Busch Lab

ZMP

A5D6S4_DANRE

Ensembl ID:
ENSDARG00000021004
Description:
LOC565774 protein [Source:UniProtKB/TrEMBL;Acc:A5D6S4]
Human Orthologue:
C5
Human Description:
complement component 5 [Source:HGNC Symbol;Acc:1331]
Mouse Orthologue:
Hc
Mouse Description:
hemolytic complement Gene [Source:MGI Symbol;Acc:MGI:96031]

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa33747 Nonsense Mutation detected in F1 DNA Not yet available
sa40586 Nonsense Mutation detected in F1 DNA Not yet available
sa17323 Nonsense Available for shipment Available now
sa20567 Nonsense Available for shipment Available now
sa20568 Essential Splice Site Available for shipment Available now
sa33748 Nonsense Mutation detected in F1 DNA Not yet available
sa33749 Nonsense Mutation detected in F1 DNA Not yet available
sa31483 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa33747
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 Nonsense 200 1050 6 25
ENSDART00000097325 Nonsense 198 1702 6 43
Genomic Location (Zv9):
Chromosome 5 (position 66665734)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62811952
GRCz11 5 63505343
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCACTGCATCTTTTATTCACAATCCAAACCCCACCAGTTATGGAATCT[G/A]GAAAATTGTGGCCACATATGCTGACAATTTTGAAACGACTGCTACTGCTG
Long Flanking Sequence:
CCCCTCTAAAACCAGCCTGGTCGACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAAGCTGGATTTTTCAGCAGGGATGTCTTTGGAAACCGGAGCACTTGAAGAAAACTGACGCTAATGCAGGGAGAACATGCATCTCAATTTTCAAAGTTGTGATATTCTTTTTGAATCACACTGTATTATAAGTAGCTGTAATTAAATTACCTAAAAATAAAAAGTTATCTCTCGCTTTACTTTAAGGGCAAAAAAAGTTATTTAGTTACAGTAGTTACTTTGTTTACTTAGTACTTGGTACTTACTGATCACTTAGTGAACTTACTAACATACTTAATTCTTTGTTACCCAAGTAAGGTTGTTGAGAATTAGTTAAGAAGCCTGCCATATGCATATATCCTAAATTTCATCATTTATTTTTATTTTTTTCATGTGTTTTTATCTTTATTTTATGTCACTGCATCTTTTATTCACAATCCAAACCCCACCAGTTATGGAATCT[G/A]GAAAATTGTGGCCACATATGCTGACAATTTTGAAACGACTGCTACTGCTGAGTTTGAGGTCAAAGAATATGGTAAGGCCGCCATTTATGTTTCAACTGGCTGTGCAGACCTTTAGAGTTTGTGAAATCTGAAATCGAGATGTTTTACAGTGTTGCCCAGTATTTCGGTCCAAATTGAGCCGGAAACCAACTACATCAGTGAAGAAAACTTTGACACTTTCAAGCTGAAGATCTCAGCCAAGTAGGTTTTCCTTTTTCTTCAATTTAACACATACAAACTACTTTTCAAAAGTATTTAAGTTAGTCATTTAAAGATTTTTATTGAGCAATGAAATATTAAAGAAACACTCCATTTAAAAAATAAAAAATAATAATTCAGCTGATCTCTGGGTCTGGCGGGAGCACTTTTTGCTTAGCTTAGTTTAACATAGATCACTAAATCAGATTAGACCATTAGCATCTCACTCAAAAATTTCATGAAAGAGCTTTAATAATTGTACT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5335
Status:
Allele not cryopreserved
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
ENSDART00000002540 Essential Splice Site 224 1050 6 25
ENSDART00000097325 Essential Splice Site 222 1702 6 43
Genomic Location (Zv9):
Chromosome 5 (position 66665807)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62811879
GRCz11 5 63505270
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAATTTTGAAACGACTGCTACTGCTGAGTTTGAGGTCAAAGAATATGG[T/C]AAGGCCGCCATTTATGTTTCAACTGGCTGTGCAGACCTTTARAGTTTGTG
Long Flanking Sequence:
AGCAGGGATGTCTTTGGAAACCGGAGCACTTGAAGAAAACTGACGCTAATGCAGGGAGAACATGCATCTCAATTTTCAAAGTTGTGATATTCTTTTTGAATCACACTGTATTATAAGTAGCTGTAATTAAATTACCTAAAAATAAAAAGTTATCTCTCGCTTTACTTTAAGGGCAAAAAAAGTTATTTAGTTACAGTAGTTACTTTGTTTACTTAGTACTTGGTACTTACTGATCACTTAGTGAACTTACTAACATACTTAATTCTTTGTTACCCAAGTAAGGTTGTTGAGAATTAGTTAAGAAGCCTGCCATATGCATATATCCTAAATTTCATCATTTATTTTTATTTTTTTCATGTGTTTTTATCTTTATTTTATGTCACTGCATCTTTTATTCACAATCCAAACCCCACCAGTTATGGAATCTGGAAAATTGTGGCCACATATGCTGACAATTTTGAAACGACTGCTACTGCTGAGTTTGAGGTCAAAGAATATGG[T/C]AAGGCCGCCATTTATGTTTCAACTGGCTGTGCAGACCTTTAGAGTTTGTGAAATCTGAAATCGAGATGTTTTACAGTGTTGCCCAGTATTTCGGTCCAAATTGAGCCGGAAACCAACTACATCAGTGAAGAAAACTTTGACACTTTCAAGCTGAAGATCTCAGCCAAGTAGGTTTTCCTTTTTCTTCAATTTAACACATACAAACTACTTTTCAAAAGTATTTAAGTTAGTCATTTAAAGATTTTTATTGAGCAATGAAATATTAAAGAAACACTCCATTTAAAAAATAAAAAATAATAATTCAGCTGATCTCTGGGTCTGGCGGGAGCACTTTTTGCTTAGCTTAGTTTAACATAGATCACTAAATCAGATTAGACCATTAGCATCTCACTCAAAAATTTCATGAAAGAGCTTTAATAATTGTACTTTTTACAGATTGACTCTTCTGTAGACTGAATATGTTGCTATTTCCTGGGTCGATATGGCTAATAACTATCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40586
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 Nonsense 272 1050 8 25
ENSDART00000097325 Nonsense 270 1702 8 43
Genomic Location (Zv9):
Chromosome 5 (position 66668064)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62809622
GRCz11 5 63503013
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCAGGGAATGCCAGTTAAATCAGCGAACATTCTGTTGAAGTTTGGATA[C/A]AGTACTCCAGAAGAAACTGTCATAATACCATCAACATATAGATCATACAT
Long Flanking Sequence:
CACATGTATGTTACTGTTTTACATGACACAAATGCTGACTTTGTAATCCCAAGCCTTTAAACTGAATAGTATGATTATTTTATTCAAAATGTACAATTTCAGCATGTTTATTTCAATACTAAACTGAAATATTAAAATTGCAGGTAACACTTTATTTTGATGGTCCATTTGAGTAATAGCAGACTGTCTTTTTAATATCTGTTGATACAGACATTCAACAGACATTTAACTATAAGACTATAAGACTATAAGAGACTTTGCAAGTACATGTCAACTTGCACTAACCCTTACCTCAATCTAACAGTCTACTTATAATCTAATGAGAATGAGTTGGCATGTAGTTGCAATGTAACTTAAATTCAACAAACATACCATCAAAATTAAGTGTGACTAAATTGCAATTGATGAAAATGACTTATATATACAGTATGTGAATATGCTGACAGGTATGTCCAGGGAATGCCAGTTAAATCAGCGAACATTCTGTTGAAGTTTGGATA[C/A]AGTACTCCAGAAGAAACTGTCATAATACCATCAACATATAGATCATACATGGTAAAGTCAGTATTCTGCTCAAGCAAGATTTAATGTTTGAGTTCAGAGAGTAAACTTTTGTTTTCTTTTTGTCTTAGCTGTATAACGGAAAAATGGAAGTGGACTTGGATATCAGGTCAGCTCTGTCATCCAAGCCTGATGCACCTCAATTCCTGAACGCCATGAAGGAAAACACATTTCTTTATGTGGAAGTTTTGCTGCAGGAGTCCACTGGTAAGGTTTAGTTATTTGTATCAACACAGGATTCAGACATTAGAGTGTCGAGTGAATAAAAGTGATGACCGTAAGCTTACTTTATTTTTTAGGTGGCCTTTCCCAGGAGGCAGTGCTCTCGCATGTGAAATTTGTCGAAACTCCATTTACCCTGAGTATAATTGCAACCCCTCCTTTCATCAAACCGGGTCTACCGTATGCTATGAGAGTAAGAAACCTGCTTTTTTATAAATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17323
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 Nonsense 509 1050 13 25
ENSDART00000097325 Nonsense 507 1702 13 43
Genomic Location (Zv9):
Chromosome 5 (position 66676688)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62800998
GRCz11 5 63494389
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTTCCWCTGGATTACTCTTCTCCCCCCCCCGCCCCCCAGATCATCTCC[A/T]AAGGAAAAGTAGTRAAATACRACACAGTCAAGCGTGTCAGTGAAAAGAGT
Long Flanking Sequence:
GGAAATAAAGCTCAGATTTAATAGATGAGGCCCACAGAACCATCAAGATGTTTACACTCTGTTGAAGTCTGAATATATCACACCTGAGCAATGCATGTGACTTCATTCTTCACATAAGAGGCGTCTTTAAGCTGCCATCACCAAAAAAAAGTATTTTATAAAAAGTCTTAAATACATTTAAAGTAGTTTGCTACTTTCTCCTTGTGTCACTTCATTGTTATTACACACAACTCATTTTTCAGATTTGATTTGTTTAATTTTTATGTTCGTATTCTTTGGGTTTTTCCCAAAATTTGGTTTATTTCCACCTCATCAGCTCCTTTAGAAATATTATTCTTAGAAAAAAACATGACGTGTTCAATATTTACTTTCCCCCACTGTAATATAGAAATACAAACCTTTATTTTGGATGTCATTATTCACTACTTTTAGTTGAAGCTCTAAAATAAAAATTTCCACTGGATTACTCTTCTCCCCCCCCCGCCCCCCAGATCATCTCC[A/T]AAGGAAAAGTAGTAAAATACGACACAGTCAAGCGTGTCAGTGAAAAGAGTCAGAGCCTCAACATTAAGATCACCCCTGACATGGTGCCGTCAGCTCGCCTGCTGGTGTATTACGTCCTGTATGGGGAGGAGAAAGCTGAGCTGGTGGCAGACTCTACATGGATCGATGTCAAGGCTAAATGTGTGAAAAACTTAAATGTAATGTCTTTTTCTCTCTCCCCAAAAATGATGCAGGTTTTATGTTGTTCACACGTTGTGAGATCTTATTCTTCTTTGAATATCTTTCAGCTGGAATTATCAACTCTCAAACTACAGGATGACTACAAACCCAAAGATAAACTGGAAATAAAGGTGTCATCTAGAAGCAAAGGAGAGTCACTGGTGGCTTTTTCTGCAGTCGATACAGCTTTATTCAACCTAAGAACTAACAAAAAGGATCCCCTGAAGAAGGTGAAAAGGCATTCATTCATTCATTCATTCATTTTACTTCGGCTTAGTCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20567
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
ENSDART00000002540 Nonsense 566 1050 13 25
ENSDART00000097325 Nonsense 564 1702 13 43
Genomic Location (Zv9):
Chromosome 5 (position 66676859)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62800827
GRCz11 5 63494218
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGGAGGAGAAAGCTGAGCTGGTGGCAGACTCTACATGGATCGATGTC[A/T]AGGCTAAATGTGTGAAAAACTTAAATGTAATGTCTTTTTCTCTCTCCCCA
Long Flanking Sequence:
ATACATTTAAAGTAGTTTGCTACTTTCTCCTTGTGTCACTTCATTGTTATTACACACAACTCATTTTTCAGATTTGATTTGTTTAATTTTTATGTTCGTATTCTTTGGGTTTTTCCCAAAATTTGGTTTATTTCCACCTCATCAGCTCCTTTAGAAATATTATTCTTAGAAAAAAACATGACGTGTTCAATATTTACTTTCCCCCACTGTAATATAGAAATACAAACCTTTATTTTGGATGTCATTATTCACTACTTTTAGTTGAAGCTCTAAAATAAAAATTTCCACTGGATTACTCTTCTCCCCCCCCCGCCCCCCAGATCATCTCCAAAGGAAAAGTAGTAAAATACGACACAGTCAAGCGTGTCAGTGAAAAGAGTCAGAGCCTCAACATTAAGATCACCCCTGACATGGTGCCGTCAGCTCGCCTGCTGGTGTATTACGTCCTGTATGGGGAGGAGAAAGCTGAGCTGGTGGCAGACTCTACATGGATCGATGTC[A/T]AGGCTAAATGTGTGAAAAACTTAAATGTAATGTCTTTTTCTCTCTCCCCAAAAATGATGCAGGTTTTATGTTGTTCACACGTTGTGAGATCTTATTCTTCTTTGAATATCTTTCAGCTGGAATTATCAACTCTCAAACTACAGGATGACTACAAACCCAAAGATAAACTGGAAATAAAGGTGTCATCTAGAAGCAAAGGAGAGTCACTGGTGGCTTTTTCTGCAGTCGATACAGCTTTATTCAACCTAAGAACTAACAAAAAGGATCCCCTGAAGAAGGTGAAAAGGCATTCATTCATTCATTCATTCATTTTACTTCGGCTTAGTCTCTATTTTAGAGGTCGCCATAGCGCAATAAACCGGCAACTATTCCAGCATATGTTTTTTTAACGCAGCAGATACCCATCCAGCTGTAACCCAGCACTGGGAAACACCCATACACACTCATTCACACACATACACTACGGATAATTACGTTTATTCAGTTCACCTATAGCTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20568
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
ENSDART00000002540 Essential Splice Site 768 1050 18 25
ENSDART00000097325 Essential Splice Site 764 1702 19 43
Genomic Location (Zv9):
Chromosome 5 (position 66683664)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62794022
GRCz11 5 63487413
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGGATCTTCGTAAAGAGAATGCAGAAAATATCATTCTAAGCCGGGCAG[G/A]TATGGATGTTTCTCACATGGCATAATATTGACTTGGATTATTAATGTGTT
Long Flanking Sequence:
TCACTCAAAACTGAAAATTGACTCACCGTGCATTTGATGAACACGAAGATAAATATGAAGAAGATATTCTAAAGAAAACTGGAAACCTGCAATCATTGACTTCCATACTATTTGTTTTTCCTACTATGGAAATCAATGGTAATTAGTTTTCAGAATATCTTCTTCATACATATATCTTGTTTTATGTTTAACAGGGAAAAGAAATTCATAAAGGTTTGGAACCACTTGAGGGTGAGTAAATAGTTAGTAAATGTACATTTTTGAGGGAACTATCTCTGAAATATCATCCATGCGAATAAAATATTTACAATATTTTAACATATAGGCCTGTATCTTTAAGTGATGTATTCCAGCAAACTCATGACAATCTTTCTGTAGCAAGAAAACGAGAAGAGATTACGAGAAGGAAAAATATTGTCGACTTGCCTTCGAGCAGTGCTGTGTATTTGCTAAGGATCTTCGTAAAGAGAATGCAGAAAATATCATTCTAAGCCGGGCAG[G/A]TATGGATGTTTCTCACATGGCATAATATTGACTTGGATTATTAATGTGTTCTTTTAAAAAGAAAGATCAAACATTCTCTTTTATGCAATGCAGCTATCGACTTTCTGATGGATGCGCCGCTGTCTCAGGTTAGGAGCTACTTCCCTGAGAGCTGGTTATGGGAGGAACACCTCAGCAAGTAGGAACACTTTCTGAACCATAATCCATTCTGTCTTTTGCAGTTAATTATAAAATTTTTAAAGGAACACTCCTAAAAAACACTTTTTTTTTTTAAATAGAGACTTTTTTTACTATTTTTTGTTTTATTTTTTGTCCATTCTGCTTATTTCTGTGTCTGGCGGGAGCACTATTAGCTTGGCTTAGCATAAATTATTGAAATGTATTAGACCAGTAGCATCTCGCTTTAAAATTTACAAAAATGCCCGATGTTTTTTTTTTTATATTTAAAGCTTGATTATCATAGTCACATCATGTATTAAGACCAACATAGTTGAGAAGTT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26604
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 Essential Splice Site 825 1050 20 25
ENSDART00000097325 Essential Splice Site 821 1702 21 43
Genomic Location (Zv9):
Chromosome 5 (position 66684680)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62793006
GRCz11 5 63486397
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTCAATCACCACATGGGAACTAAAAGCAGTTGGGGTATTCAATGAAGG[T/A]AAGCTGATGGATCTAAATATTTTGTTTTAGCACCTCCTGGTGGCTGATGT
Long Flanking Sequence:
AGCTTGGAGCTATATTCTCAGCTTAATAATAATAATAATAAAATGCATTAATGTAGGAACATCCAACCTTTCGTTTTCTGTCAGTCTTTGTAAATGACCCAAGAAAAGTCAAGATTTAAACAGAAAAAATTATCTCTTTGGTCATCGCTAAATAGATGCTAATGGTCTAATCCGCTTCTATGCGGATCTATGCTAAGCTAAGCTAAAATAATTTGTTCAAAAGTAGTAAAACTATACTGTTTAACATTACTGGAGTTTACACAACAAGCCTACTTTAGTTCCTTTAAATTTATAATTGAATACTTATAAATGAATCCTGATTAAGGCTACATCTGAGTTAATTGACTCTGTGAAGACTGTCTGTGTTGAATTGTGCTGATAATATTCTGTTTTCTTCTAATTATTGTTTTTTAAAGATCTGGTTCTGTGAGCATTAGTAAAACTCTTCCGGATTCAATCACCACATGGGAACTAAAAGCAGTTGGGGTATTCAATGAAGG[T/A]AAGCTGATGGATCTAAATATTTTGTTTTAGCACCTCCTGGTGGCTGATGTGTGTTTAAAAATGCGTATTCTCTCTTAATGGGGTATATGCCGAAGCATGCTAATAGGACTTTTAATTTGGCAGTAACCTGGGTTAAGCTCTTCCGGCAGGCCCGGCGCTACGGGGGGGCAAAGGGTGGCATTGCCCCCTCAGACAGAGTTTGTGCCCCCCCAGTTTTTATAAAGGATTGTTCACTCAAACTGAAAATTCTTTCTGTCATTAATTATTAACACTCCCGTCCTTCCAACCTTCAGAACACACATTTAAATGTTTTAAAATATATGACATAGCAATTGAATTATGAAAATAGTGATATTAAAGCTAGTCCTATAGTTCAGAGATCCGGTCCCCGCGTCAGGTCAGGTGCGGCCGTAAATAGCCTTTAAAACGCGCACACGGCGATGGAGGCGCACTCAACTCACAAGGGAGAAAATGGGTGACATGATAGGAGCAGCTTAATT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5336
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 Essential Splice Site 870 1050 21 25
ENSDART00000097325 Essential Splice Site 866 1702 22 43
ENSDART00000002540 Essential Splice Site 870 1050 21 25
ENSDART00000097325 Essential Splice Site 866 1702 22 43
Genomic Location (Zv9):
Chromosome 5 (position 66689249)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62788437
GRCz11 5 63481828
KASP Assay ID:
2259-6745.1 (used for ordering genotyping assays)
KASP Sequence:
GATTCTGCTCAAGGGTTCAGTCTACAATCAGCGCTCTTCAGGCATTAAGG[T/G]GAGAGCTTCACTTTTTATTCAGGGGGATATGTTTAAAAAAATTATATATA
Long Flanking Sequence:
AAACTAAATTGGCCTTAGTGTATGTGTATGTGGAAGGGCGTCCGCTTGCTAAAACATATGCTGGATATGTTGGCGGTTTATACCGCTGTGGCGACCCTTGATGAATGAAGAGACTAAGCCGAAGAAAAAATTAATGAATGAATAAATTAAAAGCTATGTAAGATTTCTGATTGAACAGAATACTGCAATGCTAATAAGATGGAAAATGCATGCTATTTAAATGTCATACAGTGTAAAACATAGTATTTTATTATACTTATAAAGATTTCATTATGCACATTTGATTTAAAATGATGCAGCTTTCTTAGTTTGTTTTAGGTTATTTTGGTCAGAATCTCAGACCCACCTGTTTTTTTGGTCAGGGATCTGTGTGTCGGATAAAAGGATTCCGGTGTCCCAGGACATTTGGGTGGACGTCCCGTTGCCTTATTCTATGGTTCGTGGAGAGCAGATTCTGCTCAAGGGTTCAGTCTACAATCAGCGCTCTTCAGGCATTAAGG[T/G]GAGAGCTTCACTTTTTATTCAGGGGGATATGTTTAAAAAAATTATATATAAATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTATAATAACATTAAGAAATTTAATGCATTCAAATAATCTAAGAAGAGGGCTGCAAGCAAGGATGTCACTGGTTTGAGCCTCGGCTGTGTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTCACGTGGATTTCCTCCAGGTGCTCCAGTTTCCCCCACAGTCCAAAGACACTATAGGTAAATTGGGTAGTCTAAATTATCTGTAGTGTATGTGTGTGTGAATGAGTGTGTATGGATTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATCGGCTGTGTAAAACATATGCTTGATAAGTAGGCAGTTCATTCCGCTGTGGTAACCCCAGATTATTAAAGGACTAAGCCGATAAGAAAATTAATG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa18825
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 Essential Splice Site 870 1050 21 25
ENSDART00000097325 Essential Splice Site 866 1702 22 43
ENSDART00000002540 Essential Splice Site 870 1050 21 25
ENSDART00000097325 Essential Splice Site 866 1702 22 43
Genomic Location (Zv9):
Chromosome 5 (position 66689249)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62788437
GRCz11 5 63481828
KASP Assay ID:
2259-6745.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTCTGCTCAAGGGTTCAGTCTACAATCAGCGCTCTTCAGGCATTAAGG[T/G]GAGAGCTTCACTTTTTATTCAGGGGGATATGTTTAAAAAAATTATATATA
Long Flanking Sequence:
AAACTAAATTGGCCTTAGTGTATGTGTATGTGGAAGGGCGTCCGCTTGCTAAAACATATGCTGGATATGTTGGCGGTTTATACCGCTGTGGCGACCCTTGATGAATGAAGAGACTAAGCCGAAGAAAAAATTAATGAATGAATAAATTAAAAGCTATGTAAGATTTCTGATTGAACAGAATACTGCAATGCTAATAAGATGGAAAATGCATGCTATTTAAATGTCATACAGTGTAAAACATAGTATTTTATTATACTTATAAAGATTTCATTATGCACATTTGATTTAAAATGATGCAGCTTTCTTAGTTTGTTTTAGGTTATTTTGGTCAGAATCTCAGACCCACCTGTTTTTTTGGTCAGGGATCTGTGTGTCGGATAAAAGGATTCCGGTGTCCCAGGACATTTGGGTGGACGTCCCGTTGCCTTATTCTATGGTTCGTGGAGAGCAGATTCTGCTCAAGGGTTCAGTCTACAATCAGCGCTCTTCAGGCATTAAGG[T/G]GAGAGCTTCACTTTTTATTCAGGGGGATATGTTTAAAAAAATTATATATAAATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTATAATAACATTAAGAAATTTAATGCATTCAAATAATCTAAGAAGAGGGCTGCAAGCAAGGATGTCACTGGTTTGAGCCTCGGCTGTGTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTCACGTGGATTTCCTCCAGGTGCTCCAGTTTCCCCCACAGTCCAAAGACACTATAGGTAAATTGGGTAGTCTAAATTATCTGTAGTGTATGTGTGTGTGAATGAGTGTGTATGGATTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATCGGCTGTGTAAAACATATGCTTGATAAGTAGGCAGTTCATTCCGCTGTGGTAACCCCAGATTATTAAAGGACTAAGCCGATAAGAAAATTAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33748
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
ENSDART00000002540 None None 1050 None 25
ENSDART00000097325 Nonsense 1284 1702 31 43
Genomic Location (Zv9):
Chromosome 5 (position 66704332)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62773354
GRCz11 5 63466745
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACAGTTTACGTCCTGCTTAACACTTTAACCAGAGGTGAAACCGAATA[T/G]GCAAAACCCATCTTGAACTGGTTGACACAAGATCAGAGATATGGAGGAGG
Long Flanking Sequence:
TAAAAAAAAATAGGTCTCTAAAAACACAGAAAATGTACTGGCAGTTTATTACAAGGTTTTTGTACCATGCTTTTACATCACCAAATCATACAATACATCCATTTAAACTAATAAAATGTCAATAAAAATTACATTTTCGAACTCTTCAGGGTTACAAGTTGTTGGAAGAAAAATCAAGATTGCATAATGCAATTCAAAAGCATAAATAAACCGGGAAAATAAAAAATTAACACATGAATCACGAAAAAACGGAAAACTGCAAATTTATGGATATGTTTTTACAGTATACTTCTGACCAAAACTCTTGGAAATTTTAGCACCCTTTCATATTTAATACACACCATTTTGTCCTTGTTTACAGGAAACCCACCAAGAGTCTGTTTCTGGCAAGAATCTGATACCAACATTGATCCATTAAAACCCAGCAGTGTGACAGCAAAGTCTGTGGAAACAACAGTTTACGTCCTGCTTAACACTTTAACCAGAGGTGAAACCGAATA[T/G]GCAAAACCCATCTTGAACTGGTTGACACAAGATCAGAGATATGGAGGAGGCGTCTATTCAACACAGGTATGTGTTCTTTTTTTTGTGAAGTTTACTTATTTACTAGTTTCGAGAAGATCACGTGATTATGATTGACCACAGCTGACCCCGCATTACCTAACACTTGATTCACCAATCAGATGAATCCTGTCGCACTATAAATAACCAAAGATTTTTTACTTTAAGTTATCTTCGTCTTGAAGAATTCCCCCTTTCAACACCTACTCCTACTCCCTTTCCTACATAGGGCAGCTCGGCAGCCAAGTGGTTAGCACAGTTGCCTCACAGCAAGAATGTCACCGGAGCAGTTTATATGTTTCCCGTGCTTGCCTGGGTTTCCTTCCACTGTCCAAAGACATGCAACACAAGTAAATTGACTAAATCAAATTGGCACTAAAGATGAGTTCCTAGTCAGTATTTTTTCTTTCCATAAGCAATCCCCATCTGTCGCAAATTAGGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33749
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 None None 1050 None 25
ENSDART00000097325 Nonsense 1291 1702 31 43
Genomic Location (Zv9):
Chromosome 5 (position 66704353)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62773333
GRCz11 5 63466724
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACACTTTAACCAGAGGTGAAACCGAATATGCAAAACCCATCTTGAACTG[G/A]TTGACACAAGATCAGAGATATGGAGGAGGCGTCTATTCAACACAGGTATG
Long Flanking Sequence:
AAACACAGAAAATGTACTGGCAGTTTATTACAAGGTTTTTGTACCATGCTTTTACATCACCAAATCATACAATACATCCATTTAAACTAATAAAATGTCAATAAAAATTACATTTTCGAACTCTTCAGGGTTACAAGTTGTTGGAAGAAAAATCAAGATTGCATAATGCAATTCAAAAGCATAAATAAACCGGGAAAATAAAAAATTAACACATGAATCACGAAAAAACGGAAAACTGCAAATTTATGGATATGTTTTTACAGTATACTTCTGACCAAAACTCTTGGAAATTTTAGCACCCTTTCATATTTAATACACACCATTTTGTCCTTGTTTACAGGAAACCCACCAAGAGTCTGTTTCTGGCAAGAATCTGATACCAACATTGATCCATTAAAACCCAGCAGTGTGACAGCAAAGTCTGTGGAAACAACAGTTTACGTCCTGCTTAACACTTTAACCAGAGGTGAAACCGAATATGCAAAACCCATCTTGAACTG[G/A]TTGACACAAGATCAGAGATATGGAGGAGGCGTCTATTCAACACAGGTATGTGTTCTTTTTTTTGTGAAGTTTACTTATTTACTAGTTTCGAGAAGATCACGTGATTATGATTGACCACAGCTGACCCCGCATTACCTAACACTTGATTCACCAATCAGATGAATCCTGTCGCACTATAAATAACCAAAGATTTTTTACTTTAAGTTATCTTCGTCTTGAAGAATTCCCCCTTTCAACACCTACTCCTACTCCCTTTCCTACATAGGGCAGCTCGGCAGCCAAGTGGTTAGCACAGTTGCCTCACAGCAAGAATGTCACCGGAGCAGTTTATATGTTTCCCGTGCTTGCCTGGGTTTCCTTCCACTGTCCAAAGACATGCAACACAAGTAAATTGACTAAATCAAATTGGCACTAAAGATGAGTTCCTAGTCAGTATTTTTTCTTTCCATAAGCAATCCCCATCTGTCGCAAATTAGGGAAGTTCTCGAGACCTACCTGAG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26605
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
ENSDART00000002540 None None 1050 None 25
ENSDART00000097325 Essential Splice Site 1412 1702 34 43
Genomic Location (Zv9):
Chromosome 5 (position 66708149)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62769537
GRCz11 5 63462928
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTTGACACAACCATTGACATTCATGACAGTGACCAAAACTCAGACGG[T/C]AGGTTCTGTGCTTTTGTCTACTTGTTCATACAGCACCCTTAATCTTCCTT
Long Flanking Sequence:
GTTTGTTGCGTGTAATGAGAGGAATCGGTAAAGTGAGGCAAATTAAGCCCTGGTGCCATGTTCGACAAGTCGCACTATTATGTCTTTCTTTTCTTTTTTATTCTTTTCTAACCTGTTTTAACACATTTTAATGTGTTTTTAATCACTTTTTATTATTTGTTTTTATTTTTTTATACTTGTTTCTTTTATTCCTATTTAAATAAACATGCCTTGCCTTACCTTGCCTTGTTTGGATGTTTACCAGTACTGGGCTGCGGCTGGAAGGGCATCCACTATGTACAACCTATGCTGGAATAGCTGGTGGTTCATTCTGCTGTGGCGACCTCTGAAATATAGACTAAGCCTGATTTTTCAAAGTTCTATGTATACGACCATGTTTAATTTTTAATTACCCTTTTTTGACAGCTGAAAACTGTGTATTATGTGATGACGGAAAGCAATAAAAGTTGCCTTTTTGACACAACCATTGACATTCATGACAGTGACCAAAACTCAGACGG[T/C]AGGTTCTGTGCTTTTGTCTACTTGTTCATACAGCACCCTTAATCTTCCTTCACATTGACTCAGTTCAGTTATAATCTGATTTCTTTGTAAGCAGATCCCATGCTTTTGAGTCAGCGGATTGTGGCCTGTGCAAAGTAAGTCTGTAAATTCTCCTGAATAGTCTCTGAAAAACTCATGTTATAAAATGCACTAAAATGAAAATCTAATTATGTGTAAAGATTCAAACCACCAGAGAATTCACTGGAAACTGAGTCAGCACTTACTGTGATGGAAATTAATCTGCCAACTGGAGTGACTCCAGTCCTGGAAGATCTAGATGAGGTGAAAGCCCAAATGCAGTTCATTTTCATTGAGTAAAATTCATTCTTTCAGAAAGCTAATCTTTTTATACTTCCTTTTTTTTTAGTACCAGAATGGACTTGAGTCTCGGATTTCCAACTATGAAGTTATAGGTGACAAAGTAGTGCTTCAGATAGATTCGGTGAGCATCACTCTGAATA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa26606
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 None None 1050 None 25
ENSDART00000097325 Nonsense 1540 1702 39 43
Genomic Location (Zv9):
Chromosome 5 (position 66708970)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62768716
GRCz11 5 63462107
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGCACAAAGTTGTACCAGAAACAAACCCGCAAGCTGTTACGACTCTGT[G/T]AGGAAGACCATTGTCAGTGCATGGCAGGTAAGCCATATTATAAAATATAT
Long Flanking Sequence:
GGTGAAAGCCCAAATGCAGTTCATTTTCATTGAGTAAAATTCATTCTTTCAGAAAGCTAATCTTTTTATACTTCCTTTTTTTTTAGTACCAGAATGGACTTGAGTCTCGGATTTCCAACTATGAAGTTATAGGTGACAAAGTAGTGCTTCAGATAGATTCGGTGAGCATCACTCTGAATATAATCAAGACGATTTGATCTTGTAAAACATTTTTTAAGATACATTGTTTACATGCAGATACCATCAGATAACTTCTACTGCGTGGGCTTCCGTATCCTAGAGGAATTTGAAACTGGCATGACCAAAGCCTCAGAGTTTACTGTATATGAATATCAAGCTCCAGGTAGAGTCTTTTAAAGAAATATTTAAATCATATCAGGCCAATTTTACCCACATAAAACAAGAAAACATACCAAAAAAAACATTTTTATCTTAATTTTTTAGCATTTAAGTGCACAAAGTTGTACCAGAAACAAACCCGCAAGCTGTTACGACTCTGT[G/T]AGGAAGACCATTGTCAGTGCATGGCAGGTAAGCCATATTATAAAATATATTTACCTACTGTACAAAATACTACATTTTGTTTCTTGTCATTTCTGTCATTCCTGTCCTGCTGTTATGCCATTTATTTTGGTTCTGCCTATAAATTTAGCATTCACATACTGAGTTTAAATAAATAGTTCACCCAAAAATGAAAATTTACTCACCATTTGCTCTCCCGCATGTGGTTCCATACATGTTGAACACATATTTGGAAAAATGTTAGACACTGCGTTGACTTCCATAGTAGGAAAATCAAATTGTCAATGGTTACAGGCATCCAGCATTTTTCCAAATATATTCTATTGTGTTCAACAGAAGAAGAAACAAGGGTGAGAAAATGATGACAGAATTTTAATTTTCAAGTGAAATATCCCTTTAAAGCAGGGGTCACCAATCCTGGTCCTGGAGGGCCGGTGTCCCTCCAGGGTTTAGCTCCAACTTGCCTTTACACACCTGCCTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31483
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002540 None None 1050 None 25
ENSDART00000097325 Nonsense 1696 1702 43 43
Genomic Location (Zv9):
Chromosome 5 (position 66712780)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 62764906
GRCz11 5 63458297
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACTGCAAACAATATGTCAAAGTTTTGGAAGGATTTGAATTTGAATACT[T/G]ATTAAATGGCTGTGATTTGATGTCATCTCGATAGGACTGGTACTTCATGT
Long Flanking Sequence:
TAAAGTGGCCGGTGAGTGTACATAGTAATTAATTGCATATTATGGTACATTTACCATATTTCCATATGCTATCTTTATTTAGAACAAGTAAGTTATGAAAAGCAAAGCAAAATCCATTGAGGAAACATTGCTGCTTTTTTGGTTATGCACAAATTAAAACTAGAACTAAACAAGCATTAAACACTAAAAAAATCTATAAAGAGCACTATTAGAGATAAACATGGTCATCAAATAGGATAAACGATAAAACAGATGAAATGGGAGTTTGACCTTAATCTGTTGTATTATAACTTGCATTACACTGTATAAACTCAGTATTTCACAAGATTTATTACACTACTATGTACGATGTAGCATGATTTTCTCTAAACCATGTTGCAGGTACAAGTTCCCTTTGGACTCTGAAGCTTGGGTGGACTGGTGGCCGCTTGAATCTGACTGCAGCGATGCTAACTGCAAACAATATGTCAAAGTTTTGGAAGGATTTGAATTTGAATACT[T/G]ATTAAATGGCTGTGATTTGATGTCATCTCGATAGGACTGGTACTTCATGTGTACGTTTTTATTCTTTGAAAAACAAATTCAAAATAAGAATAAAACGAAGCATTTAAATCAGTTCAACTCTTTGTAGAATCATCATTTAACAAACACCAAACATATTTAACAAAAAGTATTAGTTTTCATGTACAATTTAAAGAGAGAGTTTATTCAGAAATAAAAATGACCCACCCTTATCTTGTTCTAAATCTCTTTGACTTTCTTTCTCATGTTGAACACAGAAGAAGATATTTAGAAAAATGTTTATAACTGGAACCCATTGACTTCTATTTGTATCATTTTTTCCCCTACTATGGAAGTCAGTGGGTGCCAGCAACTAGTATTCTTCAAAATATTTTCTTTTGTATTTAACAGAATAAAGAAACAAACTCATAATGGTTTAAAATCACATGAGGTAGAATAAATGATGAGGTAATTTTCATATTTTTGGGTAACTATTCTTTTCC
Associated Phenotype:
Not determined