Busch Lab

ZMP

trim25l

Ensembl ID:
ENSDARG00000020863
ZFIN ID:
ZDB-GENE-040914-87
Description:
RING+BBOX zinc finger protein [Source:UniProtKB/TrEMBL;Acc:Q6DRJ6]
Human Orthologue:
TRIM65
Human Description:
tripartite motif-containing 65 [Source:HGNC Symbol;Acc:27316]
Mouse Orthologue:
Trim65
Mouse Description:
tripartite motif-containing 65 Gene [Source:MGI Symbol;Acc:MGI:2442815]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa10522 Essential Splice Site Available for shipment Available now
sa17056 Nonsense Available for shipment Available now
sa7022 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12188 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa10522
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
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Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039204 Essential Splice Site 250 476 2 10
ENSDART00000105278 Essential Splice Site 231 560 3 9
ENSDART00000111817 Essential Splice Site 229 576 3 8
Genomic Location (Zv9):
Chromosome 6 (position 4034338)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4003839
GRCz11 6 4164659
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGAGAGAGAGCTGAAAGACATGAAGAAAGTCGTAGACACGCTCACGG[T/G]AAACATTCAGCACACCCAGGAAACAGCTYACCTGTTAATGAGTRASAGAA
Long Flanking Sequence:
TTATATGTAGACGACGTTCACAAAAATATACAAGTAATGAATAAAATATTATGAATAAGTACAACATTACCTTTAAAATAAAGAAGAACATTTTTAAATAAGTAATAAAATCATTGTAGTGTTGTACATTTCAATGCTTAACTGCTGCTTTGCTTTATCTGGCATGACGTCACTAAACCTCAAAAAGGATCTTGCGTAGAAACAAGACGTCATTTAGAGTAATCTTCATGGTTTAAATAAAACAGACTCGCACCACTTTAAGCTTTTGCATGACAGGCTGTTTGAACGTGTCATTGTGGTTAAGTAATGATGAACTGATCTACTGTTTCTCTCACACTCGTTCCAGTCCACATTCCTTTCTATTCTGAACTTTGCTTTGTGTTAATCTTCATTGTTGTGTCAGAAAGAGCTGGGCGCAGTTCTGTCAGAGAACCATCAGAGGCTCCAGGACAGAGAGAGAGAGCTGAAAGACATGAAGAAAGTCGTAGACACGCTCACGG[T/G]AAACATTCAGCACACCCAGGAAACAGCTCACCTGTTAATGAGTGACAGAAAATTATTAGGCAACATGAATAATAAACTATTTCAAATATTTCCCAAGTCATAACATTTTTTTTTTTACCATATTTAATTAATTCCTTCGTTTATTTATTTTCCTTCAGCTTAGTCCCTTTATTCATCCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCATTTGTTTTACGCAGCAGATGCCCTCCAGCTGCAACCCAGTACATGGAAACACCCATACACTCTCATTCACACACATATAATACGGCCAATTTAGCTCATGCAATTCACCTGTAGCGCATGTGTTCGGACTAGGAAACCCACACCACAGCGGGAAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCGGGGCTCAAACCAGCGACCTTCTTGTTGTGAGGCAACATTGCGAACCAATGAGCTTTCGTGCCACATTTACTGTATTTCATTCATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17056
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039204 Nonsense 272 476 3 10
ENSDART00000105278 Nonsense 253 560 4 9
ENSDART00000111817 Nonsense 251 576 4 8
Genomic Location (Zv9):
Chromosome 6 (position 4035632)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4005133
GRCz11 6 4165953
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTGCGAGACGAWGCGGATGCTGTCCTCTCTGAGCTCCAGGAGTCAGTG[C/T]AGCGGATGCTGGATCTGCTGCTGGATGTGATGGTCTCCAGTGGGCAGGAG
Long Flanking Sequence:
ACCAGTATCTTGAAAAATAACTAGAAAATAAGACGGCACGGTAACTCAGTGGTTAGTCTCTGAGTTGCCTCACAGCAAGAAGGTTGCTGGTTTGAGTCCTGGCTGGGTCAGTCTGCATTTCTCTTTGGAGTTTGCATGTTCTCCCTGTGTTGGCGTGGGCTCCGGTTTCCCCCACAGTCCAAACACATACAATATTGGTGAATTCATTACACTAATTGGCCGTAGTGTATGAATGTGAACGAGTGTGTATGGATGTTTTTCCAGTACTGGGTTGCAGCTTGGAAGGGCATCTGCTGTGTTAAACATATGCCTGATAAGTTGGTGGTTCATTCCTCTGTGGCAGCCTCTGATGAATAAAGGGATTAAACAAAAGGAAAACGAATGAATGCATAAGTAGTACATTTTTATAGTGTTTATGTGTGTTTGTTTGTGCGTAGCGCTCCTCAGACATGGTGCGAGACGATGCGGATGCTGTCCTCTCTGAGCTCCAGGAGTCAGTG[C/T]AGCGGATGCTGGATCTGCTGCTGGATGTGATGGTCTCCAGTGGGCAGGAGAAACTCACAGAGGCCCAGGAAGTGGTCAACAAACTGGAGGCCGAAGTCAAACAGCTGAAGAGAAAAGACGGAGAGCTGAAGGAGATCATCAACTGTCCTGACAATATACACTTTCTAAAGGTCAGATGACGTGGAAATTAGATTAATTAGGGTTTTTTTATTTTGATTTATCATGAGTTTTTTTTATATAAAATACACATTTTTGAGGGCTTACAAAAAAAAGTTAATCTTAAAGTTATTGTCTGTGTCACTAAGTTCAGACCAGGGTTATTATAACTAACTAAAATTAAATAAATTTTAATAAAGTAAATAAAAGGTACAAATATAAAATAAAGTGAACTGTATTTCATTTCATTTAAATATTGAATATTTCAGGTTTTCATTTAGGGGTTGCAATCTATTCTCAGTTGTTTGAAAAAAAAATTCAATAATCAAACAAATTATAGGGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7022
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039204 Essential Splice Site 403 476 5 10
ENSDART00000105278 None None 560 None 9
ENSDART00000111817 Essential Splice Site 382 576 6 8
Genomic Location (Zv9):
Chromosome 6 (position 4037365)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4006866
GRCz11 6 4167686
KASP Assay ID:
554-5225.1 (used for ordering genotyping assays)
KASP Sequence:
GCGTTCACWGTGGCAGAACGAAACGGGCAGAAAACTGGCATCATGAAACG[T/C]RAGTGGATTTCATCACACAGCATTTGCTTTTCTGAAATAAAACTCATTTG
Long Flanking Sequence:
GAAGGTCACTGGTTTGAGCCCCAGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTGGCGTGGGTTTCCTCCGGGTCCTTTGGTTTCCCCCAGTCCAAAAACTTGCGCTATAGGTGAATTTAATAAAATAAATTGTATCATGATGTTGTCCCGGTCTCCACAGACATATCAGACTCTGTGTTGTCCGCTGGAGGCAGGAGAACTGGGAACTGTGACCGCCAACCCTGAAGCCACCTTTGATGCCGTCAGGAGCGTCATTGTCCAGTTTAGGGAGAGAGTGGAGGAGATGTGTGACCAGGAGCTGGACAAGATCAACAAGACCGGTACACACAAACACACACACACACACACACACACACACACTTAGAGCTGAAGTGGTCAGATGCATATGGAGGATCATTATCTGTGTTTCTCCTCAGTCTACAACACAACAGCGTTCACAGTGGCAGAACGAAACGGGCAGAAAACTGGCATCATGAAACG[T/C]AAGTGGATTTCATCACACAGCATTTGCTTTTCTGAAATAAAACTCATTTGGTCATGTCTGGTTATTTGTTTGTTTTAAATGAAGTTTCACAAACTAATTTCGAGAGGAGCACGTGATATGATTGACTGCAGCTGGCCACTCATCTACACTCATTGGCTAGCCAATCGGATCGATCCAAACTCACTATAAGTAACCTAGCTAAGAACTACTCCCTTATCTTCGTTTCCTGAAGAAACCCCCCATCCACCCCTTTTCCTCCTTTCCTCTTTTGCTGAGGGGAGCTCTCGAGAACACCTGACCTCGTACTCCCCTCACATGCTTTATGGACCTGGCGGGAGCCATGGGCTCAGCTATCTCCGAGCTCAGGGTTCTCTCCCGGGACAGCATGCCAAACCTGCTAACTTGCTAACAAGTTGTCAAACAGTATCTAAGTGTGAACTCTTGAAAGTAAAAAAAAAAATAAGAAAAAAGGTTGGTCCTGTATTAAACAACATTTTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12188
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039204 None None 476 None 10
ENSDART00000105278 Nonsense 451 560 7 9
ENSDART00000111817 Nonsense 470 576 8 8
Genomic Location (Zv9):
Chromosome 6 (position 4045945)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 4015644
GRCz11 6 4176464
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGCCGCTTACCTCTGACCGCTGCTACTGGGAGGTAGAGTGGAGGGGG[C/T]GRGGCTCATCTGTGGGCGTGGTCAGTGGGTCCATGCCTCGSAAAGGGGCR
Long Flanking Sequence:
GATAGATAGATAGATGAATACATACAATAAAGGAGGGATTGATAGACAGAGAGAAATATAGAAAGAACAATGGACTGATTGTACAGAATGATGGATGGATGGGCTGATGATCATATGTCATATGCTGTTGTGTGTTTGTCCTCCAGTGCGGGAGATTAACATTGACAGCATTCAGGCTGCAGAGCCCAGAAGCAGAGAAGAGTTCCTGCAGTGTGAGTTTATCATATCCTCCAGCATCTGATCCTCTGCCTGACCGCCCTTCATTCTGCTTCAGTCTCACTCTATGTTTCTCCTGTGCATCAGATGCTTGTAATCTGACTCTGGACCAAACCACAGCCCACCGCCGTCTGCTAGTGTCTGATGGAGACTCGGTGGCCACCCTGCAGCAGACCACACAGCCATACCCGGACGTCCCGCAGCGCTTCGATGGCTGGACGCAGGTGCTCTGTCTGCAGCCGCTTACCTCTGACCGCTGCTACTGGGAGGTAGAGTGGAGGGGG[C/T]GAGGCTCATCTGTGGGCGTGGTCAGTGGGTCCATGCCTCGCAAAGGGGCGGATTCGAGGGCGGGGCTTGGGTATAACAGCCAATCATGGAGTTTGGAGCTGTCTGACATGTGCTGCGCAGCCATGCACGCTAATCAGAAGGTGGAGATCCCTGTGACCTACAGCCCTCGTGTCGGGGTGTTCCTGGACAGGAGCGCAGGGACTCTGAGTTTCTATAGCGTGGATGACGAGCTGCTGCCTCTTTATAAGTTTCAGGGCTCGTTCCCGCAGTCGCTGTATGCTGCGTTCGGGGTGGGCTGTGGCGTCGGGGTCGGCCTGGATTTTGCCATGGGGCAGTTCAGCTCCACTTCAGACAGCATTAAAATATGTCCCTTGTGAGCAAAACAAATCTTTTAACAAAACAAGCGAACATACAGTACATCAACTCCGCATTCTCCATCTAAAAATTAATTTTGATTCTAACGCTTCTAGTTCACTTTTTGATTATTGTCCATAATTAGA
Associated Phenotype:
Not determined