ZMP
si:ch211-208c6.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RHY6]
Human Orthologue:
TRIM66
Human Description:
tripartite motif-containing 66 [Source:HGNC Symbol;Acc:29005]
Mouse Orthologue:
Trim66
Mouse Description:
tripartite motif-containing 66 Gene [Source:MGI Symbol;Acc:MGI:2152406]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31574 | Essential Splice Site | Available for shipment | Available now |
sa13594 | Essential Splice Site | Available for shipment | Available now |
sa45278 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18194 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31574
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076510 | Essential Splice Site | 534 | 1119 | 12 | 26 |
ENSDART00000132316 | None | None | 53 | None | 3 |
ENSDART00000132784 | None | None | 195 | None | 5 |
ENSDART00000137799 | None | None | 416 | None | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 29772817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28165340 |
GRCz11 | 7 | 28436533 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGCTGGTTCAGGGCCAGGGAGGCGATGGTCGGAGTTGTCCAGGTTTGA[A/T]GAGGGCGAGCAGGTCTCAAAGCAGTGCGGATGCACCCAGAGGACCTCGTA
Long Flanking Sequence:
AGGGCCCTTCGTGGAGCGCACATTCATCGGGCCGCCGCTTCAGACTCTGACATTTGTCGTGCCAGCGAAGGATGCAGTCGCTTGGGCTTGTCTCCAACTTCTCGCATTACTGAAATCATGACAAGAGAAGAGAAAGTCTAATCTCTGATGTGTTAATGCCGCTTATTCAAAGAAGCCTTCCGTGGCCCCAGAAGTGGGATTTACATATGATAATTGGCGCTGTAACTAAGTGGTATATTATCATCAGGAGAGTTATCGTGTTGATAGATTGTCGCGATTGTTGGTCCTTGTGCTGCAAAGCAGCGTTGTCACATTGCTCAAGGTTGTTGTTCGTCACCTCTGTTGTCACTGTTGCTATGGCTGTGGTTTGCCGCATGTGCTGTCAGATTTACTTTTAGCCTAATGAGAGTTTGGCTCTCTTGTGTAGAGATCCTCAGAGCTGGAGATGTTCGCGCTGGTTCAGGGCCAGGGAGGCGATGGTCGGAGTTGTCCAGGTTTGA[A/T]GAGGGCGAGCAGGTCTCAAAGCAGTGCGGATGCACCCAGAGGACCTCGTAAAAGGCTCTGTAAAGACAGGTCGATCAAGGATGCTCACGGCCTGGCAACAGCGACTGGGGACCAGGGATGTACAACGCAGCAGGTGAATATTTTCTTTTTCCAGAGCGTGATGAGACAAGTGCGCACTGTTAAATATACATGGTGGTTTTTGTAATGATATCATGTTTCTTCAAGGAGTGATTTTAGATCAGAGTTCTTCAAATAACTTGAACAATGTTTTTTTTTTTTCTTCAGTGTTAAGAAGCTTTTGTGGAATGGAAATATCCTAAGTCCTAAAATTAATGGCAATAATAGACTTTGTTTTTTAGATTGTAGGCCTATTAGGGAGTAGTTCTTAACCCTCCAAGAGAGGATAGAGATGTTTTGAGAGGTTTTCCATGTACACCTTAAATCAAAAATAAGTAAATAAATAAATAATATAAATAATAATAATCAGAGGCTTTTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13594
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076510 | Essential Splice Site | 588 | 1119 | 14 | 26 |
ENSDART00000132316 | None | None | 53 | None | 3 |
ENSDART00000132784 | None | None | 195 | None | 5 |
ENSDART00000137799 | None | None | 416 | None | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 29772564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28165087 |
GRCz11 | 7 | 28436280 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAYGATATCATGTTTCTTCAAGGAGTGATTTTAGATCAGAGTTCTTYAA[A/G]TAACTTGAACAATGTTTTTTTTTTTTCTTCAGTGTTAAGAAGCTTTTGTG
Long Flanking Sequence:
TATCGTGTTGATAGATTGTCGCGATTGTTGGTCCTTGTGCTGCAAAGCAGCGTTGTCACATTGCTCAAGGTTGTTGTTCGTCACCTCTGTTGTCACTGTTGCTATGGCTGTGGTTTGCCGCATGTGCTGTCAGATTTACTTTTAGCCTAATGAGAGTTTGGCTCTCTTGTGTAGAGATCCTCAGAGCTGGAGATGTTCGCGCTGGTTCAGGGCCAGGGAGGCGATGGTCGGAGTTGTCCAGGTTTGAAGAGGGCGAGCAGGTCTCAAAGCAGTGCGGATGCACCCAGAGGACCTCGTAAAAGGCTCTGTAAAGACAGGTCGATCAAGGATGCTCACGGCCTGGCAACAGCGACTGGGGACCAGGGATGTACAACGCAGCAGGTGAATATTTTCTTTTTCCAGAGCGTGATGAGACAAGTGCGCACTGTTAAATATACATGGTGGTTTTTGTAATGATATCATGTTTCTTCAAGGAGTGATTTTAGATCAGAGTTCTTCAA[A/G]TAACTTGAACAATGTTTTTTTTTTTTCTTCAGTGTTAAGAAGCTTTTGTGGAATGGAAATATCCTAAGTCCTAAAATTAATGGCAATAATAGACTTTGTTTTTTAGATTGTAGGCCTATTAGGGAGTAGTTCTTAACCCTCCAAGAGAGGATAGAGATGTTTTGAGAGGTTTTCCATGTACACCTTAAATCAAAAATAAGTAAATAAATAAATAATATAAATAATAATAATCAGAGGCTTTTTTTTATTTATTACTATTATGCCTGGTGTTTTGTATGTTGGTGTGCACGCTCACATTGGTGCCCTGTGAAGCATGAATGAAAACAGTACTCCTGTGTGTCTGCACTGAGCAGTGCATGTGAATGAATCTGCATTTTAAACGGGTCGGGTTAACCAGTGATTTAAACACCAATTCATAAAAACAGCCATTTACTTTAACAAATCCTGAACAAATCAGCCAGTTTAAGAAAATAATAATGATATTTTAAGTAGTTCTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45278
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 |
---|---|---|---|---|---|
ENSDART00000076510 | Essential Splice Site | 615 | 1119 | 16 | 26 |
ENSDART00000132316 | None | None | 53 | None | 3 |
ENSDART00000132784 | None | None | 195 | None | 5 |
ENSDART00000137799 | None | None | 416 | None | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 29770670)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28163193 |
GRCz11 | 7 | 28434386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCGCTTTTCATCATGATTCCTTTTCAAGTCCATTTCAAACCCCCCA[G/T]CCTCTGTCACAACTGTGAAAGACCAGTTCAGTGTTTACAGCTCTCTGACT
Long Flanking Sequence:
AGTCTACAGGCATTTCCCATTATTTCTCTGTTGCAATCCGGATATCACAATAATTAAGGGACATTTGAAGGGACATTTTTTGGCCCCATGATGAAAACGGGTTAAAAAATCACACAGGATGAAGTATTTTGAAAATAGGGTGGGTAGTGTGACAGAATATACAATTTGTACAGTATAAAAACCTGTACAATGTTACTTCTATGGGAAGTCCCCATAAAGAAAGCTGTTCAAGTGTGCATGTGCGTGTGCTTATGTGGTTAACTATAATAACCCTTGTGGATTATATAGGGCCTATTAGAAGGTTTAAACCACCAGTAGTCATGGCAACAAGGATGCCTGTGAACCTTTTTGGTAAACCATACTTTTAAGAAAGTATGAATAGTGCATTGATGTGAATAATTCACTACATTAATATTCATGGTAATTGACATTGATGAAATGCTCTTGACCTGAAGCGCTTTTCATCATGATTCCTTTTCAAGTCCATTTCAAACCCCCCA[G/T]CCTCTGTCACAACTGTGAAAGACCAGTTCAGTGTTTACAGCTCTCTGACTCTCCTTTTAAGTGCACAAATCCGAAGATGTACATCAAAAGAGAGATAACTGTTGTCTAGGAAACAGTTCCTTTAACCTCTTTCTAAGAACAAATGAGATGCAGCAGCCCACAGAACTGATTGTGTTCAGCTAAACAAGTTCACCTGCGTTCATATTCTCTGATTTAGTCTGCATGCTGCTGTTGTCACGTCACTGGATTCATTAATCGTCAATAAAGAGGCAGTGTTTCAAAACCTTGATGTTGCTGTTCTCTCAACTGTATCTCAGCAGGCCTGTGCACAGCTCCATGCTTCAGAGATGTTCCCAAGCAGTCACGTCGCATCTTCACTGACCACCTACAAATCCGAACCAGGTGATAAAGAAAGTCTGTCATGTTTATCTTTCAATGTACATACAATGTATGTACATACACTCAGGTGTCAAACTAGAGGGCCGCAGCCCAGCACAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18194
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 |
---|---|---|---|---|---|
ENSDART00000076510 | Nonsense | 761 | 1119 | 21 | 26 |
ENSDART00000132316 | None | None | 53 | None | 3 |
ENSDART00000132784 | None | None | 195 | None | 5 |
ENSDART00000137799 | Nonsense | 52 | 416 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 7 (position 29766932)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28159455 |
GRCz11 | 7 | 28430648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCATAGCTGTGAATCATCTGGCTCCCTTGAGGAMTCTCAGCCTCCTGTG[C/T]AAGAATTTTGCAATATAAACCAAGAGTCTGATGCRCTATCTGTTTCCAAA
Long Flanking Sequence:
ATTTATTTACCTTTAGCCCACAATCTAGTTTGTTTTTTGGCCCTTCATAAGAAAAAGTTGGGGCACCCTTGTCTTAGTAGTTAATTTTTTATTTCTGTTATTGTTTTCCACAGTGACAAAGAATCCTCGGATGGTTCCAAAGTTCCAGTTGTGTGTCTTCAGCGACTCAAGATCCTCGTATCACGACATCCACCACAGAACCATCAGAGCACAGATCCATCTTCTCAATCTGGCCTTAAACCTGAAGAAACTGTCTTGAAGGTGCTAGAAAGAGAGGCCGCTTCTCAGGTATCACTTTAACATTGATAAAATGCTTCTCTAGAAAGTTTTACATCACCCCACAGTTCATAATAATCTTTTTAATGTCCGTCAAGGGAACTTTGGATAAGGAGTCAGTTCAGGCAGAGGACAATATGTCGCCCACAGAAACGCAGCTATCACCGCAACATCTGCATAGCTGTGAATCATCTGGCTCCCTTGAGGACTCTCAGCCTCCTGTG[C/T]AAGAATTTTGCAATATAAACCAAGAGTCTGATGCGCTATCTGTTTCCAAAGATGCTGTCTTACAACCTGACGCTGAGGAGATACACTCGGATGACTCCCCATCTGATCTCATATCAGCGCCAGGCTCTGATTTCCAAACAGAATCTACAAGAGAAGCAGATGTGGAATCAGAGCTCCCTCAGGAATCTGAACTGCAAGTCGAATCTGAATCGGATGTGATTTCAGAACAGCTTCCTGAATCGGTGCTCTCCGAACAGGAAATGGAATCAGATCCAGATTCCACAGCCGAAGTGAATCTGAATCTTGAACCAGAGTGTGAATGGGAAACGGAGCAACCAGTTTCTCCACAATCTTCTGGGTTTGAGAATGTACCAGAACCTGTTGTTGAACATCAGCCTTCAGAAGAAAGTCCGGAGATTGAGAACGAGGATTTCTGTGCAGTCTGTCTAATCGGAGGAGATCTTCTTTGCTGTGACCGTTGCCCGAAGGTCTTCCACTTG
Associated Phenotype:
Not determined