ZMP
bcl9l
Ensembl ID:
ZFIN ID:
Description:
B-cell CLL/lymphoma 9-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q67FY3]
Human Orthologue:
BCL9L
Human Description:
B-cell CLL/lymphoma 9-like [Source:HGNC Symbol;Acc:23688]
Mouse Orthologue:
Bcl9l
Mouse Description:
B-cell CLL/lymphoma 9-like Gene [Source:MGI Symbol;Acc:MGI:1933114]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36718 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44897 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39214 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36718
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077357 | Nonsense | 539 | 1531 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 42300776)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 43906148 |
GRCz11 | 18 | 43899602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTAGCATGGAGGAAGCTACAAGAAGAATACTACCAGGAGAAAAGGCGA[C/T]AACATGATATGAACCCCCACCAGCATCCCCAGCATTTCCGCATAATGCCA
Long Flanking Sequence:
ATGGGCTCTCTAAGGAGCAGCTGGAACATCGTGAACGCTCTCTACAGACTCTTCGAGACATTGAGAGGTTACTTCTCCGTAGTGGAACTGGTGTTGCCCAAGAGGATCCAAGAGGTCCTAATGGCAATCCAAATGGCACTAATGTTAACAACAATAATAGTAATGATGGAGGTAGGGGTTTGGAAGATGGTGAAATTGGTGGAGGGATTCCTGGCAATTGCCATATCAACAATGCTGGTATGCCTGGTATGCCCCCTGTCGGTGGAATGAAAAAGTACGAAGAGCCATTACAGTCCATTATTTCACAGACACAGAACCTTGGTGGGCCTGGACTGGATGACTCTCTGATGGGTCCCCATCATGGTATGCCACCACATTCCCACCACCTCTCCTCACCCTCAGGATTAGACATGGGGCCCCTTCTTGGACCTGAAGGCGTAACACCAGAGCAGCTAGCATGGAGGAAGCTACAAGAAGAATACTACCAGGAGAAAAGGCGA[C/T]AACATGATATGAACCCCCACCAGCATCCCCAGCATTTCCGCATAATGCCAGAGATGGGCATGCCTGGGGGACCTCCAATGCTGATGAGGGGTCCTCCACCACCATATCATAGTAAACCTGGTGATCAGCAGTGGGGGCCTGGTCCAATGGTAGGGGGAGGAATGGGAGGGAATGCACGAATGATGGACATGAATCAGGAGGGTCCTCGCGGGCCAAGATTTCTTGGACAGATGAGAGGTCCTTCAGGGGGTGGGGGTTATCCAGAAAGCCCAGGTGGTGTATTAGGTGTAGAAGGGTTGGGGCCTCAAAGACCTCCAAGACCAGGCATGGGCTGGTTAGAGGAAATTCCTCCAAACATGGGTGGTGGAGGTCCATTTCACGGGTGCTATCCTCCAGGGGGACCTGGGGGGCCTCCCCAACACTTCCAGGGTGATTTAGATCGCCCTATGACGCGGGAAGAAATATACCGCAGAATTCATAGATTAGACTTGCAGCAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44897
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077357 | Nonsense | 582 | 1531 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 42300647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 43906019 |
GRCz11 | 18 | 43899473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGATGAGGGGTCCTCCACCACCATATCATAGTAAACCTGGTGATCAG[C/T]AGTGGGGGCCTGGTCCAATGGTAGGGGGAGGAATGGGAGGGAATGCACGA
Long Flanking Sequence:
CAAATGGCACTAATGTTAACAACAATAATAGTAATGATGGAGGTAGGGGTTTGGAAGATGGTGAAATTGGTGGAGGGATTCCTGGCAATTGCCATATCAACAATGCTGGTATGCCTGGTATGCCCCCTGTCGGTGGAATGAAAAAGTACGAAGAGCCATTACAGTCCATTATTTCACAGACACAGAACCTTGGTGGGCCTGGACTGGATGACTCTCTGATGGGTCCCCATCATGGTATGCCACCACATTCCCACCACCTCTCCTCACCCTCAGGATTAGACATGGGGCCCCTTCTTGGACCTGAAGGCGTAACACCAGAGCAGCTAGCATGGAGGAAGCTACAAGAAGAATACTACCAGGAGAAAAGGCGACAACATGATATGAACCCCCACCAGCATCCCCAGCATTTCCGCATAATGCCAGAGATGGGCATGCCTGGGGGACCTCCAATGCTGATGAGGGGTCCTCCACCACCATATCATAGTAAACCTGGTGATCAG[C/T]AGTGGGGGCCTGGTCCAATGGTAGGGGGAGGAATGGGAGGGAATGCACGAATGATGGACATGAATCAGGAGGGTCCTCGCGGGCCAAGATTTCTTGGACAGATGAGAGGTCCTTCAGGGGGTGGGGGTTATCCAGAAAGCCCAGGTGGTGTATTAGGTGTAGAAGGGTTGGGGCCTCAAAGACCTCCAAGACCAGGCATGGGCTGGTTAGAGGAAATTCCTCCAAACATGGGTGGTGGAGGTCCATTTCACGGGTGCTATCCTCCAGGGGGACCTGGGGGGCCTCCCCAACACTTCCAGGGTGATTTAGATCGCCCTATGACGCGGGAAGAAATATACCGCAGAATTCATAGATTAGACTTGCAGCAAATGTCTAGACAGCAACAGCAGGCAGGACTTGGAGGCCCTAGAATGATGGATAATCCTGGGGGACCAGGCTTCCCTAATCCTGGCATGGCTGGAGGCCCACCCTCCCGTGGTGATCCAATGGACTTTCCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39214
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 |
---|---|---|---|---|---|
ENSDART00000077357 | Nonsense | 880 | 1531 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 18 (position 42299752)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 43905124 |
GRCz11 | 18 | 43898578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATATGTATGGACCAGACCAGCCAGGTCCTCCCCATCTGAGCAGCACTT[C/A]GAGACTTAGTCACATTCCCATGAACACTGGATCAAGGGTTACAGACCTTG
Long Flanking Sequence:
ACTTGGAGGCCCTAGAATGATGGATAATCCTGGGGGACCAGGCTTCCCTAATCCTGGCATGGCTGGAGGCCCACCCTCCCGTGGTGATCCAATGGACTTTCCTGTTTCTCGGACTATAATGGGTTCTCCAATTGGTGGAGTGGGTGGAGATGGGGGCCCCACAATGAGAGACATAGTTGATTCTCCTTTAGGGGGTAACCTCAATATGAATATGGGAATGAATATAAATCAACAGCAACAGTTGCTGGCTCAGAAGTTGAGGGGAGGTCCTGGTGTTCTTGGGGAGATGTTAAATGCTGAAGACATCTCCCGCATTAGGGCTTCACAGAATGGCCGGGGTGGTGCTAACAAAGCAATGATCCCTGGCCCAGAGGGACCTCTTCAGTTCCCCAATCAGAGCTCCTTTCCCGGCGGTCAGGTTGATGGCCCATATTTACAGCAGCCAGGCCCTGATATGTATGGACCAGACCAGCCAGGTCCTCCCCATCTGAGCAGCACTT[C/A]GAGACTTAGTCACATTCCCATGAACACTGGATCAAGGGTTACAGACCTTGGGGCTCGACACCCTCCTGACCTGCCTATTAGTGTAAATCCAATGGGTTCTCCAGCTATTCCACCATCTCACCAGCTAAAATCCCCCTCTCTTAGTCAGGAGCCATCACCTCTCATGCCCTCACCCTCTGCAGCAGGCCTGAAATCACCCAGCCAGTTACCACAGAGTGGTCCAACTCACCCTCCCCTACCAGCAGCCTCTGGGGCTGGAACACCCTCTTCCACCTCAATCAAGTCCCCCCAGGTAATGGGACCTTCGCTTGGTCTTCGCTCACCATCTGGCTCCCCTGGACATCTTAAATCTCCTTCCATGCCTGTCGCTTCACCTGGCTGGACTGCCTCACCCAAGACTGCTATGCCAAGCCCTGGAGGGCCTCCTAGTGTCAAGGTCACAGGCAACGGAGGCAGCAGCTCCACTGATACAGGTAAAAGGTTTACTGAAATGTAAAAAA
Associated Phenotype:
Not determined