ZMP
ftr11
Ensembl ID:
ZFIN ID:
Description:
Si:ch211-220f13.2 protein [Source:UniProtKB/TrEMBL;Acc:A8WG25]
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 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19846 | Nonsense | Available for shipment | Available now |
| sa33000 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19846
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000005767 | Nonsense | 12 | 546 | 1 | 6 |
| ENSDART00000141989 | Nonsense | 12 | 359 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 42809861)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 42859325 |
| GRCz11 | 2 | 42708743 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTGTGCTGTAAAAAATGGCAGAATCCAGTGTTTGTTTGGCTCAGGAA[C/T]AGTTCAGCTGTTCAATCTGTCTGGATCTACTGAAGGATTCAGTGGCCATT
Long Flanking Sequence:
CGTAACTTGCTTACCCAAAGTATCTTTAAGTAAGTTATTTAAATTGTAGTCCTTTCCAAAAAGAATGTCGTAATAAATTAAAAACTATACTTTTAACCATGCGGAAAGATATCAAGTAATTCATCATAAAGAGACAATACTCACAAGATGTGCTACACCACCCTTACAAGATGTGCTACACTACATTGTTTTTGGCATTGTTAGACAAATAAAAGCTAGAAGAGGATTGACTAAATGTAGGTATCTACCATAAAAGAAGACAAAGATCTAATAATGATTTTAAAAACTTAATTGTAAAACATTTAATGTGTGACAAGGGCTGTAAACTTTTGTAGTATTTCTGTGTAACACTGACATCTAGTAGCCTCCTTGCTTATATGACTGGGTCATGTTTCAGTTCAGAGAAATCGAAACTAAACTCACGCAGTCGAAGAGTTGAGGATTCCTTTCAGTTTGTGCTGTAAAAAATGGCAGAATCCAGTGTTTGTTTGGCTCAGGAA[C/T]AGTTCAGCTGTTCAATCTGTCTGGATCTACTGAAGGATTCAGTGGCCATTCCCTGTGGACACAGTTACTGCATGAGCTGTATTTCAGACTGCTGGGATCAGGATGAGCGGAAAGGAGTCTACAGCTGCCCTCAGTGCAGACAGTCCTTCACTCCAAGACCTGCGTTAGGAAAAAACACCATGCTGACTGAAGTGATGGAGAATATCAGGAAGAGAAAATTACAAGCTGGAGATGTGGAGTGTGACGTTTGTACTGGGAGAAAATTTAAAGCTGTCAAGTCTTGTCTGGTGTGTCTGGAATCTTACTGTCAGACTCACTTTCAACGTCATGAAGAATTTCATTCTAGAAAGCGACACAAAGTGACTGATGCCACTGGACGACTGCAGGAGATGATCTGCCCTCTACATGAGAAACTACTGGAGATTTTCTGTCGAACAGATCAGTGCTGTATTTGTTATCTGTGTACAATGGATAAACACAAAAACCACGACACTGTATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33000
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000005767 | Essential Splice Site | 219 | 546 | 2 | 6 |
| ENSDART00000141989 | Essential Splice Site | 219 | 359 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 2 (position 42810607)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 42860071 |
| GRCz11 | 2 | 42709489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGACAGAAGGAGCGAGAGGAGCTGAGAGCAGCTGTAGAGTCTCACAAG[G/A]TGAGTTTTTAGCAGAAGATCAACTGTTGGCTGCTGGAAGAGCTGATTGAG
Long Flanking Sequence:
GTTTGTACTGGGAGAAAATTTAAAGCTGTCAAGTCTTGTCTGGTGTGTCTGGAATCTTACTGTCAGACTCACTTTCAACGTCATGAAGAATTTCATTCTAGAAAGCGACACAAAGTGACTGATGCCACTGGACGACTGCAGGAGATGATCTGCCCTCTACATGAGAAACTACTGGAGATTTTCTGTCGAACAGATCAGTGCTGTATTTGTTATCTGTGTACAATGGATAAACACAAAAACCACGACACTGTATCAGCTGCAGCAGAGTGGACTGACAAAAAGGTATGTGCTACAGAAATAATTTTATACATCTTTCTAACCCATTTTAAGAAACAGTTTTGATCCCACATAGCTTTTGGGATTGGGTCAACTTTCATTTTAGCTTGCATTTTGTATTCCTGCAGATTCAACTGGCTGAAATGCAAAAAACAACCCATCAGAGAATGGTGGAGAGACAGAAGGAGCGAGAGGAGCTGAGAGCAGCTGTAGAGTCTCACAAG[G/A]TGAGTTTTTAGCAGAAGATCAACTGTTGGCTGCTGGAAGAGCTGATTGAGACTCAGTTAGGACTGTCCTGCAGTCAGTCAGTGAGGAGCCCAGTGCTGGAGCATTTGAGTCCCACTAAAGCCCCTGTGGGAAGCAGGCTGTGTGGCAGCAGTAAGAGCTGAGTAAATGACTGATTCTGCTGCTTCTCTCTCTGTGTGTCCTAACAGCGCTCTGCACAGGCAGCAGTGGAGGACACTGAGAGCATCTTTACTGAGCTCATCTTCTCCTTTGAGAGAAGCTGCTCTGAGGTGACACAGCTGATCACAGATCAGCAAAAGGCTGCAGAGGGTCGAGCTGAAGAACGACTGAAGCAACTGGAACAGGAGATTGATGATCTGAGGAGAAGAAACACTGAGCTGGAGCAGCTTTCACACACAGACCATCACATCCATTTTCTCAAGGTAAAAAAGATCTCACAAACAGCACATTGAGCTTAATAAAAGTTAAGTATCTGATTTTCT
Associated Phenotype:
Not determined