ZMP
ftr01
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8E7R9]
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32855 | Nonsense | Available for shipment | Available now |
sa19690 | Nonsense | Available for shipment | Available now |
sa39783 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5717 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa32855
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 |
---|---|---|---|---|---|
ENSDART00000100524 | Nonsense | 146 | 556 | 1 | 6 |
ENSDART00000132224 | Nonsense | 146 | 355 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 11462021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11887117 |
GRCz11 | 2 | 11670716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAGAATCTGTTTAAAGACAGGAGACACAATCTATTGGATCCCACTAGA[C/T]AACTCCATGAGATGATCTGCCCAAAACACGACAAACCACTGGAAATCTAC
Long Flanking Sequence:
TGAGATAACTTGTGTTGTCAAACACATATGAACCTATCTAATCGTGTGTGTACACACAAGGTAAGATGGCAGAAGCTAGTTTTTCTCAGGACCAGTTCAGCTGCTCAGTGTGTCTGGATATCTTAAAGGGTCCAGTGACCATTCCCTGTGGACACAGTTACTGTATGAGCTGTATTACAGACTGCTGGGATCAGGAGGATCAGAAGCAAGTCTATAGCTGCCCTCAGTGCAGAAACACCTTCACTTCAAGACCTGTGTTGTGTAAGAATGTCTTGATTGATGAGATGGTGAAGAAAGTAAAGAAGACTAACTTACAAACTGCTTGTCCTGCCCATGCTCATGCTGAACCTGGAGATGTGGAGTGTGACGTCTGTCCTGGAAGAAAATATAAAGCTGTCAAGTCATGTGTGGAGTGTCTGAACTCTTACTGCCGAAGCCATCTTGAACAACACGAGAATCTGTTTAAAGACAGGAGACACAATCTATTGGATCCCACTAGA[C/T]AACTCCATGAGATGATCTGCCCAAAACACGACAAACCACTGGAAATCTACTGTCGTACTGACCTGCAGTGCATTTGTTATCGATGTTTAATGGATGAACATAAAAACCATGAAGCTGTAACAGCTGAAGCTGAGAGGACAGAGAAACAGGTATGAACTGAATTTAGTTATTATTGTGCTTATAATTCTGACTTATACTGTACATGCTAACGCACAAATCTACATTGTTATCTTGGTGTCATTTAAAAAGGAATGTAGTAGTAAATAATAGTATCATTGTTTATTAATAAATAATGGTATTATTGTTTATTTGTTGTAATTGTATATCTTCCTGCTTTTCCTACAGAAGCTTTTGGGAAGAATCCAAACAAAGTTCAAGCAAGCAATCGAGGCAAGACAGAAGGAGCTGCAGGAGCTAAGAGATGCTGTGAAGTCTTATAAGGTGAATTTTCTAACGTTTGAGGATACTTTTAAACACATTGAAGCTGACTGAAGGTTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19690
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 |
---|---|---|---|---|---|
ENSDART00000100524 | Nonsense | 168 | 556 | 1 | 6 |
ENSDART00000132224 | Nonsense | 168 | 355 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 11462087)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11887183 |
GRCz11 | 2 | 11670782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCCCAAAACACGACAAACCACTGGAAATCTACTGTCGTACTGACCTG[C/T]AGTGCATTTGTTATCGATGTTTAATGGATGAACATAAAAACCATGAAGCT
Long Flanking Sequence:
TGGCAGAAGCTAGTTTTTCTCAGGACCAGTTCAGCTGCTCAGTGTGTCTGGATATCTTAAAGGGTCCAGTGACCATTCCCTGTGGACACAGTTACTGTATGAGCTGTATTACAGACTGCTGGGATCAGGAGGATCAGAAGCAAGTCTATAGCTGCCCTCAGTGCAGAAACACCTTCACTTCAAGACCTGTGTTGTGTAAGAATGTCTTGATTGATGAGATGGTGAAGAAAGTAAAGAAGACTAACTTACAAACTGCTTGTCCTGCCCATGCTCATGCTGAACCTGGAGATGTGGAGTGTGACGTCTGTCCTGGAAGAAAATATAAAGCTGTCAAGTCATGTGTGGAGTGTCTGAACTCTTACTGCCGAAGCCATCTTGAACAACACGAGAATCTGTTTAAAGACAGGAGACACAATCTATTGGATCCCACTAGACAACTCCATGAGATGATCTGCCCAAAACACGACAAACCACTGGAAATCTACTGTCGTACTGACCTG[C/T]AGTGCATTTGTTATCGATGTTTAATGGATGAACATAAAAACCATGAAGCTGTAACAGCTGAAGCTGAGAGGACAGAGAAACAGGTATGAACTGAATTTAGTTATTATTGTGCTTATAATTCTGACTTATACTGTACATGCTAACGCACAAATCTACATTGTTATCTTGGTGTCATTTAAAAAGGAATGTAGTAGTAAATAATAGTATCATTGTTTATTAATAAATAATGGTATTATTGTTTATTTGTTGTAATTGTATATCTTCCTGCTTTTCCTACAGAAGCTTTTGGGAAGAATCCAAACAAAGTTCAAGCAAGCAATCGAGGCAAGACAGAAGGAGCTGCAGGAGCTAAGAGATGCTGTGAAGTCTTATAAGGTGAATTTTCTAACGTTTGAGGATACTTTTAAACACATTGAAGCTGACTGAAGGTTCAAAGTGATGTGATGATATGTGTCCTGATGCAAGTCCTAATTTTGCATAGTTTGACACATTCCTGTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39783
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100524 | Nonsense | 271 | 556 | 3 | 6 |
ENSDART00000132224 | None | None | 355 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 11464170)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11889266 |
GRCz11 | 2 | 11672865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGACACGACTGATCCAAGATCAGGAAAAGGCTGCAGTGAGTGAAGTT[G/T]AAAAACTCTCGGAGCAGCTGGAGGAGGAAATTGATGATCTTAGGAGGAGA
Long Flanking Sequence:
CTCCTTTTGTTACTGTATGTCTGTCGCATGGCTGTGTTTGTTTACCTTTCCTTGACAGAGCACATTCTAGTCAGCTGACCAATCAGTGAAGCCACCTGCAACCTATTATTGAGACCTACTTAAGGACTAAGTTTCCCACCTTTCAACATTCAGTTGTTCACGTCTCGGTCTGCTGTTCCCCATGACTGTTATCTTGCATTCCTTGCTACCAGAGTTGCTGTCAGCCTTTGTTCCTTGAAATTGGTACCAAGCAATTAAGCTAATAAGCTTTTTCTTGCAATTGGATGCCTTTACATTTCATCCTTGTGACCTGTCCGTAAGCGATTGCTGAAATGTTGTCCTGAGTAAAATCGTATTATGTGTGTCAACAGTGTTCTGCACAGACAGCAGTGGATGATAGTGAAAGGATCTTTACTGAACTCATCCACACCATTGAGAGAAGCCGATCTGAAGTGACACGACTGATCCAAGATCAGGAAAAGGCTGCAGTGAGTGAAGTT[G/T]AAAAACTCTCGGAGCAGCTGGAGGAGGAAATTGATGATCTTAGGAGGAGAGACTCTAAGCTGGAGCAGCTTTCACACATAGAAAATCATATTCATTTCCTCCAGGTAAACCCTAAAATACAAGACTTGGTAGGGCTGTGGTCAGGAATTCTGACAGACTTCATGTTTTATTTGCAGATGTTCCAGTATATATCTGAACACCCTAAATCTACAGACACATGTGGCATCACTGTCAGTTCCCTCATCCCTTTTCATGATGTGGTAAAGTCAATCTCTAAGCTGAAGGAAAAAGAGGGTTTCTGTAAAGAAGAGCTAGAAAAGTTCTCTGATAGAGGTAAAGTATATTCATTTACTTTTATTTTGTCTGATATTACATACAAGAATGTCTATTTCTTTTAAATGCTTATTTACATATTGATTAAAGTGTTTCTGCTACTTTTCCATAGTGACATGCAATGACATGACTCCCATCAGTGAATCAGTTCATACCCGGGAACAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5717
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000100524 | Nonsense | 450 | 556 | 6 | 6 |
ENSDART00000132224 | None | None | 355 | None | 5 |
ENSDART00000100524 | Nonsense | 450 | 556 | 6 | 6 |
ENSDART00000132224 | None | None | 355 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 11468402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11893498 |
GRCz11 | 2 | 11677097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCTGTTATTGGGAGGTTGAGTGGAGTGGAATTAAYGGTGTGTGTATAT[C/A]AGTGTCRTATAAGAGCATCAKCAGAAAGGCATTGTTTAATGAAGATATGT
Long Flanking Sequence:
CAGATCTCTGTGTGAAACTTCTTGTGCAGACAAAAATCTCACTGTACAATTACAATTAATAACAAAAATAATTCATATTTAAAACTTGTATGCTACATACAAATATAAACACAACCAACTTTTAAACCTTTTTTTTTTTTGGCGGTGGTGGGGTGAGTGACATTTGCAAAGTAATGTATAAATAGAAAAAACCATGTACACACACGCACACAGAAATATTAATTTATTCACACACTTAAACACGCACATAAGCATTCTAATAAGTAATTGTGTTTTATCTTCTCTAGGTTCCTGTCAGCTCACTCTTGATTCAAAGACAGTGAACCGTTACCTTCGTCTGTCTGAGGGAAACAAAGCAGTCAGTTTCACTGAAACACCCCAGCAGTATCGTGCTCATCCAGAAAGATTTGATGGGAGTTTTCAGGTGTTGTGTAGACAGAGTGTGTCGGAACGCTGTTATTGGGAGGTTGAGTGGAGTGGAATTAATGGTGTGTGTATAT[C/A]AGTGTCATATAAGAGCATCAGCAGAAAGGCATTGTTTAATGAAGATATGTTTGGATTCAATAGTCAGTCCTGGGGTTTGTACTGCTCTCCCTCCAATTACCTATTCATGCACAATAAGAGCAAGACTAAAATCCCTGTGTCCTCCACATCCTCTAGAGTAGGAGTGTATGTGGATCATAGGTCAGGAACTCTGCACTTCTACAGCGTCTCTGAGACTATGGCCCTCATCCATACAATCCAGACCACATTCACTCAGCCTCTATACCCTGGGTTTGGCTTAAATATCGGCTCAAATGTGAAACTGTGTCATCTAACAACATAGTAGAGAAATTTGGCATGTTACATGATGTAGCTTTGATTATTTTTATTGGGAATCTCTCACACAAGCAGTAACAATTGTGTATAATGTGTAAAAACACTAAGGACTGATGTACTGTAGCTTCTACTTACATAATCGTAGTCTGCTGTCGCAAACATGTCAATGTAAAGCTTTAACTAAC
Associated Phenotype:
Not determined