ZMP
si:ch1073-126c3.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JME7]
Human Orthologue:
C10orf96
Human Description:
chromosome 10 open reading frame 96 [Source:HGNC Symbol;Acc:30524]
Mouse Orthologue:
1700011F14Rik
Mouse Description:
RIKEN cDNA 1700011F14 gene Gene [Source:MGI Symbol;Acc:MGI:1922895]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1052 | Nonsense | F2 line generated | Not yet available |
sa13967 | Nonsense | Available for shipment | Available now |
sa35461 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1052
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081385 | Nonsense | 73 | 256 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 20665281)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 20395633 |
GRCz11 | 13 | 20526615 |
KASP Assay ID:
554-0955.1 (used for ordering genotyping assays)
KASP Sequence:
CTCAGCTGCTTTCTGAAGCCAGTCTGCAAGTTGATTTGATGACAAAACAA[C/T]GAGATCAACTGGAAAAACAGAAAGWGGAGCTCTTGGGCTTGCAGACGGAA
Long Flanking Sequence:
CCTGTGGAAATGAATGTCATGAAAGACGTGTCTAATTTTCTGCATAATATGTTTGGTCAGATCAACGTGTCCCATATAATTATGAGACATAATTTGCTTGCATTCTTTGAAGCCAGGTAGAGAGTAATTACTTAAAGGATCCTTGATGTCTTTCACACTTGACTGAGCTGGTAAAAGGGGAGAAGCAAAGACTTGAATTCAGAAGGCATTTTATGTTATGTTATGCCAATTACAGAGTGACCTACAAACAAAATGACATAAGCTTACCTTCACAAACAGCATTGGAGCCACTGATCCGTCAGATAAGCAACATTCTGTGTTGCCGCAAAGCCTTTGTTCAGCCAGTCAGAAAATAACATTGCTGTGAATGTAAAGTTTATCCAGGAGACCCTTTTGCAGAACATCTGAATGAGACACTCCTCAAATTCATGATTCGTTTGTGACCACAGGCTCAGCTGCTTTCTGAAGCCAGTCTGCAAGTTGATTTGATGACAAAACAA[C/T]GAGATCAACTGGAAAAACAGAAAGAGGAGCTCTTGGGCTTGCAGACGGAACTCAAAGACAATCTGGTATACATAAACGCATTGCATATTGTTGGAGTTAATTGCCTCTCAGTCAAACACCCTGTTAAAACACAACAAAGATAAGTTTGAAAAGGCTGCATGATATTGGAAAATCTGACATTGCGATATTTAGTTTTCTGTTAAATATATATATTGTGATATAAATAAAAATGGACTAGACAACTTGAAAAGCGCCATTTGGAAAGATTGAATTAATTATTGGGGTGATTTTGTAGGGGAGTGAATCATGCTTAAAATATTCTATAATAAAGAAATTGCAAGCAGAAATAAAAACAATGGAGCTAAGATAAAAGTGAGTATACAGTGCTTAATGGTTTTCTGGGGGAGTCTAACAGTATTTAGCTACATAAACTGAATAAATGTAAAATAGTTGCATTTCATAAATAATGAAATAAAACAAATTAAAGTAATTAAAGTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13967
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 |
---|---|---|---|---|---|
ENSDART00000081385 | Nonsense | 73 | 256 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 20665281)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 20395633 |
GRCz11 | 13 | 20526615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAGCTSCTTTCYGAAGCCAGTCTGCAAGTTGATTTGATGACAAAACAA[C/T]GAGATCAACTGGAAAAACAGAAAGWGGAGCTCTTKGGCTTGCAGACGGAA
Long Flanking Sequence:
CCTGTGGAAATGAATGTCATGAAAGACGTGTCTAATTTTCTGCATAATATGTTTGGTCAGATCAACGTGTCCCATATAATTATGAGACATAATTTGCTTGCATTCTTTGAAGCCAGGTAGAGAGTAATTACTTAAAGGATCCTTGATGTCTTTCACACTTGACTGAGCTGGTAAAAGGGGAGAAGCAAAGACTTGAATTCAGAAGGCATTTTATGTTATGTTATGCCAATTACAGAGTGACCTACAAACAAAATGACATAAGCTTACCTTCACAAACAGCATTGGAGCCACTGATCCGTCAGATAAGCAACATTCTGTGTTGCCGCAAAGCCTTTGTTCAGCCAGTCAGAAAATAACATTGCTGTGAATGTAAAGTTTATCCAGGAGACCCTTTTGCAGAACATCTGAATGAGACACTCCTCAAATTCATGATTCGTTTGTGACCACAGGCTCAGCTGCTTTCTGAAGCCAGTCTGCAAGTTGATTTGATGACAAAACAA[C/T]GAGATCAACTGGAAAAACAGAAAGAGGAGCTCTTGGGCTTGCAGACGGAACTCAAAGACAATCTGGTATACATAAACGCATTGCATATTGTTGGAGTTAATTGCCTCTCAGTCAAACACCCTGTTAAAACACAACAAAGATAAGTTTGAAAAGGCTGCATGATATTGGAAAATCTGACATTGCGATATTTAGTTTTCTGTTAAATATATATATTGTGATATAAATAAAAATGGACTAGACAACTTGAAAAGCGCCATTTGGAAAGATTGAATTAATTATTGGGGTGATTTTGTAGGGGAGTGAATCATGCTTAAAATATTCTATAATAAAGAAATTGCAAGCAGAAATAAAAACAATGGAGCTAAGATAAAAGTGAGTATACAGTGCTTAATGGTTTTCTGGGGGAGTCTAACAGTATTTAGCTACATAAACTGAATAAATGTAAAATAGTTGCATTTCATAAATAATGAAATAAAACAAATTAAAGTAATTAAAGTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35461
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081385 | Essential Splice Site | 94 | 256 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 13 (position 20665348)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 20395700 |
GRCz11 | 13 | 20526682 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGAAAGAGGAGCTCTTGGGCTTGCAGACGGAACTCAAAGACAATCTGG[T/A]ATACATAAACGCATTGCATATTGTTGGAGTTAATTGCCTCTCAGTCAAAC
Long Flanking Sequence:
TGTCCCATATAATTATGAGACATAATTTGCTTGCATTCTTTGAAGCCAGGTAGAGAGTAATTACTTAAAGGATCCTTGATGTCTTTCACACTTGACTGAGCTGGTAAAAGGGGAGAAGCAAAGACTTGAATTCAGAAGGCATTTTATGTTATGTTATGCCAATTACAGAGTGACCTACAAACAAAATGACATAAGCTTACCTTCACAAACAGCATTGGAGCCACTGATCCGTCAGATAAGCAACATTCTGTGTTGCCGCAAAGCCTTTGTTCAGCCAGTCAGAAAATAACATTGCTGTGAATGTAAAGTTTATCCAGGAGACCCTTTTGCAGAACATCTGAATGAGACACTCCTCAAATTCATGATTCGTTTGTGACCACAGGCTCAGCTGCTTTCTGAAGCCAGTCTGCAAGTTGATTTGATGACAAAACAACGAGATCAACTGGAAAAACAGAAAGAGGAGCTCTTGGGCTTGCAGACGGAACTCAAAGACAATCTGG[T/A]ATACATAAACGCATTGCATATTGTTGGAGTTAATTGCCTCTCAGTCAAACACCCTGTTAAAACACAACAAAGATAAGTTTGAAAAGGCTGCATGATATTGGAAAATCTGACATTGCGATATTTAGTTTTCTGTTAAATATATATATTGTGATATAAATAAAAATGGACTAGACAACTTGAAAAGCGCCATTTGGAAAGATTGAATTAATTATTGGGGTGATTTTGTAGGGGAGTGAATCATGCTTAAAATATTCTATAATAAAGAAATTGCAAGCAGAAATAAAAACAATGGAGCTAAGATAAAAGTGAGTATACAGTGCTTAATGGTTTTCTGGGGGAGTCTAACAGTATTTAGCTACATAAACTGAATAAATGTAAAATAGTTGCATTTCATAAATAATGAAATAAAACAAATTAAAGTAATTAAAGTTACAAAAAGTACATATTCTTGTGCCTGAATACTTTTAACTCTTTGACATGCTCCCACAGTCACAGGTAGG
Associated Phenotype:
Not determined