ZMP
ftr12
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0S539]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44544 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19847 | Nonsense | Available for shipment | Available now |
sa15836 | Nonsense | Available for shipment | Available now |
sa39910 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44544
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056161 | Nonsense | 119 | 547 | 1 | 6 |
ENSDART00000143419 | Nonsense | 119 | 291 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 42817469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42866933 |
GRCz11 | 2 | 42716351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGTTTGTACTGGAGATAAAAATAAAGCCATCAAGTCGTGTCTGGTGTG[T/A]CTGAACTCTTACTGCCAAAATCATCTTGAACAACACGAGAGTTTCTTCAG
Long Flanking Sequence:
ACATTAGTCTTAACACCACTCCTACCTTCAATGTGATTTATTACTTTATTTTTTGACTTCCTGCTCAGTGTTGAGGAGAATTCAATGGCTTTGTGTTTCTATTTCTATGGTCTAAGCTATTTTTGAGCTTCTGTATTTAGTAAAATGGCAGAATCCACACTTTCCTTGGCTCAGGATCAGTTCAACTGTTCCCTCTGTTTGGAGCTGCTAAAGGATTCAGTGGCCATTCCCTGTGGACACAGTTACTGTATGAGCTGTATTTCAGACTGCTGGGATCAGGATGAGCAGAAGGGAGTCTACAGCTGCCCTCAGTGCAGACAGACCTTCACTCCAAGACCTGCTTTAGGGAAAAACACCATGCTGACTGAAGTTGTGGAGAAACTCAAGAAGACCAAACTACAAGCTGCTCGTCCTGCTCAGTGTTACTCTGAATCTGCAGATGTGGAGTGTGGTGTTTGTACTGGAGATAAAAATAAAGCCATCAAGTCGTGTCTGGTGTG[T/A]CTGAACTCTTACTGCCAAAATCATCTTGAACAACACGAGAGTTTCTTCAGAGGTAAAAGACACAATCTGATGGACGCCACTGGACGACTGCAGGAGATGATCTGCCCTCAACATGAGAAACTACTGGAGTTCTTTTGCCGTACTGACCAGCGCTGTGTTTGTTATCTGTGTACAATGGATAAACACAAAAACCACAACACTGTATCAGCTACAGCAGAGAGGACTGACAAACAGGTATGAAATTATGCAACATAATGCGTCTTCATGTGTAATATCTACATATTTAAAGTTTGTATGAACAATTCTTACTAGTGATAAATGTAGTTTTTCTGTTAACGAATCAGTTACATATTATGCACTCTATAGAGTCAGTTGGCTGAGATGCAAAAAACAACCCATCAGCGAATCGAGGAGAAACAAAAGGAGTGTGTGGAGCTGAGAGAGGCTGTTGAGTCTTACAAGGTGAGTTTTGAGCAGAAGATCACCTGTTGGCTGCTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19847
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056161 | Nonsense | 136 | 547 | 1 | 6 |
ENSDART00000143419 | Nonsense | 136 | 291 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 42817518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42866982 |
GRCz11 | 2 | 42716400 |
KASP Assay ID:
2259-2505.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGAACTCTTACTGCCAAAATCATCTTGAACAACACGAGAGTTTCTTC[A/T]GAGGTAAAAGACACAATCTGATGGACGCCACTGGACGACTGCAGGAGATG
Long Flanking Sequence:
TTTTTGACTTCCTGCTCAGTGTTGAGGAGAATTCAATGGCTTTGTGTTTCTATTTCTATGGTCTAAGCTATTTTTGAGCTTCTGTATTTAGTAAAATGGCAGAATCCACACTTTCCTTGGCTCAGGATCAGTTCAACTGTTCCCTCTGTTTGGAGCTGCTAAAGGATTCAGTGGCCATTCCCTGTGGACACAGTTACTGTATGAGCTGTATTTCAGACTGCTGGGATCAGGATGAGCAGAAGGGAGTCTACAGCTGCCCTCAGTGCAGACAGACCTTCACTCCAAGACCTGCTTTAGGGAAAAACACCATGCTGACTGAAGTTGTGGAGAAACTCAAGAAGACCAAACTACAAGCTGCTCGTCCTGCTCAGTGTTACTCTGAATCTGCAGATGTGGAGTGTGGTGTTTGTACTGGAGATAAAAATAAAGCCATCAAGTCGTGTCTGGTGTGTCTGAACTCTTACTGCCAAAATCATCTTGAACAACACGAGAGTTTCTTC[A/T]GAGGTAAAAGACACAATCTGATGGACGCCACTGGACGACTGCAGGAGATGATCTGCCCTCAACATGAGAAACTACTGGAGTTCTTTTGCCGTACTGACCAGCGCTGTGTTTGTTATCTGTGTACAATGGATAAACACAAAAACCACAACACTGTATCAGCTACAGCAGAGAGGACTGACAAACAGGTATGAAATTATGCAACATAATGCGTCTTCATGTGTAATATCTACATATTTAAAGTTTGTATGAACAATTCTTACTAGTGATAAATGTAGTTTTTCTGTTAACGAATCAGTTACATATTATGCACTCTATAGAGTCAGTTGGCTGAGATGCAAAAAACAACCCATCAGCGAATCGAGGAGAAACAAAAGGAGTGTGTGGAGCTGAGAGAGGCTGTTGAGTCTTACAAGGTGAGTTTTGAGCAGAAGATCACCTGTTGGCTGCTGGAAGAGCTGATTGAGACTCAGTTAGCACTGTCCTGCAGTCAGTCAGTGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15836
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056161 | Nonsense | 214 | 547 | 2 | 6 |
ENSDART00000143419 | Nonsense | 214 | 291 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 42817884)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42867348 |
GRCz11 | 2 | 42716766 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGTCAGTTGGCTGAGATGCNARAAAACAACCCATCAGCRAATCGAGGRG[A/T]AACAAAAGGAGTGTGWGGAGCTGAGAGAGGCTGTTGAGTCTYACAAGGTG
Long Flanking Sequence:
CTCAGTGTTACTCTGAATCTGCAGATGTGGAGTGTGGTGTTTGTACTGGAGATAAAAATAAAGCCATCAAGTCGTGTCTGGTGTGTCTGAACTCTTACTGCCAAAATCATCTTGAACAACACGAGAGTTTCTTCAGAGGTAAAAGACACAATCTGATGGACGCCACTGGACGACTGCAGGAGATGATCTGCCCTCAACATGAGAAACTACTGGAGTTCTTTTGCCGTACTGACCAGCGCTGTGTTTGTTATCTGTGTACAATGGATAAACACAAAAACCACAACACTGTATCAGCTACAGCAGAGAGGACTGACAAACAGGTATGAAATTATGCAACATAATGCGTCTTCATGTGTAATATCTACATATTTAAAGTTTGTATGAACAATTCTTACTAGTGATAAATGTAGTTTTTCTGTTAACGAATCAGTTACATATTATGCACTCTATAGAGTCAGTTGGCTGAGATGCAAAAAACAACCCATCAGCGAATCGAGGAG[A/T]AACAAAAGGAGTGTGTGGAGCTGAGAGAGGCTGTTGAGTCTTACAAGGTGAGTTTTGAGCAGAAGATCACCTGTTGGCTGCTGGAAGAGCTGATTGAGACTCAGTTAGCACTGTCCTGCAGTCAGTCAGTGGGGAGCCCAGTGCTGGAGCACTTCCAGTCCTACTGAAGCCCCTGTGGGGAACAGGCTGTGGGAGGCAGCAGTAAGAGCTGAGTGAATGACTGATTCTGCTGCTTCTCTCTCTGTGTGTCCTAACAGTGCTCTGCACAGGCAGCAGTGGAGGACACTGAGAGGATCTTTACTGAGCTCATCCGCTTCATTGAGAGAAACCGCTCTGGGTTGACACAGCTGATCAGAGATCAGGAAAAGGCTGCAGTGAGTGGAGCTGAAGGACGACTGGAGCGACTCGAACAGGAGATTGATGATCTGAGGAGGAGAGACGCTGAGCTGGAGCAGCTTTCACACACAGACCATCACATTCATTTCCTCCAGGTAACACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39910
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056161 | Essential Splice Site | 380 | 547 | 5 | 6 |
ENSDART00000143419 | None | None | 291 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 42819336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42868800 |
GRCz11 | 2 | 42718218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACATAATTCCCACCTCTGAGCCAGAGACAATTGAGCAGTTCCAACAAT[G/T]TAAGTCTTTATCTCGAAATATAGAAACCTACATGCAATAGCTCTGGTGTT
Long Flanking Sequence:
AGTCCAAAGACATGCGGAATAGGTGAATTGGGTAAGCTAAATTGTCCATAGTGTATGTGTGTGAATAAGAGTGTATGGGTGTTTCCAGTGATGGGTTGCAGCTGGAAGGGCATCTGCTGTGTAAAACATATGCTGGATATGTTGGTGGTTTGTTCTGCTATGACAACCCACTAAGCGACTAAGCCGAAAATGAATAATTGAATATGATGTCATATCAAAGGCTTCAAAAGTACTGTATATGATTCCTAATTTTCGTAATAATCACAAATAATTGTATTGCTTTGAAAATAAATATTATGCATGCCACTGAAAGTATAACAAAGTACTGTATAGCCATTGTAGTCAAATTAAAATTAATCTTTGTGAAGTATTCAGGAAAATAATAATAATAATACATTATTTTAAAATATTGACTATTGAATGTTGTTTCTCTTCCATAGTTACAAACATAAACATAATTCCCACCTCTGAGCCAGAGACAATTGAGCAGTTCCAACAAT[G/T]TAAGTCTTTATCTCGAAATATAGAAACCTACATGCAATAGCTCTGGTGTTTAATTTGATGATTAAAAGTCAGATGGATATTATGCGTTTTATCTTCACCAGATTCCCGTCAGTTCACTTTGGATCCAAACACAGTGAATAATTACCTGGTGCTATCTGAAGATAACAGAGTAATTGATGTCATTCGAACATACCAGCAGTATCCTGATCATCCGGACAGATTTAATGCTTTTCTTCAGGTGTTGTGTAGAGAGAGTTTGTGTGGACGTTGTTACTGGGAGGTGGAGTGGAGTGGTTGGGTTGGTATATCAGTGTCGTATAAGAGCATCAGCAGGAAAGGACGGAGAACAGATTGTGAGTTTGGATGTAATGATCAGTCATGGAGTTTGTACTGCTCTGACTCCAGATGCTCGTTCTGGCACAATAACCAACCGACCAAACTGCCAGTAGTGTCCAGCTCGTCAAGAATAGGAGTGTATGTGGATCACAGTGCAGGAATTC
Associated Phenotype:
Not determined