ZMP
LOC557467
Ensembl ID:
Human Orthologue:
KBTBD11
Human Description:
kelch repeat and BTB (POZ) domain containing 11 [Source:HGNC Symbol;Acc:29104]
Mouse Orthologue:
Kbtbd11
Mouse Description:
kelch repeat and BTB (POZ) domain containing 11 Gene [Source:MGI Symbol;Acc:MGI:1922151]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15491 | Nonsense | Available for shipment | Available now |
sa8879 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12661 | Nonsense | Available for shipment | Available now |
sa12654 | Nonsense | Available for shipment | Available now |
sa2926 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa15491
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082352 | Nonsense | 33 | 468 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 27193396)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25271831 |
GRCz11 | 17 | 25290232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AYAAATCAGTATTAGCTGARAAGAGCGATTAYTTTAAGGCCAGGCTTTCT[C/T]GAGACATCCTCAMAGTAAAAGGAATGAGCTACAAGACCTTATCAGTGCTT
Long Flanking Sequence:
TTCAGACTCTGGACATCAGTTTAAGAAATACGGGTGAAGCTTCAAGTCAAAAGAACATTAGAGAAGACACAAACGGAACAAAGGTTGCTTGCAGTTTAGCACCCTCTCTATGCTTCAGGCCAGAAAACAAGGAGGAAACTGACAAACTGTCCAATGTCCTGAGAGACAGTGAGATTGTTCGGAGTCAGTTTGACATTAAAAATGTCTCTTCCACATCAGAGAACAGAAATCATTCCTACTCAGGTACCCAGGAAACGAGGTCACTTGAGAGAACCTTAGGAAGCTTTATAAATTCCTCTGAAGGAGCCAGTCAGACCAGCTACAGAACGTCATTTGGACAGACCGGGATGGAAGGGCTGAAGCAAAGTGGATCTGCAGTAAGAGAAGCTCTCTCTGCAAAAGAGGAGCCAAATTTAGTCATAGAGGTGGGCGGACAGAAAATACAAGCACACAAATCAGTATTAGCTGAAAAGAGCGATTACTTTAAGGCCAGGCTTTCT[C/T]GAGACATCCTCAAAGTAAAAGGAATGAGCTACAAGACCTTATCAGTGCTTGTAGATTATGTTTACTCTTCGCAGATGAATGTGAGCAAAGACAATATCGTGGATGTCATCACAGGGGCGAAGATCCTGCAGATGCCCTGTGCGGTGCAGGCTGCTATTGATACCATTTCCACACAGATCACACCTGAGAACTGCTACGAAATCCTAACGATCGCTAAAAAGCAACGATTAAATGAACTGAAAGAAACCGCCTATCGATTCATGAGTGACAACTTTCTGCAGGTTCTGAAAGATCCAGCTGTCTATGGACGCCTCACGGGTTCAGAGAGAGACCTCATCCTGCGCAAACGGATGGAAAGCCGCAAGTGTCTGATGGTGGCAGAAATTAATGACGTGTTTGAGCGTGTAGGAAGCCGACCGCCCAGCAGAAACAGCAGCCGTCCCCAGAGTCCCCTCTCCATCACCTCTTTTGAGGACAATCACATGATCTACTACTACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8879
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082352 | Nonsense | 98 | 468 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 27193593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25272028 |
GRCz11 | 17 | 25290429 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGCWGCTATTGATACYATTTCCACACAGATCACACCTGAGAACTGCTA[C/A]GAAATCCTAACGATYGCTAAAAAGCAACGATTAAATGAACTGAAAGAAAC
Long Flanking Sequence:
AAAAATGTCTCTTCCACATCAGAGAACAGAAATCATTCCTACTCAGGTACCCAGGAAACGAGGTCACTTGAGAGAACCTTAGGAAGCTTTATAAATTCCTCTGAAGGAGCCAGTCAGACCAGCTACAGAACGTCATTTGGACAGACCGGGATGGAAGGGCTGAAGCAAAGTGGATCTGCAGTAAGAGAAGCTCTCTCTGCAAAAGAGGAGCCAAATTTAGTCATAGAGGTGGGCGGACAGAAAATACAAGCACACAAATCAGTATTAGCTGAAAAGAGCGATTACTTTAAGGCCAGGCTTTCTCGAGACATCCTCAAAGTAAAAGGAATGAGCTACAAGACCTTATCAGTGCTTGTAGATTATGTTTACTCTTCGCAGATGAATGTGAGCAAAGACAATATCGTGGATGTCATCACAGGGGCGAAGATCCTGCAGATGCCCTGTGCGGTGCAGGCTGCTATTGATACCATTTCCACACAGATCACACCTGAGAACTGCTA[C/A]GAAATCCTAACGATCGCTAAAAAGCAACGATTAAATGAACTGAAAGAAACCGCCTATCGATTCATGAGTGACAACTTTCTGCAGGTTCTGAAAGATCCAGCTGTCTATGGACGCCTCACGGGTTCAGAGAGAGACCTCATCCTGCGCAAACGGATGGAAAGCCGCAAGTGTCTGATGGTGGCAGAAATTAATGACGTGTTTGAGCGTGTAGGAAGCCGACCGCCCAGCAGAAACAGCAGCCGTCCCCAGAGTCCCCTCTCCATCACCTCTTTTGAGGACAATCACATGATCTACTACTACAACAAGAGCAGTAAGGACTGGCACACTTTGACTGTCATGCCTGATGACATCAACACCAAGGGCTGTGGGATCTGCACTATGTACAACTACTTGTTTGTGGCCGGTGGGATCAGGGGGACTGGGGAGAAAAGCAAAGTCTCAGACAGGGTTTACTGCTATAATCCTGTCACAGACCGCTGGAGTGAAGTTAGACCCATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12661
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082352 | Nonsense | 118 | 468 | 1 | 2 |
ENSDART00000082352 | Nonsense | 118 | 468 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 27193651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25272086 |
GRCz11 | 17 | 25290487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACGATYGCTAAAAAGCAACGATTAAATGAACTGAAAGAAACCRCCTAT[C/T]GATTCATGAGTGACAACTTTCTGCAGGTTCTRAAAGATCCAGCTGTCTAT
Long Flanking Sequence:
CGAGGTCACTTGAGAGAACCTTAGGAAGCTTTATAAATTCCTCTGAAGGAGCCAGTCAGACCAGCTACAGAACGTCATTTGGACAGACCGGGATGGAAGGGCTGAAGCAAAGTGGATCTGCAGTAAGAGAAGCTCTCTCTGCAAAAGAGGAGCCAAATTTAGTCATAGAGGTGGGCGGACAGAAAATACAAGCACACAAATCAGTATTAGCTGAAAAGAGCGATTACTTTAAGGCCAGGCTTTCTCGAGACATCCTCAAAGTAAAAGGAATGAGCTACAAGACCTTATCAGTGCTTGTAGATTATGTTTACTCTTCGCAGATGAATGTGAGCAAAGACAATATCGTGGATGTCATCACAGGGGCGAAGATCCTGCAGATGCCCTGTGCGGTGCAGGCTGCTATTGATACCATTTCCACACAGATCACACCTGAGAACTGCTACGAAATCCTAACGATCGCTAAAAAGCAACGATTAAATGAACTGAAAGAAACCGCCTAT[C/T]GATTCATGAGTGACAACTTTCTGCAGGTTCTGAAAGATCCAGCTGTCTATGGACGCCTCACGGGTTCAGAGAGAGACCTCATCCTGCGCAAACGGATGGAAAGCCGCAAGTGTCTGATGGTGGCAGAAATTAATGACGTGTTTGAGCGTGTAGGAAGCCGACCGCCCAGCAGAAACAGCAGCCGTCCCCAGAGTCCCCTCTCCATCACCTCTTTTGAGGACAATCACATGATCTACTACTACAACAAGAGCAGTAAGGACTGGCACACTTTGACTGTCATGCCTGATGACATCAACACCAAGGGCTGTGGGATCTGCACTATGTACAACTACTTGTTTGTGGCCGGTGGGATCAGGGGGACTGGGGAGAAAAGCAAAGTCTCAGACAGGGTTTACTGCTATAATCCTGTCACAGACCGCTGGAGTGAAGTTAGACCCATGAACCAAGCCCGATCACAACTCAAACTCGTCTCCATGGATGGGACCCTGTACGCCATTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12654
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082352 | Nonsense | 118 | 468 | 1 | 2 |
ENSDART00000082352 | Nonsense | 118 | 468 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 27193651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25272086 |
GRCz11 | 17 | 25290487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACGATYGCTAAAAAGCAACGATTAAATGAACTGAAAGAAACCRCCTAT[C/T]GATTCATGAGTGACAACTTTCTGCAGGTTCTRAAAGATCCAGCTGTCTAT
Long Flanking Sequence:
CGAGGTCACTTGAGAGAACCTTAGGAAGCTTTATAAATTCCTCTGAAGGAGCCAGTCAGACCAGCTACAGAACGTCATTTGGACAGACCGGGATGGAAGGGCTGAAGCAAAGTGGATCTGCAGTAAGAGAAGCTCTCTCTGCAAAAGAGGAGCCAAATTTAGTCATAGAGGTGGGCGGACAGAAAATACAAGCACACAAATCAGTATTAGCTGAAAAGAGCGATTACTTTAAGGCCAGGCTTTCTCGAGACATCCTCAAAGTAAAAGGAATGAGCTACAAGACCTTATCAGTGCTTGTAGATTATGTTTACTCTTCGCAGATGAATGTGAGCAAAGACAATATCGTGGATGTCATCACAGGGGCGAAGATCCTGCAGATGCCCTGTGCGGTGCAGGCTGCTATTGATACCATTTCCACACAGATCACACCTGAGAACTGCTACGAAATCCTAACGATCGCTAAAAAGCAACGATTAAATGAACTGAAAGAAACCGCCTAT[C/T]GATTCATGAGTGACAACTTTCTGCAGGTTCTGAAAGATCCAGCTGTCTATGGACGCCTCACGGGTTCAGAGAGAGACCTCATCCTGCGCAAACGGATGGAAAGCCGCAAGTGTCTGATGGTGGCAGAAATTAATGACGTGTTTGAGCGTGTAGGAAGCCGACCGCCCAGCAGAAACAGCAGCCGTCCCCAGAGTCCCCTCTCCATCACCTCTTTTGAGGACAATCACATGATCTACTACTACAACAAGAGCAGTAAGGACTGGCACACTTTGACTGTCATGCCTGATGACATCAACACCAAGGGCTGTGGGATCTGCACTATGTACAACTACTTGTTTGTGGCCGGTGGGATCAGGGGGACTGGGGAGAAAAGCAAAGTCTCAGACAGGGTTTACTGCTATAATCCTGTCACAGACCGCTGGAGTGAAGTTAGACCCATGAACCAAGCCCGATCACAACTCAAACTCGTCTCCATGGATGGGACCCTGTACGCCATTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2926
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082352 | Nonsense | 334 | 468 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 27194301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25272736 |
GRCz11 | 17 | 25291137 |
KASP Assay ID:
554-3293.1 (used for ordering genotyping assays)
KASP Sequence:
GCCACTACATGTAACGGCGAGCTGTATGTCTCTGGAGGATCTCTGTTCTA[T/A]CGGTTGCTAAAATATGACCCTAAGAGGGACGAATGGCAGGAGTGTCCGTA
Long Flanking Sequence:
GTAGGAAGCCGACCGCCCAGCAGAAACAGCAGCCGTCCCCAGAGTCCCCTCTCCATCACCTCTTTTGAGGACAATCACATGATCTACTACTACAACAAGAGCAGTAAGGACTGGCACACTTTGACTGTCATGCCTGATGACATCAACACCAAGGGCTGTGGGATCTGCACTATGTACAACTACTTGTTTGTGGCCGGTGGGATCAGGGGGACTGGGGAGAAAAGCAAAGTCTCAGACAGGGTTTACTGCTATAATCCTGTCACAGACCGCTGGAGTGAAGTTAGACCCATGAACCAAGCCCGATCACAACTCAAACTCGTCTCCATGGATGGGACCCTGTACGCCATTGGCGGTGAATGTCTTTTCACAGTGGAGAAGTACGACCCTCGAATGGACCGCTGGACGGCGGTGGCTCCTCTACCTAAAGGAGCATTCGCTGTGGCTCACGAAGCCACTACATGTAACGGCGAGCTGTATGTCTCTGGAGGATCTCTGTTCTA[T/A]CGGTTGCTAAAATATGACCCTAAGAGGGACGAATGGCAGGAGTGTCCGTATAACAACAGCAGGAAAAAATCCACAGACATGGTGGCTCTCAAGAGCTTCATTTACAGATTTGATGTTAATCGAGAGCAGGGGATCAGCGTCTTTAAATACAACACCATTGTGAAGATGTGGCATGACTGTGCCTCCCAGCAGCAGGGCTGCACTCTGCCATTTCGATGTGCCGTTATTGATAACTGCATCTTCTGTGTAAATAAGACTCAGACTCTTGAGTTTGTTGTAGAAGACGATGGAGGTCGATTCAAAGATGAGATTCTGAAAGCACCTGTGGAGGCCAAAGGGATCTTATTCCCATTCATTCTCAGCTTGCCGGACAGAGGTGGGAGAATTGCATGAGTGGGATATTTCATCCCCACGTATGACCCTTTGGTGTCACTCCAGACGCGGAGAAAGAGAATGCCTGGTCAATATTTATAGATTAAACATTATCTCCAGAGAAGTTC
Associated Phenotype:
Not determined