ZMP
quo
Ensembl ID:
ZFIN ID:
Description:
quattro [Source:RefSeq peptide;Acc:NP_001004109]
Human Orthologue:
KIAA1755
Human Description:
KIAA1755 [Source:HGNC Symbol;Acc:29372]
Mouse Orthologue:
D630003M21Rik
Mouse Description:
RIKEN cDNA D630003M21 gene Gene [Source:MGI Symbol;Acc:MGI:3606579]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33788 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10332 | Essential Splice Site | Available for shipment | Available now |
sa26650 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17343 | Nonsense | Available for shipment | Available now |
sa7021 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33788
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109679 | Essential Splice Site | 68 | 1988 | 3 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 1886503)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 1916738 |
GRCz11 | 6 | 2050404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGAAATTATCTGCGAATCAACAAACTAGCTCTGTCTTTCTTGTTCTCT[A/T]GGCTGCATATTCCGATGTCCTGTTCCAGTGTGAGGGTTGGCCATTGTGTT
Long Flanking Sequence:
AGTTAACTACACTCGTTTCATTTGATAAAGCTGACTGTTGGGTTTTACAGTGTGGTGTTTTTTGGGGGACACCAGGACAGACAGGTCATGGACTGTATACAAAATGCACATGTACAAGAACACTGTGAATGATAAAAGAGCGAGGCAGTTATGCATTTTCATGTTTGGGTGAACTAAGCCTTTAAAGGATAAAATATGTTAGTATTCGAGGCCAGATGAAAGCAGTTTCCTGTGCAGGCATTTCGTCCATGTGGACTTTTATGGCACAGATCCCACATGCTACTTATCCTTGTCCACTCAGCACAAGATTGCTTTGTTTTATCTTCAGAAAGAACAAAGGCCTTGCAGGGCAGCTTCTTCTGAAGGGGATTCAAGAATGCTTGCGTGCAAGCCAATAAAAGGCATCAAGACCCAAACTATTAAATATCTGGTGGTCATAACATGTGTCAATCTGAAATTATCTGCGAATCAACAAACTAGCTCTGTCTTTCTTGTTCTCT[A/T]GGCTGCATATTCCGATGTCCTGTTCCAGTGTGAGGGTTGGCCATTGTGTTTGAGTGACCGTGTGGTGATCCAACTTGCCGCCATCAATCCTTTGCTACTCAGACCTGGAGATTTCTACTTGCAGGTGGAACCTTTCGGAGAACAGTCGGCCAGAATTGTCCTCAAAAGTCTTCTTGTGCAGGAAGACCTCCTGGGGCAGGAGAATCTGATCTTGCAAGCAGGTTCCAGGGTGCTGGAGTGTCCTACAATTGAAGAGACACCAATCCTCGAGACCTCTTATCCATGCATATTCACAGAGTCCTGGCTAAGGGAAATAAATGAGGGGCGTCAAGGAAATCGTCTTTCTAGATGTGTACTGTCCTCTGACAAGGGGGTTGTGAAGGTACCTTGGACCGAAGTTGCCAACCCAGAATTCCTTGACAGGCCAAAATCGAACGTCTGGCCTGATTCAAAGCCATGTTCAACCGCAACAATCCGCGTAAGAGATCTTAATACTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10332
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 |
---|---|---|---|---|---|
ENSDART00000109679 | Essential Splice Site | 1134 | 1988 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 1904276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 1934511 |
GRCz11 | 6 | 2068177 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWAAACATTCKAAATATWTTCAGTCTAAAWTGACTTCTTCTTTGTCCCCC[A/T]GGCCTCGTCTCTTGTGAAGGAGTGTAYGGAGTATTTAGATCACATGAAGT
Long Flanking Sequence:
TTTATTTTATTATTTTTTTTTTATTTAGCTTTATTTTACTTACCTTATTTCTAAGGAATGAAATTCCTTTAATTTAATTTCATTTAATTTCATTTCATTATTATTGTTTTTTTACTCTATTTTTTCCCAGAAATCTTAAAAAACATTATATATTATATATTATAAACACTAAAGACAGCAGTAATGCTGCAGAAAATTCACCTTTACACCTTTTTTCAAAGGAATAAAATTTACTTTAAATCTAACTTTTTTATTTTATTTTATTTTATTTTATTATAATAACCAGAAAAGACTTAATTTAAAAACAACATTATACTACAGTGCTCTTGAATGCTTGAGTCTTATGACAAGCATTCATTTAAAAGTGTAAAGTGTACAACTAAAATATCTCCAGTCATGTATACATTACCTAAAAACAGTCCAAACGTTATATAAAACAACCAAATATAAATAAACATTCTAAATATATTCAGTCTAAAATGACTTCTTCTTTGTCCCCC[A/T]GGCCTCGTCTCTTGTGAAGGAGTGTATGGAGTATTTAGATCACATGAAGTCCTCAAACTCCCCGATGAGCGTCTGCTGGAGTTCCCTGCATGCATTTGAGCAGCGTTTTCAACATTTCTCACCCCAGCACTTTCAGGACAGGAGCGCCGCCCTGCTGGAGAGGCTTCCGGATGGGATCTGGATGTGGAACGCAGTGCAGACTCAATGCCGAGACATCCGACAGCGGCTCTCCGAGATCCTGCAGGCCGCACACACACACAAGGACAGCCAGGACGAGGCACAATTGAACCCTGTCAGCGGTCAAACCCAAAATAGAGCCGCCGAACAGGGTGATAATGAGACACTGACGTATTTACAGTCTGCAGAGGGATCAAAGTTTGAGCAAGTAATGACTTCAAGCGTGCATGAACAATCTGCATCACGCATTCAACAATCTGTTGAATGCACAGAACAAGAAACAAGACATTTGCATGAAACTAAAGACAAATTACACAATGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26650
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 |
---|---|---|---|---|---|
ENSDART00000109679 | Nonsense | 1270 | 1988 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 1904686)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 1934921 |
GRCz11 | 6 | 2068587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCAGAGGGATCAAAGTTTGAGCAAGTAATGACTTCAAGCGTGCATGAA[C/T]AATCTGCATCACGCATTCAACAATCTGTTGAATGCACAGAACAAGAAACA
Long Flanking Sequence:
TAAAAACAGTCCAAACGTTATATAAAACAACCAAATATAAATAAACATTCTAAATATATTCAGTCTAAAATGACTTCTTCTTTGTCCCCCAGGCCTCGTCTCTTGTGAAGGAGTGTATGGAGTATTTAGATCACATGAAGTCCTCAAACTCCCCGATGAGCGTCTGCTGGAGTTCCCTGCATGCATTTGAGCAGCGTTTTCAACATTTCTCACCCCAGCACTTTCAGGACAGGAGCGCCGCCCTGCTGGAGAGGCTTCCGGATGGGATCTGGATGTGGAACGCAGTGCAGACTCAATGCCGAGACATCCGACAGCGGCTCTCCGAGATCCTGCAGGCCGCACACACACACAAGGACAGCCAGGACGAGGCACAATTGAACCCTGTCAGCGGTCAAACCCAAAATAGAGCCGCCGAACAGGGTGATAATGAGACACTGACGTATTTACAGTCTGCAGAGGGATCAAAGTTTGAGCAAGTAATGACTTCAAGCGTGCATGAA[C/T]AATCTGCATCACGCATTCAACAATCTGTTGAATGCACAGAACAAGAAACAAGACATTTGCATGAAACTAAAGACAAATTACACAATGCCTCAAGCATGCATAATGAATCTACATCACATGCTCAACAATCTGTTCAATGCACAGTCCAAAAAGCCAGTATGTTGCAGGAAACTAATAATACATCACGCAATCCAAGCATGCATAAAGACTCTGCATCACATATTCAGGAATCTGTTCAATGCACAGACCAAAACACAAGTCATTTGCATGAACCTCAAGCTATATCACACCATCCCTCTGACAGAAAGTTAAAAGAGCATCATCATAAACACTCTCACAGTGACGATGATCTCAGAAAATCAGGACGGATCCATAAGTTTGGTCAAACAGCACATTATAAAGTCTTCATCCGCTCTCAAAGTGCAGAATCCTGCTTGCGAGGCTACCGTTATAACATTCCTCTGTGCAAAACCGATGCTGCAGCCTCCTGTGTTGGAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17343
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 |
---|---|---|---|---|---|
ENSDART00000109679 | Nonsense | 1289 | 1988 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 1904744)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 1934979 |
GRCz11 | 6 | 2068645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCACRCATTCAACAAYCTGTTGAATGCAYAGAACAARAAACAAGRCATT[T/A]GCATGAAACTAAAGACAAATTACACAATGCCTCAAGCATGCATAATGMAT
Long Flanking Sequence:
TTCAGTCTAAAATGACTTCTTCTTTGTCCCCCAGGCCTCGTCTCTTGTGAAGGAGTGTATGGAGTATTTAGATCACATGAAGTCCTCAAACTCCCCGATGAGCGTCTGCTGGAGTTCCCTGCATGCATTTGAGCAGCGTTTTCAACATTTCTCACCCCAGCACTTTCAGGACAGGAGCGCCGCCCTGCTGGAGAGGCTTCCGGATGGGATCTGGATGTGGAACGCAGTGCAGACTCAATGCCGAGACATCCGACAGCGGCTCTCCGAGATCCTGCAGGCCGCACACACACACAAGGACAGCCAGGACGAGGCACAATTGAACCCTGTCAGCGGTCAAACCCAAAATAGAGCCGCCGAACAGGGTGATAATGAGACACTGACGTATTTACAGTCTGCAGAGGGATCAAAGTTTGAGCAAGTAATGACTTCAAGCGTGCATGAACAATCTGCATCACGCATTCAACAATCTGTTGAATGCACAGAACAAGAAACAAGACATT[T/A]GCATGAAACTAAAGACAAATTACACAATGCCTCAAGCATGCATAATGAATCTACATCACATGCTCAACAATCTGTTCAATGCACAGTCCAAAAAGCCAGTATGTTGCAGGAAACTAATAATACATCACGCAATCCAAGCATGCATAAAGACTCTGCATCACATATTCAGGAATCTGTTCAATGCACAGACCAAAACACAAGTCATTTGCATGAACCTCAAGCTATATCACACCATCCCTCTGACAGAAAGTTAAAAGAGCATCATCATAAACACTCTCACAGTGACGATGATCTCAGAAAATCAGGACGGATCCATAAGTTTGGTCAAACAGCACATTATAAAGTCTTCATCCGCTCTCAAAGTGCAGAATCCTGCTTGCGAGGCTACCGTTATAACATTCCTCTGTGCAAAACCGATGCTGCAGCCTCCTGTGTTGGAGCATCATTAGAAGGACTGAGCTCTGAACTCAATCAGCATGACAGTTTCTGCTCCAGCGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7021
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 |
---|---|---|---|---|---|
ENSDART00000109679 | Nonsense | 1312 | 1988 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 1904812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 1935047 |
GRCz11 | 6 | 2068713 |
KASP Assay ID:
554-5160.1 (used for ordering genotyping assays)
KASP Sequence:
AATTACACAATGCCTCAAGCATGCATAATGMATCTRCATCACATGCTCAA[C/T]AATCTGTTCAATGCACAGTCCAAAAAGCCAGTATGTTGCAGGAAACTAAT
Long Flanking Sequence:
TAGATCACATGAAGTCCTCAAACTCCCCGATGAGCGTCTGCTGGAGTTCCCTGCATGCATTTGAGCAGCGTTTTCAACATTTCTCACCCCAGCACTTTCAGGACAGGAGCGCCGCCCTGCTGGAGAGGCTTCCGGATGGGATCTGGATGTGGAACGCAGTGCAGACTCAATGCCGAGACATCCGACAGCGGCTCTCCGAGATCCTGCAGGCCGCACACACACACAAGGACAGCCAGGACGAGGCACAATTGAACCCTGTCAGCGGTCAAACCCAAAATAGAGCCGCCGAACAGGGTGATAATGAGACACTGACGTATTTACAGTCTGCAGAGGGATCAAAGTTTGAGCAAGTAATGACTTCAAGCGTGCATGAACAATCTGCATCACGCATTCAACAATCTGTTGAATGCACAGAACAAGAAACAAGACATTTGCATGAAACTAAAGACAAATTACACAATGCCTCAAGCATGCATAATGAATCTACATCACATGCTCAA[C/T]AATCTGTTCAATGCACAGTCCAAAAAGCCAGTATGTTGCAGGAAACTAATAATACATCACGCAATCCAAGCATGCATAAAGACTCTGCATCACATATTCAGGAATCTGTTCAATGCACAGACCAAAACACAAGTCATTTGCATGAACCTCAAGCTATATCACACCATCCCTCTGACAGAAAGTTAAAAGAGCATCATCATAAACACTCTCACAGTGACGATGATCTCAGAAAATCAGGACGGATCCATAAGTTTGGTCAAACAGCACATTATAAAGTCTTCATCCGCTCTCAAAGTGCAGAATCCTGCTTGCGAGGCTACCGTTATAACATTCCTCTGTGCAAAACCGATGCTGCAGCCTCCTGTGTTGGAGCATCATTAGAAGGACTGAGCTCTGAACTCAATCAGCATGACAGTTTCTGCTCCAGCGCTTCGGGATTCAGCCAAAAGTGCAGCAGTGACTGCGGATCTGAGGATCACGGCTCAGGAGTGAGATGTTCA
Associated Phenotype:
Not determined