Busch Lab

ZMP

DNER

Ensembl ID:
ENSDARG00000061031
Description:
delta/notch-like EGF repeat containing [Source:HGNC Symbol;Acc:24456]
Human Orthologue:
DNER
Human Description:
delta/notch-like EGF repeat containing [Source:HGNC Symbol;Acc:24456]
Mouse Orthologue:
Dner
Mouse Description:
delta/notch-like EGF-related receptor Gene [Source:MGI Symbol;Acc:MGI:2152889]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa14494 Nonsense Available for shipment Available now
sa43177 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa2973 Nonsense F2 line generated Not yet available
sa5643 Nonsense F2 line generated Not yet available
sa43176 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14494
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086576 Nonsense 15 688 1 13
Genomic Location (Zv9):
Chromosome 18 (position 45172095)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 46764938
GRCz11 18 46762956
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGAGATGGAGGACAGTCAGAGCACGCAGATGCAGACTCTGGAGCCGTG[G/A]GCTTATATTTGTGTCTGCAGCCGGGGCTTCACAGGGCAGAACTGTGAGGT
Long Flanking Sequence:
ATGAAGGTGTCTGACTGTTCTTGCACAGCTTCATGTACACTGACACAGCAGAAACCCTCTGAAACAGACTGGGCAAGAGGCGGAGCGTGTGTGTGTGTGTGTGTATCGTCACCTGCCGTCACTGTGAACGAGTTCCTCCCCTTTGCTCCCCTCTCTCTCTCCCTCCTCAAACACACTCAGACCTTCCAGTTTCCACAAGCGAGCGCCTGTAATCCACTGATCTCGTCTCTCCACCAGCAAACACACAGAGGTACATTAGACCGATCTGTCACCCGTCAGCATCCTCATGCAGCTCTTCATCCTTCCTCTCCTCCTCCTTCTCCTCGGGGAGATGGACGGACTCTTTGGGACCCCTCTGACGTCCAGCCCGGGCCCCGGCGAGGACCCAAGCACTGCGCCGGACCCCTGCGAGGGCCGACGTGCCTGAACGGAGGCGTCTGCAGCCGGCTGGGAGAGATGGAGGACAGTCAGAGCACGCAGATGCAGACTCTGGAGCCGTG[G/A]GCTTATATTTGTGTCTGCAGCCGGGGCTTCACAGGGCAGAACTGTGAGGTAAGATCGCCACGCACTTGATGCACTGGACGCCTTTCAGATATTTTCAGCATCATTTGGTGTGAATAAGCAGTTATAACAGTGCGCCTGCAGGAGCTTGTGTGCTGTCGGTGCTTGTGAAGGAGAGTTTTGTTGCTGTGGCAACAGGAGAGGAGTGTGTGCGCGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGCGTCTCTCTCTCTCAATTCAATTCAATAATTGCAAAGGCATTTTTAAAGTTTACATTAAAAGAACATTTTTACATACGCTCACTGGCCACTTTATTAGGTACACCTGTCCAACTTCTTTTTAACGCAAATCTCTAATTAGCCAATCACATGGCAACAACTCAATGCATTTAGCCATATAGACATGATCAAGACGATCTGCTGCAGTTCAAACAGAGCATCATAATGGGAAAGAAAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43177
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086576 Essential Splice Site 144 688 2 13
Genomic Location (Zv9):
Chromosome 18 (position 45147864)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 46740707
GRCz11 18 46738725
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCAGAGCCGGTCAGAGAGTGCTGGAGATACTGTGGGACGATCAGCAGG[T/C]GAGCAGGTGTGCGTCTGCATGCAGAAAGGGATAAGATGATACAGATTATT
Long Flanking Sequence:
AGGATATGAATTGATCTCAGCTCTCATTCTTCAAGCTCAAGTAATTGATAATCAATAGATGTTTGGCTGAAATGGGTGTTGGGTTTTGTACATCTGGAGCATTTAATAATACGCTGCAGTTTCCACCTCTCATCCATGTTGTTGTTGTTATTGGGTGCAGTTTTTTGCAGATCCGTGTGCCAGCAGTCCCTGTCTCCATGGCAACTGTAGTCAGGATGGCGAAGGGGAAGGGTTTTCATGCGAGTGCAGTGAGGGCTACAGCGGTGCCCGTTGTGACCTGCCAACCTTGACGTTTGACCTGTCCGAGTCCACCTGGGACCTCGCTGAGAGCCTCGTACCCGAGCACGCCACGCCTGCCACTCCGGCCACACCCGCCACCACCACTCAGGTGCTTCAGCCAACCACAGTCCTCACCACCACTCAAGCCCCACCCACCCTGGAGCCCTGGCAGCCCAGAGCCGGTCAGAGAGTGCTGGAGATACTGTGGGACGATCAGCAGG[T/C]GAGCAGGTGTGCGTCTGCATGCAGAAAGGGATAAGATGATACAGATTATTTTAGTAAACGAAGACTGAGGCTAAAAATTTTGGTCAAAAAACAAATTGTTAATTGAAATAAATTTTAAAAATCACAATAAATGGATGAACTAAAACTGAAATAATAAATGACAATAAAGGAAATGTAAGTGGGGTTAGCCGTGAAAATTCGCTGGGGTCAAATGCATTACCGTACTGCCCAAAAGCGTGAGAGTGCTGCTTTTGTAGTTACTAGGGTATTTTAAATGGTTGCTAGGCTGTGGGAATGCAGTTTGATAGGTGAAAATTTTATCAGCTTTTACCAAATGAACCTAAACCCTGAACCTAAACCTCTTTTTATGATGTTATGTGCTGATATAAGGCTTGTTATTTTTGTTATATGGTTGTTGGGCGCTATAAGTGGTTGCTAGGAAAAATGTACAATTTTGTTATATCACTACTTAATACCGGGTGATGCGGTGGCGCAGTGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2973
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
ENSDART00000086576 Nonsense 397 688 8 13
ENSDART00000086576 Nonsense 397 688 8 13
Genomic Location (Zv9):
Chromosome 18 (position 45124019)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 46716862
GRCz11 18 46714880
KASP Assay ID:
554-3146.1 (used for ordering genotyping assays)
KASP Sequence:
TTGWTCCCTGTGCTTCAGGGCCCTGCCATAATAAYGCCAGCTGCTCYCCA[C/T]AGGGTGCTGGTTTGGGCTWCAGCTGCACTTGTCCTGCAGGTTTCACTGGA
Long Flanking Sequence:
GATTTGGGTTAACAAAATTGACCATATTGAGTGTGTGTAGGAATGTGTGAGTGTATGAGTGTTTCCCAGTGCTGGGTTCTGGCTAGAAGGGCATCCGCTGCATGAAACATATGCTAGAATAGTTAGCGGTTCATTCCGCTGTCGTAACTCAGCTTAAAAATAAGGGACTCAGCCAAAGGAAAATGAATGAAATTAATCTCATGTGGATACTGATAGAATTTTTAATTTCCCCTCGGGATAAATGAAGTATCTATCTATCATCAATCTATCATTCATCAAGCCACCAAAGGTGGCTCCAGCAAAATCACTCCATTAAATCATTATAGTTGTATCAGAATGAATACCATCATTACAGTAATTGATGAAAACCGGTCCCTTTATGCTACAATCATAGTCTCTTCCTCTCTTTCTCTCTGTTAGGTTATCAGGGCATCATGTGTGAGCAGAAGATTGATCCCTGTGCTTCAGGGCCCTGCCATAATAATGCCAGCTGCTCCCCA[C/T]AGGGTGCTGGTTTGGGCTTCAGCTGCACTTGTCCTGCAGGTTTCACTGGACCCACCTGTGCCCAGCTGGTGGACTTCTGTGCCCTCAACCCATGCGCTCACGGCATCTGCCGCAGCATCGGCACTAGTTACCGCTGTCTGTGTGTTCCAGGTGAGAATCTCGTCTGCTTGCTGCTCAGAGCTCTGTTTCTCCCTTCTGATCCGTCTGGTTGTCATGGCAACTGCCTCCCGTGTATTGCGTGCTCAGACATCATTGTCTGTGAAGTGTGACTGCAGCAGCTGTGCAGCCAGATCAGCCCGTCCACTGATATCAACCCCGCTCGGATAAGAGCCGTCCGATGGGACCGCTGTGTTCTCCAGTGGGACTGCAAATATGCACTATGAAGGTGACACTTCTGACTACAAATGCCTGTTCCGGTGGGACTGCTGTGCTTTTCACAGTCAATGAGAACAAAATGGTCCCCATCAGAAATAATTAGCCAGTGATTTAATGGCAGCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5643
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
ENSDART00000086576 Nonsense 397 688 8 13
ENSDART00000086576 Nonsense 397 688 8 13
Genomic Location (Zv9):
Chromosome 18 (position 45124019)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 46716862
GRCz11 18 46714880
KASP Assay ID:
554-3146.1 (used for ordering genotyping assays)
KASP Sequence:
TTGWTCCCTGTGCTTCAGGGCCCTGCCATAATAAYGCCAGCTGCTCYCCA[C/T]AGGGTGCTGGTTTGGGCTWCAGCTGCACTTGTCCTGCAGGTTTCACTGGA
Long Flanking Sequence:
GATTTGGGTTAACAAAATTGACCATATTGAGTGTGTGTAGGAATGTGTGAGTGTATGAGTGTTTCCCAGTGCTGGGTTCTGGCTAGAAGGGCATCCGCTGCATGAAACATATGCTAGAATAGTTAGCGGTTCATTCCGCTGTCGTAACTCAGCTTAAAAATAAGGGACTCAGCCAAAGGAAAATGAATGAAATTAATCTCATGTGGATACTGATAGAATTTTTAATTTCCCCTCGGGATAAATGAAGTATCTATCTATCATCAATCTATCATTCATCAAGCCACCAAAGGTGGCTCCAGCAAAATCACTCCATTAAATCATTATAGTTGTATCAGAATGAATACCATCATTACAGTAATTGATGAAAACCGGTCCCTTTATGCTACAATCATAGTCTCTTCCTCTCTTTCTCTCTGTTAGGTTATCAGGGCATCATGTGTGAGCAGAAGATTGATCCCTGTGCTTCAGGGCCCTGCCATAATAATGCCAGCTGCTCCCCA[C/T]AGGGTGCTGGTTTGGGCTTCAGCTGCACTTGTCCTGCAGGTTTCACTGGACCCACCTGTGCCCAGCTGGTGGACTTCTGTGCCCTCAACCCATGCGCTCACGGCATCTGCCGCAGCATCGGCACTAGTTACCGCTGTCTGTGTGTTCCAGGTGAGAATCTCGTCTGCTTGCTGCTCAGAGCTCTGTTTCTCCCTTCTGATCCGTCTGGTTGTCATGGCAACTGCCTCCCGTGTATTGCGTGCTCAGACATCATTGTCTGTGAAGTGTGACTGCAGCAGCTGTGCAGCCAGATCAGCCCGTCCACTGATATCAACCCCGCTCGGATAAGAGCCGTCCGATGGGACCGCTGTGTTCTCCAGTGGGACTGCAAATATGCACTATGAAGGTGACACTTCTGACTACAAATGCCTGTTCCGGTGGGACTGCTGTGCTTTTCACAGTCAATGAGAACAAAATGGTCCCCATCAGAAATAATTAGCCAGTGATTTAATGGCAGCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43176
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000086576 Essential Splice Site 447 688 8 13
Genomic Location (Zv9):
Chromosome 18 (position 45123867)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 46716710
GRCz11 18 46714728
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATCTGCCGCAGCATCGGCACTAGTTACCGCTGTCTGTGTGTTCCAGG[T/C]GAGAATCTCGTCTGCTTGCTGCTCAGAGCTCTGTTTCTCCCTTCTGATCC
Long Flanking Sequence:
CTTAAAAATAAGGGACTCAGCCAAAGGAAAATGAATGAAATTAATCTCATGTGGATACTGATAGAATTTTTAATTTCCCCTCGGGATAAATGAAGTATCTATCTATCATCAATCTATCATTCATCAAGCCACCAAAGGTGGCTCCAGCAAAATCACTCCATTAAATCATTATAGTTGTATCAGAATGAATACCATCATTACAGTAATTGATGAAAACCGGTCCCTTTATGCTACAATCATAGTCTCTTCCTCTCTTTCTCTCTGTTAGGTTATCAGGGCATCATGTGTGAGCAGAAGATTGATCCCTGTGCTTCAGGGCCCTGCCATAATAATGCCAGCTGCTCCCCACAGGGTGCTGGTTTGGGCTTCAGCTGCACTTGTCCTGCAGGTTTCACTGGACCCACCTGTGCCCAGCTGGTGGACTTCTGTGCCCTCAACCCATGCGCTCACGGCATCTGCCGCAGCATCGGCACTAGTTACCGCTGTCTGTGTGTTCCAGG[T/C]GAGAATCTCGTCTGCTTGCTGCTCAGAGCTCTGTTTCTCCCTTCTGATCCGTCTGGTTGTCATGGCAACTGCCTCCCGTGTATTGCGTGCTCAGACATCATTGTCTGTGAAGTGTGACTGCAGCAGCTGTGCAGCCAGATCAGCCCGTCCACTGATATCAACCCCGCTCGGATAAGAGCCGTCCGATGGGACCGCTGTGTTCTCCAGTGGGACTGCAAATATGCACTATGAAGGTGACACTTCTGACTACAAATGCCTGTTCCGGTGGGACTGCTGTGCTTTTCACAGTCAATGAGAACAAAATGGTCCCCATCAGAAATAATTAGCCAGTGATTTAATGGCAGCATTCACAGCCTTCGGTATCTATTAGGGTTGTTTGCAAAGTAAAATTGAAGTAAAAATTTTTTTTTTGTGTGTGTGTGGGTGCATGGTGTAATTTTCACAATCAGAATAATGGCAATGCACTGTGTGTGATGGAGTCCATCTAGTAGTATCCGAGC
Associated Phenotype:
Not determined