ZMP
bcl11b
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate B-cell CLL/lymphoma 11B (Zinc finger protein) (BCL11B) [Source:U
Human Orthologue:
BCL11B
Human Description:
B-cell CLL/lymphoma 11B (zinc finger protein) [Source:HGNC Symbol;Acc:13222]
Mouse Orthologue:
Bcl11b
Mouse Description:
B-cell leukemia/lymphoma 11B Gene [Source:MGI Symbol;Acc:MGI:1929913]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2902 | Nonsense | F2 line generated | Not yet available |
sa36375 | Nonsense | Available for shipment | Available now |
sa6468 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16831 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2902
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090487 | Nonsense | 500 | 662 | 3 | 3 |
ENSDART00000144894 | Nonsense | 633 | 795 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 18005958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 18155969 |
GRCz11 | 17 | 18175805 |
KASP Assay ID:
554-2685.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCATCCCGCCACTTCATCAAAGATCCTTTCCTTGGCTTCACCGACTCC[A/T]GACAATCTCCATTCGCCACCTCCTCGGAACACTCCTCCGAGAACGGAAGC
Long Flanking Sequence:
GGCCTGAGTCAAACTTCAGCATGGACTCTGAGTTCTGTCGGAATAGGGAAAATGGCTCAAAGCCTCCTTCAGATGAGAAGACCCTTTCGTTAGGAAAGATGGTGGAAAATGTAGGGCTCAGCTCCATCCAGCAGTACAATAACTTAATAGTTGACAATCGGAAAAGGCTTCCATTCTCTAAAAGGATCTCGGAAGTGCAGAGGGAAGTGGGTGATGACGATTCAGTAGTGGGGGAAATGGACCAAGTAGAGCGGGCAACTGTGAATGGAAGGAACTGTGGCTCAGGCGACTCTTTCTCAGGCCTGTTTCCCCGCAAACCCACTCCCATAACCAGCCCCAGCCTCTCCAACTCCTCTAACAAGAGGATCAAAATTGAAAAGGATTTGGACATACCCCCAGCCCCCCTAATCCCATCTGAAAATGTCTACTCCCAGTGGCTGGTGGGCTATGCAGCATCCCGCCACTTCATCAAAGATCCTTTCCTTGGCTTCACCGACTCC[A/T]GACAATCTCCATTCGCCACCTCCTCGGAACACTCCTCCGAGAACGGAAGCTTGCGATTCTCTACGCCGCCAGGGGACCTGCTGGACGGGGGCCTCTCCGGCCGCAGTGGTACTGCTAGCGGAGGCAGCACCCCGCACCTGGGTGGGGGGCCAGGACCAGGCCGGCCTAGCTCGAAAGAGAGCCGGAGGAGTGACACCTGTGAGTACTGTGGGAAGGTGTTCAAGAACTGTAGCAATCTGACAGTGCACAGACGCAGCCACACAGGCGAGAGGCCCTACAAGTGTGAGCTTTGTAACTACGCCTGCGCCCAGAGCAGCAAGCTCACCCGCCACATGAAGACACACGGCCAGCTCGGTAAGGAAGTGTACCGCTGTGACATTTGCCAAATGCCCTTCAGCGTCTACAGCACGCTTGAGAAACACATGAAAAAGTGGCATGGGGAACATTTGATGACGAATGAGGTCAAAATTGAACAAGCAGAGAGAAGCTAAGCCAGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36375
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090487 | Nonsense | 592 | 662 | 3 | 3 |
ENSDART00000144894 | Nonsense | 725 | 795 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 18006236)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 18156247 |
GRCz11 | 17 | 18176083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAGCAATCTGACAGTGCACAGACGCAGCCACACAGGCGAGAGGCCCTA[C/A]AAGTGTGAGCTTTGTAACTACGCCTGCGCCCAGAGCAGCAAGCTCACCCG
Long Flanking Sequence:
GGCTCAGGCGACTCTTTCTCAGGCCTGTTTCCCCGCAAACCCACTCCCATAACCAGCCCCAGCCTCTCCAACTCCTCTAACAAGAGGATCAAAATTGAAAAGGATTTGGACATACCCCCAGCCCCCCTAATCCCATCTGAAAATGTCTACTCCCAGTGGCTGGTGGGCTATGCAGCATCCCGCCACTTCATCAAAGATCCTTTCCTTGGCTTCACCGACTCCAGACAATCTCCATTCGCCACCTCCTCGGAACACTCCTCCGAGAACGGAAGCTTGCGATTCTCTACGCCGCCAGGGGACCTGCTGGACGGGGGCCTCTCCGGCCGCAGTGGTACTGCTAGCGGAGGCAGCACCCCGCACCTGGGTGGGGGGCCAGGACCAGGCCGGCCTAGCTCGAAAGAGAGCCGGAGGAGTGACACCTGTGAGTACTGTGGGAAGGTGTTCAAGAACTGTAGCAATCTGACAGTGCACAGACGCAGCCACACAGGCGAGAGGCCCTA[C/A]AAGTGTGAGCTTTGTAACTACGCCTGCGCCCAGAGCAGCAAGCTCACCCGCCACATGAAGACACACGGCCAGCTCGGTAAGGAAGTGTACCGCTGTGACATTTGCCAAATGCCCTTCAGCGTCTACAGCACGCTTGAGAAACACATGAAAAAGTGGCATGGGGAACATTTGATGACGAATGAGGTCAAAATTGAACAAGCAGAGAGAAGCTAAGCCAGATTTCCTATTTTGCCTCACAATTCCTTGATTATAAAAGGGGTAGCTGGATACTCTGTTTTTTGTTTAGTTCGGTTGTTGTTTTTTGGTTGCTTGTTTGTTTGTTTTCAAGTTAATGGTTTGAGTTAGTTTTGTCCTAAGAAACTGCCATCTGAGAATGATAAAGACATTAAAGAAGTGGAAAATGCAAAAAAATAAAAATAAAAAAAGAGAGAGAGAGAGGGCGGGGGGTTAATTTGGAGACGGTATAAACCGCATATCTATGAATGGATACATTACACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6468
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090487 | Nonsense | 597 | 662 | 3 | 3 |
ENSDART00000144894 | Nonsense | 730 | 795 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 18006251)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 18156262 |
GRCz11 | 17 | 18176098 |
KASP Assay ID:
554-4595.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCACAGACGCAGCCACACAGGCGAGAGGCCCTACAAGTGTGAGCTTTG[T/A]AACTACGCCTGCGCCCAGAGCAGCAAGCTCMCCCGCCACATGAAGACACA
Long Flanking Sequence:
TTCTCAGGCCTGTTTCCCCGCAAACCCACTCCCATAACCAGCCCCAGCCTCTCCAACTCCTCTAACAAGAGGATCAAAATTGAAAAGGATTTGGACATACCCCCAGCCCCCCTAATCCCATCTGAAAATGTCTACTCCCAGTGGCTGGTGGGCTATGCAGCATCCCGCCACTTCATCAAAGATCCTTTCCTTGGCTTCACCGACTCCAGACAATCTCCATTCGCCACCTCCTCGGAACACTCCTCCGAGAACGGAAGCTTGCGATTCTCTACGCCGCCAGGGGACCTGCTGGACGGGGGCCTCTCCGGCCGCAGTGGTACTGCTAGCGGAGGCAGCACCCCGCACCTGGGTGGGGGGCCAGGACCAGGCCGGCCTAGCTCGAAAGAGAGCCGGAGGAGTGACACCTGTGAGTACTGTGGGAAGGTGTTCAAGAACTGTAGCAATCTGACAGTGCACAGACGCAGCCACACAGGCGAGAGGCCCTACAAGTGTGAGCTTTG[T/A]AACTACGCCTGCGCCCAGAGCAGCAAGCTCACCCGCCACATGAAGACACACGGCCAGCTCGGTAAGGAAGTGTACCGCTGTGACATTTGCCAAATGCCCTTCAGCGTCTACAGCACGCTTGAGAAACACATGAAAAAGTGGCATGGGGAACATTTGATGACGAATGAGGTCAAAATTGAACAAGCAGAGAGAAGCTAAGCCAGATTTCCTATTTTGCCTCACAATTCCTTGATTATAAAAGGGGTAGCTGGATACTCTGTTTTTTGTTTAGTTCGGTTGTTGTTTTTTGGTTGCTTGTTTGTTTGTTTTCAAGTTAATGGTTTGAGTTAGTTTTGTCCTAAGAAACTGCCATCTGAGAATGATAAAGACATTAAAGAAGTGGAAAATGCAAAAAAATAAAAATAAAAAAAGAGAGAGAGAGAGGGCGGGGGGTTAATTTGGAGACGGTATAAACCGCATATCTATGAATGGATACATTACACAATATTTTAAATGGAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16831
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090487 | Nonsense | 644 | 662 | 3 | 3 |
ENSDART00000144894 | Nonsense | 777 | 795 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 18006392)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 18156403 |
GRCz11 | 17 | 18176239 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAATGCCCTTCAGCGTCTACAGCACGCTTGAGAAACACATGAAAAAGTG[G/A]CATGGGGAACATTTGATGACGAATGAGRTCAAAATTGAACAAGCAGAGAG
Long Flanking Sequence:
TGGCTGGTGGGCTATGCAGCATCCCGCCACTTCATCAAAGATCCTTTCCTTGGCTTCACCGACTCCAGACAATCTCCATTCGCCACCTCCTCGGAACACTCCTCCGAGAACGGAAGCTTGCGATTCTCTACGCCGCCAGGGGACCTGCTGGACGGGGGCCTCTCCGGCCGCAGTGGTACTGCTAGCGGAGGCAGCACCCCGCACCTGGGTGGGGGGCCAGGACCAGGCCGGCCTAGCTCGAAAGAGAGCCGGAGGAGTGACACCTGTGAGTACTGTGGGAAGGTGTTCAAGAACTGTAGCAATCTGACAGTGCACAGACGCAGCCACACAGGCGAGAGGCCCTACAAGTGTGAGCTTTGTAACTACGCCTGCGCCCAGAGCAGCAAGCTCACCCGCCACATGAAGACACACGGCCAGCTCGGTAAGGAAGTGTACCGCTGTGACATTTGCCAAATGCCCTTCAGCGTCTACAGCACGCTTGAGAAACACATGAAAAAGTG[G/A]CATGGGGAACATTTGATGACGAATGAGGTCAAAATTGAACAAGCAGAGAGAAGCTAAGCCAGATTTCCTATTTTGCCTCACAATTCCTTGATTATAAAAGGGGTAGCTGGATACTCTGTTTTTTGTTTAGTTCGGTTGTTGTTTTTTGGTTGCTTGTTTGTTTGTTTTCAAGTTAATGGTTTGAGTTAGTTTTGTCCTAAGAAACTGCCATCTGAGAATGATAAAGACATTAAAGAAGTGGAAAATGCAAAAAAATAAAAATAAAAAAAGAGAGAGAGAGAGGGCGGGGGGTTAATTTGGAGACGGTATAAACCGCATATCTATGAATGGATACATTACACAATATTTTAAATGGAGCCTTTAACTGTGCAATAATTTCTGTATTTATTGGATTTTAAATATTTTGGCATGTGCAGGTTAATTTTTATTTCATAATTTTTTTATTCCATAATCTTATGATTTATTTCAAATGCTGAGATTTTTCTTTTTAAATCTAAAAG
Associated Phenotype:
Not determined