Busch Lab

ZMP

si:ch211-261c8.3

Ensembl ID:
ENSDARG00000077768
ZFIN ID:
ZDB-GENE-070705-156
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.
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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