Busch Lab

ZMP

si:ch1073-126c3.3

Ensembl ID:
ENSDARG00000039937
ZFIN ID:
ZDB-GENE-090313-1
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
sa13967 Nonsense Available for shipment Available now
sa1052 Nonsense F2 line generated Not yet available
sa35461 Essential Splice Site Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa1052
Status:
F2 line generated
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:
sa35461
Status:
Mutation detected in F1 DNA
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