ZMP
ftr58
Ensembl ID:
ZFIN IDs:
Description:
Zgc:172047 protein [Source:UniProtKB/TrEMBL;Acc:A8WFY9]
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 |
|---|---|---|---|
| sa43912 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43911 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43912
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000055085 | None | None | 241 | 2 | 6 |
| ENSDART00000056426 | Nonsense | 254 | 542 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 6972665)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 6927202 |
| GRCz11 | 23 | 6861174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCTTTATTGAGATCATCCGCTACATTGAGAGACAATGCTCTGAGCTC[A/T]AGCAGATGATCAGAGATCAGCAAAAGACTGCTGTAAGGGATGCTGAAGGG
Long Flanking Sequence:
AAATCACCAGGCGACCCCCCTTTATTGTCCCGCGACCCCTCGGGGGGTCCCGACCCCCACTTTGACAACCTCTGTGGTAGAGCATGGGCTGGTGTGGCTAACGTTACATTGCCAGGGCTGAATTTTTGTCCCGGTCCGCCTCTGGTTTGAACAGTATAACATCCAGTCCATTCTACACCAATACTGGATTCATTAAACATTCAAGTGATGTTTTTGTTATTTTAGTTTGCTATTCTTGAATTTTCCTCCAGAAAGAGCTGAAGGAGATGCAGATGAAGCTCCAACAGAGGGTCCTGCAGAGACACAAAGATCTTCAGCAGCTGAGAGGGGCTGTGGAGACTCAGAAGGTTAGTCTGGAGAAGAAGTTTAAGTCTCACTGTGTGTCACAGGCTGTGTGATTGTGATGTGTTTAACAGCGCTCTGCACAGACAGCAGTGGAGGAAACTGAGAAGATCTTTATTGAGATCATCCGCTACATTGAGAGACAATGCTCTGAGCTC[A/T]AGCAGATGATCAGAGATCAGCAAAAGACTGCTGTAAGGGATGCTGAAGGGCTCATAGAGCGACTGGAGCAGGAGATTAATGATCTGAGGAGGAGAGATGCTGAGCTGGAGCAGCTTTCACAGACACAGGATGACATGCATTTCCTGCAGGTAACAGAGATTCAGTAGAACAGAATCAAGGGGGACCTGAATAATGACTGGAGAATCAGTTTCTTTCAGATTCAATGCAATGATGTCTGGTCCTTACAGATGTTTTATAGTCACATCCAATATTCTAGATTCACATATAGTGTGCATGGCAAAAACAAGAAGATGTGCTCTTCCTGCTCACTTTATCAGTACCTAGTTATTGCACCTTCTTTTTACTATATACTACTATATACTTTATATTACTCTTCTGTCTTGTCTTTATAACGTGACTTTGTCATATTGTAAGGTGTACTTGAGGGCTTTGAAAGGTGCCCATAAATATAAGGTTTTATAATTATAATTAGAATTACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43911
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000055085 | Essential Splice Site | None | 241 | None | 6 |
| ENSDART00000056426 | Essential Splice Site | 373 | 542 | None | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 6971634)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 6926171 |
| GRCz11 | 23 | 6860143 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACACATTTACCAACACTGTTCCCGAGACCAGGAATGACTTCCTACAATG[T/A]AAGTTGCTAAGAAAATGAGCAGACAAACTCACTGAGTGTGTTTGTGTACT
Long Flanking Sequence:
TAGTTAGTATTACTCAAGTGTGTGTTTTATTAGGGTTAAAACTAAACTGTTAAACTAAACTGGCCCTGCGGGAACTGACTTTGACACTTGTGACTTATGGTAATTGCTTGAAGTGTGGAGATGAGTTTCGATTTCTGTTTTATGTAGCGTTTCCAGTCTTTCTCCGCTCCTCCTGAATCTACAGACTTTCAAACGAGTCCGCTTGGTTCTCAGTTTTCTTTTGTTGGGCTGAGAGAATCTGTTCGGCAGCTGAAAGTCAAACTGGAGGATCTCTGCAAAGAGGAGGTCAAGAAGATCACTGACAGAGGTAAAGTCCTGGAGATTCCTCTGCTCTCAGAAATGAGTTCATTCATTTGAACGTGTTTAAATCATTTAATATCATGCATGTATATCAATAGTCTTGTTCTCTCAACATTACATTTACACGATTCATGTCTGTTGATTTCTGCAGACACATTTACCAACACTGTTCCCGAGACCAGGAATGACTTCCTACAATG[T/A]AAGTTGCTAAGAAAATGAGCAGACAAACTCACTGAGTGTGTTTGTGTACTTAAGCCCAATCATAATTTCATTTTGTTCCCCTACTCCTTCTCTCTGGCCCTTAAAACAGAGTGTGAAGGGGAAGGGCTTCAAAATGTACCCCTTTAGAAATGGGACAGCACTACAACACCAGCACACGTCATCATATGTCATTGCAATCTCTCGCTTTATATAAGGTTGTCGATTGCGACTGCTGTAGTTACTCCAGTTGTGTTATTTATAGGTATTTATCTTCAGGAAATTACTAAAGGCAATGAGCTTGTGACAACATTGACATTATAGCAGACATTGTAAAAAAAAAAGTTCATTCCCAGGCACAAGACATTTCTGATAGGGTATATCAGGGTCATTGAGAGACAGATGTGAAAGTATGTTGTGGGACTACTATACAGGAGTTATTATTGGGGATGATAAATTGTGAAATTTAGTGTTTTTTGTTTTGTTAAAACTTCATAATATGA
Associated Phenotype:
Not determined