ZMP
ftr22
Ensembl ID:
ZFIN ID:
Description:
Novel protein with Zinc finger, C3HC4 type (RING finger) and B-box zinc finger domains [Source:UniPr
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 |
---|---|---|---|
sa25914 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5723 | Essential Splice Site | F2 line generated | Not yet available |
sa2070 | Essential Splice Site | F2 line generated | Not yet available |
sa19875 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25914
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098058 | None | None | 488 | None | 7 |
ENSDART00000126740 | Nonsense | 43 | 381 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 48018087)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48049751 |
GRCz11 | 2 | 47903915 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATCCCCTGTGGACACAGTTACTGTATGAGCTGCATTACTGACTGCTG[G/A]AATCAAGATGAGCAGAGGAGAGTTTACAGCTGCCCTCAGTGCAGACAGAC
Long Flanking Sequence:
GTTACGCTGCGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCCGATGTAGTGACCTGATTAATAAAGGAACTAAGCCGAAAAGAAAATGAATGAATGAAAGAATGATATAAACTGTGCAGAACACCAATAGTTCTTTAAAAATGTGATTTTGGTTCTGAAATGCACAGTGAAAATCATTATCTGGGTAAAAGTGTCTGCCATAAACAGCACAAATCAAACTAAACACTACAGCTTTTAGGTTTTTAAAATAATGAGCCTATGAGACTGACACCTAGTGGATGTTCTCTATAGTGGCCGGAAATATCTCCTTCAGAGAAAACGAAAGCGAAAGTGATTATTTCATTGAATCTGAGTGCACGTGTAGTGAAATGGCAGAATTCAATAGTAGGTGGATTCGGGACCGGTTCAGCTGTTCAGTGTGTCTGGATCTCCTGAAGGAGCCAGTGACCATCCCCTGTGGACACAGTTACTGTATGAGCTGCATTACTGACTGCTG[G/A]AATCAAGATGAGCAGAGGAGAGTTTACAGCTGCCCTCAGTGCAGACAGACCTTCACTCCAAGACCTGCTTTAAACAAGAATGTGATGCTGGCAGAAATGGTGGAGAAAGCAAAGGTGACAAGAAGAGCCCAAACAACTGACCCTGCTGTCAGTTACGCTGGAAGTGGAGATGTGGAGTGTGATGTTTGTAATGGGAGAAAACGCAAAGCTGTCAAATCCTGTCTGTTGTGTCTCGAATCTTACTGTGAAAGTCATTTTGAGTGTCATGAAGAATCGCGCTCAAAGAAACGACACAAAGTGACTGATGCCACTGGACGAATCCAGGAGATGATCTGCCCTAAACATGACCGACTGCTGGAGGTTTACTGTCGGACTGACCAGAAGTGTGTATGTTTAATGTGTGTGATGGATGAACATAAAAATCACGACACTGTTTCAGCTGAAGCAGAGAGAGCTGAGAAACAGGTATGCCATTTAAGTTCCATCCACACTGTAGAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5723
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098058 | Essential Splice Site | 17 | 488 | 2 | 7 |
ENSDART00000126740 | None | 86 | 381 | 1 | 5 |
ENSDART00000098058 | Essential Splice Site | 17 | 488 | 2 | 7 |
ENSDART00000126740 | None | 86 | 381 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 48017958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48049622 |
GRCz11 | 2 | 47903786 |
KASP Assay ID:
554-3389.1 (used for ordering genotyping assays)
KASP Sequence:
AAYGTGATGCTGGCAGAAATGGTGGAGAAAGCAAAGGTGACAAGAAGAGM[C/T]CAAACAACTGACCCTGCTGTCAGTTACGCTGGAMGTGGAGATGTGGAGTG
Long Flanking Sequence:
AATAGTTCTTTAAAAATGTGATTTTGGTTCTGAAATGCACAGTGAAAATCATTATCTGGGTAAAAGTGTCTGCCATAAACAGCACAAATCAAACTAAACACTACAGCTTTTAGGTTTTTAAAATAATGAGCCTATGAGACTGACACCTAGTGGATGTTCTCTATAGTGGCCGGAAATATCTCCTTCAGAGAAAACGAAAGCGAAAGTGATTATTTCATTGAATCTGAGTGCACGTGTAGTGAAATGGCAGAATTCAATAGTAGGTGGATTCGGGACCGGTTCAGCTGTTCAGTGTGTCTGGATCTCCTGAAGGAGCCAGTGACCATCCCCTGTGGACACAGTTACTGTATGAGCTGCATTACTGACTGCTGGAATCAAGATGAGCAGAGGAGAGTTTACAGCTGCCCTCAGTGCAGACAGACCTTCACTCCAAGACCTGCTTTAAACAAGAATGTGATGCTGGCAGAAATGGTGGAGAAAGCAAAGGTGACAAGAAGAGC[C/T]CAAACAACTGACCCTGCTGTCAGTTACGCTGGAAGTGGAGATGTGGAGTGTGATGTTTGTAATGGGAGAAAACGCAAAGCTGTCAAATCCTGTCTGTTGTGTCTCGAATCTTACTGTGAAAGTCATTTTGAGTGTCATGAAGAATCGCGCTCAAAGAAACGACACAAAGTGACTGATGCCACTGGACGAATCCAGGAGATGATCTGCCCTAAACATGACCGACTGCTGGAGGTTTACTGTCGGACTGACCAGAAGTGTGTATGTTTAATGTGTGTGATGGATGAACATAAAAATCACGACACTGTTTCAGCTGAAGCAGAGAGAGCTGAGAAACAGGTATGCCATTTAAGTTCCATCCACACTGTAGAACCCAAAAAGTGAAGGTAACTCAAACCATTTGAGGAAACCGATTGCAACAAACTATTTAAGTCCAAAAACTAATCCTAATGAGTACTGTGAACTTGCTCCATTTGAGTAAAAGAAGCAATTTGAGCACTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2070
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098058 | Essential Splice Site | 17 | 488 | 2 | 7 |
ENSDART00000126740 | None | 86 | 381 | 1 | 5 |
ENSDART00000098058 | Essential Splice Site | 17 | 488 | 2 | 7 |
ENSDART00000126740 | None | 86 | 381 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 48017958)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48049622 |
GRCz11 | 2 | 47903786 |
KASP Assay ID:
554-3389.1 (used for ordering genotyping assays)
KASP Sequence:
AAYGTGATGCTGGCAGAAATGGTGGAGAAAGCAAAGGTGACAAGAAGAGC[C/T]CAAACAACTGACCCTGCTGTCAGTTACGCTGGAAGTGGAGATGTGGAGTG
Long Flanking Sequence:
AATAGTTCTTTAAAAATGTGATTTTGGTTCTGAAATGCACAGTGAAAATCATTATCTGGGTAAAAGTGTCTGCCATAAACAGCACAAATCAAACTAAACACTACAGCTTTTAGGTTTTTAAAATAATGAGCCTATGAGACTGACACCTAGTGGATGTTCTCTATAGTGGCCGGAAATATCTCCTTCAGAGAAAACGAAAGCGAAAGTGATTATTTCATTGAATCTGAGTGCACGTGTAGTGAAATGGCAGAATTCAATAGTAGGTGGATTCGGGACCGGTTCAGCTGTTCAGTGTGTCTGGATCTCCTGAAGGAGCCAGTGACCATCCCCTGTGGACACAGTTACTGTATGAGCTGCATTACTGACTGCTGGAATCAAGATGAGCAGAGGAGAGTTTACAGCTGCCCTCAGTGCAGACAGACCTTCACTCCAAGACCTGCTTTAAACAAGAATGTGATGCTGGCAGAAATGGTGGAGAAAGCAAAGGTGACAAGAAGAGC[C/T]CAAACAACTGACCCTGCTGTCAGTTACGCTGGAAGTGGAGATGTGGAGTGTGATGTTTGTAATGGGAGAAAACGCAAAGCTGTCAAATCCTGTCTGTTGTGTCTCGAATCTTACTGTGAAAGTCATTTTGAGTGTCATGAAGAATCGCGCTCAAAGAAACGACACAAAGTGACTGATGCCACTGGACGAATCCAGGAGATGATCTGCCCTAAACATGACCGACTGCTGGAGGTTTACTGTCGGACTGACCAGAAGTGTGTATGTTTAATGTGTGTGATGGATGAACATAAAAATCACGACACTGTTTCAGCTGAAGCAGAGAGAGCTGAGAAACAGGTATGCCATTTAAGTTCCATCCACACTGTAGAACCCAAAAAGTGAAGGTAACTCAAACCATTTGAGGAAACCGATTGCAACAAACTATTTAAGTCCAAAAACTAATCCTAATGAGTACTGTGAACTTGCTCCATTTGAGTAAAAGAAGCAATTTGAGCACTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19875
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 |
---|---|---|---|---|---|
ENSDART00000098058 | Nonsense | 311 | 488 | 6 | 7 |
ENSDART00000126740 | Nonsense | 381 | 381 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 48014681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 48046345 |
GRCz11 | 2 | 47900509 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATCAACATTATTTCCAATAATGAACCCAAGACGAGGGAGGAGTTTCTA[C/T]AATGTAAGTCAATGTGGACACACACAAACACACTGGTTTGGGATCCCGTT
Long Flanking Sequence:
TGGAATTTAATGCAATTTTTTGGATCTTTGATATTTCTGTATTTTTATTCTCTCCTAGAGTTTCCAGTCTCTCTCTGAATCTCTGAAATCAGCAGCCGTCCGCAGCCCAACCGTCAGTTCTGCCCATCCTTATGAAGATGTGAGAAAATCTGTCTCTAATATGAAACAAAAACTGGAGCAGCTCTGCAAACAGGCAACAGAGCAGATATCTGGTCACGGTGAGGTGAAATAAAAGTTACTTTCAGAAAAACCTACATATTTTAACATTTATGTTAAAAAACAAACACAAAACCGTACTAATGAGAAAAAATAATTCCTGTTTGATTTACTTTTTTAATTAATACTTTTTAAAAACTAAAAATAACTTGTTCATTCCGCTGTGATCCCTGATAAACCAGGGAATAAGCTGAAGTGAGTATTCTCAATATATGTCTTGTTTTTTAGTAACATACATCAACATTATTTCCAATAATGAACCCAAGACGAGGGAGGAGTTTCTA[C/T]AATGTAAGTCAATGTGGACACACACAAACACACTGGTTTGGGATCCCGTTGGGGACTCTTTATTCAGTATATAATGATATTTCTTACTATACAGACTGTATTTTTTATCCCAAAAAAAAACATCCCCTACAGGAAACAGGCTATATATATTTTTTAGAAAATTATGTTTAAAGGTAAAAAATATAATGACTTCATTTAGGCATGTGGACATGGTCAAGACAATCTGCTGCAGTTCAAATCGAGCAGCAGAATAGGGAATAAAGTTGATTTAAGTGACTTTAAACGTGGCATGGTTGTTGGTGCCAGACTGGCTGGTCTGAGTATTTCAGAAACTGCTGATCTACTGGAATGTTCACGCACAACCAACTCTAGGGTTTACAGAGAATGCTCCTTAAAAGAGAAAATATCCAGTGAGCGGCAGTTCTGTGGGCGCAAATGCCTTGTTGATGCCCGAGGTCAGAGAATGGCCAGACTGGTTCCAGCTGATAGAAAGGCAACAG
Associated Phenotype:
Not determined