ZMP
ftr37
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens tripartite motif-containing [Source:UniProtKB/TrEMBL;Acc:B0S6J1]
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11616 | Nonsense | Available for shipment | Available now |
sa19917 | Essential Splice Site | Available for shipment | Available now |
sa31305 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11616
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061172 | Nonsense | 174 | 199 | 1 | 2 |
ENSDART00000100987 | Nonsense | 174 | 557 | 1 | 6 |
ENSDART00000134662 | Nonsense | 174 | 506 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 60171335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 59248126 |
GRCz11 | 2 | 59345352 |
KASP Assay ID:
2259-2850.1 (used for ordering genotyping assays)
KASP Sequence:
GARAAACCCCTGGAGATCTTCTGCCGCACTGATCAGCKATGTATATGTTA[T/A]CTKTGTACAATGGATCAACACAAAAACCACAAYACTGTTTYAGCTGYWGC
Long Flanking Sequence:
GTGGCTCATCATGAGTTCAGCTGTGCAGTGTGTCTGGATCTCCTGAAGGATCCAGTCTCCACTGCCTGTGGACACAATTACTGTATGAGCTGCATCACAAACTGCTGGAATCAGGAGGATCAGAAGAGAGTCTACAGCTGCCCTCAGTGCAGACAGACCTTCAGCCCCAGACCCGCTTTAGCTAAAAACACCATGCTGGCTGAAGTGCTGGAGAAACTGCAGAAGAGCAAACTACAAGCTGCTGGTCCTGCTCAGAGTCCCGCTGCATCTGGAGATGTGGAGTGTGACGTCTGTACTGGAGCCAAAAACAGAGCCGTCAAGTCCTGTCTGGTGTGTCTGAACTCTTACTGTCACACTCATTTTCAGCGCCATCAAGAGATTCACCCAGGAAATCAACACAAAGTGACTGAAGCCACTCACAAATTGAAGAAGTTGATCTGCCCTCAACATGAGAAACCCCTGGAGATCTTCTGCCGCACTGATCAGCTATGTATATGTTA[T/A]CTGTGTACAATGGATCAACACAAAAACCACAACACTGTTTCAGCTGTAGCAGAGAGGACTGAACAACAGGTAAGAACCTACTAAAGTCCAGTAATTAATAATACATGTCCCTTTAAATATATCTGTGTATTAAACTCTTTTCTTCATTAAACTCAGTTTCTAAAGGGCCACTGCCTTGTGTTTAGCTTTAATTTAATGCACCTGATCCAGATAAACAAGTCTGAAAACCACTGGTATGTGGATGGAACTAAACCGGTTGGACTGTGACTGATGCAGGCAATCAAAGCATTGGTAGTATAGTGCTGAGCATAGCTGCCTTCCAACAGCTGACCTGAGTTTGTATCCTGGTCAATCCAATGCCATTGGGTGCAGCCATGACTTAATGGTTAAACAGTTGGACTTGTGATTTAAAGGTCACAGGTTCGAGTCCCAGCACTGACAGAGATTGTTTCCCTCAATTTCACAAGGCTGAGTGGGTCCCTTGAGCAAGGAACCGATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19917
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061172 | None | None | 199 | None | 2 |
ENSDART00000100987 | None | None | 557 | None | 6 |
ENSDART00000134662 | Essential Splice Site | 360 | 506 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 60167466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 59244257 |
GRCz11 | 2 | 59341483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCTGGAGCATTTCGGCAAAAAGGAGATAAAGTTGATTTCTAGAAGAG[G/A]TCAGATTTATATTTCCTGACATGTTTCAGATGATTTTAAATGTATTTGTA
Long Flanking Sequence:
TTCTGTGTGTGTGTGTGACAGCGCTCTGCACAGGCCGCAGTGGACCACACCGAGAGGATCTTCACTCAGCTCATCTGCTGGATTGAGAGAAGCCGCTCGGAGCTCACGCAGATGATCAGAGATGGAGAAAAGACTGCAGTGAGTGGAGCTGAAGAACGACTGGAGCGACTGGAGCAGGAGATCAATGATCTGAGGAGGAGAAACGCTGAGCTGGAGCAGCTTTCACACACAGAAGATCACATCCATTTCCTCCAGGTGACACACAGGACAGTGGAAGAGCATGTGGAGCAGAGATTGTGTTTGTGTGTCTTCAGCTGCTGTTTCTGTTGTGTCTGTGTAGAGTTTGCAGTCTCTCTCTGTCCCTCCTGGATCTACAGACTCATCCAGCTTTATTAGCAGCTCTCCACTTGTTTTTGATGACATCGCTGAATCTGTGTCTCATCTGAGAGAGGATCTGGAGCATTTCGGCAAAAAGGAGATAAAGTTGATTTCTAGAAGAG[G/A]TCAGATTTATATTTCCTGACATGTTTCAGATGATTTTAAATGTATTTGTATTGTTTAACAATGTTTACTGTAAATCATCTGTTTGTCTCCACAGTGAGCAGCATTAGCAGGATTCCCGCTCCTGTACCAAAGACCCGTGAGCAGTTCCTCCAGTGTAAGTGACTCTGATCATACTGAACATTAAAGATTATAGTTATATATTGTGTTGGATTCCTTCATATGAGGCAGAGAGTCTCTGATGGCTGTAATGTGTTTTATTCTGGAACCAGCAGAAACAGTGAAAACTAGAAGTAAACACACAAATCAGCACAAAGCAGATTGATAATGAACTCTGACACCTTTACAGTTCATGATCAGGCGTTTGTGTACAGTGAACAGTAGATGAGCTGTGTAAAGTCACAGATAAACAATAATTGGCTCAGTTAACAGTTTCAAAACAAAACTTACACACCTCACTCCGCTCACCAAGGGCTGCTACAGTAGCTTTAACACGTGTAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31305
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 |
---|---|---|---|---|---|
ENSDART00000061172 | None | None | 199 | None | 2 |
ENSDART00000100987 | Nonsense | 473 | 557 | 6 | 6 |
ENSDART00000134662 | None | None | 506 | None | 6 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 60071325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 59148116 |
GRCz11 | 2 | 59245342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATCAGCAGGAAGGGTTCGGGTAATGAGTGTGGATTTGGACGCAATGAT[C/T]AGTCCTGGAGTTTGGAGTACTCTTCTCACAGTTTCTCATTCTATCATAAT
Long Flanking Sequence:
ACTTTCCTGATTCGCCTTTTCTATACTGTCCCAGTGTGTTCTGGTTTGGGGTTGAACATGTACTGAAACATTCATAGTTCTTGTTTCTTAATCAGCAAAAGTGCAAATAATATTAGAGTAAAGACATTCTGATGAACTGAAACAGATCAATAATAATACAGTCATGATTTCATTATTGTCACTCAGAAATTCATTGATATTTTTCCTGATTTTTATCTTCTTCAGATTCTCAACAGTTCACTTTGGATCCAAACACAGCGCATAACAGGCTGGTTCTGTCTGAAGGAAACACAGCGGTGGAATATAAACGTTCAGTCCAGCCGTATCCTGATCATCCAGACAGATTTGATGTTTGGCCTCAGGTGTTGTGTAGAGAGAGTGTGTGTGGACGCTCTTACTGGGAGCTGGAGTGGAGCAGAGCAAGTGTGTTAATATCAGTGTCATATAAGAGCATCAGCAGGAAGGGTTCGGGTAATGAGTGTGGATTTGGACGCAATGAT[C/T]AGTCCTGGAGTTTGGAGTACTCTTCTCACAGTTTCTCATTCTATCATAATAACATAAAGACTGATCTCCCTAAACCCTCCGTCAGCTCCTCTAGAATAGGAGTGTATGTGGATCACAGTGCAGGAACTCTGTCCTTCTACAGCGTCTCTGACACAACAATGAGCCTCATACACACACTCCACACCACATTCACACACACACTCTATCCTGGATTCTGGGTTTGTTCAAGACTGAAGCTCTGTGATCTGACAGTCTAGATTTCAAGATGTCTGAATCAGTCATCACTGCATTCTAGTTTATAATGGCCTGTTTCCTGCTAGACAGTTGATAGGGGGTTCTGGATTGGTTGCTAGGTGGTTGCTAAGGCGCTGCTAGATAGTTGTTAAGCGATTGCTAAGGTGTTGCTAGGCTATTGCTACGATGTTCTAATTGGTTGCTAAGGTGTTGCCAGTTGGTTGCTAAGGTGTTTATGGGCGGTTGCTTAGGTGTTGTTAGTTAAT
Associated Phenotype:
Not determined