ZMP
ftr64
Ensembl ID:
ZFIN IDs:
Description:
FinTRIM family protein [Source:UniProtKB/TrEMBL;Acc:B5WXY5]
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 |
---|---|---|---|
sa40578 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12729 | Nonsense | Available for shipment | Available now |
sa25315 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2248 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa40578
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 |
---|---|---|---|---|---|
ENSDART00000035360 | Nonsense | 177 | 486 | 3 | 6 |
ENSDART00000111921 | None | None | 102 | None | 2 |
Genomic Location (Zv9):
Chromosome 5 (position 62736707)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 70709032 |
GRCz11 | 4 | 71979392 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGCTCTCAGCACAGACAGCGGTGGAGGACAGTGGCAAGATCTTCACT[G/T]AGCTGATCCTCTACATTGAGAGAAGACGCTCAGAGTTCACACAGCTGATC
Long Flanking Sequence:
AGAAACAGAAAGACTTACTAAGGAGAATCCAGCAAAAAGTCCAAGAGATTCAGAAGCTGAGAGAGACTATCGAGTCACACAAGGTGAGGTGAAAGGATAACATCTTGAAAAAATTTGACATTTTAAGATTTTAATTGCTATAATCAGATCCCTGGTTCATCTGCTAACCCAGAACGCTTGAAAAAGACTAACTGTGTAGACCTTTTTTTCTGCATGCATGAGGAAAATCACACCATTATTCCAACCATACTAATACTGTAGTTAAAAACTTGAATTAATCTGTAGTGGTAATTCTATGGTATGTTATTATGGTAACTCAACAAATATATACATAAGAGATTTCTCTCTTTTGAAATAAGAGTTATAAAAACTAAGGAAGAAAAGCATACTTTGCAGTGTAGGCAGATGTGAAGAGCTGCTGCTGCAACTGATGTCAGGATTGTGTTTTATCACAGCTCTCAGCACAGACAGCGGTGGAGGACAGTGGCAAGATCTTCACT[G/T]AGCTGATCCTCTACATTGAGAGAAGACGCTCAGAGTTCACACAGCTGATCAGAGGTCAGGAAAAGGCTGCCGTGAGTCGAGCTGAAGGACTGCTGAAGCGTCTGGAGCAGGAGGTTGATGAAATGAAAAGGAGAGACTCTGAGATGAAGCAGCTTTTACAAACAGACGATCACATATACTTCCTGCAGGTAGCTTCTCTTAAAGGAACACTCCATTTTTTTGGAATTAAGCTCATTTTATAACTCCCCTAGAACCATTTTTGATTTGGCTTATAAATATAAAGAGTTATCGGTATTGTCATTTATTTATTGGTCTATATATCTGTTATCGGCTTATAAATATACATAGTTATCAGTGACAGCCATTTATTTATTGGTGTATATATCGGTTATCAGCTTATAAATATAAAGAGTTATCGGTATTGTCATTTATTTATTGGTGTATATATATATCGGTTATTGGCTTATGAATATAACAAGTTATTGGCAATGTCAGTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12729
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 |
---|---|---|---|---|---|
ENSDART00000035360 | Nonsense | 230 | 486 | 3 | 6 |
ENSDART00000111921 | None | None | 102 | None | 2 |
Genomic Location (Zv9):
Chromosome 5 (position 62736866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 70708873 |
GRCz11 | 4 | 71979233 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAGGTTGATGAAATGAAAAGGAGAGACTCTGAGATGAAGCAGCTTTTA[C/T]AAACAGACGATCACATATACTTCYTGCAGGTAGCTTCTCTTAAAGGAACA
Long Flanking Sequence:
TCTGCTAACCCAGAACGCTTGAAAAAGACTAACTGTGTAGACCTTTTTTTCTGCATGCATGAGGAAAATCACACCATTATTCCAACCATACTAATACTGTAGTTAAAAACTTGAATTAATCTGTAGTGGTAATTCTATGGTATGTTATTATGGTAACTCAACAAATATATACATAAGAGATTTCTCTCTTTTGAAATAAGAGTTATAAAAACTAAGGAAGAAAAGCATACTTTGCAGTGTAGGCAGATGTGAAGAGCTGCTGCTGCAACTGATGTCAGGATTGTGTTTTATCACAGCTCTCAGCACAGACAGCGGTGGAGGACAGTGGCAAGATCTTCACTGAGCTGATCCTCTACATTGAGAGAAGACGCTCAGAGTTCACACAGCTGATCAGAGGTCAGGAAAAGGCTGCCGTGAGTCGAGCTGAAGGACTGCTGAAGCGTCTGGAGCAGGAGGTTGATGAAATGAAAAGGAGAGACTCTGAGATGAAGCAGCTTTTA[C/T]AAACAGACGATCACATATACTTCCTGCAGGTAGCTTCTCTTAAAGGAACACTCCATTTTTTTGGAATTAAGCTCATTTTATAACTCCCCTAGAACCATTTTTGATTTGGCTTATAAATATAAAGAGTTATCGGTATTGTCATTTATTTATTGGTCTATATATCTGTTATCGGCTTATAAATATACATAGTTATCAGTGACAGCCATTTATTTATTGGTGTATATATCGGTTATCAGCTTATAAATATAAAGAGTTATCGGTATTGTCATTTATTTATTGGTGTATATATATATCGGTTATTGGCTTATGAATATAACAAGTTATTGGCAATGTCAGTTATTTATTGGTCTATATATCGGTTATCGGCTTATAAATATAAAGAGTTATCGGGAATGTCATTTATTTATTGGTCTATATATTGGTTATCGGCTCATAAATATATAGAGTTATCGGTATTGTCATTTATTTATTGGTGTATATATAGGATATTGGCTTATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25315
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035360 | Nonsense | 341 | 486 | 6 | 6 |
ENSDART00000111921 | Splice Site | None | 102 | None | 2 |
Genomic Location (Zv9):
Chromosome 5 (position 62740691)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 70705048 |
GRCz11 | 4 | 71975408 |
KASP Assay ID:
554-7354.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACGCCTTCGCCTGTCTGAAGGAAACAAACAGGCCTTCGACAGCGGCT[C/A]AGTCCAGCCGTATCCCGATCATCCAGACAGATTTGATCAGCACCTTCAGC
Long Flanking Sequence:
TGTATTTCCTACTGAAGCTTAATACCTTAATACCTACTGAACCTTGAGGCGGATGGGCTACAGCAGCAGAAGACCACACTGGGTGCCACTCCTCTCAGCTAAGAACAGGCAACTGAGGCAACAGTTCACACAGGCTTACAAAAATTGGACGAGAGAAGACTGGAGAAACGTTGCCTGCTCTGATGAGTCTCCATTTCTGATGCCACATTCGAATGCTTGGGTCAGAATTTGGCGTCAACAACATGAAAGCATGGATCCAGCCTGCCTGTATCAGCGGTTCAGGCTGGTGGTGGGGGTGTAATGGTGTTGGGGATATATTCTTGGCACACTTTGGGCCCAGTAGTACCAAATGAGTGTATGTAACGCACCTTAACAAAAATTAAATATGAAACAAATATTTTGATTTCCTCCAGATTCCCGCCAGCTCACTCTGGATCCAAACACAGCGAACAAACGCCTTCGCCTGTCTGAAGGAAACAAACAGGCCTTCGACAGCGGCT[C/A]AGTCCAGCCGTATCCCGATCATCCAGACAGATTTGATCAGCACCTTCAGCTGCTGAGCAGAGAGAGTGTGTGCGGACGCTGCTACTGGGAGCTGGACTGGAGCGGCAGTGGCGGACTCGCCGTTTCAGTGGCGTACAAGAGCATCAGGAGGAAGGGAGAAGGTGATGAGTGCGTGTTTGGGTTCAATCGCCAGTCCTGGAGCTTGTTCTACCGTCTCTCCGGGTCCTTATTTTTTCACGATAAGAAACAGATTAAACTTCACGCACCTCTCAGCTGCTGTAGATTAGGAGTGTATGTGGATCACAGAGCAGGAACTCTGTCTTTCTACAGCGTGTCTGACACATCAATGAGCCTCATCCACACCGAACAGACCACATTCACTCAGCCGCTCTATCCTGGGTTTTTACTTGCTTTCGGATCGACTATAAAGCTGCTGTGAAAAGAAGAGTACAAAATAATACACTTTTAAATCTGATATGTCAGACATACTTAAAAACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2248
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035360 | Nonsense | 374 | 486 | 6 | 6 |
ENSDART00000111921 | None | None | 102 | None | 2 |
Genomic Location (Zv9):
Chromosome 5 (position 62740790)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 70704949 |
GRCz11 | 4 | 71975309 |
KASP Assay ID:
554-3309.1 (used for ordering genotyping assays)
KASP Sequence:
GCTGCTGAGCAGAGAGAGTGTGTGCGGACGCTGCTACTGGGAGCTSGACT[G/A]GAGCGGMAGTGGCGGACTCGCCGTTTCAGTGGCGTACAAGAGCATCAGGA
Long Flanking Sequence:
TAAGAACAGGCAACTGAGGCAACAGTTCACACAGGCTTACAAAAATTGGACGAGAGAAGACTGGAGAAACGTTGCCTGCTCTGATGAGTCTCCATTTCTGATGCCACATTCGAATGCTTGGGTCAGAATTTGGCGTCAACAACATGAAAGCATGGATCCAGCCTGCCTGTATCAGCGGTTCAGGCTGGTGGTGGGGGTGTAATGGTGTTGGGGATATATTCTTGGCACACTTTGGGCCCAGTAGTACCAAATGAGTGTATGTAACGCACCTTAACAAAAATTAAATATGAAACAAATATTTTGATTTCCTCCAGATTCCCGCCAGCTCACTCTGGATCCAAACACAGCGAACAAACGCCTTCGCCTGTCTGAAGGAAACAAACAGGCCTTCGACAGCGGCTCAGTCCAGCCGTATCCCGATCATCCAGACAGATTTGATCAGCACCTTCAGCTGCTGAGCAGAGAGAGTGTGTGCGGACGCTGCTACTGGGAGCTGGACT[G/A]GAGCGGCAGTGGCGGACTCGCCGTTTCAGTGGCGTACAAGAGCATCAGGAGGAAGGGAGAAGGTGATGAGTGCGTGTTTGGGTTCAATCGCCAGTCCTGGAGCTTGTTCTACCGTCTCTCCGGGTCCTTATTTTTTCACGATAAGAAACAGATTAAACTTCACGCACCTCTCAGCTGCTGTAGATTAGGAGTGTATGTGGATCACAGAGCAGGAACTCTGTCTTTCTACAGCGTGTCTGACACATCAATGAGCCTCATCCACACCGAACAGACCACATTCACTCAGCCGCTCTATCCTGGGTTTTTACTTGCTTTCGGATCGACTATAAAGCTGCTGTGAAAAGAAGAGTACAAAATAATACACTTTTAAATCTGATATGTCAGACATACTTAAAAACAGTCCAGCCAAACTGAAGAAAAAGACATCATAGGAAATACTTCCTTACTCGTTTTAAATCGCTTGAATATTTTTGAAAAATAATTGTAAAACATTTATTGGA
Associated Phenotype:
Not determined