ZMP
zgc:101777
Ensembl ID:
ZFIN ID:
Description:
Cdc42-interacting protein 4 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q5U3Q6]
Human Orthologue:
TRIP10
Human Description:
thyroid hormone receptor interactor 10 [Source:HGNC Symbol;Acc:12304]
Mouse Orthologue:
Trip10
Mouse Description:
thyroid hormone receptor interactor 10 Gene [Source:MGI Symbol;Acc:MGI:2146901]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33322 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10290 | Nonsense | Available for shipment | Available now |
sa8614 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12704 | Nonsense | Available for shipment | Available now |
sa20149 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33322
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040855 | Nonsense | 35 | 542 | 2 | 17 |
ENSDART00000124215 | Nonsense | 35 | 592 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 55326347)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 54220163 |
GRCz11 | 3 | 54474826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGTCTGGCCTGGACCTGGTGGACAAATACATGAAGTTTGTAAAGGAG[C/T]GAACAGACATCGAACAGAATTATGCCAAGCAGCTAAGGTAAGATCTCCTT
Long Flanking Sequence:
TTTCAGTGGTTCATCTGTAATCATACAAAGCTTTAAGATCACTTTAATGTGCCAAAAATAAAGTTAAAATGACTTGGTTCAGAATTAATAACAGAAGTAACATTTTTGTGTGAACTAACCCTTTAATGCAAAAATGCATTCCACATGAGTATTTTTTTTTAATTTTTTATAACGGTTTTATTTGTTACCACTGGCATATTACTATTATTGGCGCAAAACATTACATTAAAATGAATCCATAAAATCGCACAGCTCTATTTTAGCCCGCAATGGAAATCAATAAAAAGAAAATGTAATGCGTGTAATTTGCAGACATTGTAAGCACAGCCAACCCACTTCAATCAAATGGATCTAGATCTGTGTCTGACAGCTTAAATTGAGTGGATTGACATTAATTTGCAGGCTTTTATTTTATCTTACAGGACCAATATGACATTCTTGATAAGCACACACAGTCTGGCCTGGACCTGGTGGACAAATACATGAAGTTTGTAAAGGAG[C/T]GAACAGACATCGAACAGAATTATGCCAAGCAGCTAAGGTAAGATCTCCTTATATATCTAGGCAATCTGGTTAGTCTCTGTGTTGGTGTTTACATGTATCTGCATGCTTCCCGTGTGTGTTTATCCAGAGCTGTGGCTGATTGTGAAATATTTGGGTCTCATGACTTGTTTGGTGGCTGAGCTGAACTTGCTGACACCTCTGAGCTCTAGCATTGGCTTCGGCCCAGAGGATAAGCGTTTCCTCGTCTGCTCCACCAATCATTCATGACCAGGCCTTGATCTCTGCCAGTTTCGAGCTTTACCTCGGTCTTCCCTCTGTCCCGCTGTGAGAGGAAGTAGGAGCAGACGAGCATATGACTAAGGGGATGTGGATGGAGAGAGTGAAAGTGGAGAACAGCTTAGCGTTCGTTTTGATTTCTCTTCTTGGGAGAAAAAGAAGGAAATAAATGCTCTGGTTTTGAGTACTTGATATTGGAAACATCTGACATTGCGATATTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10290
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 |
---|---|---|---|---|---|
ENSDART00000040855 | Nonsense | 42 | 542 | 2 | 17 |
ENSDART00000124215 | Nonsense | 42 | 592 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 55326324)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 54220140 |
GRCz11 | 3 | 54474803 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAAATACATGAAGTTTGTAAAGGAGCGAACAGACATCGAACAGAATTA[T/A]GCCAAGCAGCTAAGGTAAGATCTCCTTATATNNNATSNNNTAGGCAATCTGGTTAG
Long Flanking Sequence:
TACAAAGCTTTAAGATCACTTTAATGTGCCAAAAATAAAGTTAAAATGACTTGGTTCAGAATTAATAACAGAAGTAACATTTTTGTGTGAACTAACCCTTTAATGCAAAAATGCATTCCACATGAGTATTTTTTTTTAATTTTTTATAACGGTTTTATTTGTTACCACTGGCATATTACTATTATTGGCGCAAAACATTACATTAAAATGAATCCATAAAATCGCACAGCTCTATTTTAGCCCGCAATGGAAATCAATAAAAAGAAAATGTAATGCGTGTAATTTGCAGACATTGTAAGCACAGCCAACCCACTTCAATCAAATGGATCTAGATCTGTGTCTGACAGCTTAAATTGAGTGGATTGACATTAATTTGCAGGCTTTTATTTTATCTTACAGGACCAATATGACATTCTTGATAAGCACACACAGTCTGGCCTGGACCTGGTGGACAAATACATGAAGTTTGTAAAGGAGCGAACAGACATCGAACAGAATTA[T/A]GCCAAGCAGCTAAGGTAAGATCTCCTTATATATCTAGGCAATCTGGTTAGTCTCTGTGTTGGTGTTTACATGTATCTGCATGCTTCCCGTGTGTGTTTATCCAGAGCTGTGGCTGATTGTGAAATATTTGGGTCTCATGACTTGTTTGGTGGCTGAGCTGAACTTGCTGACACCTCTGAGCTCTAGCATTGGCTTCGGCCCAGAGGATAAGCGTTTCCTCGTCTGCTCCACCAATCATTCATGACCAGGCCTTGATCTCTGCCAGTTTCGAGCTTTACCTCGGTCTTCCCTCTGTCCCGCTGTGAGAGGAAGTAGGAGCAGACGAGCATATGACTAAGGGGATGTGGATGGAGAGAGTGAAAGTGGAGAACAGCTTAGCGTTCGTTTTGATTTCTCTTCTTGGGAGAAAAAGAAGGAAATAAATGCTCTGGTTTTGAGTACTTGATATTGGAAACATCTGACATTGCGATATTTTGTTTTGCTGGAATATATATTGCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8614
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040855 | Nonsense | 217 | 542 | 8 | 17 |
ENSDART00000124215 | Nonsense | 217 | 592 | 8 | 15 |
ENSDART00000040855 | Nonsense | 217 | 542 | 8 | 17 |
ENSDART00000124215 | Nonsense | 217 | 592 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 55307193)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 54201009 |
GRCz11 | 3 | 54455672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGAGTGAATCTGAAACCTACATGTATGTTTGTTCATGACAGAAGTTG[C/T]AGGACATGRATGAAMGGCGTATTAAGAAGATGGCACAGGGCTACATCCTG
Long Flanking Sequence:
AGAGGGAGTGGAGAGAAGCAGAAAAGGCTGCTCAGTATGCGGACAAAACCGATCAGGATCTCAATGCCACCAAAGCCGATGTGGAAAAGGTATTAACGTTTCACCAAAAGGTTTTGCAGGTGTCACGCACAGCTGCCGTCTCATTTCCATCATATCCAAATGCTATTGTTGTTTCCTTGTTCCTCTTTATGTACGGGTGTCTTATTTCAATTTTGCCCTTTATGTCTGCATGTAACCACAGGCCAAACAGCAGGCGCATTTGCGAACACACATAGCAGAGGATTGTAAAAACGACTATGCTGTACAACTTCAGAAGTACAACAAAGAGCAAAGTCAGTTCTACTTCACGGACATGCCCCAGATTTTCAATGTAAGAAAATCTTGCTTCGGTCCTAACATGTTGAGACGCATCTTCTCCTATCGGATTGCTGTGGGAACCATCTTGCAGAATGCAGAGTGAATCTGAAACCTACATGTATGTTTGTTCATGACAGAAGTTG[C/T]AGGACATGGATGAAAGGCGTATTAAGAAGATGGCACAGGGCTACATCCTGTTTGCCGAAACGGAGCGTCACGTCATGCCCATCATCGGGAAATGCTTAGAGGGCATGACCAGAGCTGGCACGAATGTCAACGCGAGGAATGTGAGTCTTTTTTTAAGAAAAGCACTTCCATTTTTGGCTCTTGTTAAATCAGTAGTGTCCAATCCTTTTCCTGGTAGTTCACCAACCTGCAGAGTTCACCTCCAGTCCTAATTAAACAGACCTGAACAAGCGAATGAAGGTCTTGGGGATTACTAGAATTACAACCTGGCAAATGTGCTTGGGCAGATTGGAGCTAAACTCAGCAGGACAGTGGGCCTTCTGGAGCAGGATTGACACCCAAGGCTTTCAGAGAGTATTTGAACCCCCTTCAAACAGAATCCGACAATATCTAACACTTTTTTTTTATGTTATTCAGGACTCTATGGTTCTCATAGAGCAACATAAGTCTGGTTTTGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12704
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040855 | Nonsense | 217 | 542 | 8 | 17 |
ENSDART00000124215 | Nonsense | 217 | 592 | 8 | 15 |
ENSDART00000040855 | Nonsense | 217 | 542 | 8 | 17 |
ENSDART00000124215 | Nonsense | 217 | 592 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 55307193)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 54201009 |
GRCz11 | 3 | 54455672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGAGTGAATCTGAAACCTACATGTATGTTTGTTCATGACAGAAGTTG[C/A]AGGACATGRATGAAMGGCGTATTAAGAAGATGGCACAGGGCTACATCCTG
Long Flanking Sequence:
AGAGGGAGTGGAGAGAAGCAGAAAAGGCTGCTCAGTATGCGGACAAAACCGATCAGGATCTCAATGCCACCAAAGCCGATGTGGAAAAGGTATTAACGTTTCACCAAAAGGTTTTGCAGGTGTCACGCACAGCTGCCGTCTCATTTCCATCATATCCAAATGCTATTGTTGTTTCCTTGTTCCTCTTTATGTACGGGTGTCTTATTTCAATTTTGCCCTTTATGTCTGCATGTAACCACAGGCCAAACAGCAGGCGCATTTGCGAACACACATAGCAGAGGATTGTAAAAACGACTATGCTGTACAACTTCAGAAGTACAACAAAGAGCAAAGTCAGTTCTACTTCACGGACATGCCCCAGATTTTCAATGTAAGAAAATCTTGCTTCGGTCCTAACATGTTGAGACGCATCTTCTCCTATCGGATTGCTGTGGGAACCATCTTGCAGAATGCAGAGTGAATCTGAAACCTACATGTATGTTTGTTCATGACAGAAGTTG[C/A]AGGACATGGATGAAAGGCGTATTAAGAAGATGGCACAGGGCTACATCCTGTTTGCCGAAACGGAGCGTCACGTCATGCCCATCATCGGGAAATGCTTAGAGGGCATGACCAGAGCTGGCACGAATGTCAACGCGAGGAATGTGAGTCTTTTTTTAAGAAAAGCACTTCCATTTTTGGCTCTTGTTAAATCAGTAGTGTCCAATCCTTTTCCTGGTAGTTCACCAACCTGCAGAGTTCACCTCCAGTCCTAATTAAACAGACCTGAACAAGCGAATGAAGGTCTTGGGGATTACTAGAATTACAACCTGGCAAATGTGCTTGGGCAGATTGGAGCTAAACTCAGCAGGACAGTGGGCCTTCTGGAGCAGGATTGACACCCAAGGCTTTCAGAGAGTATTTGAACCCCCTTCAAACAGAATCCGACAATATCTAACACTTTTTTTTTATGTTATTCAGGACTCTATGGTTCTCATAGAGCAACATAAGTCTGGTTTTGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20149
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040855 | Essential Splice Site | 368 | 542 | 13 | 17 |
ENSDART00000124215 | Essential Splice Site | 418 | 592 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 3 (position 55292759)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 54186575 |
GRCz11 | 3 | 54441238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGATCGACGACATGAGCAAGGAGCTGCAGAAGGAAATGGATCAGAGG[T/C]GAGTCTTTCCTGCAGCGCTCCACCACAGGGTTCCCATGGGGTCAGGGAAT
Long Flanking Sequence:
GTAAAGCATATGAGTAAAATGCAGAAAGAAAAAAAAAACAGTGGACATATTTGAAATAACTCTCTATACTGTATGCTCATTACATATCCTTTTCAAAAACCTGGAACATTCCTTTGAGTAAACTGTTTATTTATCCCACATTTCTTCTCGACACTTCTGTCATCATAATTGAAAAACGTGTTGCCAAAATCTGAAAGCCAACAGCCTATTTATGTGGTTAAAATTACGCTGGTGGTGAAACGCTACATTACAGCTTCTTCTTCTTCAAACCTGATCTCTCACTGCTGGTCTCTGGGTCACGTCTGTCACCGATCGTGGTGTTGGAGGTCTGCCTGTGTATGTGTGTGTTTGTGAGACTCTCTGTGACAGTAGATTTGATTTCTTCTCAGCCGGTGGACACAGAAGGCTTCACTCATCTTCCTCCAGAGCAGCGTCGCAAACGCCTGCAGCAGAAGATCGACGACATGAGCAAGGAGCTGCAGAAGGAAATGGATCAGAGG[T/C]GAGTCTTTCCTGCAGCGCTCCACCACAGGGTTCCCATGGGGTCAGGGAATTTCTGGAATACCATTAAATATTAAAACGTCTATTCCAGATATTGTAAGTCAGGGGACTTCTCTGTCAAGCAATATCTGTTTTTTTTGGTTGTCATGTAAAATGTTCCTTCCCATTTATTAAAATGTTTTTTTTTTTTTTTTTGTAATTGTGTGGTTTTATTGCTTTTGTGCCATGCGCTTTAGACTTTGCGCCTAGATTGTTAAAATAGAAGCTCAAAATTTAAGAGGAGCTGCTTAACACAACAGCTTTACATTTTCCTTTTCATTATACTGTAGGTCACGGAAATTTTCTATATAGTATATAGACTATAGAATAGTCTGTAAATTTTACATTTGTCTTCGAGTGGGAACCCGGTCACCAATGCCAACTCCTTTTCAGTGAAACCGCTCTGGCGGTTTACTAAACCCTCCAGTTCTCTGAGGATCTATGGCGTTGAGTGCTACGAGTGA
Associated Phenotype:
Not determined