ZMP

bcl9l

Ensembl ID:

ENSDARG00000055054

ZFIN ID:

ZDB-GENE-040927-29

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.

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.

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.

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