Busch Lab

ZMP

si:ch73-74h11.1

Ensembl ID:
ENSDARG00000062750
ZFIN ID:
ZDB-GENE-091204-215
Human Orthologues:
DSG1, DSG2, DSG3, DSG4
Human Descriptions:
desmoglein 1 [Source:HGNC Symbol;Acc:3048]
desmoglein 2 [Source:HGNC Symbol;Acc:3049]
desmoglein 3 [Source:HGNC Symbol;Acc:3050]
desmoglein 4 [Source:HGNC Symbol;Acc:21307]
Mouse Orthologues:
Dsg1a, Dsg1b, Dsg1c, Dsg2, Dsg3, Dsg4
Mouse Descriptions:
desmoglein 1 alpha Gene [Source:MGI Symbol;Acc:MGI:94930]
desmoglein 1 beta Gene [Source:MGI Symbol;Acc:MGI:2664357]
desmoglein 1 gamma Gene [Source:MGI Symbol;Acc:MGI:2664358]
desmoglein 2 Gene [Source:MGI Symbol;Acc:MGI:1196466]
desmoglein 3 Gene [Source:MGI Symbol;Acc:MGI:99499]
desmoglein 4 Gene [Source:MGI Symbol;Acc:MGI:2661061]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa19230 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12546 Essential Splice Site Available for shipment Available now
sa13085 Essential Splice Site Available for shipment Available now
sa12536 Essential Splice Site Available for shipment Available now
sa1812 Missense F2 line generated Not yet available
sa43406 Nonsense Mutation detected in F1 DNA Not yet available
sa12088 Nonsense Available for shipment Available now
sa10131 Nonsense Available for shipment Available now
sa8630 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa29325 Missense Mutation detected in F1 DNA Not yet available
sa32282 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa19230
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
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
Genomic Location (Zv9):
Chromosome 20 (position 17010378)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17070331
GRCz11 20 16969914
KASP Assay ID:
2261-4101.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGACTTTATGAGAATGTAGACTACACAAAAGAGGAATATGTGGCAAAA[G/A]TAAGCATAAGTATTTTATGTGCGACTGAACACCTGCTGCCTGGTTTTTGT
Long Flanking Sequence:
ACGCAATATTTATTTCTAAGTGTTGCAAAAAAATGCACACTTTCACTTATATGAAACACTCCAATATAATAGCTATAATTTTTTAAGTGTTCATAAATAGCCACACACACACTAATAATATAATAATATGTGTACTTTATAAATGTAAAATTTAAACATAAACCTGTCATATATGTAATTTGCATACATCAATTCATTTCAGATTTCTATATTGGTTGTTTGTTTTGTTCATTTTATCTTAAGTAGTTTCTCGTAATAGCCCAAAGAACATATAAAATAAATGATTGTGGGGTAGATATGATAGAATGAATAACTGATCATGTTTTTCAATGTCAATGCTAAACGTTGTAAATGTATAAAAAATATATATAAATTTTTTTGTTTTTTTTTAGGGATCAAAAGCCAACATCAGATCTCATCGGAAGAAGCGAGAGTGGATTCTTCCACCAACAAGACTTTATGAGAATGTAGACTACACAAAAGAGGAATATGTGGCAAAA[G/A]TAAGCATAAGTATTTTATGTGCGACTGAACACCTGCTGCCTGGTTTTTGTCACTTTGTTGGTATGTTCCCACAAGCAATGCCGGTCATTTTAGACTTTGTAGGAACATTCTTTTGGATTCCATCAGGAAAACGCCACATAAATCATGCTGAATTATTTTATATTTTTTAAATGTTTTCTGTGAGGGTCCGGATTAGGGCTAGACTTGAGCTAAGAGGACAGAATTATATTGTCCGAAGAAGAAAAAAATCTTCTATTAGAAGTCCCCATAAAACATGAAAACTCAGCATGTATGTCTGGGTCGGTGTTTGCTGGATGTTGGCCTCACTAAAAAGCATATTTTGCATATGGGTGGCCCTGATAGTCTTTCCTTGTTTGTGCAATCATCTGAAAAACACGAGATCTGGACGCACTGGTTCTTCTATAAGCTGCATATTTCACCTGTTTCATAAATTCATCCTATATGCAGCTCCATATCTGAGACTCAGCAAAAACCAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12546
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
Genomic Location (Zv9):
Chromosome 20 (position 17010378)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17070331
GRCz11 20 16969914
KASP Assay ID:
2261-4101.1 (used for ordering genotyping assays)
KASP Sequence:
CAAGACTTTATGAGAATGTAGAYTRCACAAAAGAGGAATATGTGGCAAAA[G/A]TAAGCATWAGTATTTTATGTGCGACYGAACACCTGCTGCCTGGTTTTTGT
Long Flanking Sequence:
ACGCAATATTTATTTCTAAGTGTTGCAAAAAAATGCACACTTTCACTTATATGAAACACTCCAATATAATAGCTATAATTTTTTAAGTGTTCATAAATAGCCACACACACACTAATAATATAATAATATGTGTACTTTATAAATGTAAAATTTAAACATAAACCTGTCATATATGTAATTTGCATACATCAATTCATTTCAGATTTCTATATTGGTTGTTTGTTTTGTTCATTTTATCTTAAGTAGTTTCTCGTAATAGCCCAAAGAACATATAAAATAAATGATTGTGGGGTAGATATGATAGAATGAATAACTGATCATGTTTTTCAATGTCAATGCTAAACGTTGTAAATGTATAAAAAATATATATAAATTTTTTTGTTTTTTTTTAGGGATCAAAAGCCAACATCAGATCTCATCGGAAGAAGCGAGAGTGGATTCTTCCACCAACAAGACTTTATGAGAATGTAGACTACACAAAAGAGGAATATGTGGCAAAA[G/A]TAAGCATAAGTATTTTATGTGCGACTGAACACCTGCTGCCTGGTTTTTGTCACTTTGTTGGTATGTTCCCACAAGCAATGCCGGTCATTTTAGACTTTGTAGGAACATTCTTTTGGATTCCATCAGGAAAACGCCACATAAATCATGCTGAATTATTTTATATTTTTTAAATGTTTTCTGTGAGGGTCCGGATTAGGGCTAGACTTGAGCTAAGAGGACAGAATTATATTGTCCGAAGAAGAAAAAAATCTTCTATTAGAAGTCCCCATAAAACATGAAAACTCAGCATGTATGTCTGGGTCGGTGTTTGCTGGATGTTGGCCTCACTAAAAAGCATATTTTGCATATGGGTGGCCCTGATAGTCTTTCCTTGTTTGTGCAATCATCTGAAAAACACGAGATCTGGACGCACTGGTTCTTCTATAAGCTGCATATTTCACCTGTTTCATAAATTCATCCTATATGCAGCTCCATATCTGAGACTCAGCAAAAACCAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13085
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
Genomic Location (Zv9):
Chromosome 20 (position 17010378)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17070331
GRCz11 20 16969914
KASP Assay ID:
2261-4101.1 (used for ordering genotyping assays)
KASP Sequence:
CAAGACTTTATGAGAATGTAGAYTRCACAAAAGAGGAATATGTGGCAAAA[G/A]TAAGCATWAGTATTTTATGTGCGACYGAACACCTGCTGCCTGGTTTTTGT
Long Flanking Sequence:
ACGCAATATTTATTTCTAAGTGTTGCAAAAAAATGCACACTTTCACTTATATGAAACACTCCAATATAATAGCTATAATTTTTTAAGTGTTCATAAATAGCCACACACACACTAATAATATAATAATATGTGTACTTTATAAATGTAAAATTTAAACATAAACCTGTCATATATGTAATTTGCATACATCAATTCATTTCAGATTTCTATATTGGTTGTTTGTTTTGTTCATTTTATCTTAAGTAGTTTCTCGTAATAGCCCAAAGAACATATAAAATAAATGATTGTGGGGTAGATATGATAGAATGAATAACTGATCATGTTTTTCAATGTCAATGCTAAACGTTGTAAATGTATAAAAAATATATATAAATTTTTTTGTTTTTTTTTAGGGATCAAAAGCCAACATCAGATCTCATCGGAAGAAGCGAGAGTGGATTCTTCCACCAACAAGACTTTATGAGAATGTAGACTACACAAAAGAGGAATATGTGGCAAAA[G/A]TAAGCATAAGTATTTTATGTGCGACTGAACACCTGCTGCCTGGTTTTTGTCACTTTGTTGGTATGTTCCCACAAGCAATGCCGGTCATTTTAGACTTTGTAGGAACATTCTTTTGGATTCCATCAGGAAAACGCCACATAAATCATGCTGAATTATTTTATATTTTTTAAATGTTTTCTGTGAGGGTCCGGATTAGGGCTAGACTTGAGCTAAGAGGACAGAATTATATTGTCCGAAGAAGAAAAAAATCTTCTATTAGAAGTCCCCATAAAACATGAAAACTCAGCATGTATGTCTGGGTCGGTGTTTGCTGGATGTTGGCCTCACTAAAAAGCATATTTTGCATATGGGTGGCCCTGATAGTCTTTCCTTGTTTGTGCAATCATCTGAAAAACACGAGATCTGGACGCACTGGTTCTTCTATAAGCTGCATATTTCACCTGTTTCATAAATTCATCCTATATGCAGCTCCATATCTGAGACTCAGCAAAAACCAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12536
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
ENSDART00000091076 Essential Splice Site 27 747 1 18
ENSDART00000148312 Essential Splice Site 14 277 1 6
Genomic Location (Zv9):
Chromosome 20 (position 17010378)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17070331
GRCz11 20 16969914
KASP Assay ID:
2261-4101.1 (used for ordering genotyping assays)
KASP Sequence:
CAAGACTTTATGAGAATGTAGAYTRCACAAAAGAGGAATATGTGGCAAAA[G/A]TAAGCATWAGTATTTTATGTGCGACYGAACACCTGCTGCCTGGTTTTTGT
Long Flanking Sequence:
ACGCAATATTTATTTCTAAGTGTTGCAAAAAAATGCACACTTTCACTTATATGAAACACTCCAATATAATAGCTATAATTTTTTAAGTGTTCATAAATAGCCACACACACACTAATAATATAATAATATGTGTACTTTATAAATGTAAAATTTAAACATAAACCTGTCATATATGTAATTTGCATACATCAATTCATTTCAGATTTCTATATTGGTTGTTTGTTTTGTTCATTTTATCTTAAGTAGTTTCTCGTAATAGCCCAAAGAACATATAAAATAAATGATTGTGGGGTAGATATGATAGAATGAATAACTGATCATGTTTTTCAATGTCAATGCTAAACGTTGTAAATGTATAAAAAATATATATAAATTTTTTTGTTTTTTTTTAGGGATCAAAAGCCAACATCAGATCTCATCGGAAGAAGCGAGAGTGGATTCTTCCACCAACAAGACTTTATGAGAATGTAGACTACACAAAAGAGGAATATGTGGCAAAA[G/A]TAAGCATAAGTATTTTATGTGCGACTGAACACCTGCTGCCTGGTTTTTGTCACTTTGTTGGTATGTTCCCACAAGCAATGCCGGTCATTTTAGACTTTGTAGGAACATTCTTTTGGATTCCATCAGGAAAACGCCACATAAATCATGCTGAATTATTTTATATTTTTTAAATGTTTTCTGTGAGGGTCCGGATTAGGGCTAGACTTGAGCTAAGAGGACAGAATTATATTGTCCGAAGAAGAAAAAAATCTTCTATTAGAAGTCCCCATAAAACATGAAAACTCAGCATGTATGTCTGGGTCGGTGTTTGCTGGATGTTGGCCTCACTAAAAAGCATATTTTGCATATGGGTGGCCCTGATAGTCTTTCCTTGTTTGTGCAATCATCTGAAAAACACGAGATCTGGACGCACTGGTTCTTCTATAAGCTGCATATTTCACCTGTTTCATAAATTCATCCTATATGCAGCTCCATATCTGAGACTCAGCAAAAACCAAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1812
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:
T > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091076 Missense 70 747 2 18
ENSDART00000148312 Missense 57 277 2 6
Genomic Location (Zv9):
Chromosome 20 (position 17007638)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17067591
GRCz11 20 16967174
KASP Assay ID:
554-1804.1 (used for ordering genotyping assays)
KASP Sequence:
TAATTTGTTTGTTATCAATCCTGAGAATGGTTATGTCAAAGTCACAGGTC[T/A]GCTAGACAGAGAAAAAACATCTTCATACAACGTGAGTTGTGTCCCGTGTT
Long Flanking Sequence:
AAATATGGTATATGATGTAAATTACATAAAAAACTAATAGAAAAAAATGATTAAAATAAATTAATCATAATGGCCTAGTTGTTGATAATTGTTTTTCTGTATCTATGCTAAATATGCTGAAATAAAGTATAATTGGACAAAAAAAAAAAAAAAAAAAAAGTTGGTAACACCAGTGACAAAAAATGGTTCATGCGATCTTTAGGCTCATTAAAATCATTGTGCTGTCATGTGTTTTCATAAATTCAATTGGTAATTGATTAACGTAGTCTAAGTTTAAATGTTAAATAAAGAAATAGATTTTTAGTACTTTTCCTAAACAAAAAGTGCATGTTTTCATGTTTTTTTCTTGTAATATTGTCTTGCTCTTTTCTAGATTCGCTCTGATAAAGATATTAACTGGCAGGTGGTGGAATATGGATTAACAGGTCATGGTGCCAACAAGCTACCCTATAATTTGTTTGTTATCAATCCTGAGAATGGTTATGTCAAAGTCACAGGTC[T/A]GCTAGACAGAGAAAAAACATCTTCATACAACGTGAGTTGTGTCCCGTGTTTGGGATAGTCAAAGCTACCGAAATGACAATTGACTGAAAAAATTAATTACTGAGAAACATTTTTCTTTTGTGCAGCTGACTGGCATTGCTAAATATCGTAACGGATCAATAGCTGAAGAAAACATTATGCTTAAGATTAAAGTTGAGGATCAGAATGATAACTTTCCGATATTCAGAGAGCAAAGTGGATCTGTGAAAGAAAGCAGCAAGATTGGTGGGTTCATTTATTTATTATTTTTCTGCTCTCTGAATTATGACAGATTCTCCACCACATAATTAAAATAAAAAATAACTATTCTGACATGTAATTTGTCTAAATTGATATGAATATCTTGAAACTTACAAATGAATATATTGAAGTTGAAACTTATGTCTGTGTTTCCATGTCATGTTATTTTTTGAGCTTTAAGTTTTTTTTTTTTTTTTTTGAGTTTAGCATCTGTCAATTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43406
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091076 Nonsense 127 747 3 18
ENSDART00000148312 Nonsense 114 277 3 6
Genomic Location (Zv9):
Chromosome 20 (position 17007374)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17067327
GRCz11 20 16966910
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCGATATTCAGAGAGCAAAGTGGATCTGTGAAAGAAAGCAGCAAGATT[G/T]GTGGGTTCATTTATTTATTATTTTTCTGCTCTCTGAATTATGACAGATTC
Long Flanking Sequence:
AGTCTAAGTTTAAATGTTAAATAAAGAAATAGATTTTTAGTACTTTTCCTAAACAAAAAGTGCATGTTTTCATGTTTTTTTCTTGTAATATTGTCTTGCTCTTTTCTAGATTCGCTCTGATAAAGATATTAACTGGCAGGTGGTGGAATATGGATTAACAGGTCATGGTGCCAACAAGCTACCCTATAATTTGTTTGTTATCAATCCTGAGAATGGTTATGTCAAAGTCACAGGTCTGCTAGACAGAGAAAAAACATCTTCATACAACGTGAGTTGTGTCCCGTGTTTGGGATAGTCAAAGCTACCGAAATGACAATTGACTGAAAAAATTAATTACTGAGAAACATTTTTCTTTTGTGCAGCTGACTGGCATTGCTAAATATCGTAACGGATCAATAGCTGAAGAAAACATTATGCTTAAGATTAAAGTTGAGGATCAGAATGATAACTTTCCGATATTCAGAGAGCAAAGTGGATCTGTGAAAGAAAGCAGCAAGATT[G/T]GTGGGTTCATTTATTTATTATTTTTCTGCTCTCTGAATTATGACAGATTCTCCACCACATAATTAAAATAAAAAATAACTATTCTGACATGTAATTTGTCTAAATTGATATGAATATCTTGAAACTTACAAATGAATATATTGAAGTTGAAACTTATGTCTGTGTTTCCATGTCATGTTATTTTTTGAGCTTTAAGTTTTTTTTTTTTTTTTTTGAGTTTAGCATCTGTCAATTCTGTTTTTGAAATTGAATGAATATATCAGCGCTTTAAGTTTATATCACAATTAATACTTTTATTCATATTTTTTGTATAAAATTGATTTATTATTTGATTTATATCTGGAAAAAGTCAGAAATGCAGATTAGAAAAGTCGAAATTCTTATGTACGAGTTCGAAGTTAAGGATTGTGAGATATAAAGGGAAATTTTAGGTTGGGGAAACAACCATTCTCCATTAACAGATGATACTAATTAATATGCGGTAAATTTGCATAAAATTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12088
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
ENSDART00000091076 Nonsense 258 747 6 18
ENSDART00000148312 Nonsense 245 277 6 6
Genomic Location (Zv9):
Chromosome 20 (position 17006233)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17066186
GRCz11 20 16965769
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCATGAGAATTAAAGCCCAGGACAAAGATCTGAAATTCACTGATAACTG[G/A]CTGGCAGTGTTTGACATTCWGAAAGGAAATGAAGACAATCTCWTCTCCAT
Long Flanking Sequence:
ATACAGTATAATAAAACAATCCCCTGCAGAATCAGGAAATATGTTCTCCATCGATAGAGCAACTGGGAATGTCTATGTGAAGGAGAAAATCCTGGATCGAGAGGTAACATTAAACGGATAAAAATATCCCATGATATTTGCAGGTTCATGTAAAATGCAACATGATAGTTTAAATTCAGGTTTCTGGACATTTTTTTTACAGAGACATGATAAATATACTTTAATAGTTCAGGGAGTTGATATGGACGGACATCCATCTGGCAACACAGGAACAGGCACAGTGCATATTAATATTCTGGACATAAATGACAATGTTCCCACTCTTGAGAAAGAAGAGGTAAGAACTAACAAATGGAAGTTGTTGCATTTTTAAGGTTTTGTATTTAATAGCTTTTGTTTTTCCTCTATTAGTATTCAGGCAGTGTTGATGAAGGTGTGGTTGATGTGGTTGTCATGAGAATTAAAGCCCAGGACAAAGATCTGAAATTCACTGATAACTG[G/A]CTGGCAGTGTTTGACATTCTGAAAGGAAATGAAGACAATCTCTTCTCCATTGAAACAGACCCTAAAACCAACGAGGGAATTCTAAAACTCATCAAGGTAAATGTTTTGTTTAATAAAAATACAGTCTTTTATATAATAACACTTGTTCAGGGCTCAATACAGTCATTTGTCCTATAAATTTTTGCTTTTTTTTAATGCGTAAGCTTGTAAAATGTATGATGATTTACAGTATGTGATATTTAAAAAAGGATACTTCGAGTAAGTAATAAATACTTTAAAAAACATAAACCAATACGAACTCAATATACAGTGAATCATAACTGAGTACATCACACTTTGAAAATTAATATTTGTATCCATTTCTCAATGAATATAGGCAATGCGTTTTGATTTGTGACGGGTATACTTATATATGCTGAGTACTGTATGTGTGTATACGGAGTTTAAGTCAGAATCATTAGCCTCCCTAATTTATTAACCCCCCTGTTTATTTAATTACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10131
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
ENSDART00000091076 Nonsense 258 747 6 18
ENSDART00000148312 Nonsense 245 277 6 6
Genomic Location (Zv9):
Chromosome 20 (position 17006233)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17066186
GRCz11 20 16965769
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCATGAGAATTAAAGCCCAGGACAAAGATCTGAAATTCACTGATAACTG[G/A]CTGGCAGTGTTTGACATTCWGAAAGGAAATGAAGACAATCTCWTCTCCAT
Long Flanking Sequence:
ATACAGTATAATAAAACAATCCCCTGCAGAATCAGGAAATATGTTCTCCATCGATAGAGCAACTGGGAATGTCTATGTGAAGGAGAAAATCCTGGATCGAGAGGTAACATTAAACGGATAAAAATATCCCATGATATTTGCAGGTTCATGTAAAATGCAACATGATAGTTTAAATTCAGGTTTCTGGACATTTTTTTTACAGAGACATGATAAATATACTTTAATAGTTCAGGGAGTTGATATGGACGGACATCCATCTGGCAACACAGGAACAGGCACAGTGCATATTAATATTCTGGACATAAATGACAATGTTCCCACTCTTGAGAAAGAAGAGGTAAGAACTAACAAATGGAAGTTGTTGCATTTTTAAGGTTTTGTATTTAATAGCTTTTGTTTTTCCTCTATTAGTATTCAGGCAGTGTTGATGAAGGTGTGGTTGATGTGGTTGTCATGAGAATTAAAGCCCAGGACAAAGATCTGAAATTCACTGATAACTG[G/A]CTGGCAGTGTTTGACATTCTGAAAGGAAATGAAGACAATCTCTTCTCCATTGAAACAGACCCTAAAACCAACGAGGGAATTCTAAAACTCATCAAGGTAAATGTTTTGTTTAATAAAAATACAGTCTTTTATATAATAACACTTGTTCAGGGCTCAATACAGTCATTTGTCCTATAAATTTTTGCTTTTTTTTAATGCGTAAGCTTGTAAAATGTATGATGATTTACAGTATGTGATATTTAAAAAAGGATACTTCGAGTAAGTAATAAATACTTTAAAAAACATAAACCAATACGAACTCAATATACAGTGAATCATAACTGAGTACATCACACTTTGAAAATTAATATTTGTATCCATTTCTCAATGAATATAGGCAATGCGTTTTGATTTGTGACGGGTATACTTATATATGCTGAGTACTGTATGTGTGTATACGGAGTTTAAGTCAGAATCATTAGCCTCCCTAATTTATTAACCCCCCTGTTTATTTAATTACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8630
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
ENSDART00000091076 Essential Splice Site 291 747 7 18
ENSDART00000148312 None None 277 None 6
Genomic Location (Zv9):
Chromosome 20 (position 17004258)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17064211
GRCz11 20 16963794
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATTTATACCCGTTTTATCTTTTTCCCCATGCCTGTCTACTTTCCTGAA[G/A]CCTGTTGATTTTGAAAAGGTCAAAGAGCTGGACCTCAATTTGGTTATATC
Long Flanking Sequence:
AGACAAGGCTGTTATCAACTTTTACACTACATGCCTACTGTTAAAAGTGCAGTATATTAAAGTGATAGTTCATCCCATTGTTCATCATTTATTCTTCTTCATATGGTTTTAAATCTTTATGAGTTTCTTTCTTTGTTAAACACAAAATAAGATATATGGAAGTAAGCTGGTTGATGGGACCCATTGACTTCCATAATAGGGGAAAATAATACTATGGAAGTCAGTGGGTACCAGCTGCCACCATTTTTTTTAAAATAGCTGCTTTTGTGTTCAACAGAAGAAAAAAACTCAAACAGGTTTGTGAAAAATGAGGGGTGAGTAAATCTTGACAGATTTTTTCGTTTTGAGTAAGCTATTTAATATGTGTGTGTGTGTTTCATTTTATGTTAAAGAGCCTGAGGCAATTTTGGAATTTCCTGTTACTGTTTAAATACTTAAAATTATACAATCTGATTTATACCCGTTTTATCTTTTTCCCCATGCCTGTCTACTTTCCTGAA[G/A]CCTGTTGATTTTGAAAAGGTCAAAGAGCTGGACCTCAATTTGGTTATATCAAATGTAGCTCCTTTTATAAACGGAAGTGCTTTAGAGCTGGACGTCAATCTGGACAAGGGTGGAGCAGGTGCCGGAGCAGGGGCTGGGGTGGGAGCCGGTTTGGGAGTTGGATTAGGAGTAGGGTTAGGTTTAGGGTTAGATGCTGGACTGGATGCTGGGCCGAATGCTGGACTTGGTGCAGGATTGGATTTAGGTGCTGGACTAGATGCAGGACTAGATGCTGAACTGGATGCTGGACTAGATGCTGGACTAGATGCTGGATTAGATGCTGGACTGGATGCTGGAGTGGATTTGGGTGCCGGAATGGATGCAGGTGGAGATGTTGGGCTTAAGCCTGGAGTTAATCCTGGAGCCAAGCCTGGTCCTTCACTTGGTGTCAAGCCAGGGCCAAAACCAGGGCCAAAACCAGGAACAAAACCTGGAACTAGTCCTTCTGGCAAACCTGTAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29325
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:
A > T
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091076 Missense 583 747 12 18
ENSDART00000148312 None None 277 None 6
Genomic Location (Zv9):
Chromosome 20 (position 16999009)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17058962
GRCz11 20 16958545
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCCCAGGATTAAGATTATCATACATACTTTGTGTTCTTTGCATTTTT[A/T]GTGGTACCGTTCCTTCTGCTCTTCTGCCAGTGTGGGACCGTGAATGAGTT
Long Flanking Sequence:
TGAGGACGCCGATCCAAACGCCACACCTTTCCAATTTGCTCTGATAGAAGAGGAGAGTGTCGGAAAATGGCAGATGGTGCCAATAAACGGTACAGATAAAGAAGGTTTATTGTCTTAAAACCACACAAACTCCAATAGAATTGATAGGACTTCTGTTCTTTTGTCTTATTCACAGGAACCACAGTGAGTTTTCATACACAGGAGACTTTGTGGCCTGGCATTTATGAGCTGACAGTGAAGATCACGGATGCTCAAGGTTTGGCTTGTCCAGACAACCAAAAGTTTGAGGTTGAGGTGTGCAGCTGTGAGGAAAAAAGCTCATGCGGGCCGAGGCTTGCTGCACAGCGCAGCGTCCCACTCAAAATAGGAAAGCCAGCTCTCGGCTTGTTCCTCAGCGGCGCAGCTCTACTCTTGCGTGAGTTATCCAATCACCCAAAACATTTAAACAGGCTGTCCCAGGATTAAGATTATCATACATACTTTGTGTTCTTTGCATTTTT[A/T]GTGGTACCGTTCCTTCTGCTCTTCTGCCAGTGTGGGACCGTGAATGAGTTCACAGATTTGCCATTTGACGCTAAAGAATATCTTATTCCATATCACACTGAAGGCATAGGGGAGGACAAGGTAAAAAAAAAAAAAAGTAAATAATTATAACCTGATTGGACTGGACACTGACTTTAAACAAGGGTGTCCAGTACTGTTCATGAAAGGCCAACACCCTACATATTTTTGCCAAACCAGTTTGACTAGAAGTTTCAGGGTCATATTTTATTGCAAAGGGCTCATTTCTATGATTTAGTCCATTCAAAGGGTTAACCCTTTAGTGTGAGAACTTCAAAGTAATAGAGGAACCAAAAAAAAAAAAAAATAGCTCTGCACAAAGAATTATGAGAGCAAGTTTTTTTTGCAGGTGCAAATTTGTTTTATAACTGGAGTTAACTTGTTAACAAAGGTTTGGCAGTGGAACCAAGCCTCTCTTCCTCTCCTTAACCAATCACCTACTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32282
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000091076 Essential Splice Site 631 747 14 18
ENSDART00000148312 None None 277 None 6
Genomic Location (Zv9):
Chromosome 20 (position 16996363)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 17056316
GRCz11 20 16955899
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACATAAACAATGATGGGTTAACAGAATCTGATGGCCGGATTTGGTAC[A/T]GAGAAAACACAATTTCAACGGCCAACCACCGCAACAGTGCTCTCTATTCT
Long Flanking Sequence:
ATGAAACTCATGTAAACATCCTAATCATGTTATTCTCTTAATCAGATTAAGGCAAATAATTTGATTACTAATGTCCATGTAAACGTAATCACTGATGAGCATTGTTAAGTAGATAAGGCTGAACAGCCTAGAAAAGGTAACCTTTAAATCTTTTTGAGTTTAAAAGAGGTGAGGGGAAATGTTTGGAATGCACACTAGTGAGAGTGAAGAGCTTGATTAGCTGGTTTAGGTATGTTTAATTATGGTTGAACTACACTGTGTAGGTCAGTAGGAATGGTTTAAACACGCCGGTTTTATAATGTAAAATTTTGTTTTTCGTCCTACAGGAGATTCCTGCTCTCAGTGGTCTTGCTGCTACAATAGACCAAAAGCAGCTGCTTCAGGTTTCCAACACTGTATCCAAAATGCACTTTCAAACAAGTGTTGCTAATGACTCCAGAATGCTCAACCAGGACATAAACAATGATGGGTTAACAGAATCTGATGGCCGGATTTGGTAC[A/T]GAGAAAACACAATTTCAACGGCCAACCACCGCAACAGTGCTCTCTATTCTGCATCATTCATTCAAGAAAAGCAAGACATTTATGGGGACATGGCATTAGGAGATGTCTTTCTGAATGAATACTTCTCTCAGGTATGGAATTAATTATATAGCAGCTTATTCATATTTAAGTTAATTCATAATTAAAATAGGGCGTCACGGTGGTGCAGTAGGTAGCACAATCACAGAATGAAAGACGCTGGTTCGAGCCTCAGCTGGGTCAGTTGGCTTTTCTGTGTGAAGTTTACATGTTCTCCAGGTGCTCCGTTTTCCGCCATAGTCCAAAGACATGTGCTATAGGTCAATTGCGTAAGCTTAAAGGGGTGGTCCACTATGATTTCATATTTTAAATTTTAGTTGATGTGTAATGTAGCTGTGTGAACATAAACAACATCTCTGAATGTAAAAATTTCTAAGTTCAATGCAAAGGGAGACCTTGGGTTTTTTACATAGTTAGCTTAA
Associated Phenotype:
Not determined