Busch Lab

ZMP

dennd3b

Ensembl ID:
ENSDARG00000013153
ZFIN ID:
ZDB-GENE-091230-7
Human Orthologue:
DENND3
Human Description:
DENN/MADD domain containing 3 [Source:HGNC Symbol;Acc:29134]
Mouse Orthologue:
Dennd3
Mouse Description:
DENN/MADD domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:2146009]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa11410 Nonsense Available for shipment Available now
sa42755 Nonsense Mutation detected in F1 DNA Not yet available
sa42754 Nonsense Mutation detected in F1 DNA Not yet available
sa18385 Nonsense Available for shipment Available now
sa42753 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39108 Nonsense Mutation detected in F1 DNA Not yet available
sa2847 Nonsense Available for shipment Available now
sa42752 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36176 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39107 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36175 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa11410
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035583 Nonsense 30 1262 2 25
ENSDART00000124555 None None 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 Nonsense 30 452 2 10
Genomic Location (Zv9):
Chromosome 16 (position 33204667)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30943182
GRCz11 16 30901109
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGCATGCACCCTKTGATTTSTATGTTTTCTTTATTTTSTTCAGTCTT[T/A]GTCACAACTGAATGGAAGTCCTCTTCCTCTGYTCGATCCTGAGGTTCTGC
Long Flanking Sequence:
CAGATATATTGTGCCTTAAAATGACACAATTTTTTACGTCAACTTTTTTAAAGATTTGCAGCAATATTTGTGGCATTTCTGTAATAATAAACACAAATTGACATAAATTAATTCTTCATTAGTTGTTTGACCTCTTGAACCACCTATATGAATGAAACACTGGAAAACTTTTATCTAAAGGAAATATAGTTCATTTGCTTTAATTCACTAAACTTTCTACATAAGTGTAACTGTACTTTTTTGTTCTGTATTCTCACTATAAATCAAATGGGCAATTAATATTATAGTAACCTAAAATAATAATTTCTGTAAATGATTGAAGATTATTGGAAATTATTTGGTTATGCAACAAACAAGCACGTTTGAAAAACGGGTGTCAAAATCTTAAGATCACTTTCATATGCTCAAACAGAAACATTGCTTAGTGCACTTTTTTTAGACTAATCACTATGCAGCATGCACCCTTTGATTTGTATGTTTTCTTTATTTTCTTCAGTCTT[T/A]GTCACAACTGAATGGAAGTCCTCTTCCTCTGCTCGATCCTGAGGTTCTGCAGGTCCACAGGCCTCTGTTTTGCCTTAAACAGAATGTCACGGAACCGGCTGTGGAAACCTTAAGTCCGACTCAGCAATGGTGTTCTCCGATTCAGAAAAACAACGATAAGCCCACTTTTAACACCGTAAACCCCAAGGAGGAAGCCACAGAGAATGCCAGCACTCTTAAAGAACTGGATCTGGCAGCTTTACCACAACTGTGCTTTCCAGGTGAAACAAAATTGAATGGAAATGCTTGACTTTTTTTTACTGCGGTTCAAGTCCACAAAGATATTCATACATCACACAGATTAATATTTAAAAAGTAGGGCTGCATGATATAGAAAAAAATCTGACATTTTGATTTGGCGCAATATATATTTTACTTTGACCAAATGATTTGAATGGCTCTATCTGAAAATAATTCATTAGTCTTATTATTCTATGCGCTGTGTTTGCATATGATATAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42755
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035583 Nonsense 57 1262 2 25
ENSDART00000124555 None None 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 Nonsense 57 452 2 10
Genomic Location (Zv9):
Chromosome 16 (position 33204587)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30943102
GRCz11 16 30901029
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTCGATCCTGAGGTTCTGCAGGTCCACAGGCCTCTGTTTTGCCTTAAA[C/T]AGAATGTCACGGAACCGGCTGTGGAAACCTTAAGTCCGACTCAGCAATGG
Long Flanking Sequence:
GTAATAATAAACACAAATTGACATAAATTAATTCTTCATTAGTTGTTTGACCTCTTGAACCACCTATATGAATGAAACACTGGAAAACTTTTATCTAAAGGAAATATAGTTCATTTGCTTTAATTCACTAAACTTTCTACATAAGTGTAACTGTACTTTTTTGTTCTGTATTCTCACTATAAATCAAATGGGCAATTAATATTATAGTAACCTAAAATAATAATTTCTGTAAATGATTGAAGATTATTGGAAATTATTTGGTTATGCAACAAACAAGCACGTTTGAAAAACGGGTGTCAAAATCTTAAGATCACTTTCATATGCTCAAACAGAAACATTGCTTAGTGCACTTTTTTTAGACTAATCACTATGCAGCATGCACCCTTTGATTTGTATGTTTTCTTTATTTTCTTCAGTCTTTGTCACAACTGAATGGAAGTCCTCTTCCTCTGCTCGATCCTGAGGTTCTGCAGGTCCACAGGCCTCTGTTTTGCCTTAAA[C/T]AGAATGTCACGGAACCGGCTGTGGAAACCTTAAGTCCGACTCAGCAATGGTGTTCTCCGATTCAGAAAAACAACGATAAGCCCACTTTTAACACCGTAAACCCCAAGGAGGAAGCCACAGAGAATGCCAGCACTCTTAAAGAACTGGATCTGGCAGCTTTACCACAACTGTGCTTTCCAGGTGAAACAAAATTGAATGGAAATGCTTGACTTTTTTTTACTGCGGTTCAAGTCCACAAAGATATTCATACATCACACAGATTAATATTTAAAAAGTAGGGCTGCATGATATAGAAAAAAATCTGACATTTTGATTTGGCGCAATATATATTTTACTTTGACCAAATGATTTGAATGGCTCTATCTGAAAATAATTCATTAGTCTTATTATTCTATGCGCTGTGTTTGCATATGATATAATAAATTACAAATAAAAATAAATAAACAGTATTTTATGGTTTTCTGGGGAGTTTAACAGTATTCTTTGAAGAATGAAATGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42754
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035583 Nonsense 129 1262 3 25
ENSDART00000124555 None None 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 Nonsense 129 452 3 10
Genomic Location (Zv9):
Chromosome 16 (position 33203740)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30942255
GRCz11 16 30900182
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGGTCTAAATCAGGAGGACTTCAGGTAACTAAGAAGCAAAAGGATGAA[C/T]AGTTCCATTACTTGGTCTTCACCGATGTGCTTGGAAACCAGTCTCATGGA
Long Flanking Sequence:
GATTTGAATGGCTCTATCTGAAAATAATTCATTAGTCTTATTATTCTATGCGCTGTGTTTGCATATGATATAATAAATTACAAATAAAAATAAATAAACAGTATTTTATGGTTTTCTGGGGAGTTTAACAGTATTCTTTGAAGAATGAAATGTAAAATAGCATGGTCATCGTAAAAAAAATATATATATATATTTAATAAGATCTTTGTTTTTAATCTTTAATAAGTAATTTAATCCTATAATGTGACTTTTGCACTACACACATTGTGATATCAATGCTCAAACTATATCTTGTTCAGCTCTAGTAGAAAGAGCATAACATTTGTAGAAGGTGGCAAAGGTCAGAGCCAGCACACATCAATAAAAATCAGCAATTCACACTGTAAATGTTAAATATTTCAGTGCACAGTTTCTGCAAAAGTAGTTTGAAATCAGATTTAACGCTTTTTCTTTGGTCTAAATCAGGAGGACTTCAGGTAACTAAGAAGCAAAAGGATGAA[C/T]AGTTCCATTACTTGGTCTTCACCGATGTGCTTGGAAACCAGTCTCATGGAGTAGTTCTCCAGTTCTACAGAGCAACGCAGGTCAGTTTCTTATTTATATAACCTCTCGTTGTGGTTGTGCATTGACAGATCACCTGTGCTGAATTTTACCTGCTGTTTATGAGCATTTCTCGAGTTATTGCCACTTGAAGCAGCGGTAGTTTTGTTACTGTTTGCAGATATATGTAATGTTTTGATAGTTGGTCTCAATGCCACCTTTAAATAAATAGTCATGGAGCAAACAAAGACAAACGATCCCAGCAGCAATATGTTTGGGATTGTGAGTATTTTGCAGACTAATTCACAAGATGCTGGTAATTATGCGGTTTTATATTTTAGGCACTGACATTTTCAAATAATTTTCATATGGCTGTTAAAAAGAAGGAGAAATAAACTAATAACACTAATTAATATGCCTAGTTTGCAAGTAATTTGGTTTAAAGAACGCTAATATATAGGACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18385
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
ENSDART00000035583 Nonsense 231 1262 5 25
ENSDART00000124555 None None 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 Nonsense 231 452 5 10
Genomic Location (Zv9):
Chromosome 16 (position 33201137)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30939652
GRCz11 16 30897579
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAAGGAGTTTTCTGCTAAACTATCTGTGGTCCCAGTTCCCCCTCCTGGT[C/T]AGCTGCATGTGGTGGGTTCAGAAGATCAGGAGGCWGATTAAAACTGTAAA
Long Flanking Sequence:
CACATTGCAGCCGAAAAGTCGGAAAGTTGAAAAAAGTTTTCGTTTCCTAAAAACTCTCTTAGCTTGCCATGGAGAGAAAAATATGCAGCTCATGGCCACTGACATGAGTTGAGCTGCTGGAGAATCAGAGTAGAGCTCATTAATATGCACAACTTTTCAATTATATCATATTAGGGCCCATTCCTAGGATTTACCTAAGCCACATATCTTGTATGGAGATATCGGAGAACAATTTATTATAGTGTATCAATGTGTATGGCACCTTTAATAAATTACATTGCACTCAGTTTGGGGTGTGACCTCAAAGTAATGGCAAACATATTTGTCTCCACACATTGAATGGAAGTTGTAGAAAGTACAGCACCATTTCCTCAATTATTGTTTACTGTCCTATCCACAGCCTCTTACGTGAGCTCAAAATCTGCCAGATGACTGAGATGGAGGAGCGAGCGAAGGAGTTTTCTGCTAAACTATCTGTGGTCCCAGTTCCCCCTCCTGGT[C/T]AGCTGCATGTGGTGGGTTCAGAAGATCAGGAGGCTGATTAAAACTGTAAATCCAATTTTACCCAATTGCATGTAAAATACATTTAAGCAATTTTTCTTTTCAGATGTTCATCATGCAGCCTCTGATGATTGTCCTTCCATCAAGAGAGGATCAACATCATCCTGTGGTTGATTTGGACCTTCATCTTCCATTCCTCTGCTTCAAGTCCAAAGAAGTTCTGCAGGTCTCAAATATAAATGGAAAATCAATAATTGGGGGGTTTCTTGGACAAAAATCTGGAAATCAGTCAGTTAGAGAAGCAAAAATCTCTTTTACCCTATTGTTGACCTCATGTACAAAAATTGGGTCAAAAATCTTTCGCGACTATTTTAGCAGCAGAAAAAAAAAATTATGTTTTTTTTATCTTAAAGTTTGTTGAATTTTTCTAAAATGACCCCAACATCACGACTATTTATCTATTGTCATGAAAGATGTAAACATGTGAGGTAAAATGATTGTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42753
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035583 Essential Splice Site 472 1262 11 25
ENSDART00000124555 None None 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 Essential Splice Site 419 452 10 10
Genomic Location (Zv9):
Chromosome 16 (position 33197402)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30935917
GRCz11 16 30893844
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTAGAAATAGAACCAAACTGTGTAACTAATAGCATTTTCTTTACAACA[G/T]GTCTTGGAAACACCTATTTTCCACTCCTTTTTAAAAGAACGTTTGAACAG
Long Flanking Sequence:
GTGTGTGACAAAGTTGCATTACACCATTGATGGTTTTGTATTTGTCACATTTTATGATTTTGGTGGATCTTTATGCAGAAGGAAAGGTCTTCGATTGCATTATGACCTGAATCTGTTAAATCAGAGCATATGTGGAGACCTTAATGAGCTGCGAAATCAGAGAAGATGTTGGCAACAGAGACTCAATAAGGAAATACAAAACATCAGCCTGGAGCTCCTCTTTAACATGTTTCGGTCAGTATAAGCCTGTGCAGAAATCTACTCATGACTTTTTAACAAACTAATTAAAATGTTTGTTTTTTTTTCTCAGAGATGTCAGCGATTACCTAAATTACGAACACAGAGTTTTCAATACTGATGAGTTCCTCAAGACCAGAGACCCAGAGGACCAGTCGTTTTATAAAAAAGTGATTTTCTGTGTTCTATTAAATAATACGTCTGGTCTTTGACTTTTAGAAATAGAACCAAACTGTGTAACTAATAGCATTTTCTTTACAACA[G/T]GTCTTGGAAACACCTATTTTCCACTCCTTTTTAAAAGAACGTTTGAACAGAAAAATGGATATGTTTGCCCAACTGGAGCTTAGTAATCTGACAGAAGAACAAAAGTAAGTTATGAATATAATATGTCTATGTATATGAATACCTTTTTTTGCTTTCGATAGGAGTTCCAGAGTTACATAATTGAGTACACCACATTTTAAAAATTAATATTTTTTTCCATTTCTCAGTCAATATAGGCAATGTGTTTTGATGTATTTAAACAAAACAGATTTATTAGACAGATATATTTATTAAAATAATATTTTAGTCACCAAACAAATTTAGAAATTGAAAAATAATACAATTAAATTCAATCAAAATATTGCAAAATAAATTACAACCTACAAAATTTCAATTAAATTTTTCTTTTTTTTTGGCTTCTCTTGATTTTTCTTATTTAAATTTTGTATTTAACATTTTTATATAAAATATAAATGTGGCTGTACTAGTTTTTGGACCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39108
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035583 Nonsense 769 1262 15 25
ENSDART00000124555 None None 256 None 5
ENSDART00000131356 Nonsense 30 306 1 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 None None 452 None 10
Genomic Location (Zv9):
Chromosome 16 (position 33189308)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30927823
GRCz11 16 30885750
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTACAAATTCTGGAAGGAGACTGAGGCAGAAGCCCAGGACGTTCTTT[T/A]GCCTGCTGAGGTCCTGGAGCGCCTGGACAGTAATGAGTGTGTCTACAAGC
Long Flanking Sequence:
GCTTTTCATATAAGCCACCTCTGATACCAAATGATCAACTAGAAGTCAAGTTATTATTTTTTGTTCCTAAAACTTGGATAGGTGTCAAGACTTTCGTCAGGTAGTGTAGATAGGAAGAGTAAAGAGTATGTTTCCGACAGCTGGTTTGTCCAGGTTGGGGTTTGTGGTTCTTGGCTTCTCGCGGGCAAAAGTGCAGAACGGGGGAGTGGGGGTGATTGGGGGGCCTCTAATAGTAACTTTGGGGGCCCCAAAATGGTGTGGGCCCTTAGAATCATCCTAACTCATTTTTAGTGTGTGTGTATTGCATTGTGTTGTTTCAACTCATTTTAAATAAGTAGCTTAAACAAGCAGCAAAGGTAATTTCTTTCAATGTACTGTGTTTTATAATCAAGATTTTTCTTTGGCTTTTGTAGGTGGTCAGAAGCAGATTGTTCCAGAGCTATTCAGGATGTTTTACAAATTCTGGAAGGAGACTGAGGCAGAAGCCCAGGACGTTCTTT[T/A]GCCTGCTGAGGTCCTGGAGCGCCTGGACAGTAATGAGTGTGTCTACAAGCTGTCCAGGTCTGTGAAGACCAGTTATGGTGTTGGGAAAATAGCAATGACTCAGAAAAGGATTTTTCTGCTGACCACAGGAAGTCCTGGATATGTGGACATCACAAAGTTTAGAGACATTGAGGTTTGTTCATTTTTATGTCTATAGTATACTGTTTAAACTGAGAGGTTTACGCTTGTGGTAACGGTATGAATCCTTTGAATAAAGGAAGTGAAGATCTCTGCCCCTGTACGAATTTTAAGAAATTCATCATTAAAGATCAAGAACAGCCTGAGGGATGAGATATTCGAGGCTAATTTAAAATCTGAGTGTGAACTGTGGAATCTCATGGTCAAGGAGATGTGGGCTGGCAGAATGATGGCAGACAACAATAAGGTAAAGTTAGCTTGTATTGTGATTTTTTTCTTTTTCTTTCTTTCTTACAAATCAAGTCAGTTAATCCTGACATTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2847
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
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035583 Nonsense 785 1262 15 25
ENSDART00000124555 None None 256 None 5
ENSDART00000131356 Nonsense 46 306 1 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 None None 452 None 10
Genomic Location (Zv9):
Chromosome 16 (position 33189261)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30927776
GRCz11 16 30885703
KASP Assay ID:
554-2731.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTGCCTGCTGAGGTCCTGGAGCGCCTGGACAGTAATGAGTGTGTCTAC[A/T]AGCTGTCCAGGTCTGTGAAGACCAGTTATGGTGTTGGGAAAATAGCAATG
Long Flanking Sequence:
AAGTTATTATTTTTTGTTCCTAAAACTTGGATAGGTGTCAAGACTTTCGTCAGGTAGTGTAGATAGGAAGAGTAAAGAGTATGTTTCCGACAGCTGGTTTGTCCAGGTTGGGGTTTGTGGTTCTTGGCTTCTCGCGGGCAAAAGTGCAGAACGGGGGAGTGGGGGTGATTGGGGGGCCTCTAATAGTAACTTTGGGGGCCCCAAAATGGTGTGGGCCCTTAGAATCATCCTAACTCATTTTTAGTGTGTGTGTATTGCATTGTGTTGTTTCAACTCATTTTAAATAAGTAGCTTAAACAAGCAGCAAAGGTAATTTCTTTCAATGTACTGTGTTTTATAATCAAGATTTTTCTTTGGCTTTTGTAGGTGGTCAGAAGCAGATTGTTCCAGAGCTATTCAGGATGTTTTACAAATTCTGGAAGGAGACTGAGGCAGAAGCCCAGGACGTTCTTTTGCCTGCTGAGGTCCTGGAGCGCCTGGACAGTAATGAGTGTGTCTAC[A/T]AGCTGTCCAGGTCTGTGAAGACCAGTTATGGTGTTGGGAAAATAGCAATGACTCAGAAAAGGATTTTTCTGCTGACCACAGGAAGTCCTGGATATGTGGACATCACAAAGTTTAGAGACATTGAGGTTTGTTCATTTTTATGTCTATAGTATACTGTTTAAACTGAGAGGTTTACGCTTGTGGTAACGGTATGAATCCTTTGAATAAAGGAAGTGAAGATCTCTGCCCCTGTACGAATTTTAAGAAATTCATCATTAAAGATCAAGAACAGCCTGAGGGATGAGATATTCGAGGCTAATTTAAAATCTGAGTGTGAACTGTGGAATCTCATGGTCAAGGAGATGTGGGCTGGCAGAATGATGGCAGACAACAATAAGGTAAAGTTAGCTTGTATTGTGATTTTTTTCTTTTTCTTTCTTTCTTACAAATCAAGTCAGTTAATCCTGACATTGTTTACTATGATGTCCAACACAGGCATCTCTGTTGTAATAACCATGATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42752
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035583 Essential Splice Site 961 1262 18 25
ENSDART00000124555 None None 256 None 5
ENSDART00000131356 Essential Splice Site 222 306 4 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 None None 452 None 10
Genomic Location (Zv9):
Chromosome 16 (position 33187932)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30926447
GRCz11 16 30884374
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGAACATGATGAATCCCCAGTCTGTTGATGTCCTGTTCTACTCTCCAG[G/A]TCTGCACATTTAGTGCATTAGCTATTTAGGATGTTAAAGCGTCCCTGTTA
Long Flanking Sequence:
TAATTTCCTACTGCTGGTCAAACATGCACACAGACCCACGTCCTTCCTAATGTAAAAATTGCGCTTTTAAGGTTTTAAGTCTTTTCTTTCTCCATATTTGAGTAGACATTCTTATTGCACCCTTTAAAATGCACAAAATACTTAAGCATCTTTCCTGTGACTTGTACGACTTATCAGGATCCCCAGTATGTGCAGCAGGCTTTGACCAATGTCCTTCTTATGGATGCTGTGGTGGGCTGTTTGCAGACACAGAAGAGTGTCTGCGCTGCCTCCAAACTGGCCTATCATGAAAAGCTACGACAAGAAGGTGTGTTTGAGTCTAAATGCATCAGACTCTATATCATTAAAAGATGAAGACAAGGCTGCTGTATTAAATTCTTTTATTTCCACAGTCCCTGTGATCATCCCCAGAGATACAGCATGGACACTGAAACACAAGATCAATCCATCCCAGAACATGATGAATCCCCAGTCTGTTGATGTCCTGTTCTACTCTCCAG[G/A]TCTGCACATTTAGTGCATTAGCTATTTAGGATGTTAAAGCGTCCCTGTTATATTTAAAATCAGTATTATGCTGCAAAGGTATATTTTTGATAATAGTCAAAAATACAGAGTTAAAATATGTATTTTCCTGGTCACACATTACGATAAGGTTTCATTAGTTTATTATAGTTAATGTATTTACTAAAATGATCTAATTATGAGCAATACTTGTACAGCATTCTTTAATTATAGCTTAACATTTACTAATGCTTTTCTAACATCCAAATTCATGCTTGTTAACATTAGTTAATGCACTGTGAGATGAACATGAACTGACAATGAACAACTGTATTTTTCATTAATGATAACTGAAGCCCTAGTTCAATCAAATGATTTTGTCTCGATTTTGGCACTATTTCCTTGGTGTAGTGGAGTTGTAAACAACAAATGGGCATTGTGACACAAGATTCATGACAACTGATAACATGTCTGCGACGCCTCACGACACAATCGCAGAAAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36176
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
ENSDART00000035583 Essential Splice Site 1107 1262 None 25
ENSDART00000124555 Essential Splice Site 101 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 None None 452 None 10
ENSDART00000035583 Essential Splice Site 1107 1262 None 25
ENSDART00000124555 Essential Splice Site 101 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 None None 452 None 10
Genomic Location (Zv9):
Chromosome 16 (position 33182605)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30921120
GRCz11 16 30879047
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGACAGACTGCAGTCCATTCAGATTCACAATGGAGCCTTATGGTGTGG[T/A]GAGTTTATCATCAACCTAACAAATCAAGCACTGTTGTTAACTACAAACAA
Long Flanking Sequence:
CAATAATATAAATAAATGAATGAGAAATTAAGATTATACATTATATATTATAGTATTATATAGTATAGTATACACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATTCTTCAAATATTGTGAAAATACAATAGTGAAATGATTTGGAGTTTTTTTACCAGCAGGTGGCAGCATTGTTTATCATATTTTCTCCAGATTTGTCAGCTGTACTTGTGAATACTAAGAAATGTTGTTTTGATGTTCTCTCCAAGTCGAGCGCAGGTGTACTCCTGTAGTGCAGATGGCACTGTGATCGTTTGGGACGTCCCATCTCTTAAAGTAAAGAGGCAGTTTCATCTGTCCTGTGACAGACTGCAGTCCATTCAGATTCACAATGGAGCCTTATGGTGTGG[T/A]GAGTTTATCATCAACCTAACAAATCAAGCACTGTTGTTAACTACAAACAATAGCGTTTTATTTATTTATTTACTTTCAGAGTGCTATGAAATTAACATTTTATTTAAATATTAAATATTTGAATTCTGAATTTACAATAACAATCTGAATTTATACTAATTTTTTCATTGTATGTGAAGGTGCCAGGGACTGTATAATGATGCTGAAGCCTAATGGAGATCAGCTTTGGAAAATTCACCTCCCAGACAAAATGAAAGCTACGGCCAATTTCTTCAACAGAGTTACACTGTTTCCAGAGGTTTGTTTCAGTATTTATTATATTAAAAATCAAGATTTATGATATCTCTGCGTAGTCGTTGTGTTTCATCTTTTTCTGTCTGCTGTTTCATAGTGTCTGCACAAACACGTTTAACACCCAGACAGTCAGAGAGGTCAGCCATGCCACTAAATGGTGTGAGCTGCATGAAATTATAATGTGCTCAGATATAACCAATGATCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39107
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
ENSDART00000035583 Essential Splice Site 1107 1262 None 25
ENSDART00000124555 Essential Splice Site 101 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 None None 452 None 10
ENSDART00000035583 Essential Splice Site 1107 1262 None 25
ENSDART00000124555 Essential Splice Site 101 256 None 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 None None 452 None 10
Genomic Location (Zv9):
Chromosome 16 (position 33182605)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30921120
GRCz11 16 30879047
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGACAGACTGCAGTCCATTCAGATTCACAATGGAGCCTTATGGTGTGG[T/A]GAGTTTATCATCAACCTAACAAATCAAGCACTGTTGTTAACTACAAACAA
Long Flanking Sequence:
CAATAATATAAATAAATGAATGAGAAATTAAGATTATACATTATATATTATAGTATTATATAGTATAGTATACACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATTCTTCAAATATTGTGAAAATACAATAGTGAAATGATTTGGAGTTTTTTTACCAGCAGGTGGCAGCATTGTTTATCATATTTTCTCCAGATTTGTCAGCTGTACTTGTGAATACTAAGAAATGTTGTTTTGATGTTCTCTCCAAGTCGAGCGCAGGTGTACTCCTGTAGTGCAGATGGCACTGTGATCGTTTGGGACGTCCCATCTCTTAAAGTAAAGAGGCAGTTTCATCTGTCCTGTGACAGACTGCAGTCCATTCAGATTCACAATGGAGCCTTATGGTGTGG[T/C]GAGTTTATCATCAACCTAACAAATCAAGCACTGTTGTTAACTACAAACAATAGCGTTTTATTTATTTATTTACTTTCAGAGTGCTATGAAATTAACATTTTATTTAAATATTAAATATTTGAATTCTGAATTTACAATAACAATCTGAATTTATACTAATTTTTTCATTGTATGTGAAGGTGCCAGGGACTGTATAATGATGCTGAAGCCTAATGGAGATCAGCTTTGGAAAATTCACCTCCCAGACAAAATGAAAGCTACGGCCAATTTCTTCAACAGAGTTACACTGTTTCCAGAGGTTTGTTTCAGTATTTATTATATTAAAAATCAAGATTTATGATATCTCTGCGTAGTCGTTGTGTTTCATCTTTTTCTGTCTGCTGTTTCATAGTGTCTGCACAAACACGTTTAACACCCAGACAGTCAGAGAGGTCAGCCATGCCACTAAATGGTGTGAGCTGCATGAAATTATAATGTGCTCAGATATAACCAATGATCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36175
Status:
Mutation detected in F1 DNA
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Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000035583 Essential Splice Site 1107 1262 23 25
ENSDART00000124555 Essential Splice Site 101 256 3 5
ENSDART00000131356 None None 306 None 6
ENSDART00000141403 None None 113 None 2
ENSDART00000143996 None None 452 None 10
Genomic Location (Zv9):
Chromosome 16 (position 33182435)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 30920950
GRCz11 16 30878877
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATTCTGAATTTACAATAACAATCTGAATTTATACTAATTTTTTCATT[G/T]TATGTGAAGGTGCCAGGGACTGTATAATGATGCTGAAGCCTAATGGAGAT
Long Flanking Sequence:
TAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATTCTTCAAATATTGTGAAAATACAATAGTGAAATGATTTGGAGTTTTTTTACCAGCAGGTGGCAGCATTGTTTATCATATTTTCTCCAGATTTGTCAGCTGTACTTGTGAATACTAAGAAATGTTGTTTTGATGTTCTCTCCAAGTCGAGCGCAGGTGTACTCCTGTAGTGCAGATGGCACTGTGATCGTTTGGGACGTCCCATCTCTTAAAGTAAAGAGGCAGTTTCATCTGTCCTGTGACAGACTGCAGTCCATTCAGATTCACAATGGAGCCTTATGGTGTGGTGAGTTTATCATCAACCTAACAAATCAAGCACTGTTGTTAACTACAAACAATAGCGTTTTATTTATTTATTTACTTTCAGAGTGCTATGAAATTAACATTTTATTTAAATATTAAATATTTGAATTCTGAATTTACAATAACAATCTGAATTTATACTAATTTTTTCATT[G/T]TATGTGAAGGTGCCAGGGACTGTATAATGATGCTGAAGCCTAATGGAGATCAGCTTTGGAAAATTCACCTCCCAGACAAAATGAAAGCTACGGCCAATTTCTTCAACAGAGTTACACTGTTTCCAGAGGTTTGTTTCAGTATTTATTATATTAAAAATCAAGATTTATGATATCTCTGCGTAGTCGTTGTGTTTCATCTTTTTCTGTCTGCTGTTTCATAGTGTCTGCACAAACACGTTTAACACCCAGACAGTCAGAGAGGTCAGCCATGCCACTAAATGGTGTGAGCTGCATGAAATTATAATGTGCTCAGATATAACCAATGATCTCAGGCTTTTGATTTTGTGTTTTTTAGAGACAACAGATCTGGACTAGTTTCACAGACTTTGCAGAGCTCTGCATATGGGACTTTAATGACCCTGTCAAACCACCCAAACGGCTCAAGCTTCCAAACTGCAAAGGGGTCACCTGTATGATCAAAGTGAAGAAGCAGGTAACTC
Associated Phenotype:
Not determined