Busch Lab

ZMP

ZBTB40

Ensembl ID:
ENSDARG00000091762
Description:
zinc finger and BTB domain containing 40 [Source:HGNC Symbol;Acc:29045]
Human Orthologue:
ZBTB40
Human Description:
zinc finger and BTB domain containing 40 [Source:HGNC Symbol;Acc:29045]
Mouse Orthologue:
Zbtb40
Mouse Description:
zinc finger and BTB domain containing 40 Gene [Source:MGI Symbol;Acc:MGI:2682254]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa38857 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa21957 Nonsense Available for shipment Available now
sa6217 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35138 Nonsense Mutation detected in F1 DNA Not yet available
sa38856 Nonsense Mutation detected in F1 DNA Not yet available
sa14144 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa38857
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128889 Essential Splice Site 186 1090 2 21
Genomic Location (Zv9):
Chromosome 11 (position 37286744)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36183972
GRCz11 11 36445955
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCAGTTTCTTGAGGCCTGGGATGCAGTTTCCACAGAAGAGCGACAGG[T/A]ACAATTTTAGTAGGAGAGATGAATAATCAAGAATAATTAAGACTTCATGA
Long Flanking Sequence:
TCTGTTATTCAAGTCTGTTCTGGAAAGTTCTGACAGCATCTCTATCGACACAGACCTGCTGTCCTCTCAGGAGTTTTCCTCTCTTCTGGATCTGGTGTACACCGGGAAACTGCCACCAGGAAAACACAACTTAACCCGCCTCATAGCCGCCGCAGACAGTCTGCAGATGTTTGATGTGGCTGTCGGCTGTAAAAACATCCTGACTGACCTCATGAAACAGACTGAGCCCATAGACCCACAGGTTATAAAGCCTGACAGTGTTGTGGAGCAGGTTAAAAGAGAAGAGAGGAATCTGCAAGGTAAAAGATTGAGATTTTCAGTTTGAGGTTGCTTTGTTTGAGGTGTTTTTTGTGAATTGTGTTTACGTCTGTGTTCAGAGGACAATGCAGTCGAGATGATTTCTCATGATCGAGCTGGTCTCATGAAGATCCTACAGAGAGGAAAGTCTCATGTTCAGTTTCTTGAGGCCTGGGATGCAGTTTCCACAGAAGAGCGACAGG[T/A]ACAATTTTAGTAGGAGAGATGAATAATCAAGAATAATTAAGACTTCATGAATGAAACCAACTAAGAATTGCATCTATTTGATCAAAATACTACAGATTATCCCAGTTTTTATTGAATCAATATATGTGACTTTGGACCACAAAAAAAGTCAAATTTGTTTGACCACAAAAAAGTCAAAAAGTCAAAAATTTTTTGCTATTTTTTCACATCATGTATAAGCTGTATAAATAATATTTTTAATAGGATAATGTTAGTCTCATTTGCAGCTCTCTAAATGAAGTGCTCAGCAATACTAATCAAAAATTATTTGCTGTAGGAAATTTACTAAATATCTTCATGGGACATGATCTTTCCTTAATATTCTGATGATTTTTGGAAAAATGGAAAAATTTATCATTTGGAACATTAGACTTTAGATATTTAAGATATTTAAAAATGTATTATATCATGGCAAAATTTATTTTGTGCATCAATATTTGTCTTTATTATTGTATAATCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21957
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128889 Nonsense 345 1090 9 21
Genomic Location (Zv9):
Chromosome 11 (position 37281218)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36178446
GRCz11 11 36440429
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTTTCTGTCAGGTGTAACGACAAAAGAGAGCAATGCAGTTGATTTGT[T/A]GGGAATGTATCAGAGCAGACTTGTTGAGCTGAATCTGGACCTCCAGCTCA
Long Flanking Sequence:
AGCAGGCTTCTATAAATATAAAGGTTATACATGTGGCTACATTTCTTGTAAGCTTAATAGTGCAGCTAAACAAATATTTACTAGTACACACTTATGCCACAACCAAGCTAAGCTATAAATGAGCACAGCTGGTGCACACTTGGCCTCAGTTCTCATGTGTACTTCCGAGACATATTACTTGTGAAGAAAAGTAATGAATGGTAGTGAGTGTGTTTGTTTTTTCTTAAGGCGCTTCTGCAGTGCTGTTCTGCTCCGTCATCTGCAGAGGTGCTGGAAAACTTGTTATGCAAACTCCGAGAGATGTCCATAAGTGAAGAAACGTTTCTGATTCTGCTGAATGAAGTGAAGGAAAAATCAACCGATCTGCTTCAACTCCTTGAAACTCTTAAAAACACCAGAGGTACGAACAGCAAAACACATTTCGTTATAGCGCATGTATATTTCTAACTGCTCCTTTCTGTCAGGTGTAACGACAAAAGAGAGCAATGCAGTTGATTTGT[T/A]GGGAATGTATCAGAGCAGACTTGTTGAGCTGAATCTGGACCTCCAGCTCATCAAACAAAGCCTTCAAATGGGTCCAGAGATGCCTGAAAATGACAGACAGGTACATGTGCTGCGTTGTTAGATACTTTTTTTTTAGCAAATCCCTAAGATACTTGAACTCCTCTGGTGTAAGGACTTTCGTGTAGAATTTAATGTCAGTGAATAGGGTTCAGATTTGCTAATAGTAATTACCATATTTACCCAGTTGATTGATGACATTAAAATTCATCCAAAAGTGAAAACTACTCCATAATAACAATAATAATTTCTGATTTGCATGTTTAAACATATTACTATAAAAAAAACTTGTAATACAAAATATTGTTTGGAATTCTTAAAGGGATATTTCACCCAAAAAAGGAAAATGAGCATTTACCCAGTGTTTCCCAACACTGTTCCTGAAGGCACATCACCAACAGTACATATTTTGGATGTCTGCCTTATCTGACCCATTCATTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6217
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128889 Essential Splice Site 378 1090 9 21
Genomic Location (Zv9):
Chromosome 11 (position 37281116)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36178344
GRCz11 11 36440327
KASP Assay ID:
554-4453.1 (used for ordering genotyping assays)
KASP Sequence:
CAAACAAAGCCTTCAAATGGGTCCAGAGATGCCTGAAAATGACAGACAGG[T/C]ACATGTGCTGCGTTGTTAGATACTTTTTTTTTANGCAAATCCCTAAGATAC
Long Flanking Sequence:
CCAAGCTAAGCTATAAATGAGCACAGCTGGTGCACACTTGGCCTCAGTTCTCATGTGTACTTCCGAGACATATTACTTGTGAAGAAAAGTAATGAATGGTAGTGAGTGTGTTTGTTTTTTCTTAAGGCGCTTCTGCAGTGCTGTTCTGCTCCGTCATCTGCAGAGGTGCTGGAAAACTTGTTATGCAAACTCCGAGAGATGTCCATAAGTGAAGAAACGTTTCTGATTCTGCTGAATGAAGTGAAGGAAAAATCAACCGATCTGCTTCAACTCCTTGAAACTCTTAAAAACACCAGAGGTACGAACAGCAAAACACATTTCGTTATAGCGCATGTATATTTCTAACTGCTCCTTTCTGTCAGGTGTAACGACAAAAGAGAGCAATGCAGTTGATTTGTTGGGAATGTATCAGAGCAGACTTGTTGAGCTGAATCTGGACCTCCAGCTCATCAAACAAAGCCTTCAAATGGGTCCAGAGATGCCTGAAAATGACAGACAGG[T/C]ACATGTGCTGCGTTGTTAGATACTTTTTTTTTAGCAAATCCCTAAGATACTTGAACTCCTCTGGTGTAAGGACTTTCGTGTAGAATTTAATGTCAGTGAATAGGGTTCAGATTTGCTAATAGTAATTACCATATTTACCCAGTTGATTGATGACATTAAAATTCATCCAAAAGTGAAAACTACTCCATAATAACAATAATAATTTCTGATTTGCATGTTTAAACATATTACTATAAAAAAAACTTGTAATACAAAATATTGTTTGGAATTCTTAAAGGGATATTTCACCCAAAAAAGGAAAATGAGCATTTACCCAGTGTTTCCCAACACTGTTCCTGAAGGCACATCACCAACAGTACATATTTTGGATGTCTGCCTTATCTGACCCATTCATTTCAGGTTTTGGAGTCTCTTCTAATGTTCTGATGAGTTGATTGAGTTGTGTTTGATTAGGTACAGGGGTGTCAAACTCAATTCCTGGAGGGCCGAAGCCCTGCACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35138
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128889 Nonsense 482 1090 12 21
Genomic Location (Zv9):
Chromosome 11 (position 37278152)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36175380
GRCz11 11 36437363
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCAGTGATTTTACAGTGCTTGAACAGGGTTTGAATGCAATGGATCAT[G/T]AGACAGAGAAAGTTACTGAGGTAAGAAATAAATATTGATTATTTTCTCAT
Long Flanking Sequence:
GTGTGTGGCATCTTCTACACTGAAAGAAATCTGTTTAAAAGTCGTGTTTGTGCCTGCAGTGTCTTGACTGCATTTGTATGTATTCAGTGTATTGAAGGTCTGCTGGTAGAGAAAGCAGATGCTGAGGTGTTTGAGAGGCTGATTTTAGCAGCGCTGGATGGTTCACTGCAGGCCGTCACTGCGTGGAGGATTCTCTTCTGGACAGAAACACACAATCCAGAGCTGCAGATCCTCATGCAGGAGCTCAAGGAGAAGCCAGAAGCTCAGAAACTACTCCAAACCAGTGAGAGTCAAAGAGCTTCTTAGTCACTGAGCGTCCTAAGAAAATATGGGTATTTATTAAGTACACTGTTTGTGCCTAAATCTTACACCATCATGTTTTTTTTTTCTCTTTTTTTGTAGTTAAGGACATAGATGTGCTGTTCAAGCACAAATCACTCATTCTGGAAACCATCAGTGATTTTACAGTGCTTGAACAGGGTTTGAATGCAATGGATCAT[G/T]AGACAGAGAAAGTTACTGAGGTAAGAAATAAATATTGATTATTTTCTCATTATAATTAATGAGAAAAATATACTAAAAGTGTGCAGTCTGTCCCAATCTGTATGCTTCTATTTGCAAATTGTCCAACCCAGGCTCATTCTGAAAACATACCTCTATATACATTTCTGGAGTGCGCCAAATACATCCCAGGTGCTACGTTTTTTGCAGTTTTTGTTTTCGCAGATCCACCAGAGGCCACTGTGTCTGCTTTTTGAGATCTGAAATTCTCTCACATGTGCCATTTATGCCGGCTGTTCTTGCTTAAATCCACCTTAGGCCACTGTCCACTGACTGACTGACCCCCCCTCCTCTTTCTCAAACCCAATCAATAGTATTTTCAAAAGCACTAATTGACCCACTCAGCCACTACTCTAAACCCAACTGACAATGTTAAAAAGCAATCCAGAAAAAGAAAAGCCCTTGCTTGATTTTAACCACATTTTCAGATTTTACCACATTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38856
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128889 Nonsense 764 1090 16 21
Genomic Location (Zv9):
Chromosome 11 (position 37270887)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36168115
GRCz11 11 36430098
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCGTTCGCACAGTCTATTGAACTGACACGTCACGTCCGCACACACACC[G/T]GAGACAAACCCTACGTCTGCAGAGAGTGTGGGAAAGGCTTCAAACAAGCC
Long Flanking Sequence:
ATGTCAAGAATCTGCAAACTTCTGTCCAAAAATTCTATTTAAAAAAAGCAAAAATCTGAGTTAATGTTGGTATTTGGATATGTTTTCAGTCCTGTTTAATGCTTTCAGTGTTTGTATCTTTCAGGTCTTCTATATCACAAGCGCACTGAGCACTTTGAGGAGCGCCCGTACGCCTGTGAGGAGTGTGGAGCTAAATTCGCTGCCACCTCGTCTCTAAAGAACCACATGCGTCTTCACACCGGAGAAAAGCCTTTCCACTGCAAACACTGCGACATGAGCTTCTCTGTGGCCGCCGCTCTGTCCTACCACACAAAGAAGAAGCATGCAGAGGGTACCATGCTTGCACTGCTGTTTTAAAATTTCAGGCTTTTAAGTGGAAATAAATATAATGGCAACGTGTCTGAAATTGTATGTTTGCAGGTAAAATGTACTGCTGTCAGTACTGCTCGGCCTCGTTCGCACAGTCTATTGAACTGACACGTCACGTCCGCACACACACC[G/T]GAGACAAACCCTACGTCTGCAGAGAGTGTGGGAAAGGCTTCAAACAAGCCAATGGATTATCTGTGCATCTGCAGAACTTTCACAGTAAGCAAATACACACATTTAACTCTGCATTGAGATTGGCGCAGTGGGTAGCGATGTCGCCTCACAGCAAGAAGGTTGCTGGTTCAAACCTCGACTGGGTCAGTTGACATTTCTTTGTGGAGATTCCATGGGTTTCCTTTGAGTGCTCCGGTTTCCCCCACAAGTCTAAAGACATACAGGTGCATTGTGTAAGATAAATTGTCTGTGTATGTATGTAAGGAGAGTGTATGGGTGTTTCCCGGTGATGGGTTGCAGCTGGAAGGGTATCTGCTGCGTAAAACATATGCTGGATAAGTTGGCGGTTCAGTCCGCTGTGGCGAATCCTGATTAATAAATGGACTAAGCTGAAAAGAAAATGAACGAATGAATAAACACCAATGCAGAAAATCGAATAGTAGCCATAATGTGATTTAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14144
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128889 Nonsense 953 1090 20 21
Genomic Location (Zv9):
Chromosome 11 (position 37266053)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36163281
GRCz11 11 36425264
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACYCTTTGTGTGTGTGTGTGTGTGTGTGTGKGTTCAGATGTGCAYGTGTG[G/A]AAGTGTGTGAGCTGTGACTGTTCTCTGTCCAGTGAGCAGGAGCTCCAGYA
Long Flanking Sequence:
TCGGCTCAGTTGGCCTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCCTTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGTGGTACAGGTGAATTAGGTAGGCTAAATTGTCCGTAGTGTGTGTGTAAATGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAAGGCATCCGCTGGGTAAAAACTTGCTGGATAAGTTGGTGGTTCATTCTGCTGTGGCGACCCCGGATTAATAAAGGAACTAAGCCAGCAAGAAAATGAATGAATGAATGATATTAGCAACCCCACCCTCCTTTTTTAAATTTTCATAGGAGAAACTGGTCAAAATGTTGCTGGTAAGTGCTGAGCTGCCAGTAATAATTTGAATAATTTAATGTCCACAAGCAGAGTTTATTAATTGCTAACATCACTAGTACTAGTACTGACCCTTTGTGTGTGTGTGTGTGTGTGTGTGGGTTCAGATGTGCACGTGTG[G/A]AAGTGTGTGAGCTGTGACTGTTCTCTGTCCAGTGAGCAGGAGCTCCAGCATCATGTTTGCAGTGTTCAGACTCCCGCGCTGTTCAGCTGTATGGTCTGTTCACTTCACTTCCCCTCTGAGCCTGACTTCCAGCAGCACTTCCTGTCCAAACACCTCCAGCTCGTGCAGGATGAAGCGCAGACACAGAGCTCCGCTTCACAGACGGTGAACACACACTCAACATCACACACAACTAAACATCTCCACAGGGCGGAAAATGGCCTTTTATTTCATGCCTGATTTGGTTTGGTGCTCAAGATATACAGTTGAAGGCACAATTATTAACTTAAAAAATATTTTAATATATAATTAAGTTTGGTGGCGCGGTGGCTCGGTGGTTAGCATTGTCGCCTCAAAGCAAGAAGGTCACTGGTTCGAATCCTGGCTGAGCCAGTTGGCATTTCCGTGTGGAGTTTGCATTTTCTCCCCGTTTTGGCGTGGGTTTCCTCCGGGTGCTCCAG
Associated Phenotype:
Not determined