Version: 8.0.0
Date: Tue Jan 28 2025
1,961 results for btbd7

BTBD7

(Homo sapiens)
Gene
Name: BTB domain containing 7
Synonyms: FUP1, BTB (POZ) domain containing 7, MGC48310, BTB/POZ domain-containing protein 7, DKFZp686N0544
Source: HGNC:18269
Biotype: protein coding gene
Symbol: BTBD7 (Hsa)
Symbol: BTBD7
Strict Orthology Symbols: btbd7

Btbd7

(Mus musculus)
Gene
Name: BTB domain containing 7
Synonyms: FUP1, 5730507E09Rik, RIKEN cDNA 5730507E09 gene, RIKEN cDNA E130118E17 gene, E130118E17Rik, mKIAA1525
Source: MGI:1917858
Biotype: protein coding gene
Symbol: Btbd7 (Mmu)
Symbol: Btbd7
Automated Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7).
Strict Orthology Symbols: btbd7
Alleles: Btbd7 (Mmu)...Btbd7 (Mmu)...Btbd7 (Mmu)

Btbd7

(Rattus norvegicus)
Gene
Name: BTB domain containing 7
Synonyms: BTB (POZ) domain containing 7, LOC362772, BTB/POZ domain-containing protein 7
Source: RGD:1306262
Biotype: protein coding gene
Symbol: Btbd7 (Rno)
Symbol: Btbd7
Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine
Automated Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7).
Strict Orthology Symbols: btbd7

btbd7

(Danio rerio)
Gene
Name: BTB (POZ) domain containing 7
Synonyms: wu:fd08g07, si:dkeyp-55f12.1
Source: ZFIN:ZDB-GENE-030131-4477
Biotype: protein coding gene
Symbol: btbd7 (Dre)
Symbol: btbd7
Automated Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7).
Strict Orthology Symbols: btbd7

btbd7

(Xenopus tropicalis)
Gene
Name: BTB (POZ) domain containing 7
Synonyms: BTB (POZ) domain containing 7, btbd7
Source: Xenbase:XB-GENE-6042423
Biotype: gene
Symbol: btbd7
Symbol: btbd7 (Xtr)
Automated Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7).
Synonyms: btbd7...btbd7...btbd7
Strict Orthology Symbols: btbd7

btbd7.L

(Xenopus laevis)
Gene
Name: BTB (POZ) domain containing 7
Synonyms: BTB (POZ) domain containing 7, btbd7.L
Source: Xenbase:XB-GENE-6486505
Biotype: gene
Symbol: btbd7.L (Xla)
Automated Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7).
Strict Orthology Symbols: btbd7
Symbol: btbd7.L

btbd7.S

(Xenopus laevis)
Gene
Name: BTB (POZ) domain containing 7
Synonyms: btbd7.S, BTB (POZ) domain containing 7
Source: Xenbase:XB-GENE-17345882
Biotype: gene
Symbol: btbd7.S (Xla)
Automated Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7).
Strict Orthology Symbols: btbd7
Symbol: btbd7.S

Btbd7tm1.1Kmy

(Mus musculus)
Allele/Variant
Source: MGI:6259681
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btbd7 (Mmu)
Genes: Btbd7 (Mmu)
Symbol: Btbd7tm1.1Kmy

Btbd7tm1Kmy

(Mus musculus)
Allele/Variant
Source: MGI:5908734
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btbd7 (Mmu)
Genes: Btbd7 (Mmu)
Symbol: Btbd7tm1Kmy

Btbd7em1(IMPC)Ccpcz

(Mus musculus)
Allele/Variant
Source: MGI:6385277
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Btbd7 (Mmu)
Genes: Btbd7 (Mmu)
Symbol: Btbd7em1(IMPC)Ccpcz

BTBD7P2

(Homo sapiens)
Gene
Name: BTB domain containing 7 pseudogene 2
Synonyms: Not Available
Source: HGNC:44876
Biotype: pseudogene
Symbol: BTBD7P2 (Hsa)
Symbol: BTBD7P2

BTBD7P1

(Homo sapiens)
Gene
Name: BTB domain containing 7 pseudogene 1
Synonyms: Not Available
Source: HGNC:44875
Biotype: pseudogene
Symbol: BTBD7P1 (Hsa)
Symbol: BTBD7P1

Btbd7tm1.1Kmy/Btbd7tm1.1Kmy [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J

(Mus musculus)
Model
Id: MGI:6260160
Synonyms: Not Available
Symbol: Btbd7/Btbd7 [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J (Mmu)
Genes: Btbd7 (Mmu)
Alleles: Btbd7 (Mmu)
Name: Btbd7/Btbd7 [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J

Btbd7tm1.1Kmy/Btbd7+ [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J

(Mus musculus)
Model
Id: MGI:6260161
Synonyms: Not Available
Symbol: Btbd7/Btbd7<+> [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J (Mmu)
Genes: Btbd7 (Mmu)
Alleles: Btbd7 (Mmu)
Name: Btbd7/Btbd7<+> [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J

Btbd7em1(IMPC)Ccpcz/Btbd7em1(IMPC)Ccpcz [background:] C57BL/6NCrl-Btbd7em1(IMPC)Ccpcz/Ccpcz

(Mus musculus)
Model
Id: MGI:7414801
Synonyms: Not Available
Symbol: Btbd7/Btbd7 [background:] C57BL/6NCrl-Btbd7/Ccpcz (Mmu
Genes: Btbd7 (Mmu)
Alleles: Btbd7 (Mmu)
Name: Btbd7/Btbd7 [background:] C57BL/6NCrl-Btbd7/Ccpcz

C39F7.5

(Caenorhabditis elegans)
Gene
Name: BACK domain-containing protein
Synonyms: CELE_C39F7.5
Source: WB:WBGene00016540
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human BTBD7 (BTB domain containing 7).
Automated Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7).
Strict Orthology Symbols: btbd7

CG16952

(Drosophila melanogaster)
Gene
Name: Not Available
Synonyms: Not Available
Source: FB:FBgn0030701
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human BTBD7 (BTB domain containing 7).
Strict Orthology Symbols: btbd7

regulation of branching involved in salivary gland morphogenesis

Gene Ontology
Source: GO:0060693
Synonyms: Not Available
Branch: biological process
Genes: Btbd7 (Mmu)...Btbd7 (Rno)...BTBD7 (Hsa)

morphogenesis of a branching epithelium

Gene Ontology
Source: GO:0061138
Synonyms: Not Available
Branch: biological process
Genes: Btbd7 (Rno)...Btbd7 (Mmu)...BTBD7 (Hsa)...btbd7 (Dre)

sa39282

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-16625
Genes: btbd7 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: btbd7 (Dre)

sa23720

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-17289
Genes: btbd7 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: btbd7 (Dre)

sa39283

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-16626
Genes: btbd7 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: btbd7 (Dre)

sa37046

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-5077
Genes: btbd7 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: btbd7 (Dre)

sa37045

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-5076
Genes: btbd7 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: btbd7 (Dre)

nucleus

Gene Ontology
Source: GO:0005634
Synonyms:
  • cell nucleus
  • horsetail nucleus
Branch: cellular component
Genes: BTBD7 (Hsa)...Btbd7 (Mmu)...Btbd7 (Rno)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: Btbd7 (Mmu)

(GRCh38)14:93295983T>G

(Homo sapiens)
Allele/Variant
Source: rs1180609332
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93295983T>G

(GRCh38)14:93242625T>C

(Homo sapiens)
Allele/Variant
Source: NC_000014.9:g.93242625T>C
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242625T>C

(GRCh38)14:93246086G>T

(Homo sapiens)
Allele/Variant
Source: NC_000014.9:g.93246086G>T
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93246086G>T

(GRCh38)14:93296017C>T

(Homo sapiens)
Allele/Variant
Source: rs756126969
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93296017C>T

(GRCh38)14:93242934G>A

(Homo sapiens)
Allele/Variant
Source: rs569825061
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242934G>A

(GRCh38)14:93246222T>A

(Homo sapiens)
Allele/Variant
Source: rs1260554040
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93246222T>A

(GRCh38)14:93242596G>A

(Homo sapiens)
Allele/Variant
Source: rs201912928
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242596G>A

(GRCh38)14:93248540T>C

(Homo sapiens)
Allele/Variant
Source: rs201243121
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93248540T>C

(GRCh38)14:93294920G>C

(Homo sapiens)
Allele/Variant
Source: NC_000014.9:g.93294920G>C
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93294920G>C

(GRCh38)14:93246016T>C

(Homo sapiens)
Allele/Variant
Source: rs372008556
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93246016T>C

(GRCh38)14:93242774G>A

(Homo sapiens)
Allele/Variant
Source: rs139558603
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242774G>A

(GRCh38)14:93242487G>C

(Homo sapiens)
Allele/Variant
Source: rs747016085
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242487G>C

(GRCh38)14:93242828G>T

(Homo sapiens)
Allele/Variant
Source: rs760882700
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242828G>T

(GRCh38)14:93248604G>A

(Homo sapiens)
Allele/Variant
Source: rs370542488
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93248604G>A

(GRCh38)14:93248648C>T

(Homo sapiens)
Allele/Variant
Source: rs150103724
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93248648C>T

(GRCh38)14:93294910T>C

(Homo sapiens)
Allele/Variant
Source: rs200455654
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93294910T>C

(GRCh38)14:93257298C>T

(Homo sapiens)
Allele/Variant
Source: rs377109750
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93257298C>T

(GRCh38)14:93294389C>T

(Homo sapiens)
Allele/Variant
Source: rs746181747
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93294389C>T

(GRCh38)14:93242901C>T

(Homo sapiens)
Allele/Variant
Source: rs745694971
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242901C>T

(GRCh38)14:93243010G>A

(Homo sapiens)
Allele/Variant
Source: rs2052253571
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93243010G>A

(GRCh38)14:93242725C>G

(Homo sapiens)
Allele/Variant
Source: rs147201730
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242725C>G

(GRCh38)14:93242812T>C

(Homo sapiens)
Allele/Variant
Source: rs1461316661
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242812T>C

(GRCh38)14:93242965C>G

(Homo sapiens)
Allele/Variant
Source: rs766575838
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93242965C>G

(GRCh38)14:93248597G>A

(Homo sapiens)
Allele/Variant
Source: rs200351621
Genes: BTBD7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:93248597G>A