus)
Allele/Variant
Source: rs8144886
Genes: Btg1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:31343632T>G

(mRatBN7.2)7:31342182T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320851796
Genes: Btg1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:31342182T>C

(GRCm39)10:96456879A>T

(Mus musculus)
Allele/Variant
Source: rs47932443
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96456879A>T

(GRCm39)10:96458453A>G

(Mus musculus)
Allele/Variant
Source: rs228651047
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96458453A>G

(GRCm39)10:96457482C>G

(Mus musculus)
Allele/Variant
Source: rs1133542179
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96457482C>G

(GRCm39)10:96457906C>T

(Mus musculus)
Allele/Variant
Source: rs262228211
Genes: Btg1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:96457906C>T