Busch Lab

ZMP

herc2

Ensembl ID:
ENSDARG00000073841
ZFIN ID:
ZDB-GENE-070718-6
Human Orthologue:
HERC2
Human Description:
hect domain and RLD 2 [Source:HGNC Symbol;Acc:4868]
Mouse Orthologue:
Herc2
Mouse Description:
hect (homologous to the E6-AP (UBE3A) carboxyl terminus) domain and RCC1 (CHC1)-like domain (RLD) 2

Alleles

There are 20 alleles of this gene:

Allele Name Consequence Status Availability
sa40738 Nonsense Mutation detected in F1 DNA Not yet available
sa15868 Nonsense Available for shipment Available now
sa44640 Nonsense Mutation detected in F1 DNA Not yet available
sa13507 Nonsense Available for shipment Available now
sa30874 Nonsense Mutation detected in F1 DNA Not yet available
sa13593 Nonsense Available for shipment Available now
sa13641 Nonsense Available for shipment Available now
sa40739 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33904 Nonsense Available for shipment Available now
sa33905 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33906 Nonsense Mutation detected in F1 DNA Not yet available
sa38562 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa20751 Essential Splice Site Available for shipment Available now
sa10421 Essential Splice Site Available for shipment Available now
sa20752 Nonsense Mutation detected in F1 DNA Not yet available
sa20753 Nonsense Available for shipment Available now

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26782
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Nonsense 119 4832 4 93
Genomic Location (Zv9):
Chromosome 6 (position 37715396)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37789154
GRCz11 6 37767048
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCAGCGAGCTGCGGGACTGTCTGATGGCTTTGGTAGACGACCAACAG[A/T]AGCTGTCTTCTCAGACGGCTAAGAGCACACTCTCAGCCCTGCGTCTAAGC
Long Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGCAGCTGAAGGCATTATTATTAGCCACTCTTAGAATTTATTGATTTATTTACACACTTGAATATATATATATATATATATATAATTTTAATGGCCATTTTAAGGTCAAAATTATTAGCCCCTTTAAGCTATATATTATATACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTAGCTATTAAATATATCTTATTTAGTGTTATTTATCTGCTTTTTCAAATATTCCATATTTAATGGATATATTTGCAGTTATATTGTTTATATTATTTATTTATTTATTCAACCAATAATTGTTTATAACAAATTCATGCATTTCTTTATGTATGTATGTGTAACATTTCTTTTTTCTCTCCCTTATTTGTCTAGAAACCAGCGAGCTGCGGGACTGTCTGATGGCTTTGGTAGACGACCAACAG[A/T]AGCTGTCTTCTCAGACGGCTAAGAGCACACTCTCAGCCCTGCGTCTAAGCCAGAGACTGGTGATCCTGGAGCGCTACCTCATCTCGCTCACTCACAGCATGATGGAGGAGAAGTACAAAGTACGGTGGAAGAGCCCTCCCAGTCCTCCACTCTCTGCTGTCGACAACAAAAGGTACGAGAAAAGCAGCTCTTTAATCCGGGTTACATTTTAAACCGCTCTGGGCTGCATTTCTCAAAAGCGTCAGAGTTTTACAAAAGTCGATCCTAGAATCCTTTGCTGGTAAAAGTTCTACAATCTACTTAGATTTACAGTGCTTTTGGCAACGTAGCCCCAGGAATGAAAATAATCAACCGAAATGTTTTTGTTTGTTTCCTCAGCGCTCGGCCAGTTAGTAAAGGGGTGGAAGGTTTGGCCAGGGTGGGCTCAAGGGCAGCTCTTTCCTTTGCCTTTGCATTTCTCCGCCGAGCCTGGAGATCAGGTAAGCCCTTTCCGACATGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40738
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
ENSDART00000110770 Nonsense 273 4832 7 93
Genomic Location (Zv9):
Chromosome 6 (position 37720324)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37794082
GRCz11 6 37771976
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTGACATCCATGGAAGTGCCAGTGGAAAAGCACCCAGTAACATTCCCT[T/A]GCAGGATCAGCACTTGGCCCTTGCCATCCTGCTGGAGCTCGCAGTGCAAC
Long Flanking Sequence:
TTTGTGCCCTGTCAGGAGATGATGCAGACCTGTGCAGTGAGTTACTGCAGGAGTCTCTGGATGCTCTGCGGGCTCTTCCAGAAGCTACTCTGTTTGATGAGGGCACTGTATCTCCTGTTTGGCTGGAGGTGGTTGAGAGGGCTACTAAATTTCTAAGGTTGTCTTGTCATTTACACTATTCTCAAAGCATACATATTATGATTTTGCATAAATTCTCAAAGTTTAAAGAAGTCTAAAAATATTTTTTACTCATCAATGTTTATTTATTTGATTACAAAATGAAGTGGAAAAATGTTTAATTAATGTTACAATTAAAAACAGCTTTATTTTAATATATTTAAAATATTTATAGTTAAGAAATTAATTCCTGTTATGCCATCACTTAATAAGAGAAACACAATTTGAATGATTGCTGACATTTTTAAGCTTATTTTTCTATATTTTGTTTTTTAGTGACATCCATGGAAGTGCCAGTGGAAAAGCACCCAGTAACATTCCCT[T/A]GCAGGATCAGCACTTGGCCCTTGCCATCCTGCTGGAGCTCGCAGTGCAACGAGGAACTCTCAGGTATTCAGCATGCTCTTACATGAATTTTCCAAGAAATATTGACTGTGACCAAAAGCCATTTTCACTCCTAAATTTTTATTTTAAACCTTGCGTGTACCATTAAAAAAAAAAACTTTTTTTATTTATTTATTATATATATATATATATTTTTTTTTTTTCAAGACTGAAGCATTTTCATTCATAAATCCAGTCTCTAAACTGCTTGTTCATGTTTTTGTACTGTAGTCAGCTGCTGTCTGCAGTTCTGCTGCTTCTGAGGCTCTGGGACAGTGGAACTAGAGAGATGGATAATGAGCGCTCCACCCAAGGCACCAGCGCCCCGTTACTGCCCCTCCTGCAGCGCTTCCAGAACATCCACAGCAGTAAAGAGGAGCCTGTTCCTGAAGAGGAGATTGAGGTAAGCTCACCAAACAATAGTTAGAACTTTATCTTTCTTC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26783
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Nonsense 467 4832 10 93
Genomic Location (Zv9):
Chromosome 6 (position 37725165)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37798923
GRCz11 6 37776817
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGGTTTCCTCATCCTGACCATCACTGGTGCTGTCTACACACAAAACTA[C/A]AAAAGTACTACACTAGTAAGTTTCCCTTTTATTAGATTGATTTAGTTTTT
Long Flanking Sequence:
TAAAACACGAATGAATATGTTAAAACATATGCTTGCTTGTCGTAAAAATTCGTAATAATGACAAAAATACTTATTTGTGCACCTTTTTACTTCCGTGTGCAGCCAAAATTTCTTTACCCCTTGGTTTCGAGTGTGGTCCTGAAAAATCTCTGTTTCAAGGGCTATCTAGACCTTTCCCTAAGCCCTGTGCCTTCACGCTAAAGAGAATTGGGACACTCCTACCCCTTCACGTGAATGTGTAAAACGAGGGTTTGGGGTTAGGGGAAGGGCTAAGGGGTAGAATTAGGATTGGGTCTTAATAGAGTTCATTCTCTTTCCATTTTTTAGGGGACACTGCAGGAGGTGATTGGTTGGGGTCTGCTTGGATGGAAGCCTTATGCTAATGTGAATGGACCAATTCAGTGCAAGGCACTATCAAATCTGGGTGTCACGCAGATTGTCTGCTCAGAGAAGGGTTTCCTCATCCTGACCATCACTGGTGCTGTCTACACACAAAACTA[C/A]AAAAGTACTACACTAGTAAGTTTCCCTTTTATTAGATTGATTTAGTTTTTTTTACATTACATTTCAAACCAATGCAAGTGTTTGTGTATTACTGTTGCTGGTTTGTTTGTCTTTTTTTTTTTGCATTCTAAATCAATAAACCTGTTATTTTCTTTCAGGCACCTATGCTAGTCCATGCACTGACGTCCAGGAAAATAATGAAGCTTGCAGCTCATCCTGATGGCCAGCATTATTTGGCTCTTTCAGTCAATGGAGAGGTTTTCTCCTGGGGTTGTGGAGATGGAGGCAGGCTAGGACATGGAGACACTACGTAAGAGCACACCGATGTCAGAGAGTTTCTGCAGATCTAAAGATCTTTGCCTTTCATTTAAATTTAAAGTAACATCAGCTCTTGATGTGAAGATAAATGAGTGGATTTCAATAATTATCATAATTTGAAGACCAGTTATTAAAAGGGGATGGCGGTCAGCAGGTTCACCATCATTTCAAGATTAGGTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15868
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
ENSDART00000110770 Nonsense 667 4832 14 93
Genomic Location (Zv9):
Chromosome 6 (position 37727770)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37801528
GRCz11 6 37779422
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGGTGTGCTGTGGGAGCCAGTTCTCCGTAGCGCTCACTAAAGATGGA[C/T]ARGTTTACACCTGGGGCAAAGGAGACAATCAACGACTTGGACATGGCACT
Long Flanking Sequence:
AGCAGATGGAGAGCTTCACACATGGGGCCGAGGAAACTACGGCAGACTGGGCCATGGTAAATGCAGTAGAATCCTGTTTATACCATGACATGCAGTATTTGACTTTAGGACGAAGTAAAATGACACATATGTGTTTATTGATCCTGAAGGCTCCAGTGAGGACCAGACCACTCCCATGCTAGTAACTGCACTGAAGGGGCTGAAGGTGATCGATGTGGCCTGTGGAAGCGGAGATGCTCAGACGCTTGCTGTGACTGAGAATGGTGTGATATCTGACATTTGACTGCTTTTATTGTAATGATTGAGTGAAACAATCACTTTTCTCTTGATTGCTCTTTACAGGTCAGGTATGGTCATGGGGTGATGGAGATTATGGGAAACTGGGCCGAGGGGGCAGTGATGGATGCAAAACACCAAAACTAGTGGAGAAGCTCCAGGATCTGGATATTGTGAAGGTGTGCTGTGGGAGCCAGTTCTCCGTAGCGCTCACTAAAGATGGA[C/T]AAGTTTACACCTGGGGCAAAGGAGACAATCAACGACTTGGACATGGCACTGATGAACATGTCCGCTATCCAAAACTACTTGACAGTCTGCAAGGTTCAGTGTTTTCCTTTATTTTCAAACCATTGTTTTTTTTATTTACTGGAATTACTTGTACTGAAATTACATGTTTGGTTTACTGAGGCAAACCAAACATGACAATGTCTTGACACATTTCTTAGTTTGTATCTTATGAGTATCAGATAGGTCTTTCCCTGCACTGAATAGTACTGTATATACTTTTGAAGGTAAAATTGTTAGCCCTCCTATGAAATTATTGTTTTTAAGTTATTTGCCAAGTGCTTTTTCAGGGTCTTTTATCAACACATTTTTAAAATAATAATTTGTTAGTTTTAATAACTAATTTGTCATAAATAGTTTCTTCTGCCTTTGCCATGATAAGAGTAAACTAGTGTTAAAGTGCCATCTAAGGGGTTAACTAGGGTAATTAGGCAAGTCATGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44640
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
ENSDART00000110770 Nonsense 894 4832 17 93
Genomic Location (Zv9):
Chromosome 6 (position 37732757)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37806117
GRCz11 6 37784011
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCGTGCTCCAGAGTGGCTGGTCAGTGCTACTCCCCACTGCAGAGGAA[C/T]GAGCAAGAGCCCTGTCCTCGCTGCTGCCCAATGCAGGTCAGTGCATGAAA
Long Flanking Sequence:
TTTTAGATTACAAGTGCAAAACAATCAATGTAAGGTAACAAAATCATTTAATTAGTTTTGATTTCATTTGCACTATAATTCATAAGAAATTATTATTTTTTTATTTTAATAATATTTAACCTTTGTGCTATTTTTCTACTGTTTTTTTTTATCAAACAAATGCAGTCTTGTTGAACCGAGTAGTTTAAATTTCACATTCAAACCTCTTGATGAGTTTTGTAGGCTTATTGCTTCAAAAATATCAGTTTGATTGGTAGGGAATGTCTTGGAACAGTGCTTTAAAATGGGGATTTTTGTTTTGTGTCCAGCTTCATGCAGCCATCAGTAATCAGGTGGATCCCGAGGAGCTGGGTCTGGGTCTGGGCAGTGTGCTGCTTAATAACCTCAAGCAGACGGTGGTGACTCTGGCCAGCAACGGCGGGGTGCTAAACACTGTGCAGGCTGCCGCCCAGACCGTGCTCCAGAGTGGCTGGTCAGTGCTACTCCCCACTGCAGAGGAA[C/T]GAGCAAGAGCCCTGTCCTCGCTGCTGCCCAATGCAGGTCAGTGCATGAAATCTGTGCTTGGAAAAACAGCTTGAATTAATGCTTAATACTATTGGTATCTGTTTTCCTTTATTTTTATTAAGTGTTCCATTTATTTTATCATTTGTGGATAAGTGTCATCTTGGCACCATTGTATAAAGTCAAAAAATAAGTCGAGGTCTGTTTCCAGCAGAGTGTTGTTGGTCAAAAGCATTTCTGTGTTTTTTAGCATCTGCTAATGAGATGAGTGTAAGTCCTGGCCGTCGCTTCATGATCGACCTCTTGGTTAGTAGTCTGATGGCAGATGGAGGGTTGGAGTCTGCTTTGAATGCTGCCATCACGGCCGAGATCCAGGTCAGCATGTTTTATTTAATAGTCATTTCATCATTTATTCACCCTCCATGCCTTATATCTGCAACATCCCACAGAACCCTGCCAAAAACAGACAGAGGAGGAAACAGATTCATGACCCCTCAGGGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13507
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
ENSDART00000110770 Nonsense 1088 4832 21 93
Genomic Location (Zv9):
Chromosome 6 (position 37736814)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37810174
GRCz11 6 37788068
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACTCAGARATTCWGGGAGTTGGCTCTCTCYTGAAGAAGTATATGGCTT[T/A]GCKTTGCACACACATCGGTGATATCCTTCCTGTGGCCACCAGCATTGCCC
Long Flanking Sequence:
GCCACAGTCTTAGCCAATTCAACTAGCTCGGATGCTATTGAATGAAGCTGACCAGCGCTTAACGATGACCCAAATTTGGGTGGAGACTGGTGACTTGGTGTCTCAGGGTTTTTTTTTTCTAACTAACTGAATTTGCCTGTAGTAACACTTTTTGTGTGTGTTTGTTCTGAAGGAACATTGCTTCACAGACTATAGCCCGTCTTAAGGATGTGGCCCGACGCATCTCAAATTGTCAAGACACCGAGCAGGTCAGCAAGGAGCGCTCAGCCTCTCTGGACCTGCTGCTGCGCTTTCAGAGGCTTTTGGTCTGCAAATTGTATGTCGGAGTCAATGGCACTGTGGGTGTGGGAGGATACAGTAAGTAAAAGAACTTAATTTAGTGAATTTATTATGGAAGTTATACCATCTGTACATCTAATGAGAAGCATCTCTCATTGTCACAGCTTTGAGTCACTCAGAAATTCTGGGAGTTGGCTCTCTCCTGAAGAAGTATATGGCTT[T/A]GCTTTGCACACACATCGGTGATATCCTTCCTGTGGCCACCAGCATTGCCCTCAACAGCCATCGTCACTTTGCAGAGGTGGCTCGTGTCCTTGAGGGAGATCTTACAGGTGAAATGCAGTGCTATGTCATCAGACAATAATGACTTCTGTGAAAATCCACAGAAGAATCTTGCTCTAGAAAACTTGAAAGACTTTTTATTTATTTTTTTAAATGTATTTATGTATTTATTTTAAACTTTTTAAAATGTATTATTGTTGGTATGATTTTTTTTGGAGCAAGATCCTTATAGTCTAATCCAATTAAATTATTTAAACTAAGCTAAGCTAAAAGTGCTTCCGTAACTTCTAAGCTAAGCTAAAATTTCTGAAAATGTAAAAATGTTAAAACTCAACTTTTGAACTGTTTACAAATGATCTTCCTTTAAAAGACTTGGGGTTGAACATCTTTTTTTTTTTTTTTTTTTTTTCACATATTTCTTAAAAATAATAGGTGGTGCATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30874
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Nonsense 1166 4832 22 93
Genomic Location (Zv9):
Chromosome 6 (position 37737471)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37810831
GRCz11 6 37788725
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCATTCCTCTGCTCGCTGCTCTTCTGGAGCACTTGGACCGTTTTAACTA[T/G]CTTGCACCTGGTACAGAAAGAGATGACAATGAGGATCTTGCCTGGCCTGG
Long Flanking Sequence:
CACAGAAGAATCTTGCTCTAGAAAACTTGAAAGACTTTTTATTTATTTTTTTAAATGTATTTATGTATTTATTTTAAACTTTTTAAAATGTATTATTGTTGGTATGATTTTTTTTGGAGCAAGATCCTTATAGTCTAATCCAATTAAATTATTTAAACTAAGCTAAGCTAAAAGTGCTTCCGTAACTTCTAAGCTAAGCTAAAATTTCTGAAAATGTAAAAATGTTAAAACTCAACTTTTGAACTGTTTACAAATGATCTTCCTTTAAAAGACTTGGGGTTGAACATCTTTTTTTTTTTTTTTTTTTTTTCACATATTTCTTAAAAATAATAGGTGGTGCATTTTCAGACTGTCTGGTTTCTTCACCCACCAGGTGTTCTGCTACCAGAGCTCATTGTGTCCATTGTGCTGCTGCTGACCCATGATGCTGGACTAATGCAAGAGACTGGATCCATTCCTCTGCTCGCTGCTCTTCTGGAGCACTTGGACCGTTTTAACTA[T/G]CTTGCACCTGGTACAGAAAGAGATGACAATGAGGATCTTGCCTGGCCTGGACTCATGGGTATGTGAGAAATCCCTCTAAACTATTGTTTAATGTATATGAGTTATGCTTAAATCCAATCCTATTTAACATGAATGAAATTATAGCAAATGAGATGAATTGCTATATTTATGAATTTAGTGTAAGAGAATGTGGTAGGATGGCAAATAGATAACATCTTAGTGGTAAGATGACAAAGCAAAAATGCACAATGGAGTGAAGAAACAACAGTGATTTATTAGAGAAAAGAATTCGAATTTTGAAAGAACATGACCATGTGTGCACCACATGTGGATAACGGTAATAAGCTGTAAATATATATAACATAGANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCGTTGCAGTTGCTACTCTATGTTATATATATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13593
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
ENSDART00000110770 Nonsense 1331 4832 26 93
ENSDART00000110770 Nonsense 1331 4832 26 93
Genomic Location (Zv9):
Chromosome 6 (position 37740398)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37813758
GRCz11 6 37791700
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGCATGTNAAAAAAAAAGTCACTTGCTYCTATACCTYCCAGAATGGCTC[C/T]AGTCATCYATTTTCTTYGGTGGACTTCAGACCAGTCAGATCCACTATAAT
Long Flanking Sequence:
AAATAAGAGTGGCGGAAAACTGCTTTAGGAGGATGTTTGATGGGGAAATCACCCCCCTCCCTTACGAAAAAAAAAACAACAGGAAAAAAAATAACAAGACATGATAATCAATTTATAAGAAATTTTAATTACCAACTTCAAATAAATAAAATAGCAGATAATGTAACTAGTAAAATTATTTCTAACTATTTATTGATCAGTAAATTATGTCTGGCTGAACTGTATTACATATTATCATAATAGTATTTTAGTAATGGCACAGCCAGTTGGAAGAATGAATCTAAAGTCAAAAACAATAGTATGTTGATTTGACTGGCATTCAGTTCAAAATTAATAAATTTACAATTCATTTTTTTCCCTTGATAGTTTAGTAAAGTAATGAAAAATTCAACTCATTCTGTTCTGTACTGTACTGTACTGTAGAATGACCTGTTTTTGCAAAAAGATTTTAATGCATGTAAAAAAAAAGTCACTTGCTCCTATACCTTCCAGAATGGCTC[C/T]AGTCATCTATTTTCTTCGGTGGACTTCAGACCAGTCAGATCCACTATAATTATAACGAGGAGAAGGATGAGGACCACTGCAGCTCTCCAGGGACCACCACACCAGACAAAGCCAAACTGTACTGCCGCAGAATCACCCTGAGTGATCACGCCCAGCCCTTCCTGCAGGCCATCGCTGACAACACCACCCAGGATCACACTGTGAAGGTCACAGCATTTATTTGTCTCCTCATTTAATATTATGTATAATACAGATTTCTCTTTATAAATCTAAATATTTAGTTGTTACTCTGTTAATCAAAGTCAATTCAGGATAATGTGGCATGTACTGATTTATTAATGACTGAATTGTTTTTTTTTATTTGCTACAGGACTTTTTATGCCAAATCGAGCGGTGCTGTAAACAGTACCATCTCATCACTCCCATCACTTTTCCACCTGAACATCCTGTGGAGGAAGTGGGTCGCCTGCTGCTCTGCTGCCTTCTGAAGCATCAGGATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13641
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
ENSDART00000110770 Nonsense 1331 4832 26 93
ENSDART00000110770 Nonsense 1331 4832 26 93
Genomic Location (Zv9):
Chromosome 6 (position 37740398)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37813758
GRCz11 6 37791700
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGCATGTNAAAAAAAAAGTCACTTGCTYCTATACCTYCCAGAATGGCTC[C/T]AGTCATCYATTTTCTTYGGTGGACTTCAGACCAGTCAGATCCACTATAAT
Long Flanking Sequence:
AAATAAGAGTGGCGGAAAACTGCTTTAGGAGGATGTTTGATGGGGAAATCACCCCCCTCCCTTACGAAAAAAAAAACAACAGGAAAAAAAATAACAAGACATGATAATCAATTTATAAGAAATTTTAATTACCAACTTCAAATAAATAAAATAGCAGATAATGTAACTAGTAAAATTATTTCTAACTATTTATTGATCAGTAAATTATGTCTGGCTGAACTGTATTACATATTATCATAATAGTATTTTAGTAATGGCACAGCCAGTTGGAAGAATGAATCTAAAGTCAAAAACAATAGTATGTTGATTTGACTGGCATTCAGTTCAAAATTAATAAATTTACAATTCATTTTTTTCCCTTGATAGTTTAGTAAAGTAATGAAAAATTCAACTCATTCTGTTCTGTACTGTACTGTACTGTAGAATGACCTGTTTTTGCAAAAAGATTTTAATGCATGTAAAAAAAAAGTCACTTGCTCCTATACCTTCCAGAATGGCTC[C/T]AGTCATCTATTTTCTTCGGTGGACTTCAGACCAGTCAGATCCACTATAATTATAACGAGGAGAAGGATGAGGACCACTGCAGCTCTCCAGGGACCACCACACCAGACAAAGCCAAACTGTACTGCCGCAGAATCACCCTGAGTGATCACGCCCAGCCCTTCCTGCAGGCCATCGCTGACAACACCACCCAGGATCACACTGTGAAGGTCACAGCATTTATTTGTCTCCTCATTTAATATTATGTATAATACAGATTTCTCTTTATAAATCTAAATATTTAGTTGTTACTCTGTTAATCAAAGTCAATTCAGGATAATGTGGCATGTACTGATTTATTAATGACTGAATTGTTTTTTTTTATTTGCTACAGGACTTTTTATGCCAAATCGAGCGGTGCTGTAAACAGTACCATCTCATCACTCCCATCACTTTTCCACCTGAACATCCTGTGGAGGAAGTGGGTCGCCTGCTGCTCTGCTGCCTTCTGAAGCATCAGGATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40739
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Essential Splice Site 1399 4832 26 93
Genomic Location (Zv9):
Chromosome 6 (position 37740606)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37813966
GRCz11 6 37791908
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCTGCAGGCCATCGCTGACAACACCACCCAGGATCACACTGTGAAGG[T/G]CACAGCATTTATTTGTCTCCTCATTTAATATTATGTATAATACAGATTTC
Long Flanking Sequence:
GTCTGGCTGAACTGTATTACATATTATCATAATAGTATTTTAGTAATGGCACAGCCAGTTGGAAGAATGAATCTAAAGTCAAAAACAATAGTATGTTGATTTGACTGGCATTCAGTTCAAAATTAATAAATTTACAATTCATTTTTTTCCCTTGATAGTTTAGTAAAGTAATGAAAAATTCAACTCATTCTGTTCTGTACTGTACTGTACTGTAGAATGACCTGTTTTTGCAAAAAGATTTTAATGCATGTAAAAAAAAAGTCACTTGCTCCTATACCTTCCAGAATGGCTCCAGTCATCTATTTTCTTCGGTGGACTTCAGACCAGTCAGATCCACTATAATTATAACGAGGAGAAGGATGAGGACCACTGCAGCTCTCCAGGGACCACCACACCAGACAAAGCCAAACTGTACTGCCGCAGAATCACCCTGAGTGATCACGCCCAGCCCTTCCTGCAGGCCATCGCTGACAACACCACCCAGGATCACACTGTGAAGG[T/G]CACAGCATTTATTTGTCTCCTCATTTAATATTATGTATAATACAGATTTCTCTTTATAAATCTAAATATTTAGTTGTTACTCTGTTAATCAAAGTCAATTCAGGATAATGTGGCATGTACTGATTTATTAATGACTGAATTGTTTTTTTTTATTTGCTACAGGACTTTTTATGCCAAATCGAGCGGTGCTGTAAACAGTACCATCTCATCACTCCCATCACTTTTCCACCTGAACATCCTGTGGAGGAAGTGGGTCGCCTGCTGCTCTGCTGCCTTCTGAAGCATCAGGATCTTGGTAAGCTAGAAATAGTTTGTTGTTTGAATGGCAGAAGCTAAAATCTATGTATAGTTTCCAGATTTTTACTCTTTGAACTAACCAAAAACAGTGCTGTGCATTTCACATCTCGATTTAATAGTATTTTTGTTGTCATTTATTTATTTCTTTATTGGAGGTCAGGTTTTTCTTTCATTGTTTTATGTTATTATTTGAATGTTGCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33904
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Nonsense 1463 4832 28 93
Genomic Location (Zv9):
Chromosome 6 (position 37741232)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37814592
GRCz11 6 37792534
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCCCTCTCCCTAGTTGATCAATGTGCCTTGGGTATGGACCAGGGGAAA[C/T]AGAGGTCCCTCCCGAAATCTGTGATTGATGTGTGTCGAATGGTGTATCAG
Long Flanking Sequence:
TATTAATGACTGAATTGTTTTTTTTTATTTGCTACAGGACTTTTTATGCCAAATCGAGCGGTGCTGTAAACAGTACCATCTCATCACTCCCATCACTTTTCCACCTGAACATCCTGTGGAGGAAGTGGGTCGCCTGCTGCTCTGCTGCCTTCTGAAGCATCAGGATCTTGGTAAGCTAGAAATAGTTTGTTGTTTGAATGGCAGAAGCTAAAATCTATGTATAGTTTCCAGATTTTTACTCTTTGAACTAACCAAAAACAGTGCTGTGCATTTCACATCTCGATTTAATAGTATTTTTGTTGTCATTTATTTATTTCTTTATTGGAGGTCAGGTTTTTCTTTCATTGTTTTATGTTATTATTTGAATGTTGCATTTTGTTGCTTAATTAAAAAAAAAAAAAAATCTGTTTTTTATTTGAGGGAGACATTTGTGTTCTTGTGCAGGTCATGTCGCCCTCTCCCTAGTTGATCAATGTGCCTTGGGTATGGACCAGGGGAAA[C/T]AGAGGTCCCTCCCGAAATCTGTGATTGATGTGTGTCGAATGGTGTATCAGGCCAAGTGTTCGTTGATAAAAGTGAGCATTTAAATAAGATTACTCCTGGATTATTATTTTATTGTAGTGTTCTCTTATTTTAGTGGTAATTTTTGGGAATTCATTTTTAAATTAAATCTTACAATTTGTTCAAAAACTACAACAAAACCATACGGAATCTGCAAACGTTTTTTGCTAAATCTGCGAAGAATTTTGGTAAAAATCTGCGAATTTCTGTGGAATTATTTTGGGAGTATTATAACTAAAACCTTAATATGTGACTTATTTAATGTTTAAAATGCAAATCCAATTAGATTCCTATTATTTGGTAAACAAAGCAACAAAGCAATCTCATATAATATATCTACTAAAATACAATTTATTACTGTACAAACTGCATTTTCATATTAATCAATAATATTATTGTCATTAATTTATAAACTGAATAAATAAAGATTTACAGAATTAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33905
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
ENSDART00000110770 Essential Splice Site 1595 4832 30 93
Genomic Location (Zv9):
Chromosome 6 (position 37742438)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37815798
GRCz11 6 37793734
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGCCCCGCTCCTGTTGACAAGAAGCAAACAACTGTCAAATCTGCAAAG[G/T]TTTGCCACTTTCTATTTACGTTAATTTTTTAAGTCACTGTCCTTTTAGAA
Long Flanking Sequence:
TACACAGATATATTGGGTTTAGGTGAAGCATATCATGTCTTTCTGGTTATTTACATCATAATGATTGATTATGATTTCTGTCCCTTCTATAGACACACCAGGAACAGGGTCGTTCTTATAAAGAGGTGTGCGCTCCTGTTATTGAGAGGTTGCGTTTCCTGTTTAATGAGCTACGACCTGCCGTCAGTAATGACTTGTCCATTGTGTCCAAACTCAAACTGCTGAGCTCTCAGCCTCGCTGGAAGAGGATCACACAGAAACTGATCAGAGACCGCCGCAAAAAGAGAGGTGATGAGTCTAACCAATGATTTTAAATGTGTGTAAGGATGTAGAGTCTATAATTATAGCACGTTTTGCTTGATCTTTCAGTGCCTAAAAAGTCGGAGTCAGCTGATCTGGAGGAGTGCAAGATGGAGAGGGAAGGGACCAATGAGGAACCACCTGCTCCTCTAAGCCCCGCTCCTGTTGACAAGAAGCAAACAACTGTCAAATCTGCAAAG[G/T]TTTGCCACTTTCTATTTACGTTAATTTTTTAAGTCACTGTCCTTTTAGAACTATTTAAAGGTGCAGCATGTATGATTTACACCTACCCAGTGGTTGAGGTTTTGCAGTCCAAATACAAAATATTGGATATATATTTTATATATTTTTTTTTTTCCCCACCCGGTCCTCCTGCCAACCACTTAATTCGCATGCAGGCTACCAGATTGATGACACAAACATGAGTAAGCGTGTCTGATAATTGGGTCGCACACCAGACACGCTGCTCTGTGCCACACTGTGACGCACTATGCACATCGAAGCTGTTATTAATCTCCTGTTCGCATTGCTTAGTACACAACCCTTACACAACTATGTATCGACAGGGCATCTGGTGTGCGACCCACTTTATAATGCAAGCTGTTTAGCTAATGTTTACATCTGTAATATTTGCATGATTTGCTAATTAAAGACCACCTAATGAACTTGTATCTCGTTTTGGAGGCTGCTACTGCCCTCTGTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33906
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
ENSDART00000110770 Nonsense 2185 4832 41 93
Genomic Location (Zv9):
Chromosome 6 (position 37751571)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37824931
GRCz11 6 37802867
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTAGTTCTCCTATGCTGTTTTTTCTGTCAGGCTTTGCTTGAAGACTA[T/A]CTCCCCAATGCGGAAGCAGCAGCGGTGGGCAGTCTGATGGCTGTTTTGGC
Long Flanking Sequence:
AGCTTGCTCAGCACTTGTTCTTCAGATCTGCCTCTTCTTAGGGGTATATTACTTTTGTTATTTCTTTGCTCAATGTGTTACTCCGTTCTTTTATTATAGGTCGAGCAAACTCTGATATCAGGATTTCACCTTAACATCTTTGTGACTTACAGAAGGTTCAATGCGTAGGAGGAAGTCCCGCCCCCAGGCCTCACTGACAGCCACTCATAGCAGTACTTTGGCAGAGGAAATAGTGACAGTATTGCGCACGCTTCACTCCCTCAGCCAATGGAATGCCCTGATTAATGAATACATTAACTCTCAGCTCAGTGGAATCGGGGATGTCATGGCAGGCCGACACACTGAAGTGGTAAAAGTCACATTTTTATATGTTTTTGAATTTTTGATATATTAAAGTTGACAAAATTATATTTAGGTGCTCAGTATTGATAATGAGGTATGACTAGAGGATGGTTAGTTCTCCTATGCTGTTTTTTCTGTCAGGCTTTGCTTGAAGACTA[T/A]CTCCCCAATGCGGAAGCAGCAGCGGTGGGCAGTCTGATGGCTGTTTTGGCAGTCATCGGGGGGATTGATGGACGTCTGCGTCTGGGTGGACGTGTGGTCCATGAGGAGTATGGAGAAGGCACAGTGACTCGCATCACACCTAAAGGACGAATCACTGTTCAGTTTCATGAGATGAGGAACTGCAAAGTGTGCCTGCTCAGTCAGCTCAAACCGGTACATATGCACTTACATGCAGTATTGCTTTTTGTTCATTCGTTACCCTGGAGATTCATGTTAAGAATAGTGTAGGGATGAGACAAATTTTTTCTTTCATGAAAAAATTAAAAATGACCCCAAACCTGCAAGTATAGGTGTTGACAAGTCCCTGACAAGCTATTTATTTAAAACGGCTGATACATTTAGCCAAAACTTGCATACCTAAACATTTTAATGGCAATATGTATTATAAATAATATTCATAAAGCACTTCTGCAGATATATATTAAAAATTTAAAAATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38562
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
ENSDART00000110770 Essential Splice Site 2303 4832 42 93
Genomic Location (Zv9):
Chromosome 6 (position 37752254)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37825614
GRCz11 6 37803550
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTGGAGAAACAACGCATGAAGAAATCTCTTAGTAGAGGACTTACAGG[T/C]ACAGCACATGCACAGATCCATAGAAAAACACATATTTGTTCACTTGATCA
Long Flanking Sequence:
CAAAGTGTGCCTGCTCAGTCAGCTCAAACCGGTACATATGCACTTACATGCAGTATTGCTTTTTGTTCATTCGTTACCCTGGAGATTCATGTTAAGAATAGTGTAGGGATGAGACAAATTTTTTCTTTCATGAAAAAATTAAAAATGACCCCAAACCTGCAAGTATAGGTGTTGACAAGTCCCTGACAAGCTATTTATTTAAAACGGCTGATACATTTAGCCAAAACTTGCATACCTAAACATTTTAATGGCAATATGTATTATAAATAATATTCATAAAGCACTTCTGCAGATATATATTAAAAATTTAAAAATAAAGGTTTGTGTGATGTGAATTTTGTTTTATGGATGTCTTTGCAGCTTCACATGATTCCATTCAGCGTTCAGAATCTGCCCTTCGCTGAGCCCATGCTAATGGTGTGGGCCCAGCTAGTCAACTTGGCTGGGAGCAAGCTGGAGAAACAACGCATGAAGAAATCTCTTAGTAGAGGACTTACAGG[T/C]ACAGCACATGCACAGATCCATAGAAAAACACATATTTGTTCACTTGATCAGTCCATATTTGGCCTACTTGACCTCTGCATGGTACAGGGTTCCCACACTTCCTGAAAGAACAGTACTTGAATGTCAGACATATGGTTAAGGACTGAAAAGTACTTTAGTAAAAAAAAAAACACAGGTCTTTCAAAGTGTGTGAATTACACTTTAAATTAATTTTGTTAATGCTGTTATTTGAGCAAGTGTACTGTGCTGCCATAAAAAAAGATAAATTCTTAATTTTAAAAATAATAAATTTTGTACAAGAACTGTGGGAAATAATGGACATTTGAACATTGCCAGTATCAAGTTCAACACATTTTATCACATTTTATAAACATAAAAATAAAAACGTTTCACATTTTTTGAAAATGAAACATTCTAAACATCATAATATCTCTACTATTTTAATGTAAATATTAAGTATAAGCAAACTGTTAAGAACAGTAAGGAGTTTCATGGCACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20751
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Essential Splice Site 2535 4832 46 93
Genomic Location (Zv9):
Chromosome 6 (position 37757566)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37830926
GRCz11 6 37808862
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGAGGTGCTGGAAGAGCTTGAGGAGCCTGAGCCTGCCTTTCCTGTGG[T/A]ACATACAAATACACTGATCACACAATCCAGATGTGAGGTGCTGATTCACT
Long Flanking Sequence:
CCCCCTGCTCCCATCGTCCTGCAGCTGATGGAGATGGGCTTTCAAAGGAAAAACATCGAGTTTGCTCTTAAATCACTGTCTGGAACCACAGGTGCTTCTGGAGTGCCAGGTAAAAACATAATTGCTTACGTTGGAGCATGGTATTATCATTGTCTTAAAGAAAATATCCTTTATCCTAATTTATTCATACCCTAAACATGAATAAATTAGACATGATGTATGCCGTATGTTTCAATATAGATATTTATTGTCATTTTGTCATTAAAAAATGTGTCCTAGTGATTGTTAAAAAAAACCTGTAAGAATACATAGAGCAATTTTTGCAAGCAACTGATTCTTTATTGCTTTGGTTTTAGGTGTCGAGGCATTGGTGGGCTGGTTGTTGGACCATCCAGATGTTCTCATTACAGATCTGTCGGATGCAGAGACTGTATCAGATGAATACTCTGATGAAGAGGTGCTGGAAGAGCTTGAGGAGCCTGAGCCTGCCTTTCCTGTGG[T/A]ACATACAAATACACTGATCACACAATCCAGATGTGAGGTGCTGATTCACTTGTTGTCATCAAATGTGTGGCTGACTAATGCTCTTTCATTCGCATGTCAGCCTCCTGGGGTTGTGGTGACTGAGAGTCAGACGTTTAAAAAGAGGTCGGACTTTCAGAGCAATGACGATTATGCTGTTTACGTGAGAGAGAACATTCAGGTGAGGTGTTATTCATATTCCTTAATTTTCTGGAAAATAAATAATGTGAAATCAGCTACTGGTAGCCCTGAATAAACTGAAACATTTACAATTATGTATTTTAGTTCCTGCCACTTCTCCATAGTATTCAACAGAATTCAAAACAGAAATGTAAGCGATGAATAGTATACATTAAAGCAAAATGTCACCATGTGGTAAATGAACTTCATATTCCAAATGCTTACGTTTTTTTTTCTTACATTGTTTGTTTTGTAATGTGCTTTGAAATATAAGTGAATTTACATCAGATTTTGTCATTCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10421
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Essential Splice Site 2625 4832 48 93
Genomic Location (Zv9):
Chromosome 6 (position 37758769)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37832129
GRCz11 6 37810065
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAAAGGAGGAACYTACTGGGTCCGTTACATCCACACTGAGCTGCTGGG[T/C]AATACTCTTTMTGTTCTCTTAMACATTTTTATAGGTATTTGTTAATTGAA
Long Flanking Sequence:
TATTTTTCATGTGTAATAAACCTTTAGGTTTGTTGTCTGAACAATCTCAAAATGAGCCCAAATTTATACATAAAATGAGGAAAAAGCTATAAGTCAATTATGTAAAAAAAAAAAAAAAAAGCCTTTTTTCTTGTAAATGTTTGTCGTTTTAAATGACATTTACTGGAAAAACAAGAAAAATAATAAAGAAATAATAATGAAATCAATAGTAAATTATATTATAATAACATATTTTTTCTTTTTTTTAAAGTGTTCTTTCATGATTTTTAATATTCAGATTGTGTTCTAAAGTTTGGGTGGTAACTGATCTGAGCTCCGTGTGTGTTGCAGGTGGGCATGATGGTACGGTGTTGCAGGACATATGAGGAAGTGTATGAAGGAGATGTGGGGAAAGTGATCAAGCTTGACAGAGACGGCCTGCATGACCTGAATGTTCAGTGTGACTGGCAGCAGAAAGGAGGAACTTACTGGGTCCGTTACATCCACACTGAGCTGCTGGG[T/C]AATACTCTTTCTGTTCTCTTACACATTTTTATAGGTATTTGTTAATTGAAGCTGGAATTGTGTCATTATAGAAATGTACGGTTGTATAGTTATTGAAAAAAAAATTATATAAACTTCTATTTTCCAGGGTTTCCCCCTCAGAGTTCTCCATCTCATATAAAGATTGGTGATAAAGTGCGAGTGAAGCCCTCGGTCACAACACCAAAATACAAGTGGGGGTCAGTCACTCATAGGAGTGTGGGTGTGGTCAAAGGTAACACGATTGTGTTTAAATTCAGTTCATCTTTATTTCTATAGCACTTTTACAATGTTGATTGTGTCAAAGAAGCTTAGCATGGACGAAGTTCTGGTAAATTTAAACTGCTGATCTGCTTCAGTCCAGTTTGCACAGTTTAGTACTGCTCAGTGTTATGTAAATGTCACTGTTGAAAGCTAAAACACTGAAGAGCAAATCCAAAGATACGCAGGACATTTTAATGATATGGTAATGTTAAACAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20752
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
ENSDART00000110770 Nonsense 3466 4832 66 93
Genomic Location (Zv9):
Chromosome 6 (position 37771813)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37845173
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCAGAGAGTGAGGAGAGGGTCAGTCCGCACCCCTGGATGGACAGCAAA[C/T]GAGGAGAGGTGAGGAGTTCTGCCAATTCTTGACTGTGTGTGTGTATGTAT
Long Flanking Sequence:
TTGCCATCAGAGTCTCAATAGACAGCCTTTCTATGAATATTTGCTGTATTACAACTAATGAGGTGGACTCAAAATGAACTTAAAATGCCTGTGTACTATGTAACGATTTTATTAGATAGTTTTCCAAATATTATTATGCAGTAATAGTTTTTAATATCTATGAAAGTTAGTACATATATTAATGGTTTTAGTGTATATAGGCATTTTGTTTCTGTCCATTTCAGTAATAAAACAAATATTTTAAAAAGAATTATAAAAACAGTTAAAGCAATGCAAAGCTTTGGCATCCTTTAAACACTCTCACATCTTTCACACCCCATAGAGATGCAGTGGTGGGTGCATTAATGCCATCCTGTATGATGCCTCTGGAGTGTCCCTCCAGCTCTCCGGTGCCCCCATCAGACTGTTCATCAGCTTCCAGCCCCTGTGAGGCTGAGGGTCCTGCCCTGCCCTCAGAGAGTGAGGAGAGGGTCAGTCCGCACCCCTGGATGGACAGCAAA[C/T]GAGGAGAGGTGAGGAGTTCTGCCAATTCTTGACTGTGTGTGTGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTGTGTGTGTGTGTATATATGCATGTATGCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCAGTGATTCATTTGTTCCCAAACCCCTCCTTAGCGCGAAGCTAATCTGCGCTGATTGGACCGATGACAGTCTGTTGCGATTGGTCGACTGCCTTCAGTCAGAGAATGAAATGCCAAACAGCTAATCAGCAATATAAAAGTAATCACAGTTCATACACGCTCGATAGTGTAAGGCGTGGATTTTAGCTGCCAGTGGGTCAATGTAAATACAGACTATGGACTTGAAAATACAGACGACTAACTATTTTATTGAGCAAAAACTCCAAAAACAGTTGAGGAGATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20753
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Nonsense 4262 4832 82 93
Genomic Location (Zv9):
Chromosome 6 (position 37784148)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37857508
GRCz11 6 37834714
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAAAAAGGTCATCGCAATAGCAACTGGTTCCCTTCACTGCGTTTGCTG[C/A]ACGGAGGACGGTAGGTCATTAGTATGTTTGAATTATGCTGGCCTTTGTCA
Long Flanking Sequence:
TTTAACATTTCCTATGACAAAAGCTATCCCTTTATCGTTTACAGATGGAAGCTCAAACCATTTGCGAGACAACCTATCAAAATAGTTTCAGTTTGTTTTGGTTTAATTTGAAAAATGTAATATTTCAAAGTGTTCCAAATGTTTTTTATTTTTCATAATTTGATGTTAAACTGAGTTTTTTTGTTGTATTTAATTCTACATTTTTTGATGAATAAACTAAAATGAAAAAATCTGAAAAAATAGAATTTGAGGAAAAAAGTAATAAAAATTTTGGAAAAAATAAATAATTTCATAGGACTGTACATAATGCATTGTAACATAAGCTGATGTTATATTTAGTGTGGGTAATTGTACATGTTTGTGTTTTTTAGGGGGAAGGGTGACTATCACAGACTGGGACACGGCTCAGATGATCATGTTCGCAGACCCCGGCAGGTCCAGGGTTTACAAGGCAAAAAGGTCATCGCAATAGCAACTGGTTCCCTTCACTGCGTTTGCTG[C/A]ACGGAGGACGGTAGGTCATTAGTATGTTTGAATTATGCTGGCCTTTGTCACTTTTTAGGTATTCTGTCTTCTGTTGAACCCAAAACAACATATTCTGGAGAATGTTGGAAACCAGCAGACGTTGACATCCATAGTAGGAAGAAAAAAATACTATGGAAGTCAATGGCTGCTGCTTCCCAACATACTTCAATATATTCTTTATGTTCAACAGAAGAAGGGAAAAAACAACATATTTGGAATAAATGGATGAGTAAATAACAGAATTTACATTTTTGTGTGAAGTGTCCCTTTAATGAGCTACCTTTTTTTTGTTCTCTGAGGTCCACTAATAACATTACATAGTACATTTATACATTACACAATTACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGTATTTGTATATATATTGTATTTGTATAATGTGTGTATATATATATATATATATACACACACACACACACACAC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26784
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Essential Splice Site 4394 4832 84 93
Genomic Location (Zv9):
Chromosome 6 (position 37785965)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37859325
GRCz11 6 37836530
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGTTGGCTTTGACACGCTCCGTGGAATCCTCATATCACAGGGCAAGG[T/C]GAGGTTGCAGGTAGCAGTACATGTACTGTTTTCATCCAAATGTTTCTCAA
Long Flanking Sequence:
TTAGATGTCAGAAATGATTTCAATTATTTATTATTTCGTTAAATATTAACAATTTTTAACAAAAGGATCTAATTTGTGTCAGTCACAAAAAACATATGTATAAAAAAATGTAGCTTTTAATACGATATGATACGATACAAAACAGTACAGTACAATTGAACTTTTAAAAATGAATAAGAACAATATAAGCAGTTTAAGACGCTTTGAACCACAGGACGCAGTACAGTTCAGATTATTGAAAACTTGTATTCCAGAAAGTACAATAAATATTTGTGGTTAATAATGTCATGTCTGTCTGTAGGTTCCAATGGAGTACAACCACCTGCAAGAAATCGCCATCATCGGCCTGAGGAATCGGTTACTGCTACTGCACCACATCTCTGAGCTCTTCTGCCCCTGCATCCCAATGTTTGACTTAGAAGGACGCCTGGGTGAAACTGGACATGGTGTGTCTGTTGGCTTTGACACGCTCCGTGGAATCCTCATATCACAGGGCAAGG[T/C]GAGGTTGCAGGTAGCAGTACATGTACTGTTTTCATCCAAATGTTTCTCAATTTTATTACATTTAAAATTGACTAAAATTGAAAAAATTGTGGTTTGATCATAGGGGTAAAATGTGATTTAAATATGACTTTATTTTAAGCGTATTTTAAAATAACATTTAAAGTGACTGTTTATTAATTTGTGAGGTTGCTCTGTAATTCTTAAAAGTTGTTTAGTGTTGTGAAATAAATATTGTTCCAAATATGCCAGGCAAGATTTTATAGGGGTGTGAACCTACACTGGTCTCACGGTTCGGTTTGGTTACGATTATCCTGCCAATTTGGTTCAATTCGATATCTCGGTGCATCATGGTGTATTGACGTTGCTTTCCATACACAATTAGATTTTTTCTTTACAACACAACAAAAAAATTGTATCAAAACCTATAAATATGTTTAGATATTATTTGTAATACAATTTTGTCCTTTAATACAAGCAGTCAGATATATAAACTTACTTGT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26785
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110770 Essential Splice Site 4535 4832 87 93
Genomic Location (Zv9):
Chromosome 6 (position 37790567)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 37863927
GRCz11 6 37841132
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCAGCTGCCAAATCCCCTCTGCACATCAGCATGTTCCGCTTCCTAGG[T/C]ACCAGCTGCACTCAAAACACTTTCAAGGCAGTCTGGAGTTACACAGCTGC
Long Flanking Sequence:
ATGATCACAATGATTGATACGCAAAGGCCTAATCATTGAGTGAATGTGGGCAGCGACACAATCATATTCAGAAGTTTTGGTTTGTTTACTCAAACACAGAAACTGAAATCCCACAATTCAAAAACTAAAACACGGTCTGCAGCTTTTCTGAAAGTCTCTGTTATTGAAGGTCGAAAACTCTGCAGTATTATGGAGTCTAGAACAAAAAAGCACAGCTGTAAACCCAGCCTTGCGGATGGAGGATTTTACATTAGAGAAAGAGGATGTTTATCATGTTTTTGTGTGTTTTTTTTTTTTTTTTTAGGTGAGTCGGTGGATGACTGTGGTGGCGGATACAGTGAATCTATCGCAGAAATGTGCGAGGAGCTTCAGAATGGCCTCACTCCTCTGCTCATCGTCACTCCTAATGGCAGAGACGAGTCAGGAGCGAACAGAGATTGCTTTCTGCTCAACCCAGCTGCCAAATCCCCTCTGCACATCAGCATGTTCCGCTTCCTAGG[T/C]ACCAGCTGCACTCAAAACACTTTCAAGGCAGTCTGGAGTTACACAGCTGCAGTACTTTCTTCTGTCAGATTTGGCAGTAGAGCATGCTCTGTTCTTGTATTTGTGTTTAGGGGTGCTCCTGGGCATAGCGATCCGAACAGGAAGTCCTCTTAGTCTGTATCTGGCCGAACCTGTGTGGAAACAGCTGGCAGGCATGAACCTGACCATTGCTGATCTCAGTGAGGTAAGACTGAATGTGTGTGTTTGAATCCAAAGTTATTCTATTATTGTTAACAAAATTAACATTTTAAAGGCATGCATTTAACTAAATTAAAAATACAATAGGTAGCATATTTACACTTTAATGGGTTTATTCAAATTTAATTATTTGGTCTGATTTTAGTTTTTAGACTGGATTAACAAAATGACAAAGCATTAAATGAAAAAATTCAACGTAACTGCATTGGTTTGGTTTGTTAGGGTTAACTAGGTTAGGACTGGTTTTGTCTTATTTTATCCTA
Associated Phenotype:
Not determined