ZMP
si:ch211-261c8.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
MALT1
Human Description:
mucosa associated lymphoid tissue lymphoma translocation gene 1 [Source:HGNC Symbol;Acc:6819]
Mouse Orthologue:
Malt1
Mouse Description:
mucosa associated lymphoid tissue lymphoma translocation gene 1 Gene [Source:MGI Symbol;Acc:MGI:2445
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45235 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25319 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11969 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45235
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 |
---|---|---|---|---|---|
ENSDART00000114532 | Nonsense | 114 | 817 | 3 | 17 |
ENSDART00000137534 | Nonsense | 114 | 287 | 4 | 7 |
ENSDART00000144351 | None | None | 487 | None | 8 |
The following transcripts of ENSDARG00000077768 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 69304336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 65637271 |
GRCz11 | 5 | 66316376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGACTTTTCTGTTTTTGTCTCACAGGAATTCAAATCCTGCTTCAGCCA[C/T]AGTCAGTATCTGTCATTGCCGGACACAACCTTCGCCTTAGCTGTTATGCT
Long Flanking Sequence:
GTATACATTGTGTGATTATAAGATTACTTTTGGTGATTCAGAATGCATGTTACGCGATTCAGAGTTGAGATTTTGAATTTACTTCTGCCAATTCCAAGTCTAGACCTTGCAATTCAGAGTTTAGATCTTGCTATTTCAAGTTTACAAGCTGTTATCCCAAGTTGGATCTTGCCATTCCGAGTTTAGATCTAGCTTTTCTGACTTTAGATCTTACAATTCTTAGATTAAATCTTGTCACTCTGAGTCTAAATCTTGCAATTCCGAGATTAACACTTGCCACTCCGAGTTTAGACCTTGTGATTCCGAGAGTAGATCAGATCTTGTAATTCTGAGTTTACATCTGGTGAATCAGAGTGTGTGTAATGCAGTTCAGAGTTTACGTGAAAACTATACTAATTATTACAATACTTTTCCAATGTGAAAATTAATTCCAGGTCCACATTGTGCTATTCTGACTTTTCTGTTTTTGTCTCACAGGAATTCAAATCCTGCTTCAGCCA[C/T]AGTCAGTATCTGTCATTGCCGGACACAACCTTCGCCTTAGCTGTTATGCTGTCGGTGCTTCACCTGTGCAGTTCCAGTGGTTTAAGAAAACTGAGGAGGTGTGTAGACCAATAGTTTTATAGTTTTGCATCTTTAAATGAGTTTTTATTTTGATACTAAATTGTATATTCAATTATTTATTTTTTACTGTTGATGTTTGTTAATTACTGAAATGCTCTTGCCATGAAAATAGCCTTAGTAGCTGACATGGCAATAAATAAATAATGAATGAATGAATGAATGAATGAATTATTTTGATACTATTTTAAAATTTGCTGTACGTTTCAGTTTAGTTCAATAAATAAATGGTTTGATAAGTTTTAGTTTCTTATTCTATGAACAAAATTCTTTTTAGTTTTTATATATTTATTTTCAGTTTTAGTGTAGTAATTCTACTCTAACTGAGTTGACAGAACATGTCCAGTGTGGACCAAAGCAAAGTTTAATGTTTGCACAGCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25319
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 |
---|---|---|---|---|---|
ENSDART00000114532 | Nonsense | 401 | 817 | 11 | 17 |
ENSDART00000137534 | None | None | 287 | None | 7 |
ENSDART00000144351 | Nonsense | 71 | 487 | 2 | 8 |
The following transcripts of ENSDARG00000077768 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 69316281)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 65649216 |
GRCz11 | 5 | 66328321 |
KASP Assay ID:
554-7448.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACTTTTACCCTTTTGACATTTACTCATCTCCGTAGGTTTGTTGTATTA[C/A]GCTGGACATGGTTATGAGAACTTTGGGAACAGCTTCATGGTGCCAGTCGA
Long Flanking Sequence:
AACTGTGGCGAAATATGATGCAATAATCATGTATCTCGATTAATGCTTTTTTATAATCGTTTGAAACCGAAATCTAAATCGGATTTTCAATTAATTGCAAAGCCCTTTATAATAGTGGACCATTTTTATGCCTTTTTCTACCTCAATACTTATCCTCTCCCGCGCCCCCCCCCCCCTGTGAACTCTGGCGCCCCCCTTAGGGTTGGGAGCCACTGATATAAATGGCCCACCTTGTATTTTCTGTGTATTTATTTAACGTGTTTATCATATACACTTATTTATACTGTTAGTTTATTGTTTTTTATTGTATAATTGTATACAATGCTGTACAGTGACATTGATTTCCTTGAAAGGCGCTTTAAATAAAATGTATTATTGTTATTATTACTTTTAAAAGTAACTTTACCCCAACAGATATTGTGACTACAGTATTATGTTTTTTTTTGGGGTGCACTTTTACCCTTTTGACATTTACTCATCTCCGTAGGTTTGTTGTATTA[C/A]GCTGGACATGGTTATGAGAACTTTGGGAACAGCTTCATGGTGCCAGTCGATGCCCCGAATCCCTACCGTTCAGGCAACTGTCTGTGTGTTCAGAGCATTCTGAAACTCATGCAGGAGAAGGAAACCGGTCTCAATGTCTTCCTGCTGGACATGTGCAGGAAAAGGTGAACATTTTTTGTGATATGAATTAGCATGATAATTGATTATATTGATTCTAACACCTATTATATTGTTTCAGGAACATGCACGATGACGCCATGCCAAACGTCATGCTCAAAGTTACAGCCAATATTGTGTTTGGATATGCTACGTGAGTTATCAACCAGAAAAACATATTTTTTTCTCTTTACTGACATGTTATTATTATGTAGGTAAATCAGTAGTCAACCTCGAGAGCTTGCAAATCTAAATGTGATAATAATATTTGTATGTGTAGGTTGACATTTACACTCGCAGCTCTAATGTAAATAGCTGAATCTCTCGATTTGCACACACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11969
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114532 | Essential Splice Site | 456 | 817 | 12 | 17 |
ENSDART00000137534 | None | None | 287 | None | 7 |
ENSDART00000144351 | Essential Splice Site | 126 | 487 | 3 | 8 |
The following transcripts of ENSDARG00000077768 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 69316518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 65649453 |
GRCz11 | 5 | 66328558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTAGCAWGATAATTGATTATATTGATTCTAACACYTATTATATTGTWTY[A/T]GGAACATGCACGAWGACGCCATGCCAAACGTCATGCTCMAAGTTACAGCC
Long Flanking Sequence:
TTTCTGTGTATTTATTTAACGTGTTTATCATATACACTTATTTATACTGTTAGTTTATTGTTTTTTATTGTATAATTGTATACAATGCTGTACAGTGACATTGATTTCCTTGAAAGGCGCTTTAAATAAAATGTATTATTGTTATTATTACTTTTAAAAGTAACTTTACCCCAACAGATATTGTGACTACAGTATTATGTTTTTTTTTGGGGTGCACTTTTACCCTTTTGACATTTACTCATCTCCGTAGGTTTGTTGTATTACGCTGGACATGGTTATGAGAACTTTGGGAACAGCTTCATGGTGCCAGTCGATGCCCCGAATCCCTACCGTTCAGGCAACTGTCTGTGTGTTCAGAGCATTCTGAAACTCATGCAGGAGAAGGAAACCGGTCTCAATGTCTTCCTGCTGGACATGTGCAGGAAAAGGTGAACATTTTTTGTGATATGAATTAGCATGATAATTGATTATATTGATTCTAACACCTATTATATTGTTTC[A/T]GGAACATGCACGATGACGCCATGCCAAACGTCATGCTCAAAGTTACAGCCAATATTGTGTTTGGATATGCTACGTGAGTTATCAACCAGAAAAACATATTTTTTTCTCTTTACTGACATGTTATTATTATGTAGGTAAATCAGTAGTCAACCTCGAGAGCTTGCAAATCTAAATGTGATAATAATATTTGTATGTGTAGGTTGACATTTACACTCGCAGCTCTAATGTAAATAGCTGAATCTCTCGATTTGCACACACACACATTAACACCAGTGTTTTTAACTCAAAGTTGCAGTTTAGTTATTATGTACTTATTAAATTTGATTTATTTGTATTATTTGTTTTTTTATCTATAAGGGATAAAATCACATAACATAGGGGGTCCGTTCTTCGTACCTCGCTTAAATGATCTAAGATGATTTGACAGATCCTGGATCTTTTCATCTCGATAACTGATCTCTCGCTAATTTGGTTCTTCAAACAAGTTCGCGAATCAGATT
Associated Phenotype:
Not determined